• <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 prognostic model for use before elective surgery to estimate the risk of postoperative pulmonary complications (GSU-Pulmonary Score): a development and validation study in three international cohorts
• A Rare Phenomenon of Isaacs Syndrome: A Case Report
• Altered Interoceptive Sensibility in Adults With Chronic Tic Disorder
• An Unusual Presentation of Dermatomyositis With Muscle Hypertrophy
• Anesthetic management of neuromyotonia. Description of a case
• Argyrophilic grain disease and co-pathologies in an older patient with a rapidly progressive neuropsychiatric syndrome
• Autoimmune neuromyotonia
• Bilateral Oculomotor Ocular Neuromyotonia-A Rare Case Due to Nasopharyngeal Carcinoma Radiotherapy
• 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 decision aids and computed tomography coronary angiography in patients with suspected acute coronary syndrome
• Clinical, neurophysiological and serological clues for the diagnosis of neuromyotonia and distinction from cramp-fasciculation syndrome
• Cognitive and psychiatric symptom trajectories 2-3 years after hospital admission for COVID-19: a longitudinal, prospective cohort study in the UK
• 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
• Continuous Glucose Monitoring Using the Dexcom G6 in Cardiac Surgery During the Postoperative Period
• 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
• Diagnostic Criteria for Primary Tic Disorders: Time for Reappraisal
• 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 Ca²⁺-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 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
• Generalized Peripheric Nerve Hyperexcitability with Neuropathy: Case Series with Long-Term Outcome
• Hematologic abnormalities in Aicardi Goutieres Syndrome
• 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 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
• 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
• 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
• Ocular neuromyotonia: an unusual case after radiotheraphy for nasopharyngeal carcinoma
• Ocular Neuromyotonia: Clinical Features, Diagnosis, and Outcomes
• Oculomotor Nerve Neuromyotonia: An Inflammatory Syndrome
• Oral management for a patient with trismus accompanied by Isaacs' syndrome: a case report
• 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
• 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
• 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
• Specialist physiotherapy for functional motor disorder in England and Scotland (Physio4FMD): a pragmatic, multicentre, phase 3 randomised controlled trial
• Standing genetic variation affects phenotypic heterogeneity in an SCN5A-mutation founder population with excess sudden cardiac death
• Streamlined Genetic Education and Cascade Testing in Men from Hereditary Breast Ovarian Cancer Families: A Randomized Trial
• 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
• The Association of Quality of Life with Psychosocial Factors in Adolescents with Tourette Syndrome
• The c.126C&gt;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
• The risk of malignant hyperthermia in neuromyotonia is low
• Thyroid peroxidase antibodies may induce demyelination and oculomotor neuromyotonia in the absence of thyroid eye disease
• When muscle quivers and undulates