Literature DB >> 3332806

Acetazolamide responsive hereditary paroxysmal ataxia.

J H Friedman1, P A Hollmann.   

Abstract

The fourteenth family with an apparently autosomal dominant paroxysmal ataxia is described. As in the seven families described since 1978, acetazolamide completely cured the attacks. A possible mechanism of action of acetazolamide is discussed.

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Year:  1987        PMID： 3332806     DOI： 10.1002/mds.870020110

Source DB:  PubMed          Journal:  Mov Disord        ISSN： 0885-3185            Impact factor:   10.338


  4 in total

1.  The therapeutic mode of action of 4-aminopyridine in cerebellar ataxia.

Authors:  Karina Alviña; Kamran Khodakhah
Journal:  J Neurosci       Date:  2010-05-26       Impact factor: 6.167

2.  Persistent superior oblique paresis as a manifestation of familial periodic cerebellar ataxia.

Authors:  P G Bain; G B Larkin; D M Calver; M D O'Brien
Journal:  Br J Ophthalmol       Date:  1991-10       Impact factor: 4.638

3.  Familial paroxysmal ataxia: report of a family.

Authors:  C H Hawkes
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-03       Impact factor: 10.154

4.  Familial periodic cerebellar ataxia without myokymia maps to a 19-cM region on 19p13.

Authors:  B T Teh; P Silburn; K Lindblad; R Betz; R Boyle; M Schalling; C Larsson
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025
  4 in total

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