C. Bönnemann

LGMD2A: genotype–phenotype correlations based on a large mutational survey on the calpain 3 gene

Amets Sáenz, France Leturcq, A.M. Cobo et al. · Brain · 2005 · 181 citations · Full text

Medicine, Genetics, Molecular Genetics +16

A refined diagnostic algorithm for Bethlem myopathy

Debbie Hicks, AK Lampe, Rita Barresi et al. · Neurology · 2008 · 85 citations

Medicine, Pathobiology, Pathology +17

Familial Reducing Body Myopathy with Cytoplasmic Bodies and Rigid Spine Revisited: Identification of a Second LIM Domain Mutation in FHL1

Joachim Schessl, A. Columbus, Ying Hu et al. · Neuropediatrics · 2010 · 41 citations

Life Sciences, Genetics, Molecular Genetics +14

Expansion of the <scp>GLE1</scp>‐associated arthrogryposis multiplex congenita clinical spectrum

Christopher Smith, Jillian S. Parboosingh, Kym M. Boycott et al. · Clinical Genetics · 2016 · 23 citations

Life Sciences, Genetics, Molecular Genetics +9

173rd ENMC international workshop: Congenital muscular dystrophy outcome measures 5–7 March 2010, Naarden, The Netherlands

C. Bönnemann, Anne Rutkowski, E. Mercuri et al. · Neuromuscular Disorders · 2011 · 21 citations · Full text

Medicine, Child Health, Pediatrics +9