Literature DB >> 1564494

Paroxysmal hemidystonia induced by prolonged exercise and cold.

G M Wali.   

Abstract

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Year:  1992        PMID： 1564494      PMCID： PMC1014742          DOI： 10.1136/jnnp.55.3.236

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


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  2 in total

1.  Paroxysmal kinesigenic choreoathetosis. An entity within the paroxysmal choreoathetosis syndrome. Description of 10 cases, including 1 autopsied.

Authors:  A Kertesz
Journal:  Neurology       Date:  1967-07       Impact factor: 9.910

2.  Familial paroxysmal dystonic choreoathetosis and its differentiation from related syndromes.

Authors:  J W Lance
Journal:  Ann Neurol       Date:  1977-10       Impact factor: 10.422
  2 in total
  5 in total

Review 1.  PRRT2-related disorders: further PKD and ICCA cases and review of the literature.

Authors:  Felicitas Becker; Julian Schubert; Pasquale Striano; Anna-Kaisa Anttonen; Elina Liukkonen; Eija Gaily; Christian Gerloff; Stephan Müller; Nicole Heußinger; Christoph Kellinghaus; Angela Robbiano; Anne Polvi; Simone Zittel; Tim J von Oertzen; Kevin Rostasy; Ludger Schöls; Tom Warner; Alexander Münchau; Anna-Elina Lehesjoki; Federico Zara; Holger Lerche; Yvonne G Weber
Journal:  J Neurol       Date:  2013-01-09       Impact factor: 4.849

Review 2.  Genetics of paroxysmal dyskinesias.

Authors:  Yvonne G Weber; Holger Lerche
Journal:  Curr Neurol Neurosci Rep       Date:  2009-05       Impact factor: 5.081

3.  Paroxysmal dyskinesias.

Authors:  Shyamal H Mehta; John C Morgan; Kapil D Sethi
Journal:  Curr Treat Options Neurol       Date:  2009-05       Impact factor: 3.598

4.  A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study.

Authors:  A Münchau; E M Valente; G A Shahidi; L H Eunson; M G Hanna; N P Quinn; A H Schapira; N W Wood; K P Bhatia
Journal:  J Neurol Neurosurg Psychiatry       Date:  2000-05       Impact factor: 10.154

5.  Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.

Authors:  Arvid Suls; Peter Dedeken; Karolien Goffin; Hilde Van Esch; Patrick Dupont; David Cassiman; Judith Kempfle; Thomas V Wuttke; Yvonne Weber; Holger Lerche; Zaid Afawi; Wim Vandenberghe; Amos D Korczyn; Samuel F Berkovic; Dana Ekstein; Sara Kivity; Philippe Ryvlin; Lieve R F Claes; Liesbet Deprez; Snezana Maljevic; Alberto Vargas; Tine Van Dyck; Dirk Goossens; Jurgen Del-Favero; Koen Van Laere; Peter De Jonghe; Wim Van Paesschen
Journal:  Brain       Date:  2008-06-24       Impact factor: 13.501
  5 in total

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