Classification of spinal muscular atrophies (Q72423037)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6103267%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

title

Classification of spinal muscular atrophies (English)

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26 October 2019

author name string

J Pearn

series ordinal

1

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26 October 2019

publication date

1 April 1980

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26 October 2019

language of work or name

0 references

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26 October 2019

volume

1

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26 October 2019

issue

8174

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26 October 2019

page(s)

919-922

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The gene frequency of acute Werdnig-Hoffmann disease (SMA type 1). A total population survey in North-East England

26 October 2019

cites work

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7 January 2021

Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy

1 reference

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7 January 2021

A clinical study of chronic childhood spinal muscular atrophy. A review of 141 cases

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A genetic study of subacute and chronic spinal muscular atrophy in childhood. A nosological analysis of 124 index patients

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7 January 2021

Infantile and juvenile spinal muscular atrophy

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The genetic identity of acute infantile spinal muscular atrophy

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7 January 2021

Acute Werdnig-Hoffmann disease: acute infantile spinal muscular atrophy

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7 January 2021

Distal spinal muscular atrophy. A clinical and genetic study of 8 kindreds

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7 January 2021

Autosomal dominant spinal muscular atrophy: a clinical and genetic study

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7 January 2021

Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.

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7 January 2021

A clinical and genetic study of spinal muscular atrophy of adult onset: the autosomal recessive form as a discrete disease entity

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7 January 2021

Genetic studies of acute infantile spinal muscular atrophy (SMA type I). An analysis of sex ratios, segregation ratios, and sex influence

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7 January 2021

Anterior-horn cell degeneration and gross calf hypertrophy with adolescent onset. A new spinal muscular atrophy syndrome

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7 January 2021

The benign proximal spinal progressive muscular atrophies

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7 January 2021

A genetic study of infantile and juvenile myasthenia gravis

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7 January 2021

Amyotonia congenita: a follow-up study

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7 January 2021

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

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7 January 2021

International collaborative study of the spinal muscular atrophies. Part 1. Analysis of clinical and laboratory data

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7 January 2021

International collaborative study of the spinal muscular atrophies. Part 2. Analysis of genetic data

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7 January 2021

A METHOD FOR CLUSTER ANALYSIS.

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7 January 2021

Genetic heterogeneity for dystrophia myotonica

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7 January 2021

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

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7 January 2021

A distal form of chronic spinal muscular atrophy

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7 January 2021

A study of environmental factors in relation to fatal infantile spinal muscular atrophy (SMA type I). An analysis of birth order and parental age effects, social class, seasonal influence, and clustering in time and place

1 reference

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7 January 2021

Blood selenium in chronic spinal muscular atrophy

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7 January 2021

Spinal muscular atrophy with autosomal dominant inheritance: Report of a new kindred

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7 January 2021

A clinical and genetic study of chronic proximal spinal muscular atrophy

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7 January 2021

Proximal neurogenic muscular atrophy in adolescence and adulthood with X-linked recessive inheritance: Kugelberg-Welander disease and its variant of late onset in one pedigree

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7 January 2021

Familial progressive bulbar‐spinal muscular atrophy

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7 January 2021

Benign spinal muscular atrophy arising in childhood and adolescence

1 reference

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7 January 2021

Scapuloperoneal muscular atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2880%2990847-8

7 January 2021

A Spinal Muscular Atrophy With Scapuloperoneal Distribution

1 reference

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7 January 2021

Scapuloperoneal Amytrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2880%2990847-8

7 January 2021

X-linked scapuloperoneal syndrome

1 reference

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7 January 2021

10.1016/S0140-6736(80)90847-8

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6103267%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference