Literature DB >> 1591746

Myoclonic dystonia.

S M Pueschel1, J H Friedman, T Shetty.   

Abstract

Myoclonic dystonia is a rare disorder that occurs in an hereditary and a sporadic form. The autosomal-dominantly inherited form is responsive to alcohol but not to other drugs. The sporadic form has been relatively resistant to drug treatment. We report a young man with myoclonic dystonia who displayed only little response to alcohol but improved significantly with a combination of sodium valproate for myoclonus and trihexiphenidyl hydrochloride for dystonia. His rehabilitation, however, was confounded by public authorities who thought the patient's appearance was indicative of drug use.

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Year:  1992        PMID: 1591746     DOI: 10.1007/bf00298440

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  34 in total

1.  NATURE OF AVERAGE EVOKED POTENTIALS TO SOUND AND OTHER STIMULI IN MAN.

Authors:  R G BICKFORD; J L JACOBSON; D T CODY
Journal:  Ann N Y Acad Sci       Date:  1964-05-08       Impact factor: 5.691

2.  Familial myoclonic epilepsy and its association with cerebellar disturbance.

Authors:  K B NOAD; J W LANCE
Journal:  Brain       Date:  1960-12       Impact factor: 13.501

3.  Progressive familial myoclonic epilepsy in three families: its clinical features and pathological basis.

Authors:  D G HARRIMAN; J H MILLAR; A C STEVENSON
Journal:  Brain       Date:  1955-09       Impact factor: 13.501

4.  A study of myoclonus.

Authors:  J P BRADSHAW
Journal:  Brain       Date:  1954       Impact factor: 13.501

5.  Focal contralateral myoclonus produced by inhibition of GABA action in the caudate nucleus of rats.

Authors:  D Tarsy; C J Pycock; B S Meldrum; C D Marsden
Journal:  Brain       Date:  1978-03       Impact factor: 13.501

6.  Benign juvenile myoclonic epilepsy.

Authors:  C Dean; M Hauswald
Journal:  Am J Emerg Med       Date:  1987-11       Impact factor: 2.469

7.  A clinical analysis of myoclonus epilepsy (Unverricht-Lundborg), myoclonic cerebellar dyssynergy (Hunt) and hepatolenticular degeneration (Wilson).

Authors:  G WOHLFART; O HOOK
Journal:  Acta Psychiatr Neurol Scand       Date:  1951

8.  [Familial olivo-ponto-cerebellar atrophy with myoclonus. Limits of cerebellar myoclonic dyssynergia (Ramsay-Hunt syndrome)].

Authors:  M Bonduelle; R Escourolle; P Bouygues; G Lormeau; F Gray
Journal:  Rev Neurol (Paris)       Date:  1976-02       Impact factor: 2.607

9.  Sodium valproate and clonazepam in the treatment of intractable epilepsy.

Authors:  J W Lance; M Anthony
Journal:  Arch Neurol       Date:  1977-01

10.  Myoclonic dystonia.

Authors:  J A Obeso; J C Rothwell; A E Lang; C D Marsden
Journal:  Neurology       Date:  1983-07       Impact factor: 9.910

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  3 in total

Review 1.  Substance of abuse and movement disorders: complex interactions and comorbidities.

Authors:  Andres Deik; Rachel Saunders-Pullman; Marta San Luciano
Journal:  Curr Drug Abuse Rev       Date:  2012-09

2.  Myoclonus.

Authors:  Victoria C Chang; Steven J Frucht
Journal:  Curr Treat Options Neurol       Date:  2008-05       Impact factor: 3.598

3.  A patient with genetically confirmed myoclonus-dystonia responded to anticholinergic treatment and improved spontaneously.

Authors:  Jae Hyeok Lee; Chul Hyoung Lyoo; Myung Sik Lee
Journal:  J Clin Neurol       Date:  2011-12-29       Impact factor: 3.077

  3 in total

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