(Q53711169)

English

[Sudanophilic (mitochondria) myopathy (author's transl)].

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 May 2018

http://europepmc.org/abstract/MED/4134756

[Sudanophilic (mitochondria) myopathy (author's transl)]. (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 May 2018

http://europepmc.org/abstract/MED/4134756

1 reference

based on heuristic

inferred from title

author name string

F Gullotta

1

1 reference

Europe PubMed Central

PubMed publication ID

18 May 2018

http://europepmc.org/abstract/MED/4134756

T R Payk

2

1 reference

Europe PubMed Central

PubMed publication ID

18 May 2018

http://europepmc.org/abstract/MED/4134756

A Solbach

3

1 reference

Europe PubMed Central

PubMed publication ID

18 May 2018

http://europepmc.org/abstract/MED/4134756

publication date

1 April 1974

1 reference

Europe PubMed Central

PubMed publication ID

18 May 2018

http://europepmc.org/abstract/MED/4134756

Zeitschrift fur Neurologie

1 reference

Europe PubMed Central

PubMed publication ID

18 May 2018

http://europepmc.org/abstract/MED/4134756

206

1 reference

Europe PubMed Central

PubMed publication ID

18 May 2018

http://europepmc.org/abstract/MED/4134756

4

1 reference

Europe PubMed Central

PubMed publication ID

18 May 2018

http://europepmc.org/abstract/MED/4134756

309-326

1 reference

Europe PubMed Central

PubMed publication ID

18 May 2018

http://europepmc.org/abstract/MED/4134756

Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 2. Biochemical findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipid storage myopathy: A recognizable clinicopathological entity?

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical Studies of a Patient With Pyruvate Decarboxylase Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myopathy in Cushing's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carnitine Deficiency of Human Skeletal Muscle with Associated Lipid Storage Myopathy: A New Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A myopathy associated with lipid storage

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myopathy associated with pigmentation following adrenalectomy for Cushing's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new mitochondrial myopathy in a patient with salt craving.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ultrastructural mitochondrial anomalies in myopathies and their diagnostic significance

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Skeletal-Muscle Disorder Associated with Intermittent Symptoms and a Possible Defect of Lipid Metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cortisone myopathy in rabbits: A light and electron microscopic study

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New myopathy with mitochondrial enzyme hyperactivity. Histochemical demonstration

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

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

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipid storage myopathy responsive to prednisone

1 reference

https://pubmed.ncbi.nlm.nih.gov/4134756

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 May 2018

http://europepmc.org/abstract/MED/4134756

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