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Ethylmalonic encephalopathy-report of two cases.
Heberle LC, Al Tawari AA, Ramadan DG, Ibrahim JK. Heberle LC, et al. Among authors: al tawari aa. Brain Dev. 2006 Jun;28(5):329-31. doi: 10.1016/j.braindev.2005.10.005. Epub 2006 Jan 10. Brain Dev. 2006. PMID: 16376514
Biotin-thiamine responsive basal ganglia disease: a retrospective review of the clinical, radiological and molecular findings of cases in Kuwait with novel variants.
Aburezq M, Alahmad A, Alsafi R, Al-Tawari A, Ramadan D, Shafik M, Abdelaty O, Makhseed N, Elshafie R, Ayed M, Hayat A, Dashti F, Marafi D, Albash B, Bastaki L, Alsharhan H. Aburezq M, et al. Orphanet J Rare Dis. 2023 Sep 5;18(1):271. doi: 10.1186/s13023-023-02888-y. Orphanet J Rare Dis. 2023. PMID: 37670342 Free PMC article.
Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families.
Hanna RM, Marsh SE, Swistun D, Al-Gazali L, Zaki MS, Abdel-Salam GM, Al-Tawari A, Bastaki L, Kayserili H, Rajab A, Boglárka B, Dietrich RB, Dobyns WB, Truwit CL, Sattar S, Chuang NA, Sherr EH, Gleeson JG. Hanna RM, et al. Neurology. 2011 Jan 25;76(4):373-82. doi: 10.1212/WNL.0b013e318208f492. Neurology. 2011. PMID: 21263138 Free PMC article.
What syndrome is this? Autosomal recessive type II cutis laxa.
Nanda A, Lionel J, Al-Tawari AA, Anim JT. Nanda A, et al. Among authors: al tawari aa. Pediatr Dermatol. 2004 Mar-Apr;21(2):167-70. doi: 10.1111/j.0736-8046.2004.21217.x. Pediatr Dermatol. 2004. PMID: 15078361 No abstract available.
22 results