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Wohlfart Kugelberg Welander syndrome
scientific article published on 01 May 1974
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4434270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4434270%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
title
Wohlfart Kugelberg Welander syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4434270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4434270%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
author name string
R T Ross
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4434270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4434270%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
C A Simpson
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4434270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4434270%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
S Styles
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4434270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4434270%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
publication date
1 May 1974
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4434270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4434270%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
published in
Canadian Journal of Neurological Sciences
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4434270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4434270%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
volume
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4434270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4434270%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4434270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4434270%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
page(s)
130-138
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4434270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4434270%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
cites work
Hereditary amyotrophic lateral sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary amyotrophic lateral sclerosis. Histochemical and electron microscopic study of hyaline inclusions in motor neurons
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
On the familial incidence of amyotrophic lateral sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
FAMILIAL MOTOR NEURONE DISEASE.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome preparations of leukocytes cultured from human peripheral blood
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chronic spinal muscular atrophy in adults. 1. The Kugelberg-Welander syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Histological and histochemical changes in skeletal muscle from cases of chronic juvenile and early adult spinal muscular atrophy (the Kugelberg-Welander syndrome).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epidemiologic investigations of amyotrophic lateral sclerosis. 2. Familial aggregations indicative of dominant inheritance. II.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epidemiologic investigations of amyotrophic lateral sclerosis. 2. Familial aggregations indicative of dominant inheritance. I.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Benign spinal muscular atrophy arising in childhood and adolescence
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Kugelberg-Welander Syndrome (Hereditary Proximal Spinal Muscular Atrophy)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electromyography and muscle biopsy in infantile spinal muscular atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An unusual spectrum of progressive spinal muscular atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial amyotrophic lateral sclerosis occurring in 4 generations. Report of a case
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial Proximal Spinal Muscular Atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia. A unique and partially treatable clinico-pathological entity.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
THE WOHLFART-KUGELBERG-WELANDER DISEASE; REVIEW OF THE LITERATURE AND REPORT OF A CASE.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Elevation of serum creatine phosphokinase in amyotrophic later a1 sclerosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new genetic variant of spinal muscular atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spinal muscular atrophy with autosomal dominant inheritance: Report of a new kindred
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Serum creatine phosphokinase in motor neuron disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial adult-onset proximal spinal muscular atrophy. Report of a family with type II hyperlipoproteinemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Proximal spinal muscular atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial amyotrophic lateral sclerosis. A subgroup characterized by posterior and spinocerebellar tract involvement and hyaline inclusions in the anterior horn cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0317167100019703
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1017/S0317167100019703
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4434270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4434270%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
PubMed publication ID
4434270
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4434270
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4434270%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
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