Mohammad H Al-Qahtani
Overview
Explore the profile of Mohammad H Al-Qahtani including associated specialties, affiliations and a list of published articles.
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47
Citations
392
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Recent Articles
11.
Al-Qahtani M, Yousef A, Awary B, Albuali W, Al Ghamdi M, AlOmar R, et al.
BMC Emerg Med
. 2021 Aug;
21(1):99.
PMID: 34454412
No abstract available.
12.
Al-Qahtani M, Yousef A, Awary B, Albuali W, Al Ghamdi M, AlOmar R, et al.
BMC Emerg Med
. 2021 Jun;
21(1):72.
PMID: 34154525
Background: The Emergency Repartment (ER) is one of the most used areas in healthcare institutions. Problems with over utilisation and overcrowding have been reported worldwide. This study aims at examining...
13.
Algahtani H, Shirah B, Ullah I, Al-Qahtani M, Abdulkareem A, Naseer M
Genes Dis
. 2021 Feb;
8(1):110-114.
PMID: 33569519
The nonlysosomal glucosylceramidase β2 () gene encode an enzyme that catalyzes the hydrolysis of glucosylceramide to glucose and ceramide. Mutations in the gene have been reported to cause hereditary spastic...
14.
Albuali W, Algamdi A, Hasan E, Al-Qahtani M, Yousef A, Al Ghamdi M, et al.
J Multidiscip Healthc
. 2020 Nov;
13:1507-1516.
PMID: 33204099
Purpose: Currently, several scoring systems for predicting mortality in severely ill children who require treatment in a pediatric intensive care unit (PICU) have been established. However, despite providing high-quality care,...
15.
Algahtani H, Shirah B, Daghistani M, Al-Qahtani M, Abdulkareem A, Naseer M
Neuropediatrics
. 2020 Oct;
52(2):150-152.
PMID: 33065750
No abstract available.
16.
A Novel Variant in CWF19L1 Gene in a Family with Late-Onset Autosomal Recessive Cerebellar Ataxia 17
Algahtani H, Shirah B, Almatrafi S, Al-Qahtani M, Abdulkareem A, Naseer M
Neurol Res
. 2020 Oct;
43(2):141-147.
PMID: 33012273
Introduction: Previously published studies demonstrated that mutations in cause early-onset autosomal recessive cerebellar ataxia 17. In this article, we report a novel homozygous missense variant in in two sisters who...
17.
Algahtani H, Shirah B, Albarakaty A, Al-Qahtani M, Abdulkareem A, Naseer M
J Epilepsy Res
. 2020 Sep;
10(1):40-43.
PMID: 32983954
Cerebral metabolism is primarily dependent on glucose for which a facilitated diffusion by glucose transporter protein 1 (GLUT1) across the blood-brain barrier is crucial. This GLUT1 is encoded by the...
18.
Naseer M, Abdulkareem A, Jan M, Chaudhary A, Al-Qahtani M
Pak J Med Sci
. 2020 Sep;
36(6):1425-1428.
PMID: 32968423
Objective: To study the causative variants in affected member of a Saudi family with Tay-Sachs disorder. This disorder includes paralysis, decreasing in attentiveness, seizures, blindness, motor deterioration progresses rapidly leading...
19.
Algahtani H, Shirah B, Alshareef A, Al-Qahtani M, Abdulkareem A, Naseer M
Intractable Rare Dis Res
. 2020 Aug;
9(3):151-155.
PMID: 32844072
Alzheimer's disease (AD) is the most common cause of dementia with around 50 million people suffering from this disease worldwide. Mutations in the ATP-binding cassette sub-family A member 7 ()...
20.
Algahtani H, Shirah B, Alharbi S, Al-Qahtani M, Abdulkareem A, Naseer M
J Stroke Cerebrovasc Dis
. 2020 May;
29(7):104832.
PMID: 32414585
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL; OMIM #125310) is the most common cause of monogenic familial cerebral small vessel disease. It typically manifests at middle adulthood...