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Publications by Karen Suetterlin
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
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Progressive Muscle Atrophy With Hypokalaemic Periodic Paralysis and Calcium Channel Mutation
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Hypokalaemic Periodic Paralysis Associated With Hypothyroidism
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Familial Normokalemic Periodic Paralysis Associated With Mutation in the SCN4A p.M1592V
Frontiers in Neurology
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Hypokalaemic Periodic Paralysis (A Case Report)
Medical Journal of Indonesia
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A Family With Vocal Cord Paralysis Associated With GDAP1 Mutation in Giresun, Turkey
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Hypokalaemic Thyrotoxic Periodic Paralysis
Journal of the Royal Society of Medicine
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Aggressive Gastric Cancer in a Patient With an APC Mutation and a Monoallelic MYH Mutation
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Reduced Current Density and Surface Expression of a CLCN1 Mutation Causing Dominant or Recessive Myotonia in Costa Rica
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Mutation Analysis of CACNA1S and SCN4A in Patients With Hypokalemic Periodic Paralysis
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Molecular Biology
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