(Q39573421)

13 September 2017

title

Mitochondrial abnormalities of late motor neuron degeneration following poliomyelitis and other neurogenic muscular atrophies (English)

1 reference

18 November 2022

1 reference

1 reference

18 November 2022

3

A. Bertolotto

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A91673

18 November 2022

author name string

D. Schiffer

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A91673

18 November 2022

L. Palmucci

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A91673

18 November 2022

G. Monga

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A91673

18 November 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=91673

18 November 2022

publication date

1 September 1979

1 reference

full work available at URL

13 September 2017

http://link.springer.com/content/pdf/10.1007/BF00313051.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00313051/fulltext.html

18 November 2022

1 reference

http://link.springer.com/content/pdf/10.1007/BF00313051

18 November 2022

1 reference

18 November 2022

1 reference

13 September 2017

volume

221

1 reference

13 September 2017

issue

3

1 reference

13 September 2017

page(s)

193-201

1 reference

Neuromuscular Disorder Associated With a Defect in Mitochondrial Energy Supply

13 September 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00313051

A new mitochondrial myopathy in a patient with salt craving.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00313051

21 January 2018

Mitochondrial myopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Late Muscular Atrophy after Poliomyelitis

1 reference

12 December 2020

Mitochondrial myopathy with multisystem abnormalities and normal ocular movements

1 reference

12 December 2020

Morphologic and metabolic studies in a case of oculo-cranio-somatic neuromuscular disease

1 reference

12 December 2020

Late motor neuron degeneration following poliomyelitis

1 reference

12 December 2020

Sporadic oculopharyngeal myopathy with abnormal mitochondria

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Myopathy with mitochondrial inclusions

1 reference

12 December 2020

Distal and congenital myopathy with hypertrophy of the calves. Presence of mitochondrial anomalies

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Late onset mitochondrial myopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Mitochondrial functions in five cases of human neuromuscular disorders

1 reference

12 December 2020

Skeletal muscle disease with abnormal mitochondria

1 reference

12 December 2020

Ultrastructural mitochondrial anomalies in myopathies and their diagnostic significance

1 reference

12 December 2020

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

1 reference

12 December 2020

Experimental mitochondrial myopathy produced by in vivo uncoupling of oxidative phosphorylation

1 reference

12 December 2020

Hypothyroid myopathy. Clinical, electromyographical, and ultrastructural observations

1 reference

12 December 2020

MYOPATHIC DISORDER ASSOCIATED WITH MITOCHONDRIAL ABNORMALITIES, HYPERGLYCÆMIA, AND HYPERKETONÆMIA

1 reference

12 December 2020

Myopathy with abnormal structure and function of muscle mitochondria

1 reference

12 December 2020

Giant Mitochondria in Human Muscle With Inclusions

1 reference

12 December 2020

"Megaconial" mitochondria observed in a case of chronic polymyositis

1 reference

12 December 2020

Sudanophilic mitochondrial myopathy (author's transl)

1 reference

12 December 2020

Congenital oculoskeletal myopathy with abnormal muscle and liver mitochondria

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial Myopathy With Abnormal Muscle Mitochondria

1 reference

12 December 2020

Luft's disease. Further biochemical and ultrastructural studies of skeletal muscle in the second case

1 reference

12 December 2020

Myopathies with abnormal mitochondria. A clinical, histological, and electrophysiological study

1 reference

12 December 2020

"Myopathic" Changes in Chronically Denervated Muscle

1 reference

12 December 2020

Pathological changes in muscle biopsies from patients with peroneal muscular atrophy.

1 reference

12 December 2020

The Kearns-Shy syndrome. A multisystem disease with mitochondrial abnormality demonstrated in skeletal muscle and skin

1 reference

12 December 2020

8

114

169

J. Recondo De

1966

1 reference

Therapy of myotonia;: A double-blind evaluation of diphenylhydantoin, procainamide, and placebo

18 November 2022

27

1 reference

18 November 2022

Identifiers

DOI

10.1007/BF00313051

1 reference

13 September 2017

1 reference