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Journal of Clinical Neuromuscular Disease
|
January 27, 2009
Finasteride-induced myalgia and HyperCKemia
Talal M Al-Harbi, Jennifer Kagan, Mark A Tarnopolsky
Journal of Clinical Neuromuscular Disease
|
November 19, 2016
Novel Homozygous Missense Mutation in CAPN3 Gene Detected in a Saudi Arabian Family With Limb-Girdle Muscular Dystrophy Type 2A
Talal M Al-Harbi, Sameeh O Abdulmanaʼ, Walid Dridi
The American Journal of Case Reports
|
February 10, 2015
Brain abscess following rituximab infusion in a patient with pemphigus vulgaris
Talal M Al-Harbi, Shahad A Al-Muammar, Ronald J Ellis
Journal of Clinical Neuromuscular Disease
|
August 28, 2019
Novel MFN2 Missense Mutation Induces Hereditary Axonal Motor and Sensory Neuropathy in a Saudi Arabian Family
Talal M Al-Harbi, Sameeh O Abdulmana, Shahid Bashir, et al.
Journal of Clinical Neuromuscular Disease
|
June 6, 2008
Hypogonadism is common in men with myopathies
Talal M Al-Harbi, Laura J Bainbridge, Matthew J McQueen, et al.
Neurology International
|
June 2, 2021
Fulminant Guillain-Barré Syndrome Post Hemorrhagic Stroke: Two Case Reports
Sameeh Abdulmana, Naif Al-Zahrani, Yahya Sharahely, et al.
Cureus
|
January 14, 2022
Colchicine-Induced Acute Myopathy: Case Study From Saudi Arabia
Moussa Al Megalli, Shahid Bashir, Hanaa Qadah, et al.
Frontiers in Neurology
|
December 30, 2024
Clinical presentations, electrophysiologic features, and long-term follow-up in Lambert-Eaton myasthenic syndrome: a series of six patients
Reem M Alhammad, Yafa Alshamlan, Ruwa Alneseyan, et al.
Cureus
|
June 14, 2023
Air Pollution and Its Adverse Effects on the Central Nervous System
Ameerah Ruzeeq Alhussaini, Meaad Refaay Aljabri, Zeyad T Al-Harbi, et al.
American Journal of Medical Genetics. Part A
|
October 12, 2021
Rare neurological manifestations in a Saudi Arabian patient with Ehlers-Danlos syndrome and a novel homozygous variant in the TNXB gene
Talal M Al-Harbi, Haya Al-Rammah, Naif Al-Zahrani, et al.
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Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Journal of Clinical Neuromuscular Disease
|
January 27, 2009
Finasteride-induced myalgia and HyperCKemia
Talal M Al-Harbi, Jennifer Kagan, Mark A Tarnopolsky
Journal of Clinical Neuromuscular Disease
|
November 19, 2016
Novel Homozygous Missense Mutation in CAPN3 Gene Detected in a Saudi Arabian Family With Limb-Girdle Muscular Dystrophy Type 2A
Talal M Al-Harbi, Sameeh O Abdulmanaʼ, Walid Dridi
The American Journal of Case Reports
|
February 10, 2015
Brain abscess following rituximab infusion in a patient with pemphigus vulgaris
Talal M Al-Harbi, Shahad A Al-Muammar, Ronald J Ellis
Journal of Clinical Neuromuscular Disease
|
August 28, 2019
Novel MFN2 Missense Mutation Induces Hereditary Axonal Motor and Sensory Neuropathy in a Saudi Arabian Family
Talal M Al-Harbi, Sameeh O Abdulmana, Shahid Bashir, et al.
Journal of Clinical Neuromuscular Disease
|
June 6, 2008
Hypogonadism is common in men with myopathies
Talal M Al-Harbi, Laura J Bainbridge, Matthew J McQueen, et al.
Neurology International
|
June 2, 2021
Fulminant Guillain-Barré Syndrome Post Hemorrhagic Stroke: Two Case Reports
Sameeh Abdulmana, Naif Al-Zahrani, Yahya Sharahely, et al.
Cureus
|
January 14, 2022
Colchicine-Induced Acute Myopathy: Case Study From Saudi Arabia
Moussa Al Megalli, Shahid Bashir, Hanaa Qadah, et al.
Frontiers in Neurology
|
December 30, 2024
Clinical presentations, electrophysiologic features, and long-term follow-up in Lambert-Eaton myasthenic syndrome: a series of six patients
Reem M Alhammad, Yafa Alshamlan, Ruwa Alneseyan, et al.
Cureus
|
June 14, 2023
Air Pollution and Its Adverse Effects on the Central Nervous System
Ameerah Ruzeeq Alhussaini, Meaad Refaay Aljabri, Zeyad T Al-Harbi, et al.
American Journal of Medical Genetics. Part A
|
October 12, 2021
Rare neurological manifestations in a Saudi Arabian patient with Ehlers-Danlos syndrome and a novel homozygous variant in the TNXB gene
Talal M Al-Harbi, Haya Al-Rammah, Naif Al-Zahrani, et al.
Page
of 2