About: The histographic analysis of human muscle biopsies with regard to fiber types. 4. Children's biopsies

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scientific article published on 01 June 1969

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 1969 (uk) im Juni 1969 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xunu de 1969 (ast) scientific article published on 01 June 1969 (en) գիտական հոդված հրատարակված 1969 թվականի հունիսի 1-ին (hy)
publication date	wds:Q72505897-11835817-4D5E-48D4-B662-556A69B425F5
publication date	1969-06-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q72505897-E999F368-652B-492D-A4B0-FABEC727FA64
language of work or name	English
author name string	wds:Q72505897-27CCE994-B050-4AD3-87BB-07F19A3280FF wds:Q72505897-C93C0E34-7EE5-4561-B741-C6467AEE7813
author name string	W K Engel M H Brooke
rdfs:label	The histographic analysis of human muscle biopsies with regard to fiber types. 4. Children's biopsies (en) The histographic analysis of human muscle biopsies with regard to fiber types. 4. Children's biopsies (nl)
skos:prefLabel	The histographic analysis of human muscle biopsies with regard to fiber types. 4. Children's biopsies (en) The histographic analysis of human muscle biopsies with regard to fiber types. 4. Children's biopsies (nl)
name	The histographic analysis of human muscle biopsies with regard to fiber types. 4. Children's biopsies (en) The histographic analysis of human muscle biopsies with regard to fiber types. 4. Children's biopsies (nl)
title	wds:Q72505897-6621EE0F-0B12-40F9-8761-40B29A53082B
title	The histographic analysis of human muscle biopsies with regard to fiber types. 4. Children's biopsies (en)
page(s)	wds:Q72505897-BD9AC577-3F6B-47B1-B15A-D340BD84F147
page(s)	591-605
instance of	wds:Q72505897-DC349E7C-A0B8-454B-A662-C3F031973226
instance of	scholarly article
PubMed ID	wds:Q72505897-A35AFE28-9BCC-44E4-922D-CBD7D0223A2D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/5814304
PubMed ID	5814304
published in	wds:Q72505897-8C37B68B-697B-4E97-B306-290FB20A5073
published in	Neurology
issue	wds:Q72505897-0F451259-1D96-4430-A1A5-E0183ED9E394
volume	wds:Q72505897-4C837A20-8A97-4C7F-8026-DBD0739B83E7
issue	6
volume	19
DOI	wds:Q72505897-FB2A01BC-7717-46D8-A58F-D798EEA637EA
DOI	http://dx.doi.org/10.1212/WNL.19.6.591
DOI	10.1212/WNL.19.6.591
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q72505897
is cites work of	Modeling the human MTM1 p.R69C mutation in murine Mtm1 results in exon 4 skipping and a less severe myotubular myopathy phenotype Defective myoblasts identified in Duchenne muscular dystrophy Familial focal loss of cross striations Arthrogryposis multiplex congenita: spectrum of pathologic changes Congenital fibre type disproportion myopathy. A histological diagnosis with an uncertain clinical outlook Short-term muscle power during growth and maturation Muscle fiber type transformation in nemaline myopathy and congenital fiber type disproportion. Myofiber size correlates with MTM1 mutation type and outcome in X-linked myotubular myopathy Child-adult differences in muscle activation--a review Anaerobic performance and metabolism in boys and male adolescents. A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy Multicore disease in twins Immunohistochemical study of muscle biopsy in children with cerebral palsy. Magnetic resonance imaging of mouse skeletal muscle to measure denervation atrophy Needle Biopsies of Muscle in Infants for Diagnosis and Research Severe insulin-resistant diabetes mellitus in patients with congenital muscle fiber type disproportion myopathy Congenital myopathies/dystrophies A benign form of reducing body myopathy Cross-sectional evaluation of electrical impedance myography and quantitative ultrasound for the assessment of Duchenne muscular dystrophy in a clinical trial setting Congenital cataract and mitochondrial myopathy of skeletal and heart muscle associated with lactic acidosis after exercise Obstetric lesions of the brachial plexus Skeletal Muscle Adaptability: Significance for Metabolism and Performance Muscle hypertrophy in Duchenne muscular dystrophy. A pathological and morphometric study New type of recessive X-linked muscular dystrophy: scapulo-humeral-distal muscular dystrophy with early contractures and cardiac arrhythmias Thickness and Histologic and Histochemical Properties of the Superior Pharyngeal Constrictor Muscle in Velocardiofacial Syndrome Motor unit fibre density in the extensor digitorum communis muscle. Single fibre electromyographic study in normal subjects at different ages Evaluation by exercise testing of the child with cerebral palsy. Validation of a simple, rapid, and economical technique for distinguishing type 1 and 2 fibres in fixed and frozen skeletal muscle Inhibition of activin receptor type IIB increases strength and lifespan in myotubularin-deficient mice Studies of malformation syndromes of man XIB: the cerebro-hepato-renal syndrome of zellweger: Comparative pathology The muscle fiber composition of skeletal muscle as a predictor of athletic success Comparison of clinical characteristics between congenital fiber type disproportion myopathy and congenital myopathy with type 1 fiber predominance Treatment with ActRIIB-mFc Produces Myofiber Growth and Improves Lifespan in the Acta1 H40Y Murine Model of Nemaline Myopathy. Myostatin inhibition using mRK35 produces skeletal muscle growth and tubular aggregate formation in wild type and TgACTA1D286G nemaline myopathy mice. Differential muscle hypertrophy is associated with satellite cell numbers and Akt pathway activation following activin type IIB receptor inhibition in Mtm1 p.R69C mice Selective muscle fiber type anomalies in neuromusclar disorders. An analysis of 124 consecutive muscle biopsies (author's transl) Satellite cells in human skeletal muscle; from birth to old age. Muscle fatigue during high-intensity exercise in children Congenital hypotonia revisited Electrical Impedance Myography and Its Applications in Neuromuscular Disorders Nemaline (rod) myopathy: the need for histochemical evaluation of affected families Follow-up studies in a case of unusual congenital myopathy, suggestive of nemaline type Propagation velocity of muscle action potentials in the growing normal child Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1 [High-intensity interval training for young athletes] Spatiotemporal coupling of the tongue in amyotrophic lateral sclerosis Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch families. Developmental patterns of peripheral nerve, myoneural junction and muscle: a review Congenital fiber type disproportion in identical twins Congenital fibre type disproportion with unusual clinico-pathologic manifestations Expression of growth associated protein 43 and neural cell adhesion molecule in congenital fibre type disproportion with interstitial myositis. Myogenes and Myotubes Metabolic substrates, muscle fibre composition and fibre size in late walking and normal children Histological Patterns of Muscle in Infants with Developmental Brain Abnormalities Congenital fiber type disproportion with fatal outcome: a case report Muscular changes in Engelmann's disease Congenital fiber type disproportion: severe form with marked improvement Arthrogryposis multiplex congenita in an infant with posterior agenesis of the corpus callosum Congenital type II fibre deficient myopathy Why is the electromyogram in obstetric brachial plexus lesions overly optimistic?

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