Mohammad A. Abduljabbar

A Genetic Isolate of Congenital Lipoid Adrenal Hyperplasia with Atypical Clinical Findings

Xin Chen, Bo Y. Baker, Mohammad A. Abduljabbar et al. · The Journal of Clinical Endocrinology & Metabolism · 2005 · 74 citations · Full text

Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability

Anne Raimondo, Ali Chakera, Soren K. Thomsen et al. · Human Molecular Genetics · 2014 · 64 citations · Full text

The Rising Incidence of Type 1 Diabetes Mellitus and the Role of Environmental Factors - Three Decade Experience in a Primary Care Health Center in Saudi Arabia

Mary Cherian, Kanan Alkanani, Saeed Qahtani et al. · Journal of Pediatric Endocrinology and Metabolism · 2010 · 53 citations

Persistent Hyperinsulinemic Hypoglycemia of Infancy (PHHI): Long-term Outcome Following 95% Pancreatectomy

Mary Cherian, Mohammad A. Abduljabbar · Journal of Pediatric Endocrinology and Metabolism · 2005 · 33 citations

Mutations of the AMH Type II Receptor in Two Extended Families with Persistent Müllerian Duct Syndrome: Lack of Phenotype/Genotype Correlation

Mohammad A. Abduljabbar, Khalid Taheini, Jean‐Yves Picard et al. · Hormone Research in Paediatrics · 2012 · 33 citations

Extended Families, Clinical Symptoms, Mendelian Disorder +12