(Q39947738)

reason for preferred rank

15 September 2017

On the Pathogenesis of Duchenne Muscular Dystrophy* (English)

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

21 December 2022

On the pathogenesis of duchenne muscular dystrophy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A169179

21 December 2022

0 references

G. M. Fenichel

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A169179

21 December 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=169179

21 December 2022

publication date

1 August 1975

1 reference

full work available at URL

15 September 2017

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1469-8749.1975.tb03511.x

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1975.tb03511.x/fullpdf

21 December 2022

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Developmental Medicine and Child Neurology

21 December 2022

published in

1 reference

15 September 2017

17

1 reference

15 September 2017

4

1 reference

15 September 2017

527-533

1 reference

Human Muscular Dystrophy as an Aberration of the Connective Tissue

15 September 2017

1

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Terminal innervation ratio in neuromuscular disease. I. Methods and controls

21 December 2022

3

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Neuromuscular Fatigue in Dystrophic Muscle

21 December 2022

4

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Collateral Innervation of Muscle Fibres by Motor Axons of Dystrophic Motor Units

21 December 2022

5

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Electrophysiological studies of neuromuscular transmission in hereditary 'motor end-plate disease' of the mouse.

21 December 2022

6

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Study of long-term anticholinesterase therapy. Effects on neuromuscular transmission and on motor end-plate fine structure

21 December 2022

7

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Chronic inhibition of cholinesterase as a cause of myopathy.

21 December 2022

9

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Muscular dystrophy and other myopathies. Troponin activity of natural actomyosin from skeletal muscle

21 December 2022

10

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

End-plate cholinesterase in dystrophic muscle.

21 December 2022

11

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Evidence for a role of cyclic AMP in neuromuscular transmission

21 December 2022

12

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Denervation in Murine Dystrophy

21 December 2022

13

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Experimental myopathy after microarterial embolization; comparison with childhood x-linked pseudohypertrophic muscular dystrophy

21 December 2022

14

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Ribosomal protein synthesis in Duchenne muscular dystrophy

21 December 2022

16

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Identification of carriers of Duchenne muscular dystrophy by muscle protein synthesis

21 December 2022

17

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

The numbers of limb motor neurones in the individual segments of the human lumbosacral spinal cord

21 December 2022

18

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Duchenne dystrophy. I. Morphometric study of the muscle microvasculature.

21 December 2022

19

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Duchenne dystrophy. II. Morphometric study of motor end-plate fine structure.

21 December 2022

20

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Acyl phosphatase in normal and diseased human muscle

21 December 2022

21

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Muscle adenylic acid deaminase activity: Selective decrease in early-onset Duchenne muscular dystrophy

21 December 2022

22

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

A role of cyclic AMP in a neurotrophic process

21 December 2022

25

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Adenosine 3',5'-monophosphate: electrophysiological evidence for a role in synaptic transmission

21 December 2022

26

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Denervated muscle fibres in hereditary mouse dystrophy

21 December 2022

27

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Muscular Dystrophy: Evidence for a Neural Factor

21 December 2022

28

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

An electrophysiological study of Duchenne dystrophy

21 December 2022

30

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Multiple muscle analysis of motor units in muscular dystrophy

21 December 2022

31

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Adenyl cyclase in normal and pathologic human muscle

21 December 2022

32

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Duchenne Muscular Dystrophy: Functional Ischemia Reproduces Its Characteristic Lesions

21 December 2022

33

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Catecholamines and Indoleamines in Patients With Duchenne Muscular Dystrophy

21 December 2022

34

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

A correlation of histology and amino acid incorporation studies in Duchenne muscular dystrophy

21 December 2022

37

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Serotonin and Platelet Function in Duchenne Muscular Dystrophy

21 December 2022

38

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Some electrophysiological aspects of muscular dystrophy

21 December 2022

39

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Spinal motor neurones in murine muscular dystrophy and spinal muscular atrophy: A quantitative histological study

21 December 2022

42

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Electrophysiological estimation of motor units in Duchenne muscular dystrophy

21 December 2022

43

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Muscle blood flow in Duchenne type muscular dystrophy, limb-girdle dystrophy, polymyositis, and in normal controls

21 December 2022

44

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Histopathological features of muscle in the preclinical stages of muscular dystrophy

21 December 2022

45

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Myosin from normal and dystrophic human muscle. Immunochemical and electrophoretic studies

21 December 2022

46

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Development and specialization in muscle and the biochemistry of the dystrophies

21 December 2022

47

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Functional studies of reeenerated muscles from normal and dystrophic mice

21 December 2022

49

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Tropomyosin and troponin in normal and dystrophic human muscle

21 December 2022

50

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Actomyosin alterations in Duchenne muscular dystrophy

21 December 2022

51

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Biochemical abnormalities of the sarcoplasmic reticulum in muscular dystrophy

21 December 2022

52

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Duchenne muscular dystrophy: reservations to the neurogenic hypothesis

21 December 2022

53

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Sarcoplasmic reticulum in Duchenne muscular dystrophy.

21 December 2022

55

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

The role of cyclic 3',5'-adenosine monophosphate in neuromuscular transmission

21 December 2022

56

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Total numbers of limb motor neurones in the human lumbosacral cord and an analysis of the accuracy of various sampling procedures

21 December 2022

57

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Spinal cord limb motor neurones in muscular dystrophy

21 December 2022

58

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Abnormal intrafibrillar monoamines in sex-linked muscular dystrophy

21 December 2022

59

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

Pargyline-induced myopathy with histochemical characteristics of Duchenne muscular dystrophy

21 December 2022

60

1 reference

https://api.crossref.org/works/10.1111/J.1469-8749.1975.TB03511.X

21 December 2022

Identifiers

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=169179

21 December 2022

1 reference