A novel missense mutation in the CLCN7 gene linked to benign autosomal dominant osteopetrosis: a case series

por Rashid, Ban Mousa, Rashid, Nawshirwan Gafoor, Schulz, Ansgar, Lahr, Georgia, Nore, Beston Faiek
Publicado 2013

Monogenic forms of childhood obesity due to mutations in the leptin gene

por Funcke, Jan-Bernd, von Schnurbein, Julia, Lennerz, Belinda, Lahr, Georgia, Debatin, Klaus-Michael, Fischer-Posovszky, Pamela, Wabitsch, Martin
Publicado 2014

Age-of-onset-dependent influence of NOD2 gene variants on disease behaviour and treatment in Crohn’s disease

por Posovszky, Carsten, Pfalzer, Veronika, Lahr, Georgia, Niess, Jan Hendrik, Klaus, Jochen, Mayer, Benjamin, Debatin, Klaus-Michael, von Boyen, Georg BT
Publicado 2013

NOD2 Polymorphism Predicts Response to Treatment in Crohn’s Disease—First Steps to a Personalized Therapy

por Niess, Jan Hendrik, Klaus, Jochen, Stephani, Johannes, Pflüger, Carolin, Degenkolb, Nadine, Spaniol, Ulrike, Mayer, Benjamin, Lahr, Georgia, von Boyen, Georg B. T.
Publicado 2011

Severe Early-Onset Obesity Due to Bioinactive Leptin Caused by a p.N103K Mutation in the Leptin Gene

por Wabitsch, Martin, Funcke, Jan-Bernd, von Schnurbein, Julia, Denzer, Friederike, Lahr, Georgia, Mazen, Inas, El-Gammal, Mona, Denzer, Christian, Moss, Anja, Debatin, Klaus-Michael, Gierschik, Peter, Mistry, Vanisha, Keogh, Julia M., Farooqi, I. Sadaf, Moepps, Barbara, Fischer-Posovszky, Pamela
Publicado 2015