(Q38538169)

3 September 2017

Laurence-Moon-Biedl syndrome (?) and Prader-Willi syndrome (?) in a single family (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A991874

12 August 2022

main subject

Prader–Willi syndrome

1 reference

M. Endo

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A991874

12 August 2022

Y. Tasaka

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A991874

12 August 2022

N. Matsuura

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A991874

12 August 2022

I. Matsuda

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A991874

12 August 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=991874

12 August 2022

publication date

1 November 1976

1 reference

3 September 2017

3 November 1976

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=991874

European Journal of Pediatrics

12 August 2022

published in

1 reference

3 September 2017

123

1 reference

3 September 2017

4

1 reference

3 September 2017

269-276

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00444648

3 September 2017

0 references

cites work

Retinal degeneration combined with obesity, diabetes mellitus and neurogenous deafness: a specific syndrome (not hitherto described) distinct from the Laurence-Moon-Bardet-Biedl syndrome: a clinical, endocrinological and genetic examination based on

1 reference

12 December 2020

Laurence-Moon-Biedl syndrome. Report of an unusual family

1 reference

12 December 2020

Anterior Pituitary Function in the Prader-Labhart-Willi (PLW) Syndrome

1 reference

12 December 2020

The Alström syndrome. Report of three cases with further delineation of the clinical, pathophysiological, and genetic aspects of the disorder

1 reference

12 December 2020

Prader-Willi syndrome in infant monozygotic twins

1 reference

12 December 2020

The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland. Clinical, genetic and epidemiological studies

1 reference

12 December 2020

13 cases of Laurence-Moon-Biedl syndrome

1 reference

12 December 2020

Laurence-Moon-Bardet-Biedl Syndrome in Israel

1 reference

12 December 2020

Syndrome of hypotonia-hypomentia-hypogonadism-obesity (HHHO) or Prader-Willi syndrome

1 reference

12 December 2020

The Prader-Labhart-Willi syndrome: review of the literature and report of nine cases

1 reference

12 December 2020

The Prader-Willi syndrome

1 reference

12 December 2020

Familial coexistence of diabetes mellitus, hyperlipemia, short stature, and hypogonadism

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00444648

1 reference

Dimensions Publication ID

3 September 2017

0 references

1 reference