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1  disorder distinct from chronic inflammatory demyelinating polyneuropathy.
2 lain-Barre syndrome and chronic inflammatory demyelinating polyneuropathy.
3 rse myelitis, and 1 had chronic inflammatory demyelinating polyneuropathy.
4 anti-myelin-associated glycoprotein antibody demyelinating polyneuropathy.
5 llain-Barre syndrome or chronic inflammatory demyelinating polyneuropathy.
6 %) with newly diagnosed chronic inflammatory demyelinating polyneuropathy.
7 opathy as distinct from chronic inflammatory demyelinating polyneuropathy.
8  within the spectrum of chronic inflammatory demyelinating polyneuropathy.
9 ssociation between CD and acute inflammatory demyelinating polyneuropathy (0.8; 0.3-2.1; P = .68).
10 study of rituximab in patients with anti-MAG demyelinating polyneuropathy (A-MAG-DP).
11     In chronic cases of chronic inflammatory demyelinating polyneuropathy, a concomitant axonal loss
12 ropathy and variants of chronic inflammatory demyelinating polyneuropathy, account for a proportion o
13 pathologic criteria, with acute inflammatory demyelinating polyneuropathy (AIDP) and acute motor axon
14 hina occurs in two forms: acute inflammatory demyelinating polyneuropathy (AIDP) and acute motor axon
15 ts in early stages of the acute inflammatory demyelinating polyneuropathy (AIDP) pattern of Guillain-
16                        In acute inflammatory demyelinating polyneuropathy (AIDP), the attack appears
17 ived from patients with chronic inflammatory demyelinating polyneuropathy, an autoimmune disease of t
18                            The evaluation of demyelinating polyneuropathies and the data for treatmen
19 tion indicated for a patient presenting with demyelinating polyneuropathy and concurrent papilledema.
20 focal motor neuropathy, chronic inflammatory demyelinating polyneuropathy, and dermatomyositis.
21 uillain-Barre syndrome, chronic inflammatory demyelinating polyneuropathy, and multifocal motor neuro
22                         Eleven patients with demyelinating polyneuropathy associated with monoclonal
23 a multifocal variant of chronic inflammatory demyelinating polyneuropathy but that multifocal motor n
24 inclusion-body myositis, paraproteinemic IgM demyelinating polyneuropathy, certain intractable childh
25 arre syndrome (GBS) and chronic inflammatory demyelinating polyneuropathy (CIDP) are conditions that
26                         Chronic inflammatory demyelinating polyneuropathy (CIDP) has occasionally bee
27 thirds of patients with chronic inflammatory demyelinating polyneuropathy (CIDP) need long-term intra
28  and nine patients with chronic inflammatory demyelinating polyneuropathy (CIDP) were compared with 1
29 opsies of patients with chronic inflammatory demyelinating polyneuropathy (CIDP), CIDP associated wit
30 of nerve hypertrophy in chronic inflammatory demyelinating polyneuropathy (CIDP), magnetic resonance
31 mbles the human disease chronic inflammatory demyelinating polyneuropathy (CIDP).
32 s to the human disease, chronic inflammatory demyelinating polyneuropathy (CIDP).
33 lain-Barre syndrome and chronic inflammatory demyelinating polyneuropathy (CIDP).
34 n reported as mimicking chronic inflammatory demyelinating polyneuropathy (CIDP).
35 autoimmunity resembling chronic inflammatory demyelinating polyneuropathy develops spontaneously in N
36 e (GBS), especially the classic inflammatory demyelinating polyneuropathy form, seems to involve lymp
37 ence of CMT disease and chronic inflammatory demyelinating polyneuropathy indicate that the associati
38                         Chronic inflammatory demyelinating polyneuropathy is a debilitating autoimmun
39 uillain-Barre syndrome, chronic inflammatory demyelinating polyneuropathy, multifocal motor neuropath
40 uillain-Barre syndrome, chronic inflammatory demyelinating polyneuropathy, multifocal motor neuropath
41 e immunopathogenesis of chronic inflammatory demyelinating polyneuropathy remain still fragmentary an
42                         Chronic inflammatory demyelinating polyneuropathy results from autoimmune des
43                         An acute or subacute demyelinating polyneuropathy should be considered a pote
44  were consistent with the acute inflammatory demyelinating polyneuropathy subtype of the Guillain-Bar

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