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Publications by Morad Khayat

Fatal Infantile Mitochondrial Encephalomyopathy, Hypertrophic Cardiomyopathy and Optic Atrophy Associated With a homozygousOPA1mutation

Journal of Medical Genetics

English

Mammary-Digital-Nail (MDN) Syndrome: A Novel Phenotype Maps to Human Chromosome 22q12.3–13.1

European Journal of Human Genetics

English

Related publications

FASTKD2-related Infantile Mitochondrial Encephalomyopathy

English

Bilateral Optic Atrophy With Thickened Meninges (Idiopathic Hypertrophic Pachymeningitis) - A Rare Entity

English

Hypertrophic Cardiomyopathy in Patients With Diabetes Mellitus Associated With Mitochondrial tRNALeu(UUR) Gene Mutation.

Internal Medicine

Internal Medicine

English

Optic Neuropathy Associated With Hypertrophic Cranial Pachymeningitis.

British Journal of Ophthalmology

Molecular Neuroscience

Sensory Systems

English

Ehlers-Danlos Syndrome Associated With Cardiomyopathy Hypertrophic Obstructive

Anais Brasileiros de Dermatologia

English

Mitochondrial Cardiomyopathy Presenting as Dilated Phase of Hypertrophic Cardiomyopathy Diagnosed With Histological and Genetic Analyses

Case Reports in Cardiology

Cardiovascular Medicine

English

A Case of Systemic Lupus Erythematosus Associated With Hypertrophic Cardiomyopathy

Japanese Journal of Clinical Immunology

English

Severe Infantile-Onset Cardiomyopathy Associated With a Homozygous Deletion in Desmin

Neuromuscular Disorders

English

Hypertrophic Cardiomyopathy Associated With Sudden Death During Marathon Racing.

Cardiovascular Medicine

English