Inflammatory and Autoimmune Aspects of Multisystem Inflammatory Syndrome in Children (MIS-C): A Prospective Cohort Study., PMID:38932242
Morvan Fibrillary Chorea Associated with Monoclonal B Cell Lymphocytosis., PMID:38963810
Proteinuria is a key to suspect autoimmune nodopathies., PMID:38980226
Distinct plasma metabolomic signatures differentiate autoimmune encephalitis from drug-resistant epilepsy., PMID:39012808
Anti-contact protein-associated protein 2 antibody encephalitis in children: A case report., PMID:39015900
Morvan's syndrome with hypercoagulable condition in a patient positive for anti-CASPR2 antibodies: A case report., PMID:39029039
Anti-contactin-associated protein 1 antibody-positive nodopathy presenting with central nervous system symptoms., PMID:39084134
Autoimmune Encephalitis., PMID:39088286
Antibodies in Autoimmune Neuropathies: What to Test, How to Test, Why to Test., PMID:39088795
IgG subclass shifts occurring at acute exacerbations in autoimmune nodopathies., PMID:39093334
Human cerebrospinal fluid monoclonal CASPR2 autoantibodies induce changes in electrophysiology, functional MRI, and behavior in rodent models., PMID:39142424
Different Patterns of Autoantibody Secretion by Peripheral Blood Mononuclear Cells in Autoimmune Nodopathies., PMID:39173087
Neuromyotonia., PMID:39174249
Autoantibody-mediated central nervous system channelopathies., PMID:39174251
Clinical characteristics and long-term outcome of CASPR2 antibody-associated autoimmune encephalitis in children., PMID:39183357
The difference in nerve ultrasound and motor nerve conduction studies between autoimmune nodopathy and chronic inflammatory demyelinating polyneuropathy., PMID:39205380
Characteristics of anti-contactin1 antibody positive autoimmune nodopathies combined with membranous nephropathy., PMID:39317078
MRI findings in autoimmune encephalitis., PMID:39358087
[Pathomechanism Underlying Intravenous Immunoglobulin Therapy for Chronic Inflammatory Demyelinating Polyneuropathy]., PMID:39370835
Uncommon Pediatric Immune-Mediated Epilepsy: Disease Course, Diagnosis, and Outcome - A Series of Three Cases., PMID:39377237
Contactin-4 suppresses antitumor T cell responses by engaging amyloid precursor protein., PMID:39392894
Humoral signatures of Caspr2-antibody spectrum disorder track with clinical phenotypes and outcomes., PMID:39393351
Antibody-Mediated Nodo- and Paranodopathies., PMID:39407781
Isaacs' syndrome: Clinical and paraclinical perspectives in a series of cases., PMID:39431227
A case series: Three cases of Morvan's syndrome as a rare autoimmune disorder with anti-Caspr2 antibody., PMID:39432629
Case report: target antigen and subclass switch in a patient with autoimmune nodopathy., PMID:39434877
Prevalence and clinical implications of diabetes mellitus in autoimmune nodopathies: A systematic review., PMID:39461229
Kidney injury: An overlooked manifestation in autoimmune encephalitis., PMID:39486221
Histiocytic necrotizing lymphadenitis with autoimmune encephalitis in a child: a case report., PMID:39524397
Case report: Recurring potassium channel complex autoimmunity-related neuropathic pain., PMID:39524448
Long-Term Follow Up in Anti-Contactin-1 Autoimmune Nodopathy., PMID:39601182
Quantitative proteomics analysis of cerebrospinal fluid reveals putative protein biomarkers for canine non-infectious meningoencephalomyelitis., PMID:39662837
The Discovery of Autoimmune Nodopathies and the Impact of IgG4 Antibodies in Autoimmune Neurology., PMID:39671536
CASPR2-related epilepsy: A distinctive and unrecognized form of epilepsy in adult and elderly males., PMID:39688843
Favorable long-term outcomes of autoimmune nodopathy with mycophenolate mofetil., PMID:39726762
The overlap of diabetic and inflammatory neuropathies: Epidemiology, possible mechanisms, and treatment implications., PMID:39798331
Immunotherapy-Resistant Neuropathic Pain and Fatigue Predict Quality-of-Life in Contactin-Associated Protein-Like 2 Antibody Disease., PMID:39825737
A Rare Case of Anti-Caspr2 Autoimmune Encephalitis Associated with a Testicular Mixed Germ Cell Tumor., PMID:39839164
Varied Clinical Features and Outcomes of Autoimmune Encephalitis: A Retrospective Case Series., PMID:39866989
Inter-Laboratory Validation of Nodal/Paranodal Antibody Testing., PMID:39887819
Heterogeneity of anti-Caspr2 antibodies: specificity and pathogenicity., PMID:39896527
Prevalence, clinical profiles, and prognosis of Isaacs syndrome: A nationwide survey study in Japan., PMID:40058033
Activated αβ T- and reduced mucosa-associated invariant T cells in LGI1- and CASPR2-encephalitis., PMID:40094812
Paraneoplastic Anti-Contactin-1 Autoimmune Nodopathy., PMID:40213987
Permissive central tolerance plus defective peripheral checkpoints license pathogenic memory B cells in CASPR2-antibody encephalitis., PMID:40238887
Chronic Inflammatory Demyelinating Polyneuropathy: How Pathophysiology Can Guide Treatment., PMID:40391517
Proprioceptive endings at muscle spindles as a possible target of autoantibodies., PMID:40424942
Chronic Inflammatory Demyelinating Polyneuropathy and Concurrent Membranous Nephropathy Associated With Anti-Contactin-1 Autoantibodies: A Rare Case Report With a Review of the Literature., PMID:40502862
Paraneoplastic Limbic Encephalitis in a Patient With Thymoma., PMID:40519393
Cranial Myorhythmia as a Novel Clinical Manifestation in Contactin-Associated Protein-like 2 (CASPR2) Antibody Associated Encephalitis., PMID:40525980