(Q48136727)

English

Gitelman disease associated with growth hormone deficiency, disturbances in vasopressin secretion and empty sella: a new hereditary renal tubular-pituitary syndrome?

scientific article published in August 1999

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

Gitelman disease associated with growth hormone deficiency, disturbances in vasopressin secretion and empty sella: a new hereditary renal tubular-pituitary syndrome? (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

0 references

growth hormone deficiency

1 reference

based on heuristic

inferred from title

author name string

A Bettinelli

1

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

R Rusconi

2

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

S Ciarmatori

3

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

V Righini

4

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

E Zammarchi

5

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

M A Donati

6

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

C Isimbaldi

7

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

M Bevilacqua

8

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

L Cesareo

9

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

S Tedeschi

10

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

R Garavaglia

11

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

G Casari

12

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

language of work or name

0 references

publication date

1 August 1999

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

Pediatric Research

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

46

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

2

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

232-238

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Hypomagnesaemia of hereditary renal origin

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

A Comparison of Plasma Vasopressin Measurements with a Standard Indirect Test in the Differential Diagnosis of Polyuria

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Osmoregulation of vasopressin secretion and thirst in health and disease

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Congenital hypokalemia with hypercalciuria in preterm infants: a hyperprostaglandinuric tubular syndrome different from Bartter syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Renal magnesium handling: new insights in understanding old problems

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Sexual maturation in East German girls

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Nonsteroidal antiinflammatory drugs. Renal toxicity. Review of pediatric issues

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Case Report: Familial Growth Hormone Deficiency Associated with Bartter’s Syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Bartter's syndrome with impairment of growth hormone secretion

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

The “Empty” Sella Turcica—A Manifestation of the Intrasellar Subarachnoid Space

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Relationship between the development of diaphragma sellae and the morphology of the sella turcica and its content

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

The primary empty-sella syndrome and diabetes insipidus in a child

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Vasoactive peptides in Bartter's syndrome.

1 reference

https://api.crossref.org/works/10.1203%2F00006450-199908000-00017

21 January 2018

Identifiers

10.1203/00006450-199908000-00017

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10447120

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q48136727&oldid=2209150422"