| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1046/J.1468-1331.2001.00136.X |
| P698 | PubMed publication ID | 11328326 |
| P2093 | author name string | J M Léger | |
| F Salachas | |||
| P2860 | cites work | Pathology of the motor-sensory axonal Guillain-Barré syndrome | Q57197745 |
| Sporadic amyotrophic lateral sclerosis of long duration mimicking spinal progressive muscular atrophy: a clinicopathological study | Q33593784 | ||
| Multifocal motor neuropathy with conduction block: a study of 24 patients | Q33734400 | ||
| Long term follow up of multifocal motor neuropathy with conduction block under treatment | Q33735714 | ||
| Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy | Q34023072 | ||
| Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait | Q34051849 | ||
| Chronic motor neuropathies: response to interferon-beta1a after failure of conventional therapies | Q35449950 | ||
| Intravenous immunoglobulin treatment in lower motor neuron disease associated with highly raised anti-GM1 antibodies | Q36317355 | ||
| Treatment of multifocal motor neuropathy with high dose intravenous immunoglobulins: a double blind, placebo controlled study | Q36880697 | ||
| Chronic dysimmune demyelinating polyneuropathy: a clinical and electrophysiological study of 93 patients | Q36894111 | ||
| Guillain-Barré syndrome in northern China. The spectrum of neuropathological changes in clinically defined cases | Q40438026 | ||
| The current place of high-dose immunoglobulins in the treatment of neuromuscular disorders | Q40906180 | ||
| Chronic motor neuropathies: diagnosis, therapy, and pathogenesis | Q41270462 | ||
| Human immunoglobulin treatment of multifocal motor neuropathy and polyneuropathy associated with monoclonal gammopathy | Q41663659 | ||
| Pure motor demyelinating neuropathy: deterioration after steroid treatment and improvement with intravenous immunoglobulin | Q41766911 | ||
| Multifocal acquired demyelinating neuropathy masquerading as motor neuron disease | Q43839016 | ||
| The characteristic electrodiagnostic features of Kennedy's disease | Q44881677 | ||
| Linguistic processing during repetitive transcranial magnetic stimulation | Q48555904 | ||
| Intravenous immunoglobulin therapy in multifocal motor neuropathy: a double-blind, placebo-controlled study | Q49125609 | ||
| Spinobulbar muscular atrophy can mimic ALS: the importance of genetic testing in male patients with atypical ALS. | Q50939029 | ||
| Multifocal motor neuropathy improved by IVIg: randomized, double-blind, placebo-controlled study. | Q53901414 | ||
| Motor Neuropathy with Proximal Multifocal Persistent Conduction Block, Fasciculations and Myokymia | Q56608957 | ||
| Acute motor axonal neuropathy: An antibody-mediated attack on axolemma | Q57197741 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 201-208 | |
| P577 | publication date | 2001-05-01 | |
| P1433 | published in | European Journal of Neurology | Q15757256 |
| P1476 | title | Diagnosis of motor neuropathy | |
| P478 | volume | 8 |
| Q83163196 | Acute toxic polyradiculopathy after exorbitant intracarotid substance abuse |
| Q58152606 | Bilateral hand amyotrophy with PMP-22 gene deletion |
| Q48403829 | Brainstem dysfunction in variegate porphyria |
| Q37959252 | Multifocal motor neuropathy: diagnosis, pathogenesis and treatment strategies |
| Q35979748 | Peripheral (limb) myokymic discharges in motor neuron disease |
| Q87682503 | Pure motor axonal neuropathy triggered by antituberculous therapy in an undiagnosed case of acute intermittent porphyria |
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