(Q39338106)

English

Mitochondrial changes of the skeletal muscle in the peroneal muscular atrophy (Charcot-Marie-Tooth disease). Histological and electron microscopic studies (author's transl)

scientific article published on January 1, 1975

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Mitochondrial changes of the skeletal muscle in the peroneal muscular atrophy (Charcot-Marie-Tooth disease). Histological and electron microscopic studies (author's transl) (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Mitochondrienver�nderungen im Skeletmuskel bei neuraler Muskelatrophie (Charcot-Marie-Tooth) (German)

reason for deprecated rank

marking inconsistent with the registered/official identifier/name

1 reference

10.1007/BF00312522

https://api.crossref.org/works/10.1007/BF00312522

7 April 2022

Mitochondrial changes of the skeletal muscle in the peroneal muscular atrophy (Charcot-Marie-Tooth disease). Histological and electron microscopic studies (author's transl) (English)

reason for deprecated rank

marking inconsistent with the registered/official identifier/name

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A50425

7 April 2022

muscular atrophy

1 reference

based on heuristic

inferred from title

1 reference

10.1007/BF00312522

https://api.crossref.org/works/10.1007/BF00312522

7 April 2022

author name string

G. Spalke

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A50425

7 April 2022

R. Heene

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A50425

7 April 2022

D. Herold

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A50425

7 April 2022

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=50425

7 April 2022

publication date

1 January 1975

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF00312522.pdf

Portable Document Format

1 reference

10.1007/BF00312522

https://api.crossref.org/works/10.1007/BF00312522

7 April 2022

http://link.springer.com/article/10.1007/BF00312522/fulltext.html

1 reference

10.1007/BF00312522

https://api.crossref.org/works/10.1007/BF00312522

7 April 2022

http://link.springer.com/content/pdf/10.1007/BF00312522

1 reference

10.1007/BF00312522

https://api.crossref.org/works/10.1007/BF00312522

7 April 2022

Journal of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

209

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

9-29

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

https://scigraph.springernature.com/pub.10.1007/bf00312522

0 references

Muscle fiber types: how many and what kind?

1 reference

https://api.crossref.org/works/10.1007%2FBF00312522

21 January 2018

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies

1 reference

https://api.crossref.org/works/10.1007%2FBF00312522

21 January 2018

Amyotrophic lateral sclerosis with progressive dementia and with pathologic findigs of the Creutzfeldt-Jakob syndrome.

1 reference

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21 January 2018

Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.

1 reference

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21 January 2018

A new mitochondrial myopathy in a patient with salt craving.

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21 January 2018

Mitochondrial myopathy

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A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study

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Enzymic Activities of Human Skeletal Muscle Mitochondria: A Tool in Clinical Metabolic Research

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https://pubmed.ncbi.nlm.nih.gov/50425

12 December 2020

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Nerve conduction studies in Charcot-Marie-Tooth disease

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Studies on nerve conduction in neural muscular atrophy and Friedreich's hereditary ataxia

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12 December 2020

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"Sick" motoneurones. A unifying concept of muscle disease

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Myopathy with tremor and dementia: a metabolic disorder? Case report with postmortem study

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MOTOR CONDUCTION VELOCITIES IN AMYOTROPHIC LATERAL SCLEROSIS, POLYRADICULONEURITIS AND CHARCOT-MARIE-TOOTH'S DISEASE

1 reference

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12 December 2020

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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

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[On progressive myopathy with muscle phosphorylase deficiency and giant mitochondria]

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12 December 2020

based on heuristic

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Mitochondrial ultrastructure with crystalloid inclusions in an unusual type of human myopathy

1 reference

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12 December 2020

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The histographic analysis of human muscle biopsies with regard to fiber types: I. Adult male and female

1 reference

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12 December 2020

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Charcot-Marie-Tooth disease with associated myopathy. A report of a family

1 reference

https://pubmed.ncbi.nlm.nih.gov/50425

12 December 2020

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NERVE CONDUCTION AND OTHER STUDIES IN FAMILIES WITH CHARCOT-MARIE-TOOTH DISEASE

1 reference

https://pubmed.ncbi.nlm.nih.gov/50425

12 December 2020

based on heuristic

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Peroneal Atrophy, with Signs of Friedreich's Disease.

1 reference

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12 December 2020

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The sizes of the two main histochemical fibre types in five limb muscles in man. An autopsy study

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12 December 2020

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Opthalmoplegia externa progressiva. A clinical and morphological study (author's transl)

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12 December 2020

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Electron microscopic and enzyme histochemical studies of cerebellum, ocular and skeletal muscles in chronic progressive ophthalmoplegia with cerebellar ataxia.

1 reference

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12 December 2020

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[Histological-histochemical studies on muscular changes in pseudomyopathic spinal muscular atrophy (Wohlfart-Kugelberg-Welander)].

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12 December 2020

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Segmental demyelinization in peroneal muscular atrophy: nerve fibers teased from sural nerve biopsy specimens

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The primary spino-cerebellar atrophies and their associated defects, with a study of the foot deformity.

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The fine structure of type II muscle fiber atrophy

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Oculopharyngeal muscular dystrophy. A case with abnormal mitochondria and "fingerprint" inclusions

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Myopathy with atypical mitochondria in type I skeletal muscle fibers. A histochemical and ultrastructural study

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Eaton-Lambert syndrome. Ultrastructural study of the motor end-plates

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Myopathy with mitochondrial inclusions

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Two childhood myopathies with abnormal mitochondria. I. Megaconial myopathy. II. Pleoconial myopathy

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[Ultrastructural study on progressive ocular muscular dystrophy with particular regard to mitochondrial transformation]

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Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 1. Clinical, electrophysiological and pathological findings

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Late onset mitochondrial myopathy

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Thyrotoxic hypokalemic periodic paralysis

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[Electron microscopic study of muscular lesions of neurogenic atrophy caused by injury of the anterior horn (seen in 8 cases of amyotrophic lateral sclerosis)]

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An unusual familial cerebellar syndrome.

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Mitochondrial functions in five cases of human neuromuscular disorders

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[Ovular myopathy with primary hypogonadism. Mitochondrial abnormalities in ultrastructural study]

1 reference

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Severe sensory changes, and trophic disorder, in peroneal muscular atrophy (Charcot-Marie-Tooth type)

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Electromyographic studies in amyotrophic lateral sclerosis

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1 reference

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On familial ataxia, neural amyotrophy, and their association with progressive external ophthalmoplegia.

1 reference

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Ultrastructural mitochondrial anomalies in myopathies and their diagnostic significance

1 reference

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12 December 2020

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Myopathy with mitochondrial abnormalities localizated in type I fibers. Clinical, histochemical and ultrastructural data apropos of a diffuse atrophic form with ocular onset

1 reference

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Clinical and metabolic study of a case of Eulenburg's congenital paramyotonie. Ultrastructural data concerning the muscle biopsy

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A generalized disorder of nervous system, skeletal muscle and heart resembling Refsum's disease and Hurler's syndrome. II. Ultrastructure

1 reference

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12 December 2020

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Hypothyroid myopathy. Clinical, electromyographical, and ultrastructural observations

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Progressive neuropathic (peroneal) muscular atrophy (Charcot-Marie-Tooth disease); histological findings in muscle biopsy specimens in fourteen cases, with notes on clinical diagnosis and familial occurrence

1 reference

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MYOPATHIC DISORDER ASSOCIATED WITH MITOCHONDRIAL ABNORMALITIES, HYPERGLYCÆMIA, AND HYPERKETONÆMIA

1 reference

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12 December 2020

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1 reference

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12 December 2020

based on heuristic

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Electron microscopic study of the muscle changes in diabetic amyotrophy

1 reference

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Giant Mitochondria in Human Muscle With Inclusions

1 reference

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12 December 2020

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"Megaconial" mitochondria observed in a case of chronic polymyositis

1 reference

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12 December 2020

based on heuristic

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/50425

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morphologic features of hypermetabolic mitochondrial disease. A light microscopic, histochemical and electron microscopic study

1 reference

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12 December 2020

based on heuristic

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1 reference

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12 December 2020

based on heuristic

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Autophagic glycogenosis of late onset with mitochondrial abnormalities: light and electron microscopic observations

1 reference

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based on heuristic

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1 reference

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based on heuristic

inferred from PubMed ID database lookup

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1 reference

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12 December 2020

based on heuristic

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1 reference

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12 December 2020

based on heuristic

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

1 reference

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1 reference

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12 December 2020

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Revue neurologique

12

126

81

author name string

P. Castaigne

publication date

1972

1 reference

10.1007/BF00312522

https://api.crossref.org/works/10.1007/BF00312522

7 April 2022

Revue neurologique

16

114

169

author name string

J. Recondo De

publication date

1966

1 reference

10.1007/BF00312522

https://api.crossref.org/works/10.1007/BF00312522

7 April 2022

22

43

233

author name string

A. G. Engel

publication date

1968

1 reference

10.1007/BF00312522

https://api.crossref.org/works/10.1007/BF00312522

7 April 2022

Revue neurologique

28

115

295

author name string

R. Garcin

publication date

1966

1 reference

10.1007/BF00312522

https://api.crossref.org/works/10.1007/BF00312522

7 April 2022

34

41

0 references

Identifiers

10.1007/BF00312522

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

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