Disease: CANOMAD syndrome
- A case of false positive cardiac troponin I in CANOMAD syndrome
- A syndrome of chronic ataxic polyneuropathy, ophtalmoplegia, IgM paraprotein, cold agglutinins and anti-disialosyl antibodies can cause diplopia in patients with chronic sensory polyneuropathy
- Acute and Chronic Anti-ganglioside Neuropathies: From Theory to Practice in Buenos Aires, Argentina
- Are Miller Fisher syndrome and CANDA due to a paranodopathy?
- Ataxic neuropathy associated with disialosylated antibodies: description of new clinical and biochemical forms
- CANOMAD and other chronic ataxic neuropathies with disialosyl antibodies (CANDA)
- CANOMAD Presenting as Bilateral Sixth Nerve Palsies
- Canomad presenting without ophthalmoplegia and responding to intravenous immunoglobulin
- CANOMAD responding to weekly treatment with intravenous immunoglobulin (IVIg)
- CANOMAD syndrome with respiratory failure
- CANOMAD: a neurological monoclonal gammopathy of clinical significance that benefits from B-cell-targeted therapies
- Canomad: report of a case with a 40-year history and autopsy. Is this a sensory ganglionopathy with neuromuscular junction blockade?
- Cerebrospinal fluid findings in Guillain-Barré syndrome and chronic inflammatory demyelinating polyneuropathies
- Chronic ataxic neuropathy mimicking dorsal midbrain syndrome
- CIDP mimics: a case series
- Comparison of commercial tests for detecting multiple anti-ganglioside autoantibodies in patients with well-characterized immune-mediated peripheral neuropathies
- Corrigendum to "A case of false positive cardiac troponin I in CANOMAD syndrome" [Int. J. Cardiol. 222 (2016) 359-360]
- Evolving Immunologic Perspectives in Chronic Inflammatory Demyelinating Polyneuropathy
- Facial Involuntary Movements and Respiratory Failure in CANOMAD, Responsive to IVIG Therapy
- Human IgM paraproteins demonstrate shared reactivity between Campylobacter jejuni lipopolysaccharides and human peripheral nerve disialylated gangliosides
- Identification and characterization of a monoclonal IgM reacting with disialylated gangliosides recognizing the CANOMAD syndrome
- Monosialosyl Antibody in a Case Mimicking CANOMAD Syndrome
- Neuropathies périphériques associées aux syndromes lymphoprolifératifs : spectre clinique et démarche diagnostique
- Optic neuropathy associated with CANOMAD: description of 2 cases
- Paraproteinemic neuropathies
- Polyneuropathy associated with monoclonal gammapathy: treatment perspectives
- Relapsing sensorimotor neuropathy with ophthalmoplegia, antidisialosyl antibodies, and extramembranous glomerulonephritis
- SIADH in a patient with sensory ataxic neuropathy with anti-disialosyl antibodies (CANOMAD)
- Successful treatment of CANOMAD with IVIg and rituximab
- The clinical and laboratory features of chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodies
- The Spectrum of Ocular Manifestations in Patients with Waldenström's Macroglobulinemia
- The Wide Spectrum of Pathophysiologic Mechanisms of Paraproteinemic Neuropathy
- Thromboembolic risk with IVIg: Incidence and risk factors in patients with inflammatory neuropathy