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Publications by Emma Matthews

Genotype–phenotype Association in Patients With SCN4A Mutation – Authors' Reply

The Lancet
Medicine
2019English

Mutations in XRCC1 Cause Cerebellar Ataxia and Peripheral Neuropathy

Journal of Neurology, Neurosurgery and Psychiatry
PsychiatryMental HealthNeurologySurgery
2018English

Acetazolamide Can Improve Symptoms and Signs in Ion Channel-Related Congenital Myopathy

Journal of Neurology, Neurosurgery and Psychiatry
PsychiatryMental HealthNeurologySurgery
2018English

Myotonia in a Patient With a Mutation in an S4 Arginine Residue Associated With Hypokalaemic Periodic Paralysis and a Concomitant Synonymous CLCN1 Mutation

Scientific Reports
Multidisciplinary
2019English

National Registry for Sudden Unexpected Deaths of Infants and Children in England: Why Do We Need One and Do Families Want One?

Archives of Disease in Childhood
Child HealthPediatricsPerinatology
2019English

Sodium and Chloride Channelopathies With Myositis: Coincidence or Connection?

Muscle and Nerve
Molecular NeuroscienceNeurologyPhysiologyCellular
2011English

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