review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1002/14651858.CD003217.PUB2 |
P698 | PubMed publication ID | 16034892 |
P2093 | author name string | E Nobile-Orazio | |
T Umapathi | |||
JM Léger | |||
RAC Hughes | |||
P2860 | cites work | Lower motor neuron syndromes defined by patterns of weakness, nerve conduction abnormalities, and high titers of antiglycolipid antibodies | Q28334663 |
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 | ||
Multifocal motor neuropathy: response to human immune globulin | Q34062007 | ||
Interobserver agreement for the assessment of handicap in stroke patients. | Q34176187 | ||
Multifocal motor neuropathy. | Q34204618 | ||
Chronic motor neuropathies: response to interferon-beta1a after failure of conventional therapies | Q35449950 | ||
Long term effect of intravenous immunoglobulins and oral cyclophosphamide in multifocal motor neuropathy | Q36317538 | ||
Treatment of multifocal motor neuropathy with high dose intravenous immunoglobulins: a double blind, placebo controlled study | Q36880697 | ||
Electrophysiological improvement after intravenous immunoglobulin in motor neuropathy with multifocal conduction block | Q39207150 | ||
The clinical and diagnostic role of anti-GM1 antibody testing | Q40792321 | ||
Clinical and neurophysiological assessment of immunoglobulin therapy in five patients with multifocal motor neuropathy | Q41663344 | ||
Human immunoglobulin treatment of multifocal motor neuropathy and polyneuropathy associated with monoclonal gammopathy | Q41663659 | ||
Multifocal motor neuropathy without overt conduction block | Q41702502 | ||
Pure motor demyelinating neuropathy: deterioration after steroid treatment and improvement with intravenous immunoglobulin | Q41766911 | ||
The sensitivity and specificity of anti-GM1 antibody testing | Q42553258 | ||
Treatment of IgM antibody associated polyneuropathies using rituximab | Q43069450 | ||
Plasmapheresis in multifocal motor neuropathy: a case report | Q43071840 | ||
Multifocal motor neuropathy with conduction block: is it a distinct clinical entity? | Q43583532 | ||
Multifocal acquired demyelinating neuropathy masquerading as motor neuron disease | Q43839016 | ||
A computer simulation of conduction block: effects produced by actual block versus interphase cancellation | Q43871919 | ||
Mycophenolate in treatment-resistant inflammatory neuropathies | Q44230238 | ||
Interobserver agreement in the assessment of muscle strength and functional abilities in Guillain-Barré syndrome | Q44643471 | ||
Mycophenolate mofetil in dysimmune neuropathies: a preliminary study. | Q44873430 | ||
A syndrome of asymmetric limb weakness with motor conduction block | Q44992268 | ||
Multifocal motor neuropathy with conduction block misdiagnosed as multiple entrapment neuropathies | Q46163603 | ||
The long-term effect of intravenous immunoglobulin treatment in multifocal motor neuropathy | Q48486772 | ||
Multifocal motor neuropathy: long-term clinical and electrophysiological assessment of intravenous immunoglobulin maintenance treatment | Q48536321 | ||
Intravenous immunoglobulin therapy in multifocal motor neuropathy: a double-blind, placebo-controlled study | Q49125609 | ||
How long is IVIg effective in multifocal motor neuropathy? | Q51021985 | ||
High-dose intravenous immunoglobulin therapy in multifocal motor neuropathy. | Q53771496 | ||
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 | ||
Multifocal motor neuropathy mimicking motor neuron disease: nine cases | Q59270630 | ||
Intravenous immunoglobulin treatment in multifocal motor neuropathy | Q67518467 | ||
Conduction block in clinical practice | Q68016775 | ||
Immunosuppressive treatment in multifocal motor neuropathy | Q68060632 | ||
Multifocal demyelinating motor neuropathy: cranial nerve involvement and immunoglobulin therapy | Q68075974 | ||
Chronic acquired demyelinating motor neuropathy | Q68258723 | ||
Slow resolution of multifocal weakness and fasciculation: a reversible motor neuron syndrome | Q69599049 | ||
Motor neuropathy with multifocal conduction blocks | Q69656919 | ||
A treatable multifocal motor neuropathy with antibodies to GM1 ganglioside | Q69836574 | ||
Pathological findings at the site of conduction block in multifocal motor neuropathy | Q70564756 | ||
Multifocal demyelinating neuropathy with persistent conduction block | Q70680262 | ||
Sensory nerve pathology in multifocal motor neuropathy | Q71004368 | ||
Multifocal motor neuropathy: clinical and electrophysiological findings | Q71787737 | ||
Intravenous immunoglobulin treatment in patients with motor neuron syndromes associated with anti-GM1 antibodies: a double-blind, placebo-controlled study | Q72335038 | ||
Immunosuppressive treatment of motor neuron syndromes. Attempts to distinguish a treatable disorder | Q72765673 | ||
Multifocal motor neuropathy with conduction block after Campylobacter jejuni enteritis | Q73090016 | ||
Multifocal motor neuropathy presenting as ophthalmoplegia | Q73115212 | ||
Multifocal motor neuropathy and Lewis Sumner syndrome: two distinct entities | Q73195249 | ||
Multifocal motor neuropathy and Lewis Sumner syndrome: a clinical spectrum | Q73195253 | ||
AAEM news and comments | Q73195257 | ||
Pulsed high-dose dexamethasone is not effective in patients with multifocal motor neuropathy | Q73245639 | ||
Multifocal motor neuropathy: diagnostic criteria that predict the response to immunoglobulin treatment | Q73298577 | ||
Magnetic resonance imaging of the brachial plexus in patients with multifocal motor neuropathy | Q73343604 | ||
Multifocal inflammatory demyelinating neuropathy: a distinct clinical entity? | Q73355928 | ||
Treatment of multifocal motor neuropathy with interferon-beta1A | Q73634320 | ||
79(th) ENMC International Workshop: multifocal motor neuropathy. 14-15 April 2000, Hilversum, The Netherlands | Q73739726 | ||
Natural history of 46 patients with multifocal motor neuropathy with conduction block | Q73864084 | ||
Multifocal motor neuropathy | Q74093843 | ||
Multifocal inflammatory demyelinating neuropathy: A distinct clinical entity? | Q74298491 | ||
Deterioration of multifocal motor neuropathy after plasma exchange | Q74575154 | ||
Chronic neuropathy with IgM anti-ganglioside antibodies: lack of long term response to rituximab | Q75205847 | ||
Inter-laboratory validation of an ELISA for the determination of serum anti-ganglioside antibodies | Q77343613 | ||
Multifocal acquired demyelinating sensory and motor neuropathy: the Lewis-Sumner syndrome | Q77758996 | ||
Upper limb predominant, multifocal chronic inflammatory demyelinating polyneuropathy | Q77873391 | ||
Consensus criteria for the diagnosis of multifocal motor neuropathy | Q78735138 | ||
Efficacy of cyclosporine treatment in multifocal motor neuropathy | Q79077971 | ||
Follow-up study and response to treatment in 23 patients with Lewis-Sumner syndrome | Q80407989 | ||
Multifocal motor neuropathy: decrease in conduction blocks and reinnervation with long-term IVIg | Q80847191 | ||
P921 | main subject | immunosuppression | Q1455316 |
Multifocal motor neuropathy | Q6934690 | ||
P577 | publication date | 2005-07-20 | |
P1433 | published in | Cochrane Database of Systematic Reviews | Q15750361 |
P1476 | title | Immunosuppressant and immunomodulatory treatments for multifocal motor neuropathy |