Nermin Ahmad

A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome

Mohammad Al-Haggar, Agnieszka Madej‐Pilarczyk, Janusz M. Bujnicki et al. · European Journal of Human Genetics · 2012 · 35 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Novel homozygous<i>SLC29A3</i>mutations among two unrelated Egyptian families with spectral features of H-syndrome

Mohammad Al-Haggar, Nanees Salem, Yahya Wahba et al. · Pediatric Diabetes · 2014 · 18 citations

Life Sciences, Genetics, Molecular Genetics +15

p.R672C Mutation of MYH3 Gene in an Egyptian Infant Presented with Freeman-Sheldon Syndrome

Mohammad Al-Haggar, Soheir Yahia, Kristy Damjanovich et al. · The Indian Journal of Pediatrics · 2010 · 12 citations

Life Sciences, Genetics, Molecular Genetics +13

MRI CSF flowmetry in evaluation of different neurological diseases

Nermin Ahmad, Dina H. Salama, Mohammad Al-Haggar · The Egyptian Journal of Radiology and Nuclear Medicine · 2021 · 12 citations · Full text

Medicine, Neurology, Radiology +17