Movement disorders in Friedreich's ataxia (Q35024718)

5 August 2017

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title

Movement disorders in Friedreich's ataxia (English)

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5 August 2017

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2

Joseph Jankovic

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5 August 2017

Jyh-Gong Gabriel Hou

1

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5 August 2017

publication date

1 January 2003

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Journal of the Neurological Sciences

5 August 2017

published in

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5 August 2017

volume

206

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5 August 2017

issue

1

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5 August 2017

page(s)

59-64

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Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

5 August 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Friedreich's ataxia GAA repeat expansion in patients with recessive or sporadic ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

The Friedreich ataxia GAA triplet repeat: premutation and normal alleles.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Clinical and genetic abnormalities in patients with Friedreich's ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Friedreich ataxia: an overview

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Mapping of mutation causing Friedreich's ataxia to human chromosome 9

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Frataxin gene of Friedreich's ataxia is targeted to mitochondria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

The yeast frataxin homologue mediates mitochondrial iron efflux. Evidence for a mitochondrial iron cycle

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Molecular basis of Friedreich ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Pathological study of corticospinal-tract degeneration in Friedreich's ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

The neuropathology of "typical" Friedreich's ataxia in Quebec.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Characteristic alterations of long-loop "reflexes" in patients with Friedreich's disease and late atrophy of the cerebellar anterior lobe

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Quantification of postural sway in normals and patients with cerebellar diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Control of isometric finger force in patients with cerebellar disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Extrapyramidal motor signs in degenerative ataxias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Dystonia in spinocerebellar ataxia type 6

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

CLINICAL AND PATHOLOGICAL STUDIES OF AN HEREDITARY NEUROPATHY IN MICE (DYSTONIA MUSCULORUM)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Pathologic changes in the CNS of dystonia musculorum mutant mouse: an animal model for human spinocerebellar ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Amino Acid Changes in the Mouse Mutant Dystonia Musculorum Similar to Those in Friedreich’s Ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Friedreich ataxia associated with dystonic head tremor provoked by prolonged exercise

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Incidence, natural history, and treatment of scoliosis in Friedreich's ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Friedreich's ataxia 1980. An overview of the physiopathology.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Predominantly posterior instrumentation and fusion in neuromuscular and neurogenic scoliosis in children and adolescents

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Pathomechanics and management of scoliosis in Friedreich ataxia patients: preliminary report

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansion

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Friedreich's ataxia with chorea and myoclonus caused by a compound heterozygosity for a novel deletion and the trinucleotide GAA expansion

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Ueber Ataxie mit besonderer Berücksichtigung der hereditären Formen

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Myoclonic epilepsia partialis continua and Friedreich Ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Neuropathology of myoclonus epilepsy associated with ragged-red fibers (Fukuhara's disease).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Why do some Friedreich's ataxia patients retain tendon reflexes?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Broadened Friedreich's ataxia phenotype after gene cloning. Minimal GAA expansion causes late-onset spastic ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Friedreich's ataxia presenting as adult-onset spastic paraparesis

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

Spinal deformities in patients with Friedreich ataxia: a review of 19 patients

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

inferred from DOI database lookup

7 January 2021

based on heuristic

Why do some Friedreich's ataxia patients retain tendon reflexes? A clinical, neurophysiological and molecular study

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900321-0

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-510X(02)00321-0

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5 August 2017

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