Are MuSK Antibodies the Primary Cause of Myasthenic Symptoms?
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The Myositis Autoantibody Phenotypes of the Juvenile Idiopathic Inflammatory Myopathies
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Should We Test for IgG Antibodies Against MOG in Both Serum and CSF in Patients with Suspected MOGAD?
Neurol 100:497-498, Kim,H.J. & Palace, J., 2023
Acute Rheumatic Fever: Clinical Manifestations and Diagnosis
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Aquaporin-4 Antibody-Negative Neuromyelitis Optica
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Paediatric Autoimmune Encephalopathies: Clinical Features, Laboratory Investigations and Outcomes in Patients with or without Antibodies to known Central Nervous System Autoantigens
JNNP 84:748-755, Hacohen, Y.,et al, 2013
Aquaporin-4 Antibody-Negative Neuromyelitis Optica
Neurol 80:2194-2200, 2176, Marignier, R.,et al, 2013
Longitudinally Extensive Transverse Myelitis with and Without Aquaporin 4 Antibodies
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Current Concept of Neuromyelitis Optica (NMO) and NMO Spectrum Disorders
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CSF Complements Serum for Evaluating Paraneoplastic Antibodies and NMO-IgG
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Clinicopath Conf, Acute HIV-1 Infection
NEJM 360:1540-1548, Case 11-2009, 2009
Dysphagia as the Sole Manisfestation of Myasthenia Gravis
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Myasthenia Gravis
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Congenital Myasthenic Syndromes
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Ocular Myasthenia:A Protean Disorder
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Acetylcholine Receptor Antibodies in Juvenile Myasthenia Gravis
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