PedAM
Pediatric Disease Annotations & Medicines
| Disease | polyneuropathy |
| Phenotype | C1136085|monoclonal gammopathy |
| Sentences | 13 |
| PubMedID- 24487381 | Conclusions: fcgammariiia polymorphisms are potential biomarkers for response to rituximab treatment in polyneuropathy associated with igm monoclonal gammopathy. |
| PubMedID- 23777091 | Anti-gscs antibodies can be found also in chronic inflammatory demyelinating polyneuropathy and neuropathy associated with igm monoclonal gammopathy. |
| PubMedID- 22189568 | In the remaining cohorts (monoclonal gammopathy of undetermined significance related polyneuropathy, multifocal motor neuropathy, mytonic dystrophy type-1, pompe's disease and limb-girdle muscular dystrophy), the muscles groups evaluated represented the clinical picture of each illness (see supplementary table 1 for available muscles per cohort). |
| PubMedID- 25572169 | Anti-mag neuropathy is a very rare form of acquired polyneuropathy associated with igm monoclonal gammopathy of undetermined significance (mgus). |
| PubMedID- 20124206 | Conclusion: higher age at onset and demyelination increase the risk, whereas anti-mag antibodies decrease the risk, of developing rankin scale score > or = 3 in polyneuropathy associated with immunoglobulin m monoclonal gammopathy (igm mgusp). |
| PubMedID- 26055637 | A sporadic case of late-onset familial amyloid polyneuropathy with a monoclonal gammopathy. |
| PubMedID- 23095652 | The prevalence of polyneuropathy in patients with monoclonal gammopathy of undetermined significance (mgus) has been reported to be 10-50%. |
| PubMedID- 26065001 | polyneuropathy associated with igm monoclonal gammopathy and anti-myelin associated glycoprotein (mag) antibodies is an immune-mediated demyelinating neuropathy. |
| PubMedID- 26028199 | [a case of sensory ataxic axonal polyneuropathy with igglambda monoclonal gammopathy successfully treated with intravenous immunoglobulin therapy]. |
| PubMedID- 24781837 | The objective of this study was to investigate if the clinical and electrophysiological phenotype of patients with polyneuropathy associated with igm monoclonal gammopathy (igm-pnp) is related to the presence of antibodies against gangliosides or myelin-associated glycoprotein (mag). |
| PubMedID- 22399147 | Unfortunately, polyneuropathy associated with monoclonal gammopathy is often refractory to treatment. |
| PubMedID- 24728842 | Fcγriiia (fcγriiia-v/v1158), as was suggested by a recent study in patients with a polyneuropathy associated with igm monoclonal gammopathy [69]. |
| PubMedID- 20015874 | This monoclonal gammopathy is frequently associated with polyneuropathy and antibodies against myelin protein zero, whereas the role of the t cells remains largely unknown. |
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