Prognosis of Myasthenia Gravis

J Gordon Millichap

doi:10.15844/pedneurbriefs-6-4-7

Prognosis of Myasthenia Gravis

Pediatric Neurology Briefs

Volume 6 (1992): Issue 4

By: J Gordon Millichap

Open Access

|Apr 1992

Abstract

The prognosis of myasthenia gravis (MG) was assessed retrospectively using life table analysis in 844 patients followed up for a mean period of 5 years in 3 neurological centers in Milan, Rome and Pavia, Italy.

References

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Millichap JG Dodge PR Diagnosis and treatment of myasthenia gravis in infancy, childhood, and adolescence: a study of 51 patients Neurology 1960 Nov 10 1007 1014 10.1212/WNL.10.11.1007 13770917
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Evans OB Vig V Parker CC Prematurity and early-onset juvenile myasthenia gravis Pediatr Neurol 1992 Jan-Feb 8 1 51 53 10.1016/0887-8994(92)90053-2 1558576
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Fukuyama Y Suzuki M Segawa M Studies on myasthenia gravis in childhood, especially on its clinical course and prognosis Paediatr Univ Tokyo 1970 Dec 18 57 68 5514646
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Palace J Wiles CM Newsom-Davis J 3,4-Diaminopyridine in the treatment of congenital (hereditary) myasthenia J Neurol Neurosurg Psychiatry 1991 Dec 54 12 1069 1072 10.1136/jnnp.54.12.1069 1783919
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-6-4-7 | Journal eISSN: 2166-6482

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Language: English

Page range: 29 - 31

Published on: Apr 1, 1992

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Prognosis of Myasthenia Gravis,

Anticholinesterase,

Thymectomy

© 1992 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 6 (1992): Issue 4