Algahtani HA - Search Results

1

Array-comparative genomic hybridization analysis of a cohort of Saudi patients with epilepsy.

Faheem M, Naseer MI, Chaudhary AG, Kumosani TA, Rasool M, Algahtani HA, Bibi F, Kamal MA, Al-Qahtani MH. Faheem M, et al. Among authors: algahtani ha. CNS Neurol Disord Drug Targets. 2015;14(4):468-75. doi: 10.2174/1871527314666150429111737. CNS Neurol Disord Drug Targets. 2015. PMID: 25921748

2

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

3

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

4

Chromosomal Micro-aberration in a Saudi Family with Juvenile Myoclonic Epilepsy.

Naseer MI, Rasool M, Chaudhary AG, Sogaty S, Karim S, Schulten HJ, Bibi F, Pushparaj PN, Algahtani HA, Al-Qahtani MH. Naseer MI, et al. Among authors: algahtani ha. CNS Neurol Disord Drug Targets. 2017;16(9):1010-1017. doi: 10.2174/1871527316666170731103509. CNS Neurol Disord Drug Targets. 2017. PMID: 28758580

5

Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family.

Naseer MI, Rasool M, Abdulkareem AA, Bassiouni RI, Algahtani H, Chaudhary AG, Al-Qahtani MH. Naseer MI, et al. Neurosciences (Riyadh). 2018 Oct;23(4):347-350. doi: 10.17712/nsj.2018.4.20180095. Neurosciences (Riyadh). 2018. PMID: 30351297 Free PMC article.

6

Ataxia with ocular apraxia type 2 not responding to 4-aminopyridine: A rare mutation in the SETX gene in a Saudi patient.

Algahtani H, Shirah B, Algahtani R, Naseer MI, Al-Qahtani MH, Abdulkareem AA. Algahtani H, et al. Intractable Rare Dis Res. 2018 Nov;7(4):275-279. doi: 10.5582/irdr.2018.01107. Intractable Rare Dis Res. 2018. PMID: 30560021 Free PMC article.

7

A novel mutation in CACNA1A gene in a Saudi female with episodic ataxia type 2 with no response to acetazolamide or 4-aminopyridine.

Algahtani H, Shirah B, Algahtani R, Al-Qahtani MH, Abdulkareem AA, Naseer MI. Algahtani H, et al. Intractable Rare Dis Res. 2019 Feb;8(1):67-71. doi: 10.5582/irdr.2018.01133. Intractable Rare Dis Res. 2019. PMID: 30881862 Free PMC article.

8

A very rare form of autosomal dominant progressive myoclonus epilepsy caused by a novel variant in the PRICKLE1 gene.

Algahtani H, Al-Hakami F, Al-Shehri M, Shirah B, Al-Qahtani MH, Abdulkareem AA, Naseer MI. Algahtani H, et al. Seizure. 2019 Jul;69:133-139. doi: 10.1016/j.seizure.2019.04.016. Epub 2019 Apr 19. Seizure. 2019. PMID: 31035234 Free article.

9

A novel mutation in TTN gene in a Saudi patient with bilateral facial weakness and scapular winging.

Algahtani H, Shirah B, Algahtani R, Al-Qahtani MH, Abdulkareem AA, Naseer MI. Algahtani H, et al. Intractable Rare Dis Res. 2019 May;8(2):142-145. doi: 10.5582/irdr.2019.01052. Intractable Rare Dis Res. 2019. PMID: 31218166 Free PMC article.

10

Epilepsy and driving: Local experience from Saudi Arabia.

Algahtani H, Shirah B, Algahtani R, Algahtani R. Algahtani H, et al. Epilepsy Behav. 2019 Oct;99:106401. doi: 10.1016/j.yebeh.2019.07.002. Epub 2019 Aug 24. Epilepsy Behav. 2019. PMID: 31454705

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