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American Journal of Medical Genetics. Part A|November 29, 2007
The heterozygous LMNA mutation p.R471G causes a variable phenotype with features of two types of familial partial lipodystrophyPetra Muschke, Uwe Kölsch, Sibylle Jakubiczka, et al.
Molecular Immunology|June 29, 2004
The role of adaptor proteins in lymphocyte activationMauro Togni, Jon Lindquist, Annegret Gerber, et al.
The Pediatric Infectious Disease Journal|September 23, 2017
Antibiotic Prophylaxis, Immunoglobulin Substitution and Supportive Measures Prevent Infections in MECP2 Duplication SyndromeMichael Bauer, Renate Krüger, Uwe Kölsch, et al.
Clinical and Experimental Medicine|September 5, 2023
Clinical and immunological characterisation of patients with common variable immunodeficiency related immune thrombocytopeniaNadia Somasundaram, Oliver Meyer, Carmen Scheibenbogen, et al.
Plos One|May 22, 2019
Screening and treatment for tuberculosis in a cohort of unaccompanied minor refugees in Berlin, GermanyStephanie Thee, Renate Krüger, Horst von Bernuth, et al.
Molecular and Cellular Biology|August 19, 2005
The transmembrane adapter protein SIT regulates thymic development and peripheral T-cell functionsLuca Simeoni, Vilmos Posevitz, Uwe Kölsch, et al.
Molecular and Cellular Biology|April 14, 2006
Normal T-cell development and immune functions in TRIM-deficient miceUwe Kölsch, Börge Arndt, Dirk Reinhold, et al.
The Pediatric Infectious Disease Journal|April 11, 2014
Liver abscess complicated by diaphragm perforation and pleural empyema leads to the discovery of interleukin-1 receptor-associated kinase 4 deficiencyDominik Schöndorf, Horst von Bernuth, Arne Simon, et al.
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