(Q37432025)

20 August 2017

1 reference

title

Current developments in Wolfram syndrome (English)

1 reference

20 August 2017

Mohd Ashraf Ganie

1

1 reference

PubMed ID

19344068

20 August 2017

Dilafroze Bhat

series ordinal

2

1 reference

20 August 2017

1 January 2009

1 reference

Journal of Pediatric Endocrinology and Metabolism

20 August 2017

1 reference

20 August 2017

22

1 reference

20 August 2017

1

1 reference

20 August 2017

3-10

1 reference

Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome.

20 August 2017

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Morbidity and mortality in the Wolfram syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Optic atrophy and nerve deafness in diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Documented vasopressin deficiency in a child with Wolfram syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD syndrome). A clinical study in two Sudanese families

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Predisposition of Wolfram syndrome heterozygotes to psychiatric illness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Wolfram syndrome: hereditary diabetes mellitus with brainstem and optic atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Diabetes mellitus and optic atrophy: a study of Wolfram syndrome in the Lebanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Homozygosity mapping identifies an additional locus for Wolfram syndrome on chromosome 4q

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Sodium-potassium ATPase 1 subunit is a molecular partner of Wolframin, an endoplasmic reticulum protein involved in ER stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Testing of diabetes-associated WFS1 polymorphisms in the Diabetes Prevention Program

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Two cases of Wolfram syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Inverse correlation between expression of the Wolfs Hirschhorn candidate gene Letm1 and mitochondrial volume in C. elegans and in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf-Hirschhorn syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

A novel mutation in the WFS1 gene identified in a Taiwanese family with low-frequency hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

Common variants in WFS1 confer risk of type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

The Vasopressin Precursor Is Not Processed in the Hypothalamus of Wolfram Syndrome Patients with Diabetes Insipidus: Evidence for the Involvement of PC2 and 7B2

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.1.3

21 January 2018

Identifiers

DOI

10.1515/JPEM.2009.22.1.3

1 reference

20 August 2017

1 reference

PubMed ID

19344068