Shamshad Gulab

Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10 , a Manganese Transporter in Man

Karin Tuschl, Peter T. Clayton, Sídney M. Gospe et al. · The American Journal of Human Genetics · 2012 · 378 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes

Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed et al. · Human Genetics · 2017 · 309 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Clinical profile and treatment of infantile spasms using vigabatrin and ACTH - a developing country perspective

Shahnaz Ibrahim, Shamshad Gulab, Sidra Ishaque et al. · BMC Pediatrics · 2010 · 150 citations · Full text

Medicine, Pharmacology, Pharmacotherapy +9

Frequency of intestinal parasitic infestation in children of 5-12 years of age in Abbottabad.

Akbar K. Ahmed, Babar Malik, Babar Shaheen et al. · PubMed · 2003 · 31 citations

Veterinary Medicine, Child Health, Pediatrics +17

Atypical Neurologic Phenotype and Novel SLC30A10 Mutation in Two Brothers with Hereditary Hypermanganesemia

Shamshad Gulab, Youssef Al-Said, Husam Kayyali · Neuropediatrics · 2017 · 23 citations

Life Sciences, Genetics, Neurology +17