(Q44232431)

1 December 2017

Arthrogryposis multiplex congenita: spectrum of pathologic changes (English)

1 reference

1 December 2017

Banker BQ

1

1 reference

PubMed ID

3721492

1 December 2017

language of work or name

English

0 references

publication date

1 July 1986

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1 December 2017

1 reference

1 December 2017

17

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1 December 2017

656-672

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1 December 2017

7

1 reference

Oligohydramnios, cause of the nonrenal features of Potter's syndrome, including pulmonary hypoplasia

1 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Kongenitale, atonisch-sklerotische Muskeldystrophie, ein weiterer Typus der heredodegenerativen Erkrankungen des neuromuskulären Systems

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

1 reference

7 January 2021

Amyoplasia Congenita: (Multiple congenital articular rigidity: Arthrogryposis multiplex congenita).

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

A case of arthrogryposis multiplex congenita anatomically appearing as a foetal spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Arthrogryposis multiplex due to congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Neuropathologic findings in the spinal cords of 10 infants with arthrogryposis

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Cerebro-hepato-renal syndrome of Zellweger: an inherited disorder of neuronal migration.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Cerebro-hepato-renal syndrome. Report of a case with histochemical and ultrastructural observations

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Ocular histopathologic and biochemical studies of the cerebrohepatorenal syndrome (Zellweger's syndrome) and its relationship to neonatal adrenoleukodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Striated adrenocortical cells in cerebro-hepato-renal (Zellweger) syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Neurologic aspects of the Mobius syndrome. A case study with electromyography of the extraocular and facial muscles

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Moebius's syndrome; congenital oculofacial paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Möbius syndrome due to brain stem tegmental necrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Moebius Syndrome in Kallmann Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Mobius Syndrome and Facioscapulohumeral Muscular Dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Bovine congenital arthrogryposis in New South Wales.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Congenital bovine epizootic arthrogryposis and hydranencephaly in Australia. Distribution of antibodies to Akabane virus in Australian Cattle after the 1974 epizootic

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Enzyme histochemistry on skeletal muscle of the human foetus

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Development of fiber types in human fetal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Data on the distribution of fibre types in thirty-six human muscles. An autopsy study

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

The histographic analysis of human muscle biopsies with regard to fiber types: I. Adult male and female

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

The histographic analysis of human muscle biopsies with regard to fiber types. 2. Diseases of the upper and lower motor neuron

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

The histographic analysis of human muscle biopsies with regard to fiber types: 3. Myotonias, myasthenia gravis, and hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

A histochemical study of muscle in club foot

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Neuromuscular studies in clubfoot.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

A case of amyoplasia congenita, with pathological report

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Part I. Amyoplasia: A common, sporadic condition with congenital contractures

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Part II. Amyoplasia: Twinning in amyoplasia—a specific type of arthrogryposis with an apparent excess of discordantly affected identical twins

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Infantile muscular atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Congenital non-progressive peripheral neuropathy with arthrogryposis multiplex

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

A dominantly inherited lower motor neuron disorder presenting at birth with associated arthrogryposis

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Arthrogryposis multiplex congenita. Report of two cases of a radicular type with familial incidence.

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Arthrogryposis following treatment of maternal tetanus with muscle relaxants

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Arthrogryposis Multiplex Congenita due to Congenital Myasthenia

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Experimental clubfoot and arthrogryposis multiplex congenita

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Congenital muscular dystrophy (CMD) - a collagen formative disease?

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Maturational defect of regenerating muscle fibers in cases with duchenne and congenital muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Light and electron microscopic studies of congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Congenital dystrophia myotonica

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Clinical effects of myotonic dystrophy on pregnancy and the neonate

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Maturational arrest of fetal muscle in neonatal myotonic dystrophy. A pathologic study of four cases

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

[Neonatal forms of Steinert's mytonic dystrophy]

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

Congenital abnormalities in newborn lambs after infection of pregnant sheep with Akabane virus

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

The muscles in club foot--a histological histochemical and electron microscopic study

1 reference

https://api.crossref.org/works/10.1016%2FS0046-8177%2886%2980177-0

7 January 2021

10.1016/S0046-8177(86)80177-0

Identifiers

DOI

1 reference

1 December 2017

1 reference

PubMed ID

3721492