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Neurology
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Peripheral neuropathy

Citations 191-200 of 339 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Near-infrared spectrophotoscopy of finger venules in assessment of autonomic dysfunction
K. Obayashi, Y. Ando, M. Nakamura, T. Yamashita, M. Ueda, K. Haraoka, H. Terazaki, and M. Uchino
Neurology 2004; 63: 164-166. [Abstract] [Full text] [PDF]  

EDITORIALS
Thalidomide neuropathy: Too much or too long?
Stuart C. Apfel and Douglas W. Zochodne
Neurology 2004; 62: 2158-2159. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Thalidomide neurotoxicity: Prospective study in patients with lupus erythematosus
C. Briani, G. Zara, R. Rondinone, S. Della Libera, M. Ermani, S. Ruggero, A. Ghirardello, S. Zampieri, and A. Doria
Neurology 2004; 62: 2288-2290. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Thalidomide sensory neurotoxicity: A clinical and neurophysiologic study
G. Cavaletti, A. Beronio, L. Reni, E. Ghiglione, A. Schenone, C. Briani, G. Zara, D. Cocito, G. Isoardo, P. Ciaramitaro, R. Plasmati, F. Pastorelli, M. Frigo, M. Piatti, and M. Carpo
Neurology 2004; 62: 2291-2293. [Abstract] [Full text] [PDF]  

ARTICLES
Immunoglobulin improves a model of acute motor axonal neuropathy by preventing axonal degeneration
Y. Nishimoto, M. Koga, M. Kamijo, K. Hirata, and N. Yuki
Neurology 2004; 62: 1939-1944. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Doxifluridine-induced neurotoxicity with normal dihydropyrimidine dehydrogenase activity
Dong Wook Kim, Han-Joon Kim, Dong-Eog Kim, and Jae-Kyu Roh
Neurology 2004; 62: 2136-2137. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Chronic cough due to Thr124Met mutation in the peripheral myelin protein zero (MPZ gene)
Robert H. Baloh, Joanna C. Jen, Gilbert Kim, and Robert W. Baloh
Neurology 2004; 62: 1905-1906. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Vasculitic mononeuritis multiplex induced by valacyclovir
Luis F. Pary, Angela Henszel, and Praful Kelkar
Neurology 2004; 62: 1906-1907. [Full text] [PDF]  

ARTICLES
Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene
N. Bissar-Tadmouri, E. Nelis, S. Züchner, Y. Parman, F. Deymeer, P. Serdaroglu, P. De Jonghe, V. Van Gerwen, V. Timmerman, J. M. Schröder, and E. Battaloglu
Neurology 2004; 62: 1522-1525. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Serum S100ß increases in marathon runners reflect extracranial release rather than glial damage
M. Hasselblatt, F. C. Mooren, N. von Ahsen, K. Keyvani, A. Fromme, K. Schwarze-Eicker, V. Senner, and W. Paulus
Neurology 2004; 62: 1634-1636. [Abstract] [Full text] [PDF]  

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* Collected Resources Home

* Related collections:
 Neuromuscular disease
 All Neuromuscular Disease
 Anterior nerve cell disease
 Amyotrophic lateral sclerosis
 Myasthenia
 Lambert-Eaton syndrome
 Peripheral neuropathy
 Carpal tunnel syndrome
 Cranial neuropathy
 Guillain-Barre syndrome
 Chronic inflammatory demyelinating polyneuropathy
 Transverse myelitis
 Muscle disease


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