(Q36714235)

15 August 2017

Vasopressin function in familial cranial diabetes insipidus (English)

1 reference

15 August 2017

0 references

1 reference

P. H. Baylis

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7279821

11 April 2024

G. L. Robertson

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7279821

11 April 2024

language of work or name

English

0 references

publication date

1 January 1981

1 reference

PMCID

2424765

full work available at URL

15 August 2017

https://pmj.bmj.com/content/57/663/36.full.pdf

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7279821

https://europepmc.org/articles/PMC2424765

11 April 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7279821

https://europepmc.org/articles/PMC2424765?pdf=render

11 April 2024

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7279821

https://academic.oup.com/pmj/article-pdf/57/663/36/50215966/postgradmedj-57-36.pdf

11 April 2024

file format

Portable Document Format

1 reference

Crossref

DOI

10.1136/PGMJ.57.663.36

https://api.crossref.org/works/10.1136/PGMJ.57.663.36

Postgraduate Medical Journal

11 April 2024

published in

1 reference

15 August 2017

57

1 reference

15 August 2017

36-40

1 reference

15 August 2017

663

1 reference

Two different mutations of the X-chromosome causing diabetes insipidus

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2424765

Development and Clinical Application of a New Method for the Radioimmunoassay of Arginine Vasopressin in Human Plasma

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2424765

Pedigrees with diabetes insipidus, diabetes mellitus, and optic atrophy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2424765

Genetic Approaches to the Study of the Regulation and Actions of Vasopressin

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2424765

The regulation of vasopressin function in health and disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2424765

Diabetes insipidus, diabetes mellitus, optic atrophy and deafness. A clinical and genetic study

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2424765

Hereditary hypothalamic diabetes insipidus in rats (Brattleboro strain). A useful experimental model.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2424765

Recessive inheritance of diabetes: the syndrome of diabetes insipidus, diabetes mellitus, optic atrophy and deafness.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2424765

HEREDITARY IDIOPATHIC DIABETES INSIPIDUS. A CASE REPORT WITH AUTOPSY FINDINGS.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2424765

Hereditary diabetes insipidus: unusual urinary tract changes

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2424765

Dominant inheritance of diabetes insipidus; a family study

20 October 2018

1 reference

12 December 2020

Hereditary diabetes insipidus: report of 20 cases in seven generations

1 reference

12 December 2020

Familial diabetes insipidus; report of one of fourteen cases in four generations

1 reference

12 December 2020

Primary or idiopathic diabetes insipidus: a system disease

1 reference

12 December 2020

A water deprivation test for the differential diagnosis of polyuria

1 reference

12 December 2020

The use of hypertonic saline infusions in the differential diagnosis of diabetes insipidus and psychogenic polydipsia

series ordinal

4

1 reference

Crossref

DOI

10.1136/PGMJ.57.663.36

https://api.crossref.org/works/10.1136/PGMJ.57.663.36

11 April 2024

Identifiers

DOI

10.1136/PGMJ.57.663.36

1 reference

15 August 2017

1 reference

15 August 2017

1 reference

PMCID

2424765