Disease: Myasthenia- familial
- A family with early onset myopathy caused by MEGF10 gene defect and literature review
- A novel <em>DOK7</em> mutation causing congenital myasthenic syndrome with limb-girdle weakness: case series of three family members
- A novel DOK7 mutation causing congenital myasthenic syndrome with limb-girdle weakness: case series of three family members
- A Rare Case of Lambert-Eaton Myasthenia Syndrome Associated with Non-Hodgkin's Lymphoma: A Case Report and Review of the Literature
- Altered gut microbiota and metabolites in untreated myasthenia gravis patients
- Analysis of clinical characteristics and related genetic variation of juvenile myasthenia gravis
- Antibody Response to HERV-K and HERV-W Envelope Epitopes in Patients with Myasthenia Gravis
- Association between systemic lupus erythematosus and myasthenia gravis: A population-based National Study
- Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis
- Associations between autoimmune diseases and amyotrophic lateral sclerosis: a register-based study
- Autoimmune Diseases in Patients With Myotonic Dystrophy Type 2
- Causal relationship between gut microbiota and myasthenia gravis: a bidirectional mendelian randomization study
- Causal relationship between gut microbiota and myasthenia gravis: a two-sample Mendelian randomization study
- Clinical characteristics of anti-CV2 antibody-associated neurological diseases
- Clinical delineation of myasthenia gravis in the Kingdom of Bahrain
- Clinical spectrum of myasthenia gravis: An institute experience over 8 years from North East India
- Clinical, Histological, and Genetic Features of 25 Patients with Autosomal Dominant Progressive External Ophthalmoplegia (ad-PEO)/PEO-Plus Due to <em>TWNK</em> Mutations
- Comparative the efficacy and acceptability of immunosuppressive agents for myasthenia gravis: A protocol for systematic review and network meta-analysis
- Comparison of Short-Term Post-Thymectomy Outcomes by Time-Weighted Dosages of Drug Requirements between Thymoma and Non-Thymoma Myasthenia Gravis Patients
- Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian families
- DCAF12 and HSPA1A May Serve as Potential Diagnostic Biomarkers for Myasthenia Gravis
- Decision for early tracheostomy in respiratory failure of a paralyzed myasthenia gravis patient with sepsis-induced pneumonia: A case report
- Developing the health state classification system for a condition-specific preference-based measure for patients with myasthenia gravis
- Development and characterization of agonistic antibodies targeting the Ig-like 1 domain of MuSK
- Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy
- Downregulation of DNMT3a expression by RNAi and its effect on NF-κBs expression of thymic epithelial cells
- Dynamics of patents, orphan drug designation, licensing, and revenues from drugs for rare diseases: The market expansion of eculizumab
- Effect of Fufang Huangqi Decoction on the Gut Microbiota in Patients With Class I or II Myasthenia Gravis
- Effects of Qishen Dihuang Granules on Intestinal Microbiota in Experimental Autoimmune Myasthenia Gravis Model Rats
- Evidence for genetic causal relationships between gut microbiome, metabolites, and myasthenia gravis: a bidirectional Mendelian randomization study
- Exacerbation Rate in Generalized Myasthenia Gravis and Its Predictors
- Experience of Daily Life with Generalized Myasthenia Gravis: A Qualitative Investigation and Assessment of Instrument Content Validity
- Explainable machine learning model for identifying key gut microbes and metabolites biomarkers associated with myasthenia gravis
- Factors associated with the disease family burden of caregivers of myasthenia gravis patients in northwestern China: A cross-sectional study
- Familial autoimmunity in patients with idiopathic inflammatory myopathies
- Family Game Show-style Didactic for Teaching Nervous System Disorders during Emergency Medicine Training
- Fetal Surveillance in Pregnancies with Myasthenia Gravis
- Five-Month Trial of Whole-Food Plant-Based Diet in a Patient With Coexisting Myasthenia Gravis and Lambert-Eaton Myasthenic Syndrome
- FOXM1: Functional Roles of FOXM1 in Non-Malignant Diseases
- Fracture Risk in Patients with Myasthenia Gravis: A Population-Based Cohort Study
- Genetic analysis of a Chinese pedigree affected with atypical Charcot-Marie-Tooth disease type 1A due to duplication of PMP22 gene
- GFPT1-Associated Congenital Myasthenic Syndrome Mimicking a Glycogen Storage Disease - Diagnostic Pitfalls in Myopathology Solved by Next-Generation-Sequencing
- Idiopathic multicentric Castleman disease and associated autoimmune and autoinflammatory conditions: practical guidance for diagnosis
- Immune checkpoint inhibitor-induced myocarditis with myasthenia gravis overlap syndrome: A case report and literature review
- Impact of the COVID-19 Pandemic on People Living With Rare Diseases and Their Families: Results of a National Survey
- Implications of COVID-19 On A Rapidly Growing Thymoma Case
- Improving the efficacy of exome sequencing at a quaternary care referral centre: novel mutations, clinical presentations and diagnostic challenges in rare neurogenetic diseases
- In sickness and in health: when myasthenia gravis is a conjugal matter
- Investigating the possible association between NLRP3 gene polymorphisms and myasthenia gravis
- Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies
- JNO Literature Commentary
- Lipin 1 deficiency causes adult-onset myasthenia with motor neuron dysfunction in humans and neuromuscular junction defects in zebrafish
- Lower BAFF Levels in Myasthenic Patients Treated with Glucocorticoids
- Machine learning strategy for identifying altered gut microbiomes for diagnostic screening in myasthenia gravis
- Major histocompatibility complex (MHC) associations with diseases in ethnic groups of the Arabian Peninsula
- Mechanisms of Congenital Myasthenia Caused by Three Mutations in the <em>COLQ</em> Gene
- Mechanisms of Congenital Myasthenia Caused by Three Mutations in the COLQ Gene
- Mendelian randomization study revealed a gut microbiota-neuromuscular junction axis in myasthenia gravis
- Mental health in myasthenia gravis patients and its impact on caregiver burden
- Metagenome-wide association study of gut microbiome revealed potential microbial marker set for diagnosis of pediatric myasthenia gravis
- Myasthenia gravis and economic burden: Exploring the impact of family dynamics on financial strain
- Myasthenia Gravis and Pregnancy: Toronto Specialty Center Experience
- Myasthenia gravis-Gender aspects and family planning
- Myasthenic crisis-induced Takotsubo cardiomyopathy in an elderly man: A case report of an underestimated but deadly combination
- Neuromuscular Diseases Care in the Era of COVID-19
- Neuromyelitis Optica Spectrum Disorder
- New acute onset of ocular myasthenia gravis after COVID-19 vaccine: A case report
- Nivolumab-Induced Myasthenia Gravis Concomitant With Myocarditis, Myositis, and Hepatitis
- Nivolumab, a Double-Edged Sword: A Case Report of Nivolumab-Induced Myasthenia Gravis
- Outcome of therapeutic plasma exchange in Myasthenia gravis patients
- Pediatric Neuromuscular Diseases
- Perry Syndrome with a Novel Mutation and a Rare Presentation: First Report from India
- POTEE mutation as a potential predictive biomarker for immune checkpoint inhibitors in lung adenocarcinoma
- Pregnancy loss and risk of multiple sclerosis and autoimmune neurological disorder: A nationwide cohort study
- Prenatal diagnosis of isolated bilateral clubfoot: Is amniocentesis indicated?
- Prevalence of depression among Iranian patients with myasthenia gravis during 2017-2018
- Provisional practice recommendation for the management of myopathy in VCP-associated multisystem proteinopathy
- Psychopharmacological Treatments for Mental Disorders in Patients with Neuromuscular Diseases: A Scoping Review
- Ptosis Correction
- Ptosis Correction
- Rechallenge of immune checkpoint inhibitors in a case with adverse events inducing myasthenia gravis
- Retrospective study on the safety of COVID-19 vaccination in myasthenia gravis
- Rituximab in the Management of Refractory Myasthenia Gravis and Variability of Its Efficacy in Anti-MuSK Positive and Anti-AChR Positive Myasthenia Gravis
- Role of Toll-Like Receptors in Neuroimmune Diseases: Therapeutic Targets and Problems
- Seronegative Ocular Myasthenia Gravis in an Older Woman With Transient Dizziness and Diplopia
- Serum Pentaxin 3 (PTX3) Promotes NLRP3 Inflammasome and Pyroptosis in Patients with Up-Regulated Myasthenia Gravis
- Serum pentraxin 3 concentration correlates with disease severity in patients with myasthenia gravis
- Socio-Economic Burden of Myasthenia Gravis: A Cost-of-Illness Study in Bulgaria
- Special Issue: Immune-Mediated Neurological Disorders
- The association of chemotherapy-induced peripheral neuropathy with reduced executive function in chemotherapy-treated cancer survivors: A cross-sectional study
- The burden of myasthenia gravis - highlighting the impact on family planning and the role of social support
- The investigation of killer-cell immunoglobulin-like receptors (KIRs) and their HLA ligands in Iranian patients with myasthenia gravis
- The Parallel World of Dyspnea: A Case Report
- The role of thymectomy in myasthenia gravis: A programmatic approach to thymectomy and perioperative management of myasthenia gravis
- Thyrotoxic hypokalemic periodic paralysis and COVID-19 infection
- Transient Neonatal Myasthenia Gravis Born to a Mother with Asymptomatic MG: A Case Report
- Transient Neonatal Myasthenia Gravis: A Case Report
- Understanding the Symptom Burden and Impact of Myasthenia Gravis from the Patient's Perspective: A Qualitative Study
- Unraveling the Immune Microenvironment of Thymic Epithelial Tumors: Implications for Autoimmunity and Treatment
- Whole-exome sequencing and human leukocyte antigen analysis in familial myasthenia gravis with thymoma: Case report and literature review