Disease: Pseudomyotonia
- <em>HINT1</em>-Associated Axonal Neuropathy with Neuromyotonia
- A nanobody recognizes a unique conserved epitope and potently neutralizes SARS-CoV-2 omicron variants
- A novel mutation in HINT1 gene causes autosomal recessive axonal neuropathy with neuromyotonia, effective treatment with carbamazepine and review of the literature
- A platform technology for generating subunit vaccines against diverse viral pathogens
- A practical use of noninvasive tests in clinical practice to identify high-risk patients with nonalcoholic steatohepatitis
- A randomized, double-blind, placebo- and positive-controlled crossover study of the effects of durlobactam on cardiac repolarization in healthy subjects
- A Rare Phenomenon of Isaacs Syndrome: A Case Report
- Adapting Medication for Type 2 Diabetes to a Low Carbohydrate Diet
- Altered Interoceptive Sensibility in Adults With Chronic Tic Disorder
- An Unusual Case of Muscle Twitching: Its LGI1
- An Unusual Presentation of Dermatomyositis With Muscle Hypertrophy
- Anesthetic management of neuromyotonia. Description of a case
- Anti-voltage-Gated Potassium Channel (VGKC) Antibodies and Acquired Neuromyotonia in Patients with Immune Dysregulation, Polyendocrinopathy, Enteropathy X-Lined (IPEX) Syndrome
- Argyrophilic grain disease and co-pathologies in an older patient with a rapidly progressive neuropsychiatric syndrome
- Autoimmune neuromyotonia
- Canadian Rheumatology Association Meeting Quebec City Convention Centre Quebec City, Quebec, Canada February 8-11, 2023
- Characterization and comparison of novel adjuvants for a prefusion clamped MERS vaccine
- Clinical characteristics with inflammation profiling of long COVID and association with 1-year recovery following hospitalisation in the UK: a prospective observational study
- Clinical Correlates of Health-Related Quality of Life in Adults With Chronic Tic Disorder
- Clinical, neurophysiological and serological clues for the diagnosis of neuromyotonia and distinction from cramp-fasciculation syndrome
- Comment on: Proposal for a new diagnostic classification of photodistributed Stevens-Johnson syndrome and toxic epidermal necrolysis
- Comparison of clinical features between patients with anti-synthetase syndrome and dermatomyositis: Results from the MYONET registry
- Complete protection by a single-dose skin patch-delivered SARS-CoV-2 spike vaccine
- Consensus statement on blocking interleukin-6 receptor and interleukin-6 in inflammatory conditions: an update
- Conversion of Superior Oblique Myokymia to Superior Oblique Neuromyotonia in a Patient With History of Superior Oblique Palsy
- CORR Insights®: What Factors Are Associated With Revision Cubital Tunnel Release Within 3 Years?
- Correlation Between Postvaccination Anti-Spike Antibody Titers and Protection Against Breakthrough Severe Acute Respiratory Syndrome Coronavirus 2 Infection: A Population-Based Longitudinal Study
- Cross-disorder comparison of sensory over-responsivity in chronic tic disorders and obsessive-compulsive disorder
- De novo variants identified by trio whole exome sequencing of bladder exstrophy epispadias complex
- Demystifying the spontaneous phenomena of motor hyperexcitability
- Differential Analysis of Gly211Val and Gly286Val Mutations Affecting Sarco(endo)plasmic Reticulum Ca(2+)-ATPase (SERCA1) in Congenital Pseudomyotonia Romagnola Cattle
- Differential Analysis of Gly211Val and Gly286Val Mutations Affecting Sarco(endo)plasmic Reticulum Ca<sup>2+</sup>-ATPase (SERCA1) in Congenital Pseudomyotonia Romagnola Cattle
- Dimensional Assessment of Depression and Anxiety in a Clinical Sample of Adults With Chronic Tic Disorder
- Does spatial perspective in virtual reality affect imitation accuracy in stroke patients?
- Early computed tomography coronary angiography in patients with suspected acute coronary syndrome: randomised controlled trial
- Early Outcomes of SARS-CoV-2 Infection in a Multisite Prospective Cohort of Inpatient Veterans
- Effectiveness of therapeutic plasma exchange in case of rare neurological disorder Isaacs syndrome
- Electrodiagnostic Assessment of Hyperexcitable Nerve Disorders
- EULAR recommendations for the management and vaccination of people with rheumatic and musculoskeletal diseases in the context of SARS-CoV-2: the November 2021 update
- Evaluation of Autoantibody Binding to Cardiac Tissue in Multisystem Inflammatory Syndrome in Children and COVID-19 Vaccination-Induced Myocarditis
- Exploration of Gross Motor Function in Aicardi-Goutieres Syndrome
- Generalized myokymia, or neuromyotonia, or both in dogs with or without spinocerebellar ataxia
- Hematologic abnormalities in Aicardi Goutieres Syndrome
- HINT1 founder mutation causing axonal neuropathy with neuromyotonia in South America: A case report
- HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling
- HINT1 neuropathy: Expanding the genotype and phenotype spectrum
- HINT1-related neuropathy in Greek patients with Charcot-Marie-Tooth disease
- Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour
- Identification of High Risk NAFLD Patients in Endocrinology Clinics
- Identification of High-Risk Patients With Nonalcoholic Fatty Liver Disease in Endocrinology Clinics
- Inflammatory myopathy occurring shortly after severe acute respiratory syndrome coronavirus 2 vaccination: two case reports
- Isaacs syndrome with LGI1 and CASPR2 antibodies after HPV vaccination: A case report
- Isaacs' syndrome as the initial presentation of malignant thymoma and associated with double-positive voltage-gated potassium channel complex antibodies, a case report
- Large-scale phenotyping of patients with long COVID post-hospitalization reveals mechanistic subtypes of disease
- Leucine-rich Glioma-inactivated 1 Encephalitis Followed by Isaacs Syndrome: Alternating Presence of Pathogenic Autoantibodies to Leucine-rich Glioma-inactivated 1 and Contactin-associated Protein-like 2
- Long COVID research: an update from the PHOSP-COVID Scientific Summit
- Mercury poisoning complicated by acquired neuromyotonia syndrome: A case report
- Monoclonal Antibodies Specific for SARS-CoV-2 Spike Protein Suitable for Multiple Applications for Current Variants of Concern
- Morvan Syndrome Converted from Isaacs' Syndrome after Thymectomy with Positivity for Both Anti-LGI1 and Anti-CASPR2 Antibodies
- Morvan's syndrome Presenting with Psychiatric Manifestations - A Case Report and Review of the Literature
- Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case report
- Neonatal Outcomes after Combined Opioid and Nicotine Exposure in Utero: A Scoping Review
- Neuromuscular junction disorders beyond myasthenia gravis
- Neuromuscular Ultrasound Findings of Myokymia in a Young Woman With Generalized Anti-LGI-1 and Anti-Caspr2 Antibodies Negative Isaac Syndrome
- Neuromyotonia: a skin-deep problem
- Nonalcoholic Fatty Liver Disease
- Occult bowel cancer presenting as Morvan syndrome
- Ocular Neuromyotonia in Children and Adolescents Following Radiation Treatment of Pediatric Brain Tumors
- Ocular neuromyotonia: a review of diagnosis and treatment
- Outcomes of 10 years of PSA screening for prostate cancer in Norwegian men with Lynch syndrome
- Overall survival in the OlympiA phase III trial of adjuvant olaparib in patients with germline pathogenic variants in BRCA1/2 and high-risk, early breast cancer
- Paraneoplastic autoimmune neurologic disorders associated with thymoma
- Paraneoplastic neuropathies and peripheral nerve hyperexcitability disorders
- Perspectives from Adults with Tourette Syndrome on Research Priorities and Registry Development: A Focus Group Study
- Post-acute COVID-19 neuropsychiatric symptoms are not associated with ongoing nervous system injury
- Post-Irradiation Facial Neuromyotonia/Myokymia: A Hemifacial Spasm Mimic
- Preclinical development of a molecular clamp-stabilised subunit vaccine for severe acute respiratory syndrome coronavirus 2
- Prostate Cancer Predisposition
- Rare diseases in the differential diagnosis of myalgia
- Rare diseases in the differential diagnosis of myalgia
- Respiratory infections and type 1 diabetes: Potential roles in pathogenesis
- Retinal Vasculitis in a Patient With Isaacs Syndrome and Inclusion Body Myositis
- Rituximab Was Effective in Relieving Symptoms of Isaacs Syndrome: A Case Report
- SARS-CoV-2 neutralizing antibodies: Longevity, breadth, and evasion by emerging viral variants
- Senolytic therapy alleviates physiological human brain aging and COVID-19 neuropathology
- Short communication: Prevalence of deleterious variants causing recessive disorders in Italian Chianina, Marchigiana and Romagnola cattle
- Simultaneous Ocular Motor Neuromyotonia and Aberrant Regeneration in Metastatic Cavernous Sinus Disease
- Six generations of CHMP2B-mediated Frontotemporal Dementia: Clinical features, predictive testing, progression, and survival
- Standing genetic variation affects phenotypic heterogeneity in an SCN5A-mutation founder population with excess sudden cardiac death
- Surgical treatment of craniovertebral junction instability in children with Down syndrome: a systematic review
- Symptom-based stratification of patients with primary Sjögren's syndrome: multi-dimensional characterisation of international observational cohorts and reanalyses of randomised clinical trials
- Systematic Review of the Clinical Characteristics and Management of Isaac Syndrome
- Tacrolimus as a therapeutic option in patients with acquired neuromyotonia
- Teaching Video NeuroImage: Clenched Fists as an Unusual Presentation of Focal Neuromyotonia
- The Association of Quality of Life with Psychosocial Factors in Adolescents with Tourette Syndrome
- The c.126C>A(p.(Cys42Ter)) SLC7A10 nonsense variant is a candidate causative variant for paradoxical pseudomyotonia in English Cocker and Springer Spaniels
- The c.126C>A(p.(Cys42Ter)) SLC7A10 nonsense variant is a candidate causative variant for paradoxical pseudomyotonia in English Cocker and Springer Spaniels
- The interferon gene signature as a clinically relevant biomarker in autoimmune rheumatic disease
- Thyroid peroxidase antibodies may induce demyelination and oculomotor neuromyotonia in the absence of thyroid eye disease
- When muscle quivers and undulates