Literature DB >> 3460301

Hereditary ataxias. Occurrence and clinical features.

L Werdelin.   

Abstract

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Year:  1986        PMID： 3460301

Source DB:  PubMed          Journal:  Acta Neurol Scand Suppl        ISSN： 0065-1427


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  6 in total

1.  Spinocerebellar ataxia: multipoint linkage analysis of genes associated with the disease locus.

Authors:  P J Wilkie; L J Schut; S S Rich
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

2.  Degenerative neurological disorders associated with deficiency of glutamate dehydrogenase.

Authors:  V S Kostić; L Mojsilović; M Stojanović
Journal:  J Neurol       Date:  1989-02       Impact factor: 4.849

3.  Evoked potentials in hereditary spastic paraplegia.

Authors:  I M Sawhney; S K Bansal; P K Upadhyay; J S Chopra
Journal:  Ital J Neurol Sci       Date:  1993-09

4.  Significance of MRI-confirmed atrophy of the cranial spinal cord in Friedreich's ataxia.

Authors:  K Wessel; G Schroth; H C Diener; W Müller-Forell; J Dichgans
Journal:  Eur Arch Psychiatry Neurol Sci       Date:  1989

5.  Prevalence of hereditary ataxias and spastic paraplegias in Molise, a region of Italy.

Authors:  A Filla; G De Michele; R Marconi; L Bucci; C Carillo; A E Castellano; L Iorio; C Kniahynicki; F Rossi; G Campanella
Journal:  J Neurol       Date:  1992-07       Impact factor: 4.849

6.  An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15.

Authors:  Geert Vander Stichele; Alexandra Durr; Grace Yoon; Rebecca Schüle; Craig Blackstone; Giovanni Esposito; Connor Buffel; Inês Oliveira; Christian Freitag; Stephane van Rooijen; Stéphanie Hoffmann; Leen Thielemans; Belinda S Cowling
Journal:  BMC Neurol       Date:  2022-03-24       Impact factor: 2.474
  6 in total

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