A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis
Absent T-cell immunity resulting in life-threatening infections provides a clear rationale for hematopoetic stem cell transplantation (HSCT) in patients with severe combined immunodeficiency (SCID). Combined immunodeficiencies (CIDs) and “atypical” SCID show reduced, not absent T-cell immunity. If a...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Speckmann, Carsten [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2017 |
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| Schlagwörter: |
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| Umfang: |
11803 |
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| Übergeordnetes Werk: |
Enthalten in: Antidiabetic treatment in elderly patients with low performance status admitted to internal medicine ward - Papakitsou, I. ELSEVIER, 2022, official publication of the American Academy of Allergy, Asthma and Immunology, Amsterdam [u.a.] |
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| Übergeordnetes Werk: |
volume:139 ; year:2017 ; number:4 ; pages:1302-13104 ; extent:11803 |
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| DOI / URN: |
10.1016/j.jaci.2016.07.040 |
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| 520 | |a Absent T-cell immunity resulting in life-threatening infections provides a clear rationale for hematopoetic stem cell transplantation (HSCT) in patients with severe combined immunodeficiency (SCID). Combined immunodeficiencies (CIDs) and “atypical” SCID show reduced, not absent T-cell immunity. If associated with infections or autoimmunity, they represent profound combined immunodeficiency (P-CID), for which outcome data are insufficient for unambiguous early transplant decisions. | ||
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10.1016/j.jaci.2016.07.040 doi GBVA2017001000003.pica (DE-627)ELV014717816 (ELSEVIER)S0091-6749(16)30965-4 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 44.85 bkl Speckmann, Carsten verfasserin aut A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis 2017 11803 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Absent T-cell immunity resulting in life-threatening infections provides a clear rationale for hematopoetic stem cell transplantation (HSCT) in patients with severe combined immunodeficiency (SCID). Combined immunodeficiencies (CIDs) and “atypical” SCID show reduced, not absent T-cell immunity. If associated with infections or autoimmunity, they represent profound combined immunodeficiency (P-CID), for which outcome data are insufficient for unambiguous early transplant decisions. hematopoietic stem cell transplantation Elsevier T-cell deficiency Elsevier natural history Elsevier combined immunodeficiency Elsevier Doerken, Sam oth Aiuti, Alessandro oth Albert, Michael H. oth Al-Herz, Waleed oth Allende, Luis M. oth Scarselli, Alessia oth Avcin, Tadej oth Perez-Becker, Ruy oth Cancrini, Caterina oth Cant, Andrew oth Di Cesare, Silvia oth Finocchi, Andrea oth Fischer, Alain oth Gaspar, H. Bobby oth Ghosh, Sujal oth Gennery, Andrew oth Gilmour, Kimberly oth González-Granado, Luis I. oth Martinez-Gallo, Monica oth Hambleton, Sophie oth Hauck, Fabian oth Hoenig, Manfred oth Moshous, Despina oth Neven, Benedicte oth Niehues, Tim oth Notarangelo, Luigi oth Picard, Capucine oth Rieber, Nikolaus oth Schulz, Ansgar oth Schwarz, Klaus oth Seidel, Markus G. oth Soler-Palacin, Pere oth Stepensky, Polina oth Strahm, Brigitte oth Vraetz, Thomas oth Warnatz, Klaus oth Winterhalter, Christine oth Worth, Austen oth Fuchs, Sebastian oth Uhlmann, Annette oth Ehl, Stephan oth Enthalten in Elsevier Papakitsou, I. ELSEVIER Antidiabetic treatment in elderly patients with low performance status admitted to internal medicine ward 2022 official publication of the American Academy of Allergy, Asthma and Immunology Amsterdam [u.a.] (DE-627)ELV000021164 volume:139 year:2017 number:4 pages:1302-13104 extent:11803 https://doi.org/10.1016/j.jaci.2016.07.040 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.85 Kardiologie Angiologie VZ AR 139 2017 4 1302-13104 11803 045F 610 |
| spelling |
10.1016/j.jaci.2016.07.040 doi GBVA2017001000003.pica (DE-627)ELV014717816 (ELSEVIER)S0091-6749(16)30965-4 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 44.85 bkl Speckmann, Carsten verfasserin aut A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis 2017 11803 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Absent T-cell immunity resulting in life-threatening infections provides a clear rationale for hematopoetic stem cell transplantation (HSCT) in patients with severe combined immunodeficiency (SCID). Combined immunodeficiencies (CIDs) and “atypical” SCID show reduced, not absent T-cell immunity. If associated with infections or autoimmunity, they represent profound combined immunodeficiency (P-CID), for which outcome data are insufficient for unambiguous early transplant decisions. hematopoietic stem cell transplantation Elsevier T-cell deficiency Elsevier natural history Elsevier combined immunodeficiency Elsevier Doerken, Sam oth Aiuti, Alessandro oth Albert, Michael H. oth Al-Herz, Waleed oth Allende, Luis M. oth Scarselli, Alessia oth Avcin, Tadej oth Perez-Becker, Ruy oth Cancrini, Caterina oth Cant, Andrew oth Di Cesare, Silvia oth Finocchi, Andrea oth Fischer, Alain oth Gaspar, H. Bobby oth Ghosh, Sujal oth Gennery, Andrew oth Gilmour, Kimberly oth González-Granado, Luis I. oth Martinez-Gallo, Monica oth Hambleton, Sophie oth Hauck, Fabian oth Hoenig, Manfred oth Moshous, Despina oth Neven, Benedicte oth Niehues, Tim oth Notarangelo, Luigi oth Picard, Capucine oth Rieber, Nikolaus oth Schulz, Ansgar oth Schwarz, Klaus oth Seidel, Markus G. oth Soler-Palacin, Pere oth Stepensky, Polina oth Strahm, Brigitte oth Vraetz, Thomas oth Warnatz, Klaus oth Winterhalter, Christine oth Worth, Austen oth Fuchs, Sebastian oth Uhlmann, Annette oth Ehl, Stephan oth Enthalten in Elsevier Papakitsou, I. ELSEVIER Antidiabetic treatment in elderly patients with low performance status admitted to internal medicine ward 2022 official publication of the American Academy of Allergy, Asthma and Immunology Amsterdam [u.a.] (DE-627)ELV000021164 volume:139 year:2017 number:4 pages:1302-13104 extent:11803 https://doi.org/10.1016/j.jaci.2016.07.040 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.85 Kardiologie Angiologie VZ AR 139 2017 4 1302-13104 11803 045F 610 |
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10.1016/j.jaci.2016.07.040 doi GBVA2017001000003.pica (DE-627)ELV014717816 (ELSEVIER)S0091-6749(16)30965-4 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 44.85 bkl Speckmann, Carsten verfasserin aut A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis 2017 11803 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Absent T-cell immunity resulting in life-threatening infections provides a clear rationale for hematopoetic stem cell transplantation (HSCT) in patients with severe combined immunodeficiency (SCID). Combined immunodeficiencies (CIDs) and “atypical” SCID show reduced, not absent T-cell immunity. If associated with infections or autoimmunity, they represent profound combined immunodeficiency (P-CID), for which outcome data are insufficient for unambiguous early transplant decisions. hematopoietic stem cell transplantation Elsevier T-cell deficiency Elsevier natural history Elsevier combined immunodeficiency Elsevier Doerken, Sam oth Aiuti, Alessandro oth Albert, Michael H. oth Al-Herz, Waleed oth Allende, Luis M. oth Scarselli, Alessia oth Avcin, Tadej oth Perez-Becker, Ruy oth Cancrini, Caterina oth Cant, Andrew oth Di Cesare, Silvia oth Finocchi, Andrea oth Fischer, Alain oth Gaspar, H. Bobby oth Ghosh, Sujal oth Gennery, Andrew oth Gilmour, Kimberly oth González-Granado, Luis I. oth Martinez-Gallo, Monica oth Hambleton, Sophie oth Hauck, Fabian oth Hoenig, Manfred oth Moshous, Despina oth Neven, Benedicte oth Niehues, Tim oth Notarangelo, Luigi oth Picard, Capucine oth Rieber, Nikolaus oth Schulz, Ansgar oth Schwarz, Klaus oth Seidel, Markus G. oth Soler-Palacin, Pere oth Stepensky, Polina oth Strahm, Brigitte oth Vraetz, Thomas oth Warnatz, Klaus oth Winterhalter, Christine oth Worth, Austen oth Fuchs, Sebastian oth Uhlmann, Annette oth Ehl, Stephan oth Enthalten in Elsevier Papakitsou, I. ELSEVIER Antidiabetic treatment in elderly patients with low performance status admitted to internal medicine ward 2022 official publication of the American Academy of Allergy, Asthma and Immunology Amsterdam [u.a.] (DE-627)ELV000021164 volume:139 year:2017 number:4 pages:1302-13104 extent:11803 https://doi.org/10.1016/j.jaci.2016.07.040 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.85 Kardiologie Angiologie VZ AR 139 2017 4 1302-13104 11803 045F 610 |
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10.1016/j.jaci.2016.07.040 doi GBVA2017001000003.pica (DE-627)ELV014717816 (ELSEVIER)S0091-6749(16)30965-4 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 44.85 bkl Speckmann, Carsten verfasserin aut A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis 2017 11803 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Absent T-cell immunity resulting in life-threatening infections provides a clear rationale for hematopoetic stem cell transplantation (HSCT) in patients with severe combined immunodeficiency (SCID). Combined immunodeficiencies (CIDs) and “atypical” SCID show reduced, not absent T-cell immunity. If associated with infections or autoimmunity, they represent profound combined immunodeficiency (P-CID), for which outcome data are insufficient for unambiguous early transplant decisions. hematopoietic stem cell transplantation Elsevier T-cell deficiency Elsevier natural history Elsevier combined immunodeficiency Elsevier Doerken, Sam oth Aiuti, Alessandro oth Albert, Michael H. oth Al-Herz, Waleed oth Allende, Luis M. oth Scarselli, Alessia oth Avcin, Tadej oth Perez-Becker, Ruy oth Cancrini, Caterina oth Cant, Andrew oth Di Cesare, Silvia oth Finocchi, Andrea oth Fischer, Alain oth Gaspar, H. Bobby oth Ghosh, Sujal oth Gennery, Andrew oth Gilmour, Kimberly oth González-Granado, Luis I. oth Martinez-Gallo, Monica oth Hambleton, Sophie oth Hauck, Fabian oth Hoenig, Manfred oth Moshous, Despina oth Neven, Benedicte oth Niehues, Tim oth Notarangelo, Luigi oth Picard, Capucine oth Rieber, Nikolaus oth Schulz, Ansgar oth Schwarz, Klaus oth Seidel, Markus G. oth Soler-Palacin, Pere oth Stepensky, Polina oth Strahm, Brigitte oth Vraetz, Thomas oth Warnatz, Klaus oth Winterhalter, Christine oth Worth, Austen oth Fuchs, Sebastian oth Uhlmann, Annette oth Ehl, Stephan oth Enthalten in Elsevier Papakitsou, I. ELSEVIER Antidiabetic treatment in elderly patients with low performance status admitted to internal medicine ward 2022 official publication of the American Academy of Allergy, Asthma and Immunology Amsterdam [u.a.] (DE-627)ELV000021164 volume:139 year:2017 number:4 pages:1302-13104 extent:11803 https://doi.org/10.1016/j.jaci.2016.07.040 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.85 Kardiologie Angiologie VZ AR 139 2017 4 1302-13104 11803 045F 610 |
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10.1016/j.jaci.2016.07.040 doi GBVA2017001000003.pica (DE-627)ELV014717816 (ELSEVIER)S0091-6749(16)30965-4 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 44.85 bkl Speckmann, Carsten verfasserin aut A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis 2017 11803 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Absent T-cell immunity resulting in life-threatening infections provides a clear rationale for hematopoetic stem cell transplantation (HSCT) in patients with severe combined immunodeficiency (SCID). Combined immunodeficiencies (CIDs) and “atypical” SCID show reduced, not absent T-cell immunity. If associated with infections or autoimmunity, they represent profound combined immunodeficiency (P-CID), for which outcome data are insufficient for unambiguous early transplant decisions. hematopoietic stem cell transplantation Elsevier T-cell deficiency Elsevier natural history Elsevier combined immunodeficiency Elsevier Doerken, Sam oth Aiuti, Alessandro oth Albert, Michael H. oth Al-Herz, Waleed oth Allende, Luis M. oth Scarselli, Alessia oth Avcin, Tadej oth Perez-Becker, Ruy oth Cancrini, Caterina oth Cant, Andrew oth Di Cesare, Silvia oth Finocchi, Andrea oth Fischer, Alain oth Gaspar, H. Bobby oth Ghosh, Sujal oth Gennery, Andrew oth Gilmour, Kimberly oth González-Granado, Luis I. oth Martinez-Gallo, Monica oth Hambleton, Sophie oth Hauck, Fabian oth Hoenig, Manfred oth Moshous, Despina oth Neven, Benedicte oth Niehues, Tim oth Notarangelo, Luigi oth Picard, Capucine oth Rieber, Nikolaus oth Schulz, Ansgar oth Schwarz, Klaus oth Seidel, Markus G. oth Soler-Palacin, Pere oth Stepensky, Polina oth Strahm, Brigitte oth Vraetz, Thomas oth Warnatz, Klaus oth Winterhalter, Christine oth Worth, Austen oth Fuchs, Sebastian oth Uhlmann, Annette oth Ehl, Stephan oth Enthalten in Elsevier Papakitsou, I. ELSEVIER Antidiabetic treatment in elderly patients with low performance status admitted to internal medicine ward 2022 official publication of the American Academy of Allergy, Asthma and Immunology Amsterdam [u.a.] (DE-627)ELV000021164 volume:139 year:2017 number:4 pages:1302-13104 extent:11803 https://doi.org/10.1016/j.jaci.2016.07.040 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.85 Kardiologie Angiologie VZ AR 139 2017 4 1302-13104 11803 045F 610 |
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Enthalten in Antidiabetic treatment in elderly patients with low performance status admitted to internal medicine ward Amsterdam [u.a.] volume:139 year:2017 number:4 pages:1302-13104 extent:11803 |
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Enthalten in Antidiabetic treatment in elderly patients with low performance status admitted to internal medicine ward Amsterdam [u.a.] volume:139 year:2017 number:4 pages:1302-13104 extent:11803 |
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Antidiabetic treatment in elderly patients with low performance status admitted to internal medicine ward |
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Speckmann, Carsten @@aut@@ Doerken, Sam @@oth@@ Aiuti, Alessandro @@oth@@ Albert, Michael H. @@oth@@ Al-Herz, Waleed @@oth@@ Allende, Luis M. @@oth@@ Scarselli, Alessia @@oth@@ Avcin, Tadej @@oth@@ Perez-Becker, Ruy @@oth@@ Cancrini, Caterina @@oth@@ Cant, Andrew @@oth@@ Di Cesare, Silvia @@oth@@ Finocchi, Andrea @@oth@@ Fischer, Alain @@oth@@ Gaspar, H. Bobby @@oth@@ Ghosh, Sujal @@oth@@ Gennery, Andrew @@oth@@ Gilmour, Kimberly @@oth@@ González-Granado, Luis I. @@oth@@ Martinez-Gallo, Monica @@oth@@ Hambleton, Sophie @@oth@@ Hauck, Fabian @@oth@@ Hoenig, Manfred @@oth@@ Moshous, Despina @@oth@@ Neven, Benedicte @@oth@@ Niehues, Tim @@oth@@ Notarangelo, Luigi @@oth@@ Picard, Capucine @@oth@@ Rieber, Nikolaus @@oth@@ Schulz, Ansgar @@oth@@ Schwarz, Klaus @@oth@@ Seidel, Markus G. @@oth@@ Soler-Palacin, Pere @@oth@@ Stepensky, Polina @@oth@@ Strahm, Brigitte @@oth@@ Vraetz, Thomas @@oth@@ Warnatz, Klaus @@oth@@ Winterhalter, Christine @@oth@@ Worth, Austen @@oth@@ Fuchs, Sebastian @@oth@@ Uhlmann, Annette @@oth@@ Ehl, Stephan @@oth@@ |
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A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis |
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Absent T-cell immunity resulting in life-threatening infections provides a clear rationale for hematopoetic stem cell transplantation (HSCT) in patients with severe combined immunodeficiency (SCID). Combined immunodeficiencies (CIDs) and “atypical” SCID show reduced, not absent T-cell immunity. If associated with infections or autoimmunity, they represent profound combined immunodeficiency (P-CID), for which outcome data are insufficient for unambiguous early transplant decisions. |
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Absent T-cell immunity resulting in life-threatening infections provides a clear rationale for hematopoetic stem cell transplantation (HSCT) in patients with severe combined immunodeficiency (SCID). Combined immunodeficiencies (CIDs) and “atypical” SCID show reduced, not absent T-cell immunity. If associated with infections or autoimmunity, they represent profound combined immunodeficiency (P-CID), for which outcome data are insufficient for unambiguous early transplant decisions. |
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Absent T-cell immunity resulting in life-threatening infections provides a clear rationale for hematopoetic stem cell transplantation (HSCT) in patients with severe combined immunodeficiency (SCID). Combined immunodeficiencies (CIDs) and “atypical” SCID show reduced, not absent T-cell immunity. If associated with infections or autoimmunity, they represent profound combined immunodeficiency (P-CID), for which outcome data are insufficient for unambiguous early transplant decisions. |
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