| Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man K Tuschl, PT Clayton, SM Gospe, S Gulab, S Ibrahim, P Singhi, R Aulakh, ... The American Journal of Human Genetics 90 (3), 457-466, 2012 | 384 | 2012 |
| The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes D Monies, M Abouelhoda, M AlSayed, Z Alhassnan, M Alotaibi, H Kayyali, ... Human genetics 136, 921-939, 2017 | 268 | 2017 |
| Lessons learned from large-scale, first-tier clinical exome sequencing in a highly consanguineous population D Monies, M Abouelhoda, M Assoum, N Moghrabi, R Rafiullah, ... The American Journal of Human Genetics 104 (6), 1182-1201, 2019 | 251 | 2019 |
| Frequency of intestinal parasitic infestation in children of 5–12 years of age in Abbottabad AK Ahmed, B Malik, B Shaheen, G Yasmeen, JB Dar, AK Mona, S Gulab, ... Journal of Ayub Medical College Abbottabad 15 (2), 2003 | 63 | 2003 |
| Clinical profile and treatment of infantile spasms using vigabatrin and ACTH-a developing country perspective S Ibrahim, S Gulab, S Ishaque, T Saleem BMC pediatrics 10, 1-9, 2010 | 46 | 2010 |
| Atypical neurologic phenotype and novel SLC30A10 mutation in two brothers with hereditary hypermanganesemia S Gulab, HR Kayyali, Y Al-Said Neuropediatrics 49 (01), 072-075, 2018 | 16 | 2018 |
| Cerebral sinus venous thrombosis due to asparaginase therapy Y Alsaid, S Gulab, M Bayoumi, S Baeesa Case reports in hematology 2013 (1), 841057, 2013 | 10 | 2013 |
| Brain calcinosis and seizures in an adolescent boy Anwar-ul-Haq, S Ibrahim, S Gulab, T Saleem, S Ishaque Clinical pediatrics 49 (12), 1160-1163, 2010 | 4 | 2010 |
| Rett syndrome: A classic presentation S Ibrahim, SG Khan Journal of Pediatric Neurology 6 (2), 191-194, 2008 | 3 | 2008 |
| CEREBELLAR SWELLING: A RARE PRESENTATION OF: FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS M Alali, S Shamshad, K Husam, B Mahamed, MS Bin Mahfoodh, ... PEDIATRIC BLOOD & CANCER 62, S1-S1, 2015 | | 2015 |
| Hereditary Hypermanganesemia: a new potentially treatable metabolic disorder in four Pakistani siblings SG Khan, S Ibrahim, K Ahmed ANNALS OF NEUROLOGY 76, S177-S177, 2014 | | 2014 |
| Case Report Cerebral Sinus Venous Thrombosis due to Asparaginase Therapy Y Alsaid, S Gulab, M Bayoumi, S Baeesa | | 2013 |
| Pratibha Singhi, Roosy Aulakh, Reinaldo T. Ribeiro, Orlando G. Barsottini, Maha S. Zaki, Maria Luz Del Rosario, Sarah Dyack, Victoria Price, Andrea Rideout, Kevin Gordon, Ron A … K Tuschl, PT Clayton, SM Gospe Jr, S Gulab, S Ibrahim The American Journal of Human Genetics 90, 457-466, 2012 | | 2012 |
| Pediatrics Neurolgy S Gulab Pakistan Journal of Neurological Sciences (PJNS) 5 (1), 55-57, 2010 | | 2010 |
| FREQUENCY OF INTESTINAL PARASITIC INFESIATION IN AK Mona, S Gulab, M Ayub J Ayub Med Coll Abbottabad 15 (2), 2, 2003 | | 2003 |
| Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man SM Gospe Jr, SG Khan, MS Zaki, PB Mills | | |
| Pratibha Singhi, 4 Roosy Aulakh, 5 Reinaldo T. Ribeiro, 6 Orlando G. Barsottini, 6 Maha S. Zaki, 7 Maria Luz Del Rosario, 8 Sarah Dyack, 9 Victoria Price, 9 Andrea Rideout, 9 … K Tuschl, PT Clayton, SM Gospe Jr, S Gulab, S Ibrahim | | |
