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Central diabetes insipidus
scientific article
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instance of
scholarly article
1 reference
stated in
PubMed
title
Central diabetes insipidus
(English)
1 reference
stated in
PubMed
main subject
diabetes insipidus
1 reference
based on heuristic
inferred from title
author name string
Arima H
series ordinal
1
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stated in
PubMed
Azuma Y
series ordinal
2
1 reference
stated in
PubMed
Morishita Y
series ordinal
3
1 reference
stated in
PubMed
Hagiwara D
series ordinal
4
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stated in
PubMed
language of work or name
English
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stated in
PubMed
publication date
December 2016
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stated in
PubMed
number of pages
10
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based on heuristic
inferred from page(s)
published in
Nagoya journal of medical science
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stated in
PubMed
volume
78
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stated in
PubMed
issue
4
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PubMed
page(s)
349-358
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PubMed
cites work
Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus-benefit of genetic testing.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Identification of five novel arginine vasopressin gene mutations in patients with familial neurohypophyseal diabetes insipidus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Identification of a Novel Deletion in AVP-NPII Gene in a Patient with Central Diabetes Insipidus.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
A novel AVP gene mutation in a Turkish family with neurohypophyseal diabetes insipidus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
AVP-NPII gene mutations and clinical characteristics of the patients with autosomal dominant familial central diabetes insipidus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Arginine vasopressin neuronal loss results from autophagy-associated cell death in a mouse model for familial neurohypophysial diabetes insipidus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Dilatative uropathy as a manifestation of neurohypophyseal diabetes insipidus due to a novel mutation in the arginine vasopressin-neurophysin-II gene.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
A novel variation in the AVP gene resulting in familial neurohypophyseal diabetes insipidus in a large Italian kindred
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Diabetes insipidus--diagnosis and management.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Familial forms of diabetes insipidus: clinical and molecular characteristics
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Familial neurohypophyseal diabetes insipidus due to a novel mutation in the arginine vasopressin-neurophysin II gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Growth retardation in untreated autosomal dominant familial neurohypophyseal diabetes insipidus caused by one recurring and two novel mutations in the vasopressin-neurophysin II gene.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Polyuria and polydipsia in a young child: diagnostic considerations and identification of novel mutation causing familial neurohypophyseal diabetes insipidus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Utility of AVP gene testing in familial neurohypophyseal diabetes insipidus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Mutation of Glu78 of the AVP-NPII gene impairs neurophysin as a carrier protein for arginine vasopressin in a family with neurohypophyseal diabetes insipidus.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Clinical insights into adipsic diabetes insipidus: a large case series.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Familial neurohypophyseal diabetes insipidus--an update
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Posterior lobe of the pituitary gland: correlation between signal intensity on T1-weighted MR images and vasopressin concentration
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
29 September 2017
Quality of life in the patients with central diabetes insipidus assessed by Nagasaki Diabetes Insipidus Questionnaire
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
2 June 2018
Regulation of vasopressin synthesis and release by area postrema in rats.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
2 June 2018
Adipsia increases risk of death in patients with central diabetes insipidus.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
27 November 2018
Efficacy and safety of desmopressin orally disintegrating tablet in patients with central diabetes insipidus: results of a multicenter open-label dose-titration study.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
27 November 2018
Clinical and molecular analysis of a Chinese family with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel missense mutation in the vasopressin-neurophysin II gene.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
27 November 2018
Progressive polyuria without vasopressin neuron loss in a mouse model for familial neurohypophysial diabetes insipidus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
27 November 2018
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene in a Brazilian family
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
27 November 2018
A novel heterozygous missense mutation in the vasopressin moiety is identified in a Japanese person with neurohypophyseal diabetes insipidus.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
27 November 2018
Hyperintensity of posterior pituitary on MR T1WI in a boy with central diabetes insipidus caused by missense mutation of neurophysin II gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
27 November 2018
Rapid and sensitive vasopressin heteronuclear RNA responses to changes in plasma osmolality.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
27 November 2018
Heredtary and idiopathic types of diabetes insipidus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5159460
retrieved
27 November 2018
Lymphocytic infundibuloneurohypophysitis as a cause of central diabetes insipidus
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/28008190
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Late-onset familial neurohypophyseal diabetes insipidus due to a novel mutation in the AVP gene
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/28008190
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/28008190
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Prevalence, predictors and patterns of postoperative polyuria and hyponatraemia in the immediate course after transsphenoidal surgery for pituitary adenomas
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/28008190
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Comparison of incidence of hyponatremia between intranasal and oral desmopressin in patients with central diabetes insipidus
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/28008190
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A novel deletion partly removing the AVP gene causes autosomal recessive inheritance of early-onset neurohypophyseal diabetes insipidus
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/28008190
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Induction of glucocorticoid receptor expression in hypothalamic magnocellular vasopressin neurons during chronic hypoosmolality
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/28008190
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.18999/NAGJMS.78.4.349
0 references
PMCID
5159460
1 reference
stated in
PubMed
PubMed ID
28008190
1 reference
stated in
PubMed
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