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C Timmann

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Zeitschrift Fur Rheumatologie|October 16, 2009
[Molecular diagnostics of hereditary fever syndromes. Familial Mediterranean fever (FMF), hyperimmunoglobulin D syndrome (HIDS), tumor necrosis factor receptor-associated periodic syndrome (TRAPS), cryopyrin-associated periodic syndrome (CAPS: FCAS, MWS, NOMID/CINCA)]C Timmann, R Horstmann
Journal of Immunology (Baltimore, Md. : 1950)|February 15, 1991
Two major serum components antigenically related to complement factor H are different glycosylation forms of a single protein with no factor H-like complement regulatory functionsC Timmann, M Leippe, R D Horstmann
Der Internist|July 10, 2004
[Hereditary periodic fever]P Lamprecht, C Timmann, K Ahmadi-Simab, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 15, 1992
Two additional human serum proteins structurally related to complement factor H. Evidence for a family of factor H-related genesC Skerka, C Timmann, R D Horstmann, et al.
Mutation Research|July 27, 2001
Two novel mutations R653H and E230K in the Mediterranean fever gene associated with diseaseC Timmann, B Muntau, K Kuhne, et al.
Clinical and Experimental Immunology|December 21, 2004
Relevance of ex vivo blood lymphocyte assay for in vivo lymphocyte functionN W Brattig, C Timmann, R S Abraha, et al.
European Journal of Pediatrics|August 21, 2012
Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric populationE Lainka, M Bielak, P Lohse, et al.
QJM : Monthly Journal of the Association of Physicians|August 20, 2004
High mortality of infant bacteraemia clinically indistinguishable from severe malariaJ A Evans, A Adusei, C Timmann, et al.
Klinische Padiatrie|November 9, 2010
Analysis of cryopyrin-associated periodic syndromes (CAPS) in German children: epidemiological, clinical and genetic characteristicsE Lainka, U Neudorf, P Lohse, et al.
Rheumatology International|November 1, 2011
Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German childrenE Lainka, U Neudorf, P Lohse, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Zeitschrift Fur Rheumatologie|October 16, 2009
[Molecular diagnostics of hereditary fever syndromes. Familial Mediterranean fever (FMF), hyperimmunoglobulin D syndrome (HIDS), tumor necrosis factor receptor-associated periodic syndrome (TRAPS), cryopyrin-associated periodic syndrome (CAPS: FCAS, MWS, NOMID/CINCA)]C Timmann, R Horstmann
Journal of Immunology (Baltimore, Md. : 1950)|February 15, 1991
Two major serum components antigenically related to complement factor H are different glycosylation forms of a single protein with no factor H-like complement regulatory functionsC Timmann, M Leippe, R D Horstmann
Der Internist|July 10, 2004
[Hereditary periodic fever]P Lamprecht, C Timmann, K Ahmadi-Simab, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 15, 1992
Two additional human serum proteins structurally related to complement factor H. Evidence for a family of factor H-related genesC Skerka, C Timmann, R D Horstmann, et al.
Mutation Research|July 27, 2001
Two novel mutations R653H and E230K in the Mediterranean fever gene associated with diseaseC Timmann, B Muntau, K Kuhne, et al.
Clinical and Experimental Immunology|December 21, 2004
Relevance of ex vivo blood lymphocyte assay for in vivo lymphocyte functionN W Brattig, C Timmann, R S Abraha, et al.
European Journal of Pediatrics|August 21, 2012
Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric populationE Lainka, M Bielak, P Lohse, et al.
QJM : Monthly Journal of the Association of Physicians|August 20, 2004
High mortality of infant bacteraemia clinically indistinguishable from severe malariaJ A Evans, A Adusei, C Timmann, et al.
Klinische Padiatrie|November 9, 2010
Analysis of cryopyrin-associated periodic syndromes (CAPS) in German children: epidemiological, clinical and genetic characteristicsE Lainka, U Neudorf, P Lohse, et al.
Rheumatology International|November 1, 2011
Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German childrenE Lainka, U Neudorf, P Lohse, et al.
Pageof 2