El-Kiki H - Search Results

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Hereditary tyrosinemia type 1 from a single center in Egypt: clinical study of 22 cases.

El-Karaksy H, Fahmy M, El-Raziky M, El-Koofy N, El-Sayed R, Rashed MS, El-Kiki H, El-Hennawy A, Mohsen N. El-Karaksy H, et al. Among authors: el kiki h. World J Pediatr. 2011 Aug;7(3):224-31. doi: 10.1007/s12519-011-0287-3. Epub 2011 Jun 1. World J Pediatr. 2011. PMID: 21633861

Enhanced MRI in early undifferentiated oligoarthritis of the knee joints: improvements already visible after 2 months of DMARDs treatment.

Emad Y, Ragab Y, Shaarawy A, Raafat H, El-Kiki HA, Rasker JJ. Emad Y, et al. Among authors: el kiki ha. Clin Rheumatol. 2008 Sep;27(9):1177-82. doi: 10.1007/s10067-008-0935-8. Epub 2008 Jun 18. Clin Rheumatol. 2008. PMID: 18563513

Screening for TSEN54 Variants in Egyptian Patients with Pontocerebellar Malformations.

Emam BA, Abdel-Hamid MS, Eid M, Girgis M, Ragab OA, Zaki MS, El-Kiki H, Abdel-Hady S, Abdel-Salam GMH. Emam BA, et al. Among authors: el kiki h. Mol Syndromol. 2024 Dec;15(6):474-480. doi: 10.1159/000539364. Epub 2024 Jun 20. Mol Syndromol. 2024. PMID: 39634246

Enzyme replacement therapy and bony changes in Egyptian paediatric Gaucher disease patients.

El-Beshlawy A, Ragab L, Youssry I, Yakout K, El-Kiki H, Eid K, Mansour IM, Abd El-Hamid S, Yang M, Mistry PK. El-Beshlawy A, et al. Among authors: el kiki h. J Inherit Metab Dis. 2006 Feb;29(1):92-8. doi: 10.1007/s10545-006-0121-6. J Inherit Metab Dis. 2006. PMID: 16601874

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