(Q35150707)

6 August 2017

title

Chronic generalized spinal muscular atrophy of infancy and childhood. Arrested Werdnig-Hoffman disease (English)

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6 August 2017

main subject

spinal muscular atrophy

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Werdnig–Hoffmann disease

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Pearn JH

1

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6 August 2017

Wilson J

series ordinal

2

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6 August 2017

language of work or name

English

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publication date

1 October 1973

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Archives of Disease in Childhood

6 August 2017

published in

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6 August 2017

volume

48

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6 August 2017

issue

10

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6 August 2017

page(s)

768-774

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The amyotonia congenita syndrome

6 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.

28 July 2018

1 reference

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The Reliability of Paediatric Case-History Milestones

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

The Denver developmental screening test

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

A distal form of chronic spinal muscular atrophy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

The nosology of the spinal muscular atrophies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

Patients' subjective interpretation of risks offered in genetic counselling

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

Acute Werdnig-Hoffmann disease: acute infantile spinal muscular atrophy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

Parental acceptance of the handicapped child (illustrated with recorded case extracts).

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

Motor handicapped children: a study from a Swedish county

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

Progressive spinal muscular atrophy in infancy and childhood.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

A graphic method for the evaluation of motor development in infants.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

INFANTILE MUSCULAR ATROPHY. A PROSPECTIVE STUDY WITH PARTICULAR REFERENCE TO A SLOWLY PROGRESSIVE VARIETY

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

Scapuloperoneal muscular atrophy

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

Norms for Four Standard Developmental Milestones by Sex, Social Class and Place in Family

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

Neurogenic muscular atrophy of infancy with prolonged survival. The variable course of Werdnig-Hoffmann Disease

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

The Genetic Relationship of Progressive Muscular Dystrophy (Duchenne Type) and Mental Retardation

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1648514

Benign spinal muscular atrophy arising in childhood and adolescence

27 September 2018

1 reference

12 December 2020

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations

1 reference

12 December 2020

Heritable spinal muscular atrophies

1 reference

12 December 2020

Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease)

1 reference

12 December 2020

Fetal movements and Werdnig-Hoffmann disease

1 reference

12 December 2020

Infantile muscular atrophy

1 reference

12 December 2020

Identifiers

DOI

10.1136/ADC.48.10.768

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6 August 2017

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6 August 2017

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