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Publications by F Brancati
Severe Infantile Hyperkalaemic Periodic Paralysis and Paramyotonia Congenita: Broadening the Clinical Spectrum Associated With the T704M Mutation in SCN4A
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Related publications
Overlap of Periodic Paralysis and Paramyotonia Congenita Caused by SCN4A Gene Mutations
Channels
Medicine
Biochemistry
Biophysics
Familial Normokalemic Periodic Paralysis Associated With Mutation in the SCN4A p.M1592V
Frontiers in Neurology
Neurology
Mutation Analysis of CACNA1S and SCN4A in Patients With Hypokalemic Periodic Paralysis
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
SCN4A p.R675Q Mutation Leading to Normokalemic Periodic Paralysis: A Family Report and Literature Review
Frontiers in Neurology
Neurology
Hyperkalaemic Ascending Paralysis
Journal of the Royal Society of Medicine
Medicine
A Variety of Paramyotonia Congenita
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Hypokalaemic Periodic Paralysis Associated With Hypothyroidism
Indian Journal of Physical Medicine and Rehabilitation
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
Progressive Muscle Atrophy With Hypokalaemic Periodic Paralysis and Calcium Channel Mutation
Aktuelle Neurologie
Neurology
