Literature DB >> 8739381

3,4-Diaminopyridine, an orphan drug, in the symptomatic treatment of Lambert-Eaton myasthenic syndrome.

J Molgó1, J M Guglielmi.   

Abstract

The Lambert-Eaton myasthenic syndrome (LEMS) is a rare autoimmune disease of peripheral cholinergic transmission that results in muscle weakness and autonomic dysfunction, due to impaired acetylcholine release. A review of available clinical information indicates that 3,4-diaminopyridine (3,4-DAP) used either alone or in conjunction with other therapies was effective in treating the motor and the autonomic deficits in patients with primary and paraneoplastic LEMS of varying degrees of severity. A survey of the medical literature indicates that about 150 patients have been treated worldwide with 3,4-DAP. The general view is that 3,4-DAP is well tolerated in short- or long-term treatments, with only mild side effects. 3,4-DAP is an orphan drug approved for clinical use in many european countries that lacks adoptive parents because its exploitation is not profitable.

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Year:  1996        PMID: 8739381     DOI: 10.1007/bf02346385

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  25 in total

1.  Guanidine and neuromuscular transmission. I. Effect on transmitter release occurring spontaneously and in response to single nerve stimuli.

Authors:  M A Kamenskaya; D Elmqvist; S Thesleff
Journal:  Arch Neurol       Date:  1975-08

2.  4-aminopyridine--a new drug tested in the treatment of Eaton-Lambert syndrome.

Authors:  H Lundh; O Nilsson; I Rosén
Journal:  J Neurol Neurosurg Psychiatry       Date:  1977-11       Impact factor: 10.154

Review 3.  Review of evidence for loss of motor nerve terminal calcium channels in Lambert-Eaton myasthenic syndrome.

Authors:  A G Engel
Journal:  Ann N Y Acad Sci       Date:  1991       Impact factor: 5.691

4.  IgG from patients with Lambert-Eaton syndrome blocks voltage-dependent calcium channels.

Authors:  Y I Kim; E Neher
Journal:  Science       Date:  1988-01-22       Impact factor: 47.728

5.  Lambert-Eaton myasthenic syndrome: immunoglobulin G inhibition of Ca2+ flux in tumor cells correlates with disease severity.

Authors:  B Lang; A Vincent; N M Murray; J Newsom-Davis
Journal:  Ann Neurol       Date:  1989-03       Impact factor: 10.422

6.  Decreased calcium currents in motor nerve terminals of mice with Lambert-Eaton myasthenic syndrome.

Authors:  D O Smith; M W Conklin; P J Jensen; W D Atchison
Journal:  J Physiol       Date:  1995-08-15       Impact factor: 5.182

7.  Practical aspects of 3,4-diaminopyridine treatment of the Lambert-Eaton myasthenic syndrome.

Authors:  H Lundh; O Nilsson; I Rosén; S Johansson
Journal:  Acta Neurol Scand       Date:  1993-08       Impact factor: 3.209

8.  Treatment of Lambert-Eaton syndrome: 3,4-diaminopyridine and pyridostigmine.

Authors:  H Lundh; O Nilsson; I Rosén
Journal:  Neurology       Date:  1984-10       Impact factor: 9.910

9.  The Lambert-Eaton myasthenic syndrome. A review of 50 cases.

Authors:  J H O'Neill; N M Murray; J Newsom-Davis
Journal:  Brain       Date:  1988-06       Impact factor: 13.501

10.  The mode of action of guanidine on mouse motor nerve terminals.

Authors:  J Molgó; A Mallart
Journal:  Neurosci Lett       Date:  1988-06-29       Impact factor: 3.046

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  1 in total

1.  Lambert-Eaton Myasthenic Syndrome.

Authors:  John Newsom-Davis
Journal:  Curr Treat Options Neurol       Date:  2001-03       Impact factor: 3.598

  1 in total

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