(Q54504607)

30 May 2018

title

[Friedreich's ataxia with peripheral nerve involvement resembling peroneal muscular atrophy]. (English)

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30 May 2018

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H C Hopf

1

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30 May 2018

F K Port

series ordinal

2

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30 May 2018

publication date

1 January 1968

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30 May 2018

Deutsche Zeitschrift fur Nervenheilkunde

published in

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30 May 2018

volume

194

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30 May 2018

issue

1

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30 May 2018

page(s)

1-16

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30 May 2018

[Forms of heredo-ataxia of children and adolescents with severe involvement of the spinobulbomesencephalic motor nuclei.]

cites work

1 reference

12 December 2020

CHANGES IN NERVE CONDUCTION VELOCITY IN PATIENTS WITH NEUROPATHY AND NEURITIS. ON THE CLASSIFICATION OF DISEASES OF THE PERIPHERAL NERVES ACCORDING TO THE EMG

1 reference

12 December 2020

Three Brothers, illustrating an Unusual Form of Family Paralysis (Familial Lateral Sclerosis with Amyotrophy).

1 reference

12 December 2020

NERVE CONDUCTION TIMES IN NEUROLOGICAL DIAGNOSIS. EVIDENCE OF NEUROPATHIC COMPONENT IN SOME CASES OF SPINOCEREBELLAR DEGENERATION

1 reference

12 December 2020

[Neural muscle atrophy and Friedreich's tabes; observations through the study of another family of Berne]

1 reference

12 December 2020

Report of a family suffering from Friedreich's disease, peroneal muscular atrophy, and schizophrenia

1 reference

12 December 2020

[Friedrich's ataxia complicated by muscular atrophy; the effect of exogenous factors on the severity of heredo-familial abiotrophic processes]

1 reference

12 December 2020

Peroneal Atrophy, with Signs of Friedreich's Disease.

1 reference

12 December 2020

Familial peroneal muscular atrophy and its association with the familial ataxias and tremor and longevity

1 reference

12 December 2020

[HEREDO-DEGENERATIVE ATAXIA ASSOCIATED WITH HYPACUSIA.]

1 reference

12 December 2020

[Heredoataxia and neural muscular atrophy; case report]

1 reference

12 December 2020

FAMILIAL SYNDROME COMBINING ATAXIA, DEAFNESS AND OLIGOPHRENIA. MYOCARDIAL SCLEROSIS WITH FATAL DEVELOPMENT IN ONE OF THE CHILDREN

1 reference

12 December 2020

Connections between neural muscle atrophy and hereditary ataxia (Friedreich)

1 reference

12 December 2020

[Contribution to the study of heredo-familial dystrophic syndrome; case of the association of Charcot-Marie type of amyotrophia with Friedreich's disease]

1 reference

12 December 2020

[Distal amyotrophy of the Charcot-Marie type with nystagmus; clinical study and muscle biopsies]

1 reference

12 December 2020

NEW RESEARCH ON NEURAL MUSCULAR ATROPHY IN A FAMILY OF BERNE

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12 December 2020

A kinship with the Roussy-Levy syndrome

1 reference

12 December 2020

[An unusual spino-cerebellar heredo-degenerative sequence.]

1 reference

12 December 2020

[Amyotrophia in Friedreich's disease.]

1 reference

12 December 2020

An unusual familial cerebellar syndrome.

1 reference

12 December 2020

[On the genesis of peripheral-atrophic paralysis in spinal heredo-ataxia]

1 reference

12 December 2020

On a possible relationship between hereditary ataxia and peroneal muscular atrophy; with a critical review of the problems of intermediate forms in the degenerative disorders of the central nervous system

1 reference

12 December 2020

[Unusual form of familial disease of the nervous system, related to Friedreich's and Charcot-Marie diseases; two anatomoclinical observations]

1 reference

12 December 2020

Conduction velocity of nerves in a family with Charcot-Marie-Tooth disease: detection of latent involvement

1 reference

12 December 2020

Familial ataxia, deaf-mutism, and muscular wasting

1 reference

12 December 2020

[Case of Friedreich disease with Charcot-Marie amyotrophy clinical study.]

1 reference

12 December 2020

Extreme slowing of nerve conduction in peroneal muscular atrophy

1 reference

12 December 2020

MOTOR NERVE CONDUCTION VELOCITY DETERMINATION

1 reference

12 December 2020

Heredofamilial cerebellar ataxia with spastic paralysis and spinal muscular atrophy; report of two cases of an unusual syndrome

1 reference

12 December 2020

[Study of hereditary areflexic dystasia; present condition of four of the first seven cases of Roussy and Mlle. Lévy thirty years after the first publication of these authors]

1 reference

12 December 2020

[A family with Roussy-Levy syndrome.]

1 reference

12 December 2020

ELECTROMYOGRAPHIC STUDIES IN PERONEAL MUSCULAR ATROPHY: CHARCOT- MARIE-TOOTH DISEASE

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12 December 2020

Identifiers

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30 May 2018