(Q43045657)

English

Clinical features and molecular analysis of arginine-vasopressin neurophysin II gene in long-term follow-up patients with idiopathic central diabetes insipidus

scientific article published in March 2010

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 November 2017

Clinical features and molecular analysis of arginine-vasopressin neurophysin II gene in long-term follow-up patients with idiopathic central diabetes insipidus (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 November 2017

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Jose Antunes-Rodrigues

3

object named as

Jose Antunes-Rodrigues

1 reference

Europe PubMed Central

PubMed publication ID

12 November 2017

author name string

Sergio L Batista

1

1 reference

Europe PubMed Central

PubMed publication ID

12 November 2017

Ayrton C Moreira

2

1 reference

Europe PubMed Central

PubMed publication ID

12 November 2017

Margaret de Castro

4

1 reference

Europe PubMed Central

PubMed publication ID

12 November 2017

Lucila L K Elias

5

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Europe PubMed Central

PubMed publication ID

12 November 2017

Paula C L Elias

6

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Europe PubMed Central

PubMed publication ID

12 November 2017

publication date

1 March 2010

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Europe PubMed Central

PubMed publication ID

12 November 2017

Arquivos Brasileiros de Endocrinologia e Metabologia

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Europe PubMed Central

PubMed publication ID

12 November 2017

54

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Europe PubMed Central

PubMed publication ID

12 November 2017

3

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Europe PubMed Central

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12 November 2017

269-273

1 reference

Europe PubMed Central

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12 November 2017

Familial neurohypophyseal diabetes insipidus--an update

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Molecular basis of autosomal dominant neurohypophyseal diabetes insipidus. Cellular toxicity caused by the accumulation of mutant vasopressin precursors within the endoplasmic reticulum

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Autosomal recessive familial neurohypophyseal diabetes insipidus with continued secretion of mutant weakly active vasopressin.

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Expression of three different mutations in the arginine vasopressin gene suggests genotype-phenotype correlation in familial neurohypophyseal diabetes insipidus kindreds

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Progressive decline of vasopressin secretion in familial autosomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin‐neurophysin II gene

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Clinical and molecular analysis of three families with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel and recurrent mutations in the vasopressin-neurophysin II gene

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Mechanism of endoplasmic reticulum retention of mutant vasopressin precursor caused by a signal peptide truncation associated with diabetes insipidus.

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Mutant vasopressin precursors that cause autosomal dominant neurohypophyseal diabetes insipidus retain dimerization and impair the secretion of wild-type proteins.

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Central diabetes insipidus. 22 years' experience.

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Etiologies of central diabetes insipidus in children

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Recognition of Partial Defects in Antidiuretic Hormone Secretion

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

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/10.1590%2FS0004-27302010000300004

21 January 2018

Endocrine disorders in pediatric - onset Langerhans Cell Histiocytosis.

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Clinical, hormonal and imaging findings in 27 children with central diabetes insipidus.

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Autosomal dominant neurohypophyseal diabetes insipidus with linkage to chromosome 20p13 but without mutations in the AVP-NPII gene

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Central diabetes insipidus and autoimmunity: relationship between the occurrence of antibodies to arginine vasopressin-secreting cells and clinical, immunological, and radiological features in a large cohort of patients with central diabetes insipid

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Vasopressin cell surface antibodies in central diabetes insipidus detected on cultured human foetal hypothalamus.

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Idiopathic central diabetes insipidus in children and young adults is commonly associated with vasopressin-cell antibodies and markers of autoimmunity.

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Magnetic resonance imaging of the hypothalamic-neurohypophyseal system

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Idiopathic central diabetes insipidus is associated with abnormal blood supply to the posterior pituitary gland caused by vascular impairment of the inferior hypophyseal artery system

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302010000300004

21 January 2018

Identifiers

10.1590/S0004-27302010000300004

1 reference

Europe PubMed Central

PubMed publication ID

12 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 November 2017

ResearchGate publication ID

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