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| Found 42 studies with search of: | Paraneoplastic Syndromes |
| Rank | Status | Study | ||||
|---|---|---|---|---|---|---|
| 1 | Recruiting |
Immunotherapy of the Paraneoplastic Syndromes
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| 2 | Completed |
Studies of Neurological Paraneoplastic Syndromes
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| 3 | Recruiting |
The Study of Immune Cell (T Cell) Activity in Patients With Paraneoplastic Neurologic Syndromes
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| 4 | Recruiting |
Study of Cytokines in Children With Opsoclonus-Myoclonus Syndrome
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| 5 | Recruiting |
MC-5A for Chemotherapy Induced Peripheral Neuropathy
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| 6 | Recruiting |
3,4-Diaminopyridine Use in Lambert-Eaton Myasthenic Syndrome(LEMS) and Congenital Myasthenic Syndromes (CMS)
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| 7 | Recruiting |
Use of 3, 4-Diaminopyridine in Lambert Eaton Myasthenic Syndrome
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| 8 | Recruiting |
Efficacy of Albuterol in the Treatment of Congenital Myasthenic Syndromes
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| 9 | Available |
Treatment of Lambert-Eaton Syndrome With 3,4 DAP
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| 10 | Available |
Treatment of Lambert-Eaton Myasthenic Syndrome (LEMS) With 3, 4 DAP
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| 11 | Enrolling by invitation |
Effectiveness of 3,4-Diaminopyridine in Lambert-Eaton Myasthenic Syndrome
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| 12 | Available |
Treatment of Lambert-Eaton Syndrome With 3,4 Diaminopyridine
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| 13 | Available |
Use Of 3,4-Diaminopyridine (3,4-DAP) In The Treatment Of Lambert Eaton Myasthenic Syndrome
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| 14 | Completed |
Pregnancy Outcomes in Congenital Myasthenie Syndrome
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| 15 | Recruiting |
A Phase 3 Study of Amifampridine Phosphate in Patients With Lambert Eaton Myasthenic Syndrome (LEMS)
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| 16 | Completed |
Randomized Study of 3,4-Diaminopyridine for Lambert-Eaton Myasthenic Syndrome
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| 17 | Completed |
Effectiveness of Rituximab in Pediatric OMS Patients.
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| 18 | Recruiting |
Cyclophosphamide and Prednisone With or Without Immunoglobulin in Treating Abnormal Muscle Movement in Children With Neuroblastoma
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| 19 | Unknown † |
Phase III Randomized, Double-Blind, Sham-Controlled Study of Plasma Exchange for Acute Severe Attacks of Inflammatory Demyelinating Disease Refractory to Intravenous Methylprednisolone
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| 20 | Enrolling by invitation |
Ephedrine for the Treatment of Congenital Myasthenia
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