✦ LIBER ✦

Characterisation of autoantibodies to peripheral myelin protein 22 in patients with hereditary and acquired neuropathies

✍ Scribed by Marie-Françoise Ritz; Jeannette Lechner-Scott; Rodney J Scott; Peter Fuhr; Nass Malik; Beat Erne; Verdon Taylor; Ueli Suter; Nicole Schaeren-Wiemers; Andreas J Steck

Book ID: 114139030
Publisher: Elsevier Science
Year: 2000
Tongue: English
Weight: 575 KB
Volume: 104
Category: Article
ISSN: 0165-5728
DOI: 10.1016/s0165-5728(99)00250-7

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A novel 3′-splice site mutation in perip

A novel 3′-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies

✍ J Meuleman; A Pou-Serradell; A Löfgren; C Ceuterick; J.J Martin; V Timmerman; C 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 297 KB

Expression of peripheral myelin protein-

Expression of peripheral myelin protein-22 (PMP22)-mRNA in hereditary motor and sensory neuropathy type 1 (HMSN 1)

✍ H. Grehl; T. Liehr; B. Neundörfer; B. Rautenstrauβ 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 258 KB

Immunoreactive myelin basic protein in c

Immunoreactive myelin basic protein in cerebrospinal fluid of patients with peripheral neuropathies

✍ Dr David R. Cornblath; John W. Griffin; Gihan I. Tennekoon 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 English ⚖ 270 KB 👁 2 views

Deletion in chromosome 17p11.2 including

Deletion in chromosome 17p11.2 including the peripheral myelin protein-22 (PMP-22) gene in hereditary neuropathy with liability to pressure palsies

✍ Fujio Umehara; Takashirou Kiwaki; Hiroo Yoshikawa; Tomoya Nishimura; Masanori Na 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 740 KB

A possible novel isoform of peripheral m

A possible novel isoform of peripheral myelin P0 protein: a target antigen recognized by an autoantibody in a patient with malignant lymphoma and peripheral neuropathy

✍ Kazuyuki Ishida; Hiroaki Takeuchi; Ryosuke Takahashi; Kazunori Yoshimura; Masahi 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 200 KB

Recurrent brachial plexus palsies as the

Recurrent brachial plexus palsies as the only clinical expression of hereditary neuropathy with liability to pressure palsies associated with a de novo deletion of the peripheral myelin protein-22 gene

✍ Florian Stögbauer; Peter Young; Max Kerschensteiner; E. Bernd Ringelstein; Gerd 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 72 KB 👁 2 views

There is phenotypic heterogeneity in patients with hereditary neuropathy with liability to pressure palsies. In rare cases, recurrent brachial plexopathy is the only expression of the disease. We describe a patient with three episodes of plexus brachialis palsy and a de novo deletion of the peripher