(Q52087505)

21 April 2018

title

Troyer syndrome revisited. A clinical and radiological study of a complicated hereditary spastic paraplegia. (English)

1 reference

21 April 2018

1 reference

1

1 reference

21 April 2018

author name string

Harold Cross

2

1 reference

21 April 2018

Heema Patel

3

1 reference

21 April 2018

Michael A Patton

4

1 reference

21 April 2018

Alan Valentine

5

1 reference

21 April 2018

Andrew H Crosby

6

1 reference

21 April 2018

publication date

1 September 2004

1 reference

21 April 2018

published in

Journal of Neurology

1 reference

21 April 2018

volume

251

1 reference

21 April 2018

issue

9

1 reference

21 April 2018

page(s)

1105-1110

1 reference

21 April 2018

Troyer syndrome: a combination of central brain abnormality and motor neuron disease?

cites work

1 reference

12 December 2020

Hereditary spastic paraparesis with distal muscle wasting, microcephaly, mental retardation, arachnodactyly and tremors: New entity?

1 reference

12 December 2020

Strümpell's familial spastic paraplegia: genetics and neuropathology

1 reference

12 December 2020

Familial spastic paraplegia, axonal sensory-motor polyneuropathy and bulbar amyotrophy with facial dysmorphia: new cases of Troyer-like syndrome

1 reference

12 December 2020

A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members.

1 reference

12 December 2020

Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15.

1 reference

12 December 2020

The mast syndrome. A recessively inherited form of presenile dementia with motor disturbances

1 reference

12 December 2020

Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 families

1 reference

12 December 2020

Is the transportation highway the right road for hereditary spastic paraplegia?

1 reference

12 December 2020

SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.

1 reference

12 December 2020

Hereditary (familial) spastic paraplegia; further clinical and pathologic observations.

1 reference

12 December 2020

Phenotypic and genotypic heterogeneity in hereditary motor neuronopathy type V: a clinical, electrophysiological and genetic study

1 reference

12 December 2020

ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF

1 reference

12 December 2020

Familial spastic paraplegia with distal muscle wasting in the Old Order Amish; atypical Troyer syndrome or “new” syndrome*

1 reference

12 December 2020

Hereditary spastic paraplegias

1 reference

12 December 2020

The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting

1 reference

12 December 2020

Troyer Syndrome: report of the first "non-Amish" sibship and review

1 reference

12 December 2020

Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia

1 reference

12 December 2020

The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype

1 reference

12 December 2020

Hereditary spastic paraparesis: a review of new developments.

1 reference

12 December 2020

GENETIC STUDIES OF THE AMISH, BACKGROUND AND POTENTIALITIES

1 reference

12 December 2020

Complicated hereditary spastic paraparesis with cerebral white matter lesions

1 reference

12 December 2020

Autosomal recessive paraparesis with amyotrophy of hands and feet and white matter lesions.

1 reference

12 December 2020

Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15.

1 reference

12 December 2020

A survey of neurological disorders in a genetic isolate

1 reference

12 December 2020

Clinical heterogeneity of autosomal recessive spastic paraplegias: analysis of 106 patients in 46 families.

1 reference

12 December 2020

X-linked pure familial spastic paraparesis. Characterization of a large kindred with magnetic resonance imaging studies

1 reference

12 December 2020

10.1007/S00415-004-0491-3

Identifiers

DOI

1 reference

21 April 2018

1 reference

21 April 2018