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Muscle Biopsies in Neuromuscular Diseases
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
4875469
retrieved
16 September 2017
review article
1 reference
stated in
Europe PubMed Central
title
Muscle Biopsies in Neuromuscular Diseases
(English)
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
main subject
biopsy
0 references
author name string
W. K. Engel
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
4875469
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4875469
retrieved
13 March 2023
language of work or name
English
1 reference
stated in
National Center for Biotechnology Information
PubMed ID
4875469
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=4875469
retrieved
13 March 2023
publication date
1 November 1967
1 reference
stated in
Europe PubMed Central
PubMed ID
4875469
retrieved
16 September 2017
full work available at URL
https://api.elsevier.com/content/article/PII:S0031395516320673?httpAccept=text/xml
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
https://api.elsevier.com/content/article/PII:S0031395516320673?httpAccept=text/plain
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
published in
Pediatric Clinics of North America
1 reference
stated in
Europe PubMed Central
PubMed ID
4875469
retrieved
16 September 2017
volume
14
1 reference
stated in
Europe PubMed Central
PubMed ID
4875469
retrieved
16 September 2017
issue
4
1 reference
stated in
Europe PubMed Central
PubMed ID
4875469
retrieved
16 September 2017
page(s)
963-995
1 reference
stated in
Europe PubMed Central
PubMed ID
4875469
retrieved
16 September 2017
cites work
Dermatomyositis (systemic angiopathy) of childhood
series ordinal
3
1 reference
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Familial non-progressive myopathy with muscle cramps after exercise. A new disease associated with cores in the muscle fibres.
series ordinal
4
1 reference
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Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Myopathia distalis juvenilis hereditaria
series ordinal
6
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
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13 March 2023
Thyroid function and myasthenia gravis
series ordinal
12
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
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13 March 2023
A CLINICAL APPROACH TO THE MYOPATHIES
series ordinal
13
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Focal myopathic changes produced by electromyographic and hypodermic needles. "Needle myopathy".
series ordinal
18
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
MITOCHONDRIAL AGGREGATES IN MUSCLE DISEASE
series ordinal
20
1 reference
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Muscle Target Fibres, a Newly Recognized Sign of Denervation
series ordinal
23
1 reference
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Histochemical studies of denervated or tenotomized cat muscle: illustrating difficulties in relating experimental animal conditions to human neuromuscular diseases
series ordinal
26
1 reference
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
RAPID EXAMINATION OF MUSCLE TISSUE. AN IMPROVED TRICHROME METHOD FOR FRESH-FROZEN BIOPSY SECTIONS
series ordinal
27
1 reference
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Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Neuropathy in Tangier disease. Alpha-Lipoprotein deficiency manifesting as familial recurrent neuropathy and intestinal lipid storage.
series ordinal
28
1 reference
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Central core disease-an investigation of a rare muscle cell abnormality.
series ordinal
30
1 reference
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Muscle lesions in myasthenia gravis. Discussion
series ordinal
34
1 reference
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Protein abnormalities in neuromuscular diseases. I.
series ordinal
35
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
NEMALINE MYOPATHY; A SECOND CASE
series ordinal
39
1 reference
stated in
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Myopathies in search of a name: benign congenital forms
series ordinal
41
1 reference
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
HISTOCHEMISTRY OF MUSCLE IN INFANTILE SPINAL MUSCULAR ATROPHY
series ordinal
42
1 reference
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Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
A syndrome characterized by myokymia, myotonia, muscular wasting and increased perspiration
series ordinal
43
1 reference
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
The prognostic value of the muscle biopsy in the floppy infant.
series ordinal
45
1 reference
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
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13 March 2023
Pathological changes in muscle biopsies from patients with peroneal muscular atrophy.
series ordinal
47
1 reference
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease).
series ordinal
49
1 reference
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
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13 March 2023
A MYOPATHY PRESENTING IN ADULT LIFE WITH FEATURES SUGGESTIVE OF GLYCOGEN STORAGE DISEASE.
series ordinal
51
1 reference
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.
series ordinal
52
1 reference
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DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
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
series ordinal
55
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
POMPE'S DISEASE (DIFFUSE GLYCOGENOSIS) WITH NEURONAL STORAGE
series ordinal
56
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Antibodies to muscle and thymus in nonmyasthenic patients with thymoma. Clinical evaluation
series ordinal
57
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Critical reappraisal of the use of edrophonium (tensilon) chloride tests in myasthenia gravis and significance of clinical classification
series ordinal
60
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Polymyositis and related disorders
series ordinal
61
1 reference
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Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
A metabolic myopathy due to absence of muscle phosphorylase
series ordinal
62
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
A third type of periodic paralysis, with normokalemia and favourable response to sodium chloride
series ordinal
63
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Ocular myopathy sensitive to curare.
series ordinal
67
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
A new myopathy due to glycolytic abnormalities
series ordinal
69
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in the muscle
series ordinal
70
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Ultrastructural studies of muscle in McArdle's disease
series ordinal
71
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
NEMALINE MYOPATHY
series ordinal
73
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Two childhood myopathies with abnormal mitochondria. I. Megaconial myopathy. II. Pleoconial myopathy
series ordinal
74
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
A new congenital non-progressive myopathy
series ordinal
75
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Myotubular Myopathy
series ordinal
77
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Refsum's disease--a recently characterized lipidosis involving the nervous system. Combined clinical staff conference at the National Institutes of Health
series ordinal
78
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Congenital myopathy--A fifty-year follow-up.
series ordinal
82
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Amyotonia congenita: a follow-up study
series ordinal
83
1 reference
stated in
Crossref
DOI
10.1016/S0031-3955(16)32067-3
reference URL
https://api.crossref.org/works/10.1016/S0031-3955(16)32067-3
retrieved
13 March 2023
Identifiers
DOI
10.1016/S0031-3955(16)32067-3
1 reference
stated in
National Center for Biotechnology Information
PubMed ID
4875469
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=4875469
retrieved
13 March 2023
PubMed ID
4875469
1 reference
stated in
Europe PubMed Central
PubMed ID
4875469
retrieved
16 September 2017
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