Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2
Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In child...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Bonne, Nicolas-Xavier [verfasserIn] |
|---|
| Format: |
E-Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
2014transfer abstract |
|---|
| Schlagwörter: |
|---|
| Umfang: |
5 |
|---|
| Übergeordnetes Werk: |
Enthalten in: The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics - 2011, Amsterdam [u.a.] |
|---|---|
| Übergeordnetes Werk: |
volume:9 ; year:2014 ; number:1 ; pages:22-26 ; extent:5 |
| Links: |
|---|
| DOI / URN: |
10.1016/j.pedex.2013.12.004 |
|---|
| Katalog-ID: |
ELV033838097 |
|---|
| LEADER | 01000caa a22002652 4500 | ||
|---|---|---|---|
| 001 | ELV033838097 | ||
| 003 | DE-627 | ||
| 005 | 20230625195150.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 180603s2014 xx |||||o 00| ||eng c | ||
| 024 | 7 | |a 10.1016/j.pedex.2013.12.004 |2 doi | |
| 028 | 5 | 2 | |a GBVA2014009000013.pica |
| 035 | |a (DE-627)ELV033838097 | ||
| 035 | |a (ELSEVIER)S1871-4048(13)00059-2 | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 082 | 0 | |a 610 | |
| 082 | 0 | 4 | |a 610 |q DE-600 |
| 082 | 0 | 4 | |a 510 |q VZ |
| 082 | 0 | 4 | |a 540 |q VZ |
| 084 | |a 58.30 |2 bkl | ||
| 100 | 1 | |a Bonne, Nicolas-Xavier |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2 |
| 264 | 1 | |c 2014transfer abstract | |
| 300 | |a 5 | ||
| 336 | |a nicht spezifiziert |b zzz |2 rdacontent | ||
| 337 | |a nicht spezifiziert |b z |2 rdamedia | ||
| 338 | |a nicht spezifiziert |b zu |2 rdacarrier | ||
| 520 | |a Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. | ||
| 520 | |a Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. | ||
| 650 | 7 | |a ERM |2 Elsevier | |
| 650 | 7 | |a PSC |2 Elsevier | |
| 650 | 7 | |a SDS |2 Elsevier | |
| 650 | 7 | |a LOH |2 Elsevier | |
| 650 | 7 | |a SRT |2 Elsevier | |
| 650 | 7 | |a CPERH |2 Elsevier | |
| 650 | 7 | |a NF2 |2 Elsevier | |
| 650 | 7 | |a PTA |2 Elsevier | |
| 650 | 7 | |a VS |2 Elsevier | |
| 700 | 1 | |a Baroncini, Marc |4 oth | |
| 700 | 1 | |a Aboukais, Rabih |4 oth | |
| 700 | 1 | |a Lorenz, Mark Brandt |4 oth | |
| 700 | 1 | |a Broly, Franck |4 oth | |
| 700 | 1 | |a Dubrulle, Frédérique |4 oth | |
| 700 | 1 | |a Lejeune, Jean-Paul |4 oth | |
| 700 | 1 | |a Vincent, Christophe |4 oth | |
| 773 | 0 | 8 | |i Enthalten in |n Elsevier Science |t The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics |d 2011 |g Amsterdam [u.a.] |w (DE-627)ELV020823398 |
| 773 | 1 | 8 | |g volume:9 |g year:2014 |g number:1 |g pages:22-26 |g extent:5 |
| 856 | 4 | 0 | |u https://doi.org/10.1016/j.pedex.2013.12.004 |3 Volltext |
| 912 | |a GBV_USEFLAG_U | ||
| 912 | |a GBV_ELV | ||
| 912 | |a SYSFLAG_U | ||
| 912 | |a SSG-OLC-PHA | ||
| 936 | b | k | |a 58.30 |j Biotechnologie |q VZ |
| 951 | |a AR | ||
| 952 | |d 9 |j 2014 |e 1 |h 22-26 |g 5 | ||
| 953 | |2 045F |a 610 | ||
| author_variant |
n x b nxb |
|---|---|
| matchkey_str |
bonnenicolasxavierbaroncinimarcaboukaisr:2014----:otrocruainshmctoenhlhoade |
| hierarchy_sort_str |
2014transfer abstract |
| bklnumber |
58.30 |
| publishDate |
2014 |
| allfields |
10.1016/j.pedex.2013.12.004 doi GBVA2014009000013.pica (DE-627)ELV033838097 (ELSEVIER)S1871-4048(13)00059-2 DE-627 ger DE-627 rakwb eng 610 610 DE-600 510 VZ 540 VZ 58.30 bkl Bonne, Nicolas-Xavier verfasserin aut Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2 2014transfer abstract 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. ERM Elsevier PSC Elsevier SDS Elsevier LOH Elsevier SRT Elsevier CPERH Elsevier NF2 Elsevier PTA Elsevier VS Elsevier Baroncini, Marc oth Aboukais, Rabih oth Lorenz, Mark Brandt oth Broly, Franck oth Dubrulle, Frédérique oth Lejeune, Jean-Paul oth Vincent, Christophe oth Enthalten in Elsevier Science The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics 2011 Amsterdam [u.a.] (DE-627)ELV020823398 volume:9 year:2014 number:1 pages:22-26 extent:5 https://doi.org/10.1016/j.pedex.2013.12.004 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 58.30 Biotechnologie VZ AR 9 2014 1 22-26 5 045F 610 |
| spelling |
10.1016/j.pedex.2013.12.004 doi GBVA2014009000013.pica (DE-627)ELV033838097 (ELSEVIER)S1871-4048(13)00059-2 DE-627 ger DE-627 rakwb eng 610 610 DE-600 510 VZ 540 VZ 58.30 bkl Bonne, Nicolas-Xavier verfasserin aut Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2 2014transfer abstract 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. ERM Elsevier PSC Elsevier SDS Elsevier LOH Elsevier SRT Elsevier CPERH Elsevier NF2 Elsevier PTA Elsevier VS Elsevier Baroncini, Marc oth Aboukais, Rabih oth Lorenz, Mark Brandt oth Broly, Franck oth Dubrulle, Frédérique oth Lejeune, Jean-Paul oth Vincent, Christophe oth Enthalten in Elsevier Science The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics 2011 Amsterdam [u.a.] (DE-627)ELV020823398 volume:9 year:2014 number:1 pages:22-26 extent:5 https://doi.org/10.1016/j.pedex.2013.12.004 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 58.30 Biotechnologie VZ AR 9 2014 1 22-26 5 045F 610 |
| allfields_unstemmed |
10.1016/j.pedex.2013.12.004 doi GBVA2014009000013.pica (DE-627)ELV033838097 (ELSEVIER)S1871-4048(13)00059-2 DE-627 ger DE-627 rakwb eng 610 610 DE-600 510 VZ 540 VZ 58.30 bkl Bonne, Nicolas-Xavier verfasserin aut Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2 2014transfer abstract 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. ERM Elsevier PSC Elsevier SDS Elsevier LOH Elsevier SRT Elsevier CPERH Elsevier NF2 Elsevier PTA Elsevier VS Elsevier Baroncini, Marc oth Aboukais, Rabih oth Lorenz, Mark Brandt oth Broly, Franck oth Dubrulle, Frédérique oth Lejeune, Jean-Paul oth Vincent, Christophe oth Enthalten in Elsevier Science The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics 2011 Amsterdam [u.a.] (DE-627)ELV020823398 volume:9 year:2014 number:1 pages:22-26 extent:5 https://doi.org/10.1016/j.pedex.2013.12.004 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 58.30 Biotechnologie VZ AR 9 2014 1 22-26 5 045F 610 |
| allfieldsGer |
10.1016/j.pedex.2013.12.004 doi GBVA2014009000013.pica (DE-627)ELV033838097 (ELSEVIER)S1871-4048(13)00059-2 DE-627 ger DE-627 rakwb eng 610 610 DE-600 510 VZ 540 VZ 58.30 bkl Bonne, Nicolas-Xavier verfasserin aut Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2 2014transfer abstract 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. ERM Elsevier PSC Elsevier SDS Elsevier LOH Elsevier SRT Elsevier CPERH Elsevier NF2 Elsevier PTA Elsevier VS Elsevier Baroncini, Marc oth Aboukais, Rabih oth Lorenz, Mark Brandt oth Broly, Franck oth Dubrulle, Frédérique oth Lejeune, Jean-Paul oth Vincent, Christophe oth Enthalten in Elsevier Science The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics 2011 Amsterdam [u.a.] (DE-627)ELV020823398 volume:9 year:2014 number:1 pages:22-26 extent:5 https://doi.org/10.1016/j.pedex.2013.12.004 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 58.30 Biotechnologie VZ AR 9 2014 1 22-26 5 045F 610 |
| allfieldsSound |
10.1016/j.pedex.2013.12.004 doi GBVA2014009000013.pica (DE-627)ELV033838097 (ELSEVIER)S1871-4048(13)00059-2 DE-627 ger DE-627 rakwb eng 610 610 DE-600 510 VZ 540 VZ 58.30 bkl Bonne, Nicolas-Xavier verfasserin aut Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2 2014transfer abstract 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. ERM Elsevier PSC Elsevier SDS Elsevier LOH Elsevier SRT Elsevier CPERH Elsevier NF2 Elsevier PTA Elsevier VS Elsevier Baroncini, Marc oth Aboukais, Rabih oth Lorenz, Mark Brandt oth Broly, Franck oth Dubrulle, Frédérique oth Lejeune, Jean-Paul oth Vincent, Christophe oth Enthalten in Elsevier Science The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics 2011 Amsterdam [u.a.] (DE-627)ELV020823398 volume:9 year:2014 number:1 pages:22-26 extent:5 https://doi.org/10.1016/j.pedex.2013.12.004 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 58.30 Biotechnologie VZ AR 9 2014 1 22-26 5 045F 610 |
| language |
English |
| source |
Enthalten in The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics Amsterdam [u.a.] volume:9 year:2014 number:1 pages:22-26 extent:5 |
| sourceStr |
Enthalten in The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics Amsterdam [u.a.] volume:9 year:2014 number:1 pages:22-26 extent:5 |
| format_phy_str_mv |
Article |
| bklname |
Biotechnologie |
| institution |
findex.gbv.de |
| topic_facet |
ERM PSC SDS LOH SRT CPERH NF2 PTA VS |
| dewey-raw |
610 |
| isfreeaccess_bool |
false |
| container_title |
The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics |
| authorswithroles_txt_mv |
Bonne, Nicolas-Xavier @@aut@@ Baroncini, Marc @@oth@@ Aboukais, Rabih @@oth@@ Lorenz, Mark Brandt @@oth@@ Broly, Franck @@oth@@ Dubrulle, Frédérique @@oth@@ Lejeune, Jean-Paul @@oth@@ Vincent, Christophe @@oth@@ |
| publishDateDaySort_date |
2014-01-01T00:00:00Z |
| hierarchy_top_id |
ELV020823398 |
| dewey-sort |
3610 |
| id |
ELV033838097 |
| language_de |
englisch |
| fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV033838097</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230625195150.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">180603s2014 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.pedex.2013.12.004</subfield><subfield code="2">doi</subfield></datafield><datafield tag="028" ind1="5" ind2="2"><subfield code="a">GBVA2014009000013.pica</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV033838097</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S1871-4048(13)00059-2</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">610</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">610</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">510</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">540</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">58.30</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Bonne, Nicolas-Xavier</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2014transfer abstract</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">5</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">ERM</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">PSC</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">SDS</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">LOH</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">SRT</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">CPERH</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">NF2</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">PTA</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">VS</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Baroncini, Marc</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Aboukais, Rabih</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Lorenz, Mark Brandt</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Broly, Franck</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Dubrulle, Frédérique</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Lejeune, Jean-Paul</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Vincent, Christophe</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="n">Elsevier Science</subfield><subfield code="t">The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics</subfield><subfield code="d">2011</subfield><subfield code="g">Amsterdam [u.a.]</subfield><subfield code="w">(DE-627)ELV020823398</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:9</subfield><subfield code="g">year:2014</subfield><subfield code="g">number:1</subfield><subfield code="g">pages:22-26</subfield><subfield code="g">extent:5</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1016/j.pedex.2013.12.004</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="936" ind1="b" ind2="k"><subfield code="a">58.30</subfield><subfield code="j">Biotechnologie</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">9</subfield><subfield code="j">2014</subfield><subfield code="e">1</subfield><subfield code="h">22-26</subfield><subfield code="g">5</subfield></datafield><datafield tag="953" ind1=" " ind2=" "><subfield code="2">045F</subfield><subfield code="a">610</subfield></datafield></record></collection>
|
| author |
Bonne, Nicolas-Xavier |
| spellingShingle |
Bonne, Nicolas-Xavier ddc 610 ddc 510 ddc 540 bkl 58.30 Elsevier ERM Elsevier PSC Elsevier SDS Elsevier LOH Elsevier SRT Elsevier CPERH Elsevier NF2 Elsevier PTA Elsevier VS Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2 |
| authorStr |
Bonne, Nicolas-Xavier |
| ppnlink_with_tag_str_mv |
@@773@@(DE-627)ELV020823398 |
| format |
electronic Article |
| dewey-ones |
610 - Medicine & health 510 - Mathematics 540 - Chemistry & allied sciences |
| delete_txt_mv |
keep |
| author_role |
aut |
| collection |
elsevier |
| remote_str |
true |
| illustrated |
Not Illustrated |
| topic_title |
610 610 DE-600 510 VZ 540 VZ 58.30 bkl Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2 ERM Elsevier PSC Elsevier SDS Elsevier LOH Elsevier SRT Elsevier CPERH Elsevier NF2 Elsevier PTA Elsevier VS Elsevier |
| topic |
ddc 610 ddc 510 ddc 540 bkl 58.30 Elsevier ERM Elsevier PSC Elsevier SDS Elsevier LOH Elsevier SRT Elsevier CPERH Elsevier NF2 Elsevier PTA Elsevier VS |
| topic_unstemmed |
ddc 610 ddc 510 ddc 540 bkl 58.30 Elsevier ERM Elsevier PSC Elsevier SDS Elsevier LOH Elsevier SRT Elsevier CPERH Elsevier NF2 Elsevier PTA Elsevier VS |
| topic_browse |
ddc 610 ddc 510 ddc 540 bkl 58.30 Elsevier ERM Elsevier PSC Elsevier SDS Elsevier LOH Elsevier SRT Elsevier CPERH Elsevier NF2 Elsevier PTA Elsevier VS |
| format_facet |
Elektronische Aufsätze Aufsätze Elektronische Ressource |
| format_main_str_mv |
Text Zeitschrift/Artikel |
| carriertype_str_mv |
zu |
| author2_variant |
m b mb r a ra m b l mb mbl f b fb f d fd j p l jpl c v cv |
| hierarchy_parent_title |
The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics |
| hierarchy_parent_id |
ELV020823398 |
| dewey-tens |
610 - Medicine & health 510 - Mathematics 540 - Chemistry |
| hierarchy_top_title |
The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics |
| isfreeaccess_txt |
false |
| familylinks_str_mv |
(DE-627)ELV020823398 |
| title |
Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2 |
| ctrlnum |
(DE-627)ELV033838097 (ELSEVIER)S1871-4048(13)00059-2 |
| title_full |
Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2 |
| author_sort |
Bonne, Nicolas-Xavier |
| journal |
The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics |
| journalStr |
The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics |
| lang_code |
eng |
| isOA_bool |
false |
| dewey-hundreds |
600 - Technology 500 - Science |
| recordtype |
marc |
| publishDateSort |
2014 |
| contenttype_str_mv |
zzz |
| container_start_page |
22 |
| author_browse |
Bonne, Nicolas-Xavier |
| container_volume |
9 |
| physical |
5 |
| class |
610 610 DE-600 510 VZ 540 VZ 58.30 bkl |
| format_se |
Elektronische Aufsätze |
| author-letter |
Bonne, Nicolas-Xavier |
| doi_str_mv |
10.1016/j.pedex.2013.12.004 |
| dewey-full |
610 510 540 |
| title_sort |
posterior circulation ischemic stroke in childhood and neurofibromatosis type 2 |
| title_auth |
Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2 |
| abstract |
Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. |
| abstractGer |
Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. |
| abstract_unstemmed |
Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2. |
| collection_details |
GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA |
| container_issue |
1 |
| title_short |
Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2 |
| url |
https://doi.org/10.1016/j.pedex.2013.12.004 |
| remote_bool |
true |
| author2 |
Baroncini, Marc Aboukais, Rabih Lorenz, Mark Brandt Broly, Franck Dubrulle, Frédérique Lejeune, Jean-Paul Vincent, Christophe |
| author2Str |
Baroncini, Marc Aboukais, Rabih Lorenz, Mark Brandt Broly, Franck Dubrulle, Frédérique Lejeune, Jean-Paul Vincent, Christophe |
| ppnlink |
ELV020823398 |
| mediatype_str_mv |
z |
| isOA_txt |
false |
| hochschulschrift_bool |
false |
| author2_role |
oth oth oth oth oth oth oth |
| doi_str |
10.1016/j.pedex.2013.12.004 |
| up_date |
2024-07-06T19:36:09.651Z |
| _version_ |
1803859598666366976 |
| fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV033838097</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230625195150.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">180603s2014 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.pedex.2013.12.004</subfield><subfield code="2">doi</subfield></datafield><datafield tag="028" ind1="5" ind2="2"><subfield code="a">GBVA2014009000013.pica</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV033838097</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S1871-4048(13)00059-2</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">610</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">610</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">510</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">540</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">58.30</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Bonne, Nicolas-Xavier</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Posterior circulation ischemic stroke in childhood and neurofibromatosis type 2</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2014transfer abstract</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">5</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Neurofibromatosis 2 (NF2) is a genetically inherited tumor predisposition syndrome. It predisposes to the development of multiple tumors of the central nervous system including schwannomas, meningiomas and ependymomas. Bilateral vestibular schwannomas (VS) are pathognomonic for the disease. In childhood, non-auditory symptoms often mark the onset of the NF2, such as facial palsy, peripheral neuropathy, and neurosurgical emergencies. In this article, we describe the case of a 6-year-old child presenting with an ischemic brain-stem stroke, who was later diagnosed with NF2. We report the clinical and genetic findings and review the previous literature on vasculopathy reported in association with NF2, with a focus on the symptoms presenting at disease onset. For our case patient, an unpublished germline mutation resulting in frameshift (c.876_877insT) was identified on blood screening. We report our full multidisciplinary assessment with vascular angiography, volumetric MRI and audiometry. Vasculopathy is not currently included in the criteria traditionally used for diagnosis of NF2. We suggest that vascular stroke in childhood may be considered a presenting symptom for NF2.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">ERM</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">PSC</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">SDS</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">LOH</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">SRT</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">CPERH</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">NF2</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">PTA</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">VS</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Baroncini, Marc</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Aboukais, Rabih</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Lorenz, Mark Brandt</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Broly, Franck</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Dubrulle, Frédérique</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Lejeune, Jean-Paul</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Vincent, Christophe</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="n">Elsevier Science</subfield><subfield code="t">The inviscid and non-resistive limit in the cauchy problem for 3-D nonhomogeneous incompressible magneto-hydrodynamics</subfield><subfield code="d">2011</subfield><subfield code="g">Amsterdam [u.a.]</subfield><subfield code="w">(DE-627)ELV020823398</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:9</subfield><subfield code="g">year:2014</subfield><subfield code="g">number:1</subfield><subfield code="g">pages:22-26</subfield><subfield code="g">extent:5</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1016/j.pedex.2013.12.004</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="936" ind1="b" ind2="k"><subfield code="a">58.30</subfield><subfield code="j">Biotechnologie</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">9</subfield><subfield code="j">2014</subfield><subfield code="e">1</subfield><subfield code="h">22-26</subfield><subfield code="g">5</subfield></datafield><datafield tag="953" ind1=" " ind2=" "><subfield code="2">045F</subfield><subfield code="a">610</subfield></datafield></record></collection>
|
| score |
7.399884 |