Angham Al Mutair

Wolcott-Rallison Syndrome Is the Most Common Genetic Cause of Permanent Neonatal Diabetes in Consanguineous Families

Oscar Rubio‐Cabezas, Ann‐Marie Patch, Jayne A.L. Minton et al. · The Journal of Clinical Endocrinology & Metabolism · 2009 · 146 citations · Full text

Proposal for a Standardized Protocol for <sup>18</sup>F-DOPA-PET (PET/CT) in Congenital Hyperinsulinism

Klaus Mohnike, Oliver Blankenstein, Henrik Thybo Christesen et al. · Hormone Research in Paediatrics · 2006 · 69 citations · Full text

Positron Emission Tomography, Standardized Protocol, Congenital Hyperinsulinism +5

Four novel cases of permanent neonatal diabetes mellitus caused by homozygous mutations in the glucokinase gene

Kate Bennett, Chela James, Angham Al Mutair et al. · Pediatric Diabetes · 2010 · 42 citations

Glucokinase Gene, Novel Cases, Homozygous Mutations +14

Puberty Onset among Boys in Riyadh, Saudi Arabia

Ibrahim Al Alwan, Naila Felimban, Yasmin Altwaijri et al. · Clinical Medicine Insights Pediatrics · 2010 · 15 citations · Full text

Variable phenotype in five patients with Wolcott-Rallison syndrome due to the same EIF2AK3 (c.1259delA) mutation

Manal Al-Shawi, Angham Al Mutair, Sian Ellard et al. · Journal of Pediatric Endocrinology and Metabolism · 2012 · 13 citations

Wolcott-rallison Syndrome, Genetics, Genetic Epidemiology +16