Shirah BH - Search Results

1

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.

2

Neurological Complications of Middle East Respiratory Syndrome Coronavirus: A Report of Two Cases and Review of the Literature.

Algahtani H, Subahi A, Shirah B. Algahtani H, et al. Case Rep Neurol Med. 2016;2016:3502683. doi: 10.1155/2016/3502683. Epub 2016 Apr 28. Case Rep Neurol Med. 2016. PMID: 27239356 Free PMC article.

3

Nosocomial herpes simplex encephalitis: A challenging diagnosis.

Algahtani H, Shirah B, Hmoud M, Subahi A. Algahtani H, et al. J Infect Public Health. 2017 May-Jun;10(3):343-347. doi: 10.1016/j.jiph.2016.08.004. Epub 2016 Sep 24. J Infect Public Health. 2017. PMID: 27686257 Free article.

4

Transverse myelitis-like presentation of methanol intoxication: A case report and review of the literature.

Algahtani H, Shirah B, Ahmad R, Abobaker H, Hmoud M. Algahtani H, et al. J Spinal Cord Med. 2018 Jan;41(1):72-76. doi: 10.1080/10790268.2016.1226005. Epub 2016 Oct 6. J Spinal Cord Med. 2018. PMID: 27707395 Free PMC article. Review.

5

Congenital insensitivity to pain with anhidrosis: A report of two siblings with a novel mutation in (TrkA) NTRK1 gene in a Saudi family.

Algahtani H, Naseer MI, Al-Qahtani M, Abdulrahman SA, Boker F, Shirah B. Algahtani H, et al. J Neurol Sci. 2016 Nov 15;370:35-38. doi: 10.1016/j.jns.2016.09.016. Epub 2016 Sep 9. J Neurol Sci. 2016. PMID: 27772781

6

Neurological Manifestations of Acute Posterior Multifocal Placoid Pigment Epitheliopathy.

Algahtani H, Alkhotani A, Shirah B. Algahtani H, et al. J Clin Neurol. 2016 Oct;12(4):460-467. doi: 10.3988/jcn.2016.12.4.460. J Clin Neurol. 2016. PMID: 27819416 Free PMC article.

7

Bilateral Numb Chin Syndrome as the Initial Presentation of Burkitt's Lymphoma/Leukemia: A Report of Two Cases and Review of the Literature.

Algahtani H, Shirah B, Bassuni W, Adas R. Algahtani H, et al. Case Rep Hematol. 2016;2016:3791045. doi: 10.1155/2016/3791045. Epub 2016 Nov 1. Case Rep Hematol. 2016. PMID: 27882251 Free PMC article.

8

Biotin-thiamine-responsive basal ganglia disease: catastrophic consequences of delay in diagnosis and treatment.

Algahtani H, Ghamdi S, Shirah B, Alharbi B, Algahtani R, Bazaid A. Algahtani H, et al. Neurol Res. 2017 Feb;39(2):117-125. doi: 10.1080/01616412.2016.1263176. Epub 2016 Dec 1. Neurol Res. 2017. PMID: 27905264

9

Autosomal Recessive Cerebellar Ataxia type 1 mimicking multiple sclerosis: A report of two siblings with a novel mutation in SYNE1 gene in a Saudi family.

Algahtani H, Marzouk Y, Algahtani R, Salman S, Shirah B. Algahtani H, et al. J Neurol Sci. 2017 Jan 15;372:97-100. doi: 10.1016/j.jns.2016.11.036. Epub 2016 Nov 17. J Neurol Sci. 2017. PMID: 28017257

10

Posterior Reversible Encephalopathy Syndrome: Local Experience From Saudi Arabia.

Algahtani H, Algahtani A, Aldarmahi A, Hmoud M, Marzuk Y, Shirah B. Algahtani H, et al. Neurohospitalist. 2017 Jan;7(1):24-29. doi: 10.1177/1941874416665762. Epub 2016 Aug 31. Neurohospitalist. 2017. PMID: 28042366 Free PMC article.

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