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Publications by Alexa K. Craig

Dravet Syndrome: Patients With Co-Morbid SCN1A Gene Mutations and Mitochondrial Electron Transport Chain Defects

Seizure : the journal of the British Epilepsy Association

English

Related publications

Clinical and Genetic Factors Predicting Dravet Syndrome in Infants With SCN1A Mutations

English

Analysis of SCN1A Mutation and Parental Origin in Patients With Dravet Syndrome

Journal of Human Genetics

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Expecting the Unexpected: Lack of in Vivo Network Defects in an Scn1a Model of Dravet Syndrome

Epilepsy Currents

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Co-Morbid Disorders in Tourette Syndrome

Behavioural Neurology

Physiological Psychology

Neuropsychology

English

Drug Screening in Scn1a Zebrafish Mutant Identifies Clemizole as a Potential Dravet Syndrome Treatment

Nature Communications

Molecular Biology

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Four Novel Thymidine Phosphorylase Gene Mutations in Mitochondrial Neurogastrointestinal Encephalomyopathy Syndrome (MNGIE) Patients

European Journal of Human Genetics

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Cerebral Mitochondrial Electron Transport Chain Dysfunction in Multiple System Atrophy and Parkinson’s Disease

Scientific Reports

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Mutations in the FGFR2 Gene in Mexican Patients With Apert Syndrome

Genetics and Molecular Research

Molecular Biology

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Frequency of Mitochondrial Transfer RNA Mutations and Deletions in 225 Patients Presenting With Respiratory Chain Deficiencies

Journal of Medical Genetics

English