Literature DB >> 3713739

Treatment of hypersomnolence in myotonic dystrophy with a CNS stimulant.

F G van der Meché, J M Boogaard, B van den Berg.   

Abstract

A 42-year-old man with myotonic dystrophy developed severe hypersomnolence during the year prior to admission for acute respiratory insufficiency. However, his hypersomnolence could be attributed to a central dysfunction, and during a follow-up period of 3 years, was successfully treated with methylphenidate.

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Year:  1986        PMID： 3713739     DOI： 10.1002/mus.880090410

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN： 0148-639X            Impact factor:   3.217


  3 in total

1.  Pulmonary function and resting breathing pattern in myotonic dystrophy.

Authors:  J M Bogaard; F G van der Meché; I Hendriks; C Ververs
Journal:  Lung       Date:  1992       Impact factor: 2.584

2.  Neuronal cell loss in the dorsal raphe nucleus and the superior central nucleus in myotonic dystrophy: a clinicopathological correlation.

Authors:  S Ono; F Kanda; K Takahashi; Y Fukuoka; K Jinnai; H Kurisaki; S Mitake; T Inagaki; K Nagao
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

3.  Daytime sleep in myotonic dystrophy is not caused by sleep apnoea.

Authors:  F G van der Meché; J M Bogaard; J C van der Sluys; R J Schimsheimer; C C Ververs; H F Busch
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-05       Impact factor: 10.154
  3 in total

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