(Q33629025)

English

Muscle fibre type composition, motoneuron firing properties, axonal conduction velocity and refractory period for foot extensor motor units in dystrophia myotonica

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Muscle fibre type composition, motoneuron firing properties, axonal conduction velocity and refractory period for foot extensor motor units in dystrophia myotonica (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

author name string

Borg J

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Edström L

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Butler-Browne GS

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Thornell LE

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 August 1987

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Neurology, Neurosurgery and Psychiatry

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

50

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1036-1044

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Axonal refractory period of single short toe extensor motor units in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032233

21 June 2018

Contractile properties of muscles in myotonic dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032233

21 June 2018

Effects of prior activity on the conduction in single motor units in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032233

21 June 2018

Refractory period of single motor nerve fibres in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032233

21 June 2018

Electrophysiological study of dystrophia myotonica

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032233

21 June 2018

Muscle fiber types: how many and what kind?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032233

21 June 2018

The intramuscular nerve endings in dystrophia myotonica--a biopsy study by vital staining and electron microscopy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032233

21 June 2018

Effect of exercise on the motor unit

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032233

21 June 2018

Are muscle fibers denervated in myotonic dystrophy?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032233

21 June 2018

Motor neuron firing range, axonal conduction velocity, and muscle fiber histochemistry in neuromuscular diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032233

21 June 2018

Histochemical and histopathological changes in skeletal muscle in late-onset hereditary distal myopathy (Welander)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032233

21 June 2018

The histology of the neuromuscular junction in dystrophia myotonica.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032233

30 October 2018

Abnormal use of remaining motor units during locomotion in peroneal palsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032233

30 October 2018

Conduction velocity and refractory period of single motor nerve fibres in motor neuron disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032233

30 October 2018

An electron microscopic study of myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative study of the myotonic state. Correlative biochemical, histoenzymological and electrical investigations

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Histochemical and ultrastructural study of muscle biopsies in 3 cases of dystrophia myotonica in the newborn child

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peripheral Nerve Morphometry in Myotonic Dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Satellite cells and muscle regeneration in diseased human skeletal muscles

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Axonal conduction velocity and voluntary discharge properties of individual short toe extensor motor units in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myosin types in human skeletal muscle fibers

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital myotonic dystrophy: fiber type abnormalities in two cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three myosin heavy-chain isozymes appear sequentially in rat muscle development

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Embryonic and foetal myosins in human skeletal muscle. The presence of foetal myosins in duchenne muscular dystrophy and infantile spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fetal myosin heavy chains in regenerating muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Denervation of newborn rat muscles does not block the appearance of adult fast myosin heavy chain

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myosin isozyme transitions occurring during the postnatal development of the rat soleus muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transformation of fibre types in muscular dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle fibre type composition in distal myopathy (Welander)

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Promiscuous expression of myosin in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factors affecting the activity of adenosine triphosphatase and other phosphatases as measured by histochemical techniques

1 reference

https://pubmed.ncbi.nlm.nih.gov/3655808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JNNP.50.8.1036

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

0 references

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