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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. Among authors: hayat a. 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.
White Matter Sexual Dimorphism of the Adult Human Brain.
Bourisly AK, Gejo G, Hayat AA, Alsarraf L, Dashti FM, Di Paola M. Bourisly AK, et al. Among authors: hayat aa. Transl Neurosci. 2017 May 31;8:49-53. doi: 10.1515/tnsci-2017-0009. eCollection 2017. Transl Neurosci. 2017. PMID: 28729918 Free PMC article.
Gastroenteropancreatic neuroendocrine neoplasms: current development, challenges, and clinical perspectives.
Zhang XB, Fan YB, Jing R, Getu MA, Chen WY, Zhang W, Dong HX, Dakal TC, Hayat A, Cai HJ, Ashrafizadeh M, Abd El-Aty AM, Hacimuftuoglu A, Liu P, Li TF, Sethi G, Ahn KS, Ertas YN, Chen MJ, Ji JS, Ma L, Gong P. Zhang XB, et al. Among authors: hayat a. Mil Med Res. 2024 Jun 4;11(1):35. doi: 10.1186/s40779-024-00535-6. Mil Med Res. 2024. PMID: 38835066 Free article. Review.
Clinical and genetic investigation of 14 families with various forms of short stature syndromes.
Khan FU, Khan H, Ullah K, Nawaz S, Abdullah, Khan MJ, Ahmed S, Ilyas M, Ali A, Ullah I, Sohail A, Hussain S, Ahmad F, Faisal, Sufyan R, Hayat A, Hanif T, Bibi F, Hayat M, Ullah R, Khan IU, Ali RH, Hasni MS, Ali H, Bilal M, Peralta S, Buchert R, Zehri Z, Hassan G, Liaqat K, Zahid M, Shah K, Mikitie O, Haack TB, Ji W, Lakhani SA, Ansar M, Ahmad W. Khan FU, et al. Among authors: hayat a. Clin Genet. 2024 May 22. doi: 10.1111/cge.14550. Online ahead of print. Clin Genet. 2024. PMID: 38774940
410 results