Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members

Gespeichert in:

Autor*in:	Glanville, James [verfasserIn] Taibjee, Saleem Crow, Yanick Davis, Penny Ryder, Clive Southwood, Taunton

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2011

Schlagwörter:	Systemic Lupus Erythematosus Developmental Delay Auditory Hallucination Leukodystrophy Acute Encephalopathy

Anmerkung:	© Glanville et al; licensee BioMed Central Ltd. 2011

Übergeordnetes Werk:	Enthalten in: Pediatric rheumatology - London : BioMed Central, 2003, 9(2011), Suppl 1 vom: 14. Sept.
Übergeordnetes Werk:	volume:9 ; year:2011 ; number:Suppl 1 ; day:14 ; month:09

Links:	Volltext

DOI / URN:	10.1186/1546-0096-9-S1-P283

Katalog-ID:	SPR029049628

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allfields	10.1186/1546-0096-9-S1-P283 doi (DE-627)SPR029049628 (SPR)1546-0096-9-S1-P283-e DE-627 ger DE-627 rakwb eng Glanville, James verfasserin aut Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Glanville et al; licensee BioMed Central Ltd. 2011 Systemic Lupus Erythematosus (dpeaa)DE-He213 Developmental Delay (dpeaa)DE-He213 Auditory Hallucination (dpeaa)DE-He213 Leukodystrophy (dpeaa)DE-He213 Acute Encephalopathy (dpeaa)DE-He213 Taibjee, Saleem aut Crow, Yanick aut Davis, Penny aut Ryder, Clive aut Southwood, Taunton aut Enthalten in Pediatric rheumatology London : BioMed Central, 2003 9(2011), Suppl 1 vom: 14. Sept. (DE-627)527833746 (DE-600)2279468-2 1546-0096 nnns volume:9 year:2011 number:Suppl 1 day:14 month:09 https://dx.doi.org/10.1186/1546-0096-9-S1-P283 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2011 Suppl 1 14 09
spelling	10.1186/1546-0096-9-S1-P283 doi (DE-627)SPR029049628 (SPR)1546-0096-9-S1-P283-e DE-627 ger DE-627 rakwb eng Glanville, James verfasserin aut Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Glanville et al; licensee BioMed Central Ltd. 2011 Systemic Lupus Erythematosus (dpeaa)DE-He213 Developmental Delay (dpeaa)DE-He213 Auditory Hallucination (dpeaa)DE-He213 Leukodystrophy (dpeaa)DE-He213 Acute Encephalopathy (dpeaa)DE-He213 Taibjee, Saleem aut Crow, Yanick aut Davis, Penny aut Ryder, Clive aut Southwood, Taunton aut Enthalten in Pediatric rheumatology London : BioMed Central, 2003 9(2011), Suppl 1 vom: 14. Sept. (DE-627)527833746 (DE-600)2279468-2 1546-0096 nnns volume:9 year:2011 number:Suppl 1 day:14 month:09 https://dx.doi.org/10.1186/1546-0096-9-S1-P283 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2011 Suppl 1 14 09
allfields_unstemmed	10.1186/1546-0096-9-S1-P283 doi (DE-627)SPR029049628 (SPR)1546-0096-9-S1-P283-e DE-627 ger DE-627 rakwb eng Glanville, James verfasserin aut Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Glanville et al; licensee BioMed Central Ltd. 2011 Systemic Lupus Erythematosus (dpeaa)DE-He213 Developmental Delay (dpeaa)DE-He213 Auditory Hallucination (dpeaa)DE-He213 Leukodystrophy (dpeaa)DE-He213 Acute Encephalopathy (dpeaa)DE-He213 Taibjee, Saleem aut Crow, Yanick aut Davis, Penny aut Ryder, Clive aut Southwood, Taunton aut Enthalten in Pediatric rheumatology London : BioMed Central, 2003 9(2011), Suppl 1 vom: 14. Sept. (DE-627)527833746 (DE-600)2279468-2 1546-0096 nnns volume:9 year:2011 number:Suppl 1 day:14 month:09 https://dx.doi.org/10.1186/1546-0096-9-S1-P283 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2011 Suppl 1 14 09
allfieldsGer	10.1186/1546-0096-9-S1-P283 doi (DE-627)SPR029049628 (SPR)1546-0096-9-S1-P283-e DE-627 ger DE-627 rakwb eng Glanville, James verfasserin aut Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Glanville et al; licensee BioMed Central Ltd. 2011 Systemic Lupus Erythematosus (dpeaa)DE-He213 Developmental Delay (dpeaa)DE-He213 Auditory Hallucination (dpeaa)DE-He213 Leukodystrophy (dpeaa)DE-He213 Acute Encephalopathy (dpeaa)DE-He213 Taibjee, Saleem aut Crow, Yanick aut Davis, Penny aut Ryder, Clive aut Southwood, Taunton aut Enthalten in Pediatric rheumatology London : BioMed Central, 2003 9(2011), Suppl 1 vom: 14. Sept. (DE-627)527833746 (DE-600)2279468-2 1546-0096 nnns volume:9 year:2011 number:Suppl 1 day:14 month:09 https://dx.doi.org/10.1186/1546-0096-9-S1-P283 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2011 Suppl 1 14 09
allfieldsSound	10.1186/1546-0096-9-S1-P283 doi (DE-627)SPR029049628 (SPR)1546-0096-9-S1-P283-e DE-627 ger DE-627 rakwb eng Glanville, James verfasserin aut Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Glanville et al; licensee BioMed Central Ltd. 2011 Systemic Lupus Erythematosus (dpeaa)DE-He213 Developmental Delay (dpeaa)DE-He213 Auditory Hallucination (dpeaa)DE-He213 Leukodystrophy (dpeaa)DE-He213 Acute Encephalopathy (dpeaa)DE-He213 Taibjee, Saleem aut Crow, Yanick aut Davis, Penny aut Ryder, Clive aut Southwood, Taunton aut Enthalten in Pediatric rheumatology London : BioMed Central, 2003 9(2011), Suppl 1 vom: 14. Sept. (DE-627)527833746 (DE-600)2279468-2 1546-0096 nnns volume:9 year:2011 number:Suppl 1 day:14 month:09 https://dx.doi.org/10.1186/1546-0096-9-S1-P283 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2011 Suppl 1 14 09
language	English
source	Enthalten in Pediatric rheumatology 9(2011), Suppl 1 vom: 14. Sept. volume:9 year:2011 number:Suppl 1 day:14 month:09
sourceStr	Enthalten in Pediatric rheumatology 9(2011), Suppl 1 vom: 14. Sept. volume:9 year:2011 number:Suppl 1 day:14 month:09
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Systemic Lupus Erythematosus Developmental Delay Auditory Hallucination Leukodystrophy Acute Encephalopathy
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container_title	Pediatric rheumatology
authorswithroles_txt_mv	Glanville, James @@aut@@ Taibjee, Saleem @@aut@@ Crow, Yanick @@aut@@ Davis, Penny @@aut@@ Ryder, Clive @@aut@@ Southwood, Taunton @@aut@@
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author	Glanville, James
spellingShingle	Glanville, James misc Systemic Lupus Erythematosus misc Developmental Delay misc Auditory Hallucination misc Leukodystrophy misc Acute Encephalopathy Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members
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topic_title	Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members Systemic Lupus Erythematosus (dpeaa)DE-He213 Developmental Delay (dpeaa)DE-He213 Auditory Hallucination (dpeaa)DE-He213 Leukodystrophy (dpeaa)DE-He213 Acute Encephalopathy (dpeaa)DE-He213
topic	misc Systemic Lupus Erythematosus misc Developmental Delay misc Auditory Hallucination misc Leukodystrophy misc Acute Encephalopathy
topic_unstemmed	misc Systemic Lupus Erythematosus misc Developmental Delay misc Auditory Hallucination misc Leukodystrophy misc Acute Encephalopathy
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title	Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members
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title_full	Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members
author_sort	Glanville, James
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author_browse	Glanville, James Taibjee, Saleem Crow, Yanick Davis, Penny Ryder, Clive Southwood, Taunton
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author-letter	Glanville, James
doi_str_mv	10.1186/1546-0096-9-S1-P283
title_sort	phenotypic variation in familial chilblain lupus (fcl) and aicardi-goutières syndrome (ags) associated with trex1 mutation in 4 family members
title_auth	Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members
abstract	© Glanville et al; licensee BioMed Central Ltd. 2011
abstractGer	© Glanville et al; licensee BioMed Central Ltd. 2011
abstract_unstemmed	© Glanville et al; licensee BioMed Central Ltd. 2011
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container_issue	Suppl 1
title_short	Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members
url	https://dx.doi.org/10.1186/1546-0096-9-S1-P283
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author2	Taibjee, Saleem Crow, Yanick Davis, Penny Ryder, Clive Southwood, Taunton
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up_date	2024-07-03T23:13:19.228Z
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Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members

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