Nursing and Health Professions
Patient
100%
Diseases
28%
Thomsen Disease
28%
Periodic Paralysis
21%
Onset Age
14%
Inpatient
14%
Weakness
14%
Muscle Biopsy
14%
Myotonia
14%
Hypokalemic Periodic Paralysis
14%
Diagnosis
7%
Clinical Feature
7%
Isotopes of Potassium
7%
Absence
7%
Myopathy
7%
Coding
7%
Potassium Blood Level
7%
Ion Channel
7%
Calcium Channel
7%
Potassium Channel
7%
Acetazolamide
7%
Medicine and Dentistry
Diseases
28%
Thomsen Disease
28%
Gene
21%
Periodic Paralysis
21%
Phenotype
14%
Genotype
14%
Muscle Biopsy
14%
Onset Age
14%
Hypokalemic Periodic Paralysis
14%
Myotonia
14%
Weakness
14%
Clinical Feature
7%
Diagnosis
7%
Sodium Channel
7%
Potassium
7%
Diet
7%
Senescence
7%
Myopathy
7%
Orphan Disorder
7%
Ion Channel
7%
Calcium Channel
7%
Potassium Channel
7%
Acetazolamide
7%
Therapeutic Procedure
7%
Absence
7%
Biochemistry, Genetics and Molecular Biology
Mutation
50%
Paramyotonia congenita
28%
Nested Gene
21%
Phenotype
14%
Genotyping
14%
Coding Region
14%
Hypokalemic Periodic Paralysis
14%
Hyperkalemic Periodic Paralysis
14%
Sodium Channel
7%
Senescence
7%
Periodic Paralysis
7%
KCNE3
7%
Muscle Level
7%
Potassium Blood Level
7%
Potassium Channel
7%
Acetazolamide
7%
Age
7%