PReS-FINAL-2196: The clinical significance of the Q703K mutation of NLRP3 gene. A multicentric national study

Gespeichert in:

Autor*in:	Naselli, A [verfasserIn] Cantarini, L Insalaco, A Alessio, M Tommasini, A Gallizzi, R Signa, S Lucherini, OM Caroli, F Ceccherini, I Martini, A Gattorno, M

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2013

Schlagwörter:	Steroid Normal Control Clinical History National Study Pathogenic Role

Anmerkung:	© Naselli et al.; licensee BioMed Central Ltd. 2013

Übergeordnetes Werk:	Enthalten in: Pediatric rheumatology - London : BioMed Central, 2003, 11(2013), Suppl 2 vom: 05. Dez.
Übergeordnetes Werk:	volume:11 ; year:2013 ; number:Suppl 2 ; day:05 ; month:12

Links:	Volltext

DOI / URN:	10.1186/1546-0096-11-S2-P186

Katalog-ID:	SPR029059933

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allfields_unstemmed	10.1186/1546-0096-11-S2-P186 doi (DE-627)SPR029059933 (SPR)1546-0096-11-S2-P186-e DE-627 ger DE-627 rakwb eng Naselli, A verfasserin aut PReS-FINAL-2196: The clinical significance of the Q703K mutation of NLRP3 gene. A multicentric national study 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Naselli et al.; licensee BioMed Central Ltd. 2013 Steroid (dpeaa)DE-He213 Normal Control (dpeaa)DE-He213 Clinical History (dpeaa)DE-He213 National Study (dpeaa)DE-He213 Pathogenic Role (dpeaa)DE-He213 Cantarini, L aut Insalaco, A aut Alessio, M aut Tommasini, A aut Gallizzi, R aut Signa, S aut Lucherini, OM aut Caroli, F aut Ceccherini, I aut Martini, A aut Gattorno, M aut Enthalten in Pediatric rheumatology London : BioMed Central, 2003 11(2013), Suppl 2 vom: 05. Dez. (DE-627)527833746 (DE-600)2279468-2 1546-0096 nnns volume:11 year:2013 number:Suppl 2 day:05 month:12 https://dx.doi.org/10.1186/1546-0096-11-S2-P186 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 11 2013 Suppl 2 05 12
allfieldsGer	10.1186/1546-0096-11-S2-P186 doi (DE-627)SPR029059933 (SPR)1546-0096-11-S2-P186-e DE-627 ger DE-627 rakwb eng Naselli, A verfasserin aut PReS-FINAL-2196: The clinical significance of the Q703K mutation of NLRP3 gene. A multicentric national study 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Naselli et al.; licensee BioMed Central Ltd. 2013 Steroid (dpeaa)DE-He213 Normal Control (dpeaa)DE-He213 Clinical History (dpeaa)DE-He213 National Study (dpeaa)DE-He213 Pathogenic Role (dpeaa)DE-He213 Cantarini, L aut Insalaco, A aut Alessio, M aut Tommasini, A aut Gallizzi, R aut Signa, S aut Lucherini, OM aut Caroli, F aut Ceccherini, I aut Martini, A aut Gattorno, M aut Enthalten in Pediatric rheumatology London : BioMed Central, 2003 11(2013), Suppl 2 vom: 05. Dez. (DE-627)527833746 (DE-600)2279468-2 1546-0096 nnns volume:11 year:2013 number:Suppl 2 day:05 month:12 https://dx.doi.org/10.1186/1546-0096-11-S2-P186 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 11 2013 Suppl 2 05 12
allfieldsSound	10.1186/1546-0096-11-S2-P186 doi (DE-627)SPR029059933 (SPR)1546-0096-11-S2-P186-e DE-627 ger DE-627 rakwb eng Naselli, A verfasserin aut PReS-FINAL-2196: The clinical significance of the Q703K mutation of NLRP3 gene. A multicentric national study 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Naselli et al.; licensee BioMed Central Ltd. 2013 Steroid (dpeaa)DE-He213 Normal Control (dpeaa)DE-He213 Clinical History (dpeaa)DE-He213 National Study (dpeaa)DE-He213 Pathogenic Role (dpeaa)DE-He213 Cantarini, L aut Insalaco, A aut Alessio, M aut Tommasini, A aut Gallizzi, R aut Signa, S aut Lucherini, OM aut Caroli, F aut Ceccherini, I aut Martini, A aut Gattorno, M aut Enthalten in Pediatric rheumatology London : BioMed Central, 2003 11(2013), Suppl 2 vom: 05. Dez. (DE-627)527833746 (DE-600)2279468-2 1546-0096 nnns volume:11 year:2013 number:Suppl 2 day:05 month:12 https://dx.doi.org/10.1186/1546-0096-11-S2-P186 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 11 2013 Suppl 2 05 12
language	English
source	Enthalten in Pediatric rheumatology 11(2013), Suppl 2 vom: 05. Dez. volume:11 year:2013 number:Suppl 2 day:05 month:12
sourceStr	Enthalten in Pediatric rheumatology 11(2013), Suppl 2 vom: 05. Dez. volume:11 year:2013 number:Suppl 2 day:05 month:12
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spellingShingle	Naselli, A misc Steroid misc Normal Control misc Clinical History misc National Study misc Pathogenic Role PReS-FINAL-2196: The clinical significance of the Q703K mutation of NLRP3 gene. A multicentric national study
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topic_title	PReS-FINAL-2196: The clinical significance of the Q703K mutation of NLRP3 gene. A multicentric national study Steroid (dpeaa)DE-He213 Normal Control (dpeaa)DE-He213 Clinical History (dpeaa)DE-He213 National Study (dpeaa)DE-He213 Pathogenic Role (dpeaa)DE-He213
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title	PReS-FINAL-2196: The clinical significance of the Q703K mutation of NLRP3 gene. A multicentric national study
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title_full	PReS-FINAL-2196: The clinical significance of the Q703K mutation of NLRP3 gene. A multicentric national study
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author_browse	Naselli, A Cantarini, L Insalaco, A Alessio, M Tommasini, A Gallizzi, R Signa, S Lucherini, OM Caroli, F Ceccherini, I Martini, A Gattorno, M
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author-letter	Naselli, A
doi_str_mv	10.1186/1546-0096-11-S2-P186
title_sort	pres-final-2196: the clinical significance of the q703k mutation of nlrp3 gene. a multicentric national study
title_auth	PReS-FINAL-2196: The clinical significance of the Q703K mutation of NLRP3 gene. A multicentric national study
abstract	© Naselli et al.; licensee BioMed Central Ltd. 2013
abstractGer	© Naselli et al.; licensee BioMed Central Ltd. 2013
abstract_unstemmed	© Naselli et al.; licensee BioMed Central Ltd. 2013
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container_issue	Suppl 2
title_short	PReS-FINAL-2196: The clinical significance of the Q703K mutation of NLRP3 gene. A multicentric national study
url	https://dx.doi.org/10.1186/1546-0096-11-S2-P186
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author2	Cantarini, L Insalaco, A Alessio, M Tommasini, A Gallizzi, R Signa, S Lucherini, OM Caroli, F Ceccherini, I Martini, A Gattorno, M
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PReS-FINAL-2196: The clinical significance of the Q703K mutation of NLRP3 gene. A multicentric national study

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