Alsinani A[au] - Search Results

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Year	Number of Results
2012	2
2015	1
2021	1
2023	0

Page 1

Case Report: Surgical Management in Acute Subdural Hematoma Induced by Chronic Myelogenous Leukemia.

Moshref R, Alsinani TA, Al-Sinani A. Moshref R, et al. Am J Case Rep. 2021 Aug 24;22:e932787. doi: 10.12659/AJCR.932787. Am J Case Rep. 2021. PMID: 34426567 Free PMC article.

A novel leprechaunism mutation, Cys807Arg, in an Arab infant: a rare cause of hypoglycaemia.

Baqir ZS, Al-Lawati TT, Al Hussaini SO, Al-Sinani A, Al-Said K, Al-Rashdi I. Baqir ZS, et al. Paediatr Int Child Health. 2012 Aug;32(3):183-5. doi: 10.1179/2046905512Y.0000000004. Paediatr Int Child Health. 2012. PMID: 22824672

Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutation.

Shaheen R, Alazami AM, Alshammari MJ, Faqeih E, Alhashmi N, Mousa N, Alsinani A, Ansari S, Alzahrani F, Al-Owain M, Alzayed ZS, Alkuraya FS. Shaheen R, et al. Among authors: alsinani a. J Med Genet. 2012 Oct;49(10):630-5. doi: 10.1136/jmedgenet-2012-101142. J Med Genet. 2012. PMID: 23054245

A Novel Mutation Causing 17-β-Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Omani Child: First Case Report and Review of Literature.

Al-Sinani A, Mula-Abed WA, Al-Kindi M, Al-Kusaibi G, Al-Azkawi H, Nahavandi N. Al-Sinani A, et al. Oman Med J. 2015 Mar;30(2):129-34. doi: 10.5001/omj.2015.27. Oman Med J. 2015. PMID: 25960839 Free PMC article.

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