Shirah BH - Search Results

1

Clinical whole Exome Sequencing Reveals Novel Homozygous Missense Variant in the PMPCA Gene causing Autosomal Recessive Spinocerebellar Ataxia.

Bagabir HA, Abdulkareem AA, Muthaffar OY, Shirah BH, Naseer MI. Bagabir HA, et al. Among authors: shirah bh. Pak J Med Sci. 2024 Nov;40(10):2243-2250. doi: 10.12669/pjms.40.10.10474. Pak J Med Sci. 2024. PMID: 39554679 Free PMC article.

2

Whole exome sequencing of a novel homozygous missense variant in PALB2 gene leading to Fanconi anaemia complementation group.

Abdulkareem AA, Shirah BH, Bagabir HA, Haque A, Naseer MI. Abdulkareem AA, et al. Among authors: shirah bh. Biomed Rep. 2024 Mar 1;20(4):67. doi: 10.3892/br.2024.1756. eCollection 2024 Apr. Biomed Rep. 2024. PMID: 38476606 Free PMC article.

3

Tumor-like manifestation of central nervous system Scedosporium infection.

Shirah BH. Shirah BH. Neurol Sci. 2024 Jul;45(7):3561-3562. doi: 10.1007/s10072-024-07411-0. Epub 2024 Feb 22. Neurol Sci. 2024. PMID: 38386234 No abstract available.

4

Perception of Neurologists on Intraoperative Neurophysiological Monitoring in Saudi Arabia.

Algahtani HA, Shirah BH, Albeladi YK, Albeladi RK. Algahtani HA, et al. Among authors: shirah bh. Acta Neurol Taiwan. 2024 Dec 30;33(4):161-164. Acta Neurol Taiwan. 2024. PMID: 37994002 Free article.

5

Guillain-Barré Syndrome Following the BNT162b2 mRNA COVID-19 Vaccine.

Algahtani HA, Shirah BH, Albeladi YK, Albeladi RK. Algahtani HA, et al. Among authors: shirah bh. Acta Neurol Taiwan. 2023 Jun 30;32(2):82-85. Acta Neurol Taiwan. 2023. PMID: 37198513 Free article.

6

Phenotypic Classification of Eye Colour and Developmental Validation of the Irisplex System on Population Living in Malakand Division, Pakistan.

Rahat MA, Akbar F, Rasool A, Ilyas M, Rakha A, Shams S, Jelani M, Bibi F, Shirah BH, Abdulkareem AA, Naseer MI, Israr M. Rahat MA, et al. Among authors: shirah bh. Biomedicines. 2023 Apr 20;11(4):1228. doi: 10.3390/biomedicines11041228. Biomedicines. 2023. PMID: 37189847 Free PMC article.

7

Automated pupillometry in space neuroscience.

Shirah BH, Sen J, Naaman NK, Pandya S. Shirah BH, et al. Life Sci Space Res (Amst). 2023 May;37:1-2. doi: 10.1016/j.lssr.2023.01.004. Epub 2023 Jan 18. Life Sci Space Res (Amst). 2023. PMID: 37087173

8

Whole Exome Sequencing Reveals a Novel Homozygous Variant in the Ganglioside Biosynthetic Enzyme, ST3GAL5 Gene in a Saudi Family Causing Salt and Pepper Syndrome.

Abdulkareem AA, Shirah BH, Naseer MI. Abdulkareem AA, et al. Among authors: shirah bh. Genes (Basel). 2023 Jan 30;14(2):354. doi: 10.3390/genes14020354. Genes (Basel). 2023. PMID: 36833282 Free PMC article.

9

Cerebral fat embolism syndrome: diagnostic challenges and catastrophic outcomes: a case series.

Algahtani HA, Shirah BH, Abdelghaffar N, Alahmari F, Alhadi W, Alqahtani SA. Algahtani HA, et al. Among authors: shirah bh. J Yeungnam Med Sci. 2023 Apr;40(2):207-211. doi: 10.12701/jyms.2022.00360. Epub 2022 Sep 7. J Yeungnam Med Sci. 2023. PMID: 36069083 Free PMC article.

10

Epilepsy and Hearing Loss in a Patient with a Rare Heterozygous Variant in the CACNA1H Gene.

Algahtani HA, Shirah BH, Samman A, Alhazmi A. Algahtani HA, et al. Among authors: shirah bh. J Epilepsy Res. 2022 Jun 30;12(1):33-35. doi: 10.14581/jer.22006. eCollection 2022 Jun. J Epilepsy Res. 2022. PMID: 35910327 Free PMC article.

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