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Chronic inflammatory demyelinating polyneuropathy

PARK p-adrenergic receptor kinase CIDP chronic inflammatory demyelinating polyneuropathy... [Pg.963]

Chronic inflammatory demyelinating polyneuropathy is sometimes associated with malignancy [123]. The reported incidence of carcinoma in chronic inflammatory demyelinating polyneuropathy varies from 4 to 10% [100, 124]. [Pg.157]

Elderly patients with chronic inflammatory demyelinating polyneuropathy and a subacute onset and poor response to treatment are particularly prone to harboring an underlying malignancy [125],... [Pg.158]

Antoine JC, Mosnier JF, Lapras J, Convers P, Absi L, Laurent B, et al. Chronic inflammatory demyelinating polyneuropathy associated with carcinoma. J Neurol Neurosurg Psychiatry 1996 60(2) 188-190. [Pg.178]

Hies Z, Kondo T, Newcombe J, Oka N, Tabita T, Yamamura T (2000) Differential expression of NK T cell V alpha 24J alpha Q invariant TCR chain in the lesions of multiple sclerosis and chronic inflammatory demyelinating polyneuropathy. J Immun 164 4375 381. [Pg.56]

Yamamoto M, Ito Y, Mitsuma N, Li M, Hattori N, Sobue G (2002) Parallel expression of neurotrophic factors and their receptors in chronic inflammatory demyelinating polyneuropathy. Muscle Nerve 25 601-604. [Pg.262]

Takigawa T, Yasuda H, Terada M, Haneda M, Kashiwagi A Saito T, Saida T, Kitasato H, Kikkawa R (2000) The sera from GMl gan-glioside antibody positive patients with Guillain-Barre syndrome or chronic inflammatory demyelinating polyneuropathy blocks Na+ currents in rat single myehnated nerve fibers. Intern Med 39 123-127. [Pg.280]

Various forms of interferon alfa-induced neuropathy have been reported (SED-14,1249), but chronic inflammatory demyelinating polyneuropathy has seldom been described (61,62). [Pg.1796]

A chronic inflammatory demyelinating polyneuropathy was considered to have been caused by tacrolimus in a 62-year-old patient (30). [Pg.3281]

Matsrrmuro K, Izumo S, Umehara F, et al. Chronic inflammatory demyelinating polyneuropathy Histological and immu-nopathological studies on biopsied sural nerves. J Neurol Sci. 1994 127 170-178. [Pg.889]

In a patient who does have a close family history of diabetes-2, a glucocorticoid should be avoided if possible, because it can increase insulin resistance and make manifest diabetes-2 glucose dysmetabo-lism. Accordingly, asking about a close family history of diabetes-2 is very important in managing a chronic immune dysschwannian polyneuropathy (CIDP) (sometimes less precisely called chronic inflammatory demyelinating polyneuropathy), or other dysimmune patient. [Pg.36]

Treatment Because of the sensory abnormalities, dysschwannian nerve conductions, elevated CSF protein, aspects of denervation-reinnervation in the muscle biopsy, and the diabetes-2 in both parents, we considered that our patient probably had coexisting genetico-diahetoid-2 dysimmune neuropathy," a type of chronic immune dysschwannian polyneuropathy (CIDP) (sometimes less precisely called chronic inflammatory demyelinating polyneuropathy, Chapter 2). We therefore treated her using/WG, and she was remarkably benefited her walking ability and endurance greatly improved, she did not require frequent rests, and was able to ascend steps much more easily. [Pg.61]


See other pages where Chronic inflammatory demyelinating polyneuropathy is mentioned: [Pg.58]    [Pg.645]    [Pg.696]    [Pg.423]    [Pg.157]    [Pg.773]    [Pg.257]    [Pg.591]    [Pg.1725]    [Pg.1726]    [Pg.1796]    [Pg.879]    [Pg.1106]    [Pg.494]   
See also in sourсe #XX -- [ Pg.58 ]

See also in sourсe #XX -- [ Pg.645 ]

See also in sourсe #XX -- [ Pg.157 ]

See also in sourсe #XX -- [ Pg.2245 ]




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