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Publications by Qiuling Sang
Familial Normokalemic Periodic Paralysis Associated With Mutation in the SCN4A p.M1592V
Frontiers in Neurology
Neurology
Related publications
SCN4A p.R675Q Mutation Leading to Normokalemic Periodic Paralysis: A Family Report and Literature Review
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
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
Familial Hypokalemic Periodic Paralysis
Journal of the Neurological Sciences
Neurology
Familial Hypokalemic Periodic Paralysis: Case Report
Eurasian Journal of Family Medicine
Hypokalaemic Periodic Paralysis Associated With Hypothyroidism
Indian Journal of Physical Medicine and Rehabilitation
Familial Hypokalemic Periodic Paralysis With Myotonic Phenomenon : Case Report
Journal of Neurology and Neurological Disorders
Familial Hypokalemic Periodic Paralysis: A Case Report
Journal of Dr. Behcet Uz Children's Hospital
Overlap of Periodic Paralysis and Paramyotonia Congenita Caused by SCN4A Gene Mutations
Channels
Medicine
Biochemistry
Biophysics
