(Q39660923)

reason for deprecated rank

13 September 2017

title

Hereditary motor neuron disease: the proximal, adult, sex-linked form (or Kennedy disease). Clinical and neuroendocrinologic observations (English)

marking inconsistent with the registered/official identifier/name

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A108363

reason for deprecated rank

26 April 2022

Motoneuropathie héréditaire: La forme proximale de l'adulte liéé au sexe (ou maladie de kennedy) (French)

marking inconsistent with the registered/official identifier/name

1 reference

https://api.crossref.org/works/10.1016/0022-510X(79)90094-7

25 November 2022

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A108363

26 April 2022

1 reference

https://api.crossref.org/works/10.1016/0022-510X(79)90094-7

25 November 2022

author name string

J. Schoenen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A108363

26 April 2022

P. J. Delwaide

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A108363

26 April 2022

J. J. Legros

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A108363

26 April 2022

P. Franchimont

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A108363

26 April 2022

language of work or name

French

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=108363

26 April 2022

publication date

1 May 1979

1 reference

full work available at URL

13 September 2017

number of pages

15

1 reference

based on heuristic

inferred from page(s)

https://api.elsevier.com/content/article/PII:0022510X79900947?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0022-510X(79)90094-7

https://api.elsevier.com/content/article/PII:0022510X79900947?httpAccept=text/plain

25 November 2022

1 reference

https://api.crossref.org/works/10.1016/0022-510X(79)90094-7

Journal of the Neurological Sciences

25 November 2022

published in

1 reference

13 September 2017

volume

41

1 reference

13 September 2017

issue

3

1 reference

13 September 2017

page(s)

343-357

1 reference

Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait

13 September 2017

cites work

3

1 reference

https://api.crossref.org/works/10.1016/0022-510X(79)90094-7

Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.

25 November 2022

5

1 reference

https://api.crossref.org/works/10.1016/0022-510X(79)90094-7

Neurogenic Muscular Atrophy Simulating Muscular Dystrophy

25 November 2022

6

1 reference

https://api.crossref.org/works/10.1016/0022-510X(79)90094-7

THE WOHLFART-KUGELBERG-WELANDER DISEASE; REVIEW OF THE LITERATURE AND REPORT OF A CASE.

25 November 2022

9

1 reference

https://api.crossref.org/works/10.1016/0022-510X(79)90094-7

X-linked spinal and bulbar muscular atrophy of late onset. A separate type of motor neuron disease?

25 November 2022

10

1 reference

https://api.crossref.org/works/10.1016/0022-510X(79)90094-7

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

25 November 2022

11

1 reference

https://api.crossref.org/works/10.1016/0022-510X(79)90094-7

HEREDITARY PROXIMAL NEUROGENIC MUSCULAR ATROPHY IN ADULT

25 November 2022

12

1 reference

https://api.crossref.org/works/10.1016/0022-510X(79)90094-7

25 November 2022

Identifiers

1 reference

13 September 2017

1 reference