Disease: Continuous muscle fiber activity hereditary
- A case of neuromyotonia and axonal motor neuropathy: A report of a HINT1 mutation in the United States
- A Novel Variant in the HINT1 Gene in a Girl with Autosomal Recessive Axonal Neuropathy with Neuromyotonia: Thorough Neurological Examination Gives the Clue
- AAEM minimonograph #44: diseases associated with excess motor unit activity
- AAEM minimonograph #46: neurogenic muscle hypertrophy
- Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurologic phenotype
- Axonal neuropathy with neuromyotonia: there is a HINT
- Clinical and electrophysiological characterization of myokymia and neuromyotonia in Jack Russell Terriers
- Clinical Reasoning: A 6-Year-Old Boy With Muscle Twitching
- Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
- Continuous muscle activity, Morvan's syndrome and limbic encephalitis: ionic or non ionic disorders?
- Deleterious BRCA1/2 mutations in an urban population of Black women
- Diabetes and breast cancer among women with BRCA1 and BRCA2 mutations
- Disparities in uptake of BRCA1/2 genetic testing in a randomized trial of telephone counseling
- Familial spastic paraplegia with syndrome of continuous muscle fiber activity (Isaacs)
- Generalized myokymia, or neuromyotonia, or both in dogs with or without spinocerebellar ataxia
- Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
- Genetic basis of cancer of the kidney: disease-specific approaches to therapy
- Genetic testing for hereditary breast and ovarian cancer and the USPSTF recommendations
- Hereditary channelopathies in neurology
- Hereditary continuous muscle fiber activity
- Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies
- Hereditary myokymia and periodic ataxia
- HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling
- HINT1-related neuropathy in Greek patients with Charcot-Marie-Tooth disease
- How Far Do We Go With Genetic Evaluation? Gene, Panel, and Tumor Testing
- Identification of a novel NBN truncating mutation in a family with hereditary prostate cancer
- Immune-mediated neuromyotonia (Isaacs' syndrome)--clinical aspects and pathomechanism
- Immunological associations of acquired neuromyotonia (Isaacs' syndrome). Report of five cases and literature review
- Information and support needs of young women regarding breast cancer risk and genetic testing: adapting effective interventions for a novel population
- Late-onset hereditary axonal neuropathies
- Morvan's syndrome: peripheral and central nervous system and cardiac involvement with antibodies to voltage-gated potassium channels
- Motor unit hyperactivity states (a correlative clinico-electromyographical study)
- Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case report
- Myokymia and neuromyotonia in 37 Jack Russell terriers
- Myokymia and neuromyotonia in veterinary medicine: a comparison with peripheral nerve hyperexcitability syndrome in humans
- Neurological potassium channelopathies
- Neuromyotonia in a dachshund with clinical and electrophysiological signs of spinocerebellar ataxia
- Neuromyotonia in mice with hereditary myelinopathies
- Novel mutations in HINT1 gene cause autosomal recessive axonal neuropathy with neuromyotonia in two cases of sensorimotor neuropathy and one case of motor neuropathy
- Novel mutations in HINT1 gene cause the autosomal recessive axonal neuropathy with neuromyotonia
- Outcomes of 10 years of PSA screening for prostate cancer in Norwegian men with Lynch syndrome
- Prostate Cancer Predisposition
- Recurrent fevers
- Reifenstein's syndrome: hereditary familial hypogonadism with hypospadias and gynecomastia
- Role of Genetic Testing for Inherited Prostate Cancer Risk: Philadelphia Prostate Cancer Consensus Conference 2017
- Six generations of CHMP2B-mediated Frontotemporal Dementia: Clinical features, predictive testing, progression, and survival
- Spectrum of peripheral neuropathy in eastern India
- Streamlined Genetic Education and Cascade Testing in Men from Hereditary Breast Ovarian Cancer Families: A Randomized Trial