Motor neuron degeneration in a 20-week male fetus: spinal muscular atrophy type 0. (Q54505730)

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1 January 2020

title

Motor neuron degeneration in a 20-week male fetus: spinal muscular atrophy type 0 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17598601%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

main subject

spinal muscular atrophy

1 reference

1 reference

Harvey B Sarnat

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17598601%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Cynthia L Trevenen

series ordinal

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17598601%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

publication date

1 May 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17598601%20AND%20SRC:MED&resulttype=core&format=json

Canadian Journal of Neurological Sciences

1 January 2020

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17598601%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

volume

34

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1 January 2020

issue

2

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1 January 2020

page(s)

215-220

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17598601%20AND%20SRC:MED&resulttype=core&format=json

Infantile muscular atrophy

1 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006077

7 January 2021

Spinal muscular atrophy type I combined with atrial septal defect in three sibs.

1 reference

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7 January 2021

Diminutive fetal left ventricle at mid‐gestation associated with persistent left superior vena cava and coronary sinus dilatation

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006077

7 January 2021

Changing a diagnosis: the importance of neonatal autopsy

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006077

7 January 2021

Refined physical map of the spinal muscular atrophy gene (SMA) region at 5q13 based on YAC and cosmid contiguous arrays.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006077

7 January 2021

Spinal muscle atrophy type 1 (Werdnig-Hoffman disease) with complex cardiac malformation

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006077

7 January 2021

Identification and characterization of a spinal muscular atrophy-determining gene

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006077

7 January 2021

Pontocerebellar hypoplasia associated with infantile motor neuron disease (Norman's disease).

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006077

7 January 2021

Mutation of gene in spinal muscular atrophy respiratory distress type I

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https://api.crossref.org/works/10.1017%2FS0317167100006077

7 January 2021

"Marden-Walker syndrome": neuropathologic findings in two siblings

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006077

7 January 2021

Ubiquitin immunohistochemistry suggests classic motor neuron disease, motor neuron disease with dementia, and frontotemporal dementia of the motor neuron disease type represent a clinicopathologic spectrum.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006077

7 January 2021

Severe lethal spinal muscular atrophy variant with arthrogryposis

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https://api.crossref.org/works/10.1017%2FS0317167100006077

7 January 2021

Neuronal-specific roles of the survival motor neuron protein: evidence from survival motor neuron expression patterns in the developing human central nervous system

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https://api.crossref.org/works/10.1017%2FS0317167100006077

7 January 2021

Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006077

7 January 2021

Spinal muscular atrophy combined with congenital heart disease: a report of two cases.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006077

7 January 2021

10.1017/S0317167100006077

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17598601%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

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