(Q41529330)

2 October 2017

title

The heterogeneity of distal arthrogryposis (English)

1 reference

2 October 2017

G. Hageman

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6091488

3 August 2023

F. G. Jennekens

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6091488

3 August 2023

J. K. Vette

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6091488

3 August 2023

J. Willemse

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6091488

3 August 2023

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=6091488

3 August 2023

publication date

1 January 1984

1 reference

full work available at URL

2 October 2017

https://api.elsevier.com/content/article/PII:S0387760484800406?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0387-7604(84)80040-6

https://api.elsevier.com/content/article/PII:S0387760484800406?httpAccept=text/plain

3 August 2023

1 reference

https://api.crossref.org/works/10.1016/S0387-7604(84)80040-6

3 August 2023

published in

Brain and Development

1 reference

2 October 2017

volume

6

1 reference

2 October 2017

issue

3

1 reference

2 October 2017

page(s)

273-283

1 reference

Arthrogryposis multiplex congenita. Case due to disease of the anterior horn cells

2 October 2017

cites work

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Arthrogryposis multiplex congenita. Review with comment

3 August 2023

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Increased Collagen Synthesis in Arthrogryposis Multiplex Congenita

3 August 2023

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The role of movement in the development of joints and related structures: the head and neck in the chick embryo

3 August 2023

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Concepts of multiple congenital contractures (arthrogryposis) in man and animals

3 August 2023

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The distal arthrogryposes: delineation of new entities--review and nosologic discussion

3 August 2023

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Autosomal-dominant inheritance of distal arthrogryposis

3 August 2023

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The clinical spectrum of congenital contractural arachnodactyly. A case with congenital heart disease

3 August 2023

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Hereditary contractures of the fingers (camptodactyly)

3 August 2023

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Camptodactyly, cleft palate, and club foot. A syndrome showing the autosomal-dominant pattern of inheritance

3 August 2023

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Camptodactyly, cleft palate, and club foot (the Gordon syndrome). A report of a large pedigree

3 August 2023

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Central core disease in one of identical twins

3 August 2023

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Central core disease with congenital hip dislocation: study of two families

3 August 2023

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Malignant Hyperthermia and Central Core Disease in a Child With Congenital Dislocating Hips

3 August 2023

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Central core disease-an investigation of a rare muscle cell abnormality

3 August 2023

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Correlative histochemical study of skeletal muscle after suprasegmental denervation, peripheral nerve section, and skeletal fixation

3 August 2023

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Enzyme histochemistry of skeletal muscle

3 August 2023

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Central core disease: histochemical and ultrastructural study of muscle biopsies of father and daughter

3 August 2023

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An approach to clinical dysmorphology

3 August 2023

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Fatal neonatal nemaline myopathy with multiple congenital anomalies

3 August 2023

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Abnormal Dermatoglyphics in Arthrogryposis Multiplex Congenita

3 August 2023

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Significance of dermatoglyphics and skin grooves in the diagnosis of arthromyogryposis multiplex congenita

3 August 2023

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A dominantly inherited form of arthrogryposis multiplex congenita with unusual dermatoglyphics

3 August 2023

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Some congenital abnormalities: Possibly due to embryonic peripheral neuropathy

3 August 2023

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Congenital non-progressive peripheral neuropathy with arthrogryposis multiplex

3 August 2023

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Arthrogryposis multiplex congenita. Simultaneous involvement of peripheral nerve and skeletal muscle

3 August 2023

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Lower motor neuron deficit in arthrogryposis. An EMG study

3 August 2023

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Neurogenic arthrogryposis in one identical twin

3 August 2023

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Arthrogryposis multiplex congenita: neurogenic type with autosomal recessive inheritance

3 August 2023

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Central core disease. Study of a family with five affected generations

3 August 2023

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Central core disease of muscle with focal wasting

3 August 2023

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Arthrogryposis multiplex congenita. Search for prenatal factors in 66 sporadic cases

3 August 2023

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3 August 2023

Identifiers

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6091488

3 August 2023

1 reference