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Publications by Bader Shirah

A Novel Mutation in CACNA1A Gene in a Saudi Female With Episodic Ataxia Type 2 With No Response to Acetazolamide or 4-Aminopyridine

Intractable and Rare Diseases Research

English

Post-Partum Headache Caused by Dual Pathology: A Message to the Anesthetist

English

Related publications

Identification of a Novel Nonsense Mutation p.Tyr1957Ter of CACNA1A in a Chinese Family With Episodic Ataxia 2

Multidisciplinary

English

A Novel KCNA1 Mutation in a Family With Episodic Ataxia and Malignant Hyperthermia

Molecular Neuroscience

English

Detection of a Novel Mutation in the CACNA1A Gene

Twin Research and Human Genetics

English

Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency: A Novel Mutation With Prominent Ataxia

Movement Disorders Clinical Practice

English

Pearls & Oy-Sters: Episodic Ataxia Type 2

English

Identification of a Novel MEN1 Gene Mutation in Saudi Arabian Patient With Multiple Endocrine Tumors

Endocrinology&Metabolism International Journal

English

A Novel POLG Gene Mutation in a Patient With SANDO

Journal of Experimental and Integrative Medicine

Alternative Medicine

English

A Novel Missense Mutation T101N in the Melanocortin-4 Receptor Gene Associated With Obesity

Genetics and Molecular Research

Molecular Biology

English

Progressive Ataxia Due to a Missense Mutation in a Calcium-Channel Gene

American Journal of Human Genetics

English