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Publications by Juraj Stanik

Mutations in SURF1 Are Important Genetic Causes of Leigh Syndrome in Slovak Patients

Endocrine Regulations

English

Related publications

Light and Electron Microscopy Characteristics of the Muscle of Patients With SURF1 Gene Mutations Associated With Leigh Disease

Journal of Clinical Pathology

Forensic Medicine

English

The Prevalence of Mitochondrial DNA Mutations in Leigh Syndrome in a Brazilian Series

Medical Express

English

Leigh Syndrome

English

Hematologically Important Mutations: Shwachman–Diamond Syndrome

Blood Cells, Molecules, and Diseases

Molecular Medicine

Molecular Biology

English

Clinical Case of Leigh Syndrome in an Infant

INTERNATIONAL NEUROLOGICAL JOURNAL

English

A Mutation in MT-TW Causes a tRNA Processing Defect and Reduced Mitochondrial Function in a Family With Leigh Syndrome

Molecular Medicine

Molecular Biology

English

Novel GRN Mutations in Patients With Corticobasal Syndrome

Scientific Reports

Multidisciplinary

English

Identification of Novel Genetic Causes of Rett Syndrome-Likephenotypes

Journal of Medical Genetics

English

Mitochondrial DNA-associated Leigh Syndrome

English