(Q43955531)

28 November 2017

title

Evaluation of insulin resistant diabetes mellitus in Alström syndrome: a long-term prospective follow-up of three siblings (English)

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28 November 2017

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Satman I

1

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28 November 2017

Yilmaz MT

2

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28 November 2017

Gürsoy N

3

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28 November 2017

Karşidağ K

4

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28 November 2017

Dinççağ N

5

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28 November 2017

Ovali T

6

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28 November 2017

Karadeniz S

7

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28 November 2017

Uysal V

8

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28 November 2017

Buğra Z

9

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28 November 2017

Okten A

10

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28 November 2017

Devrim S

11

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28 November 2017

publication date

1 June 2002

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Diabetes Research and Clinical Practice

28 November 2017

published in

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28 November 2017

volume

56

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28 November 2017

issue

3

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28 November 2017

page(s)

189-196

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Familial syndrome of primary testicular insufficiency with normal virilization, blindness, deafness and metabolic abnormalities

28 November 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0168-8227%2802%2900004-9

7 January 2021

Hepatic dysfunction in Alström disease

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8227%2802%2900004-9

7 January 2021

Genealogy, natural history, and phenotype of Alström syndrome in a large Acadian kindred and three additional families

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8227%2802%2900004-9

7 January 2021

Impaired insulin-induced RNA synthesis secondary to a genetically defective insulin receptor.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8227%2802%2900004-9

7 January 2021

Impaired glucose tolerance leads to delayed diagnosis of Alström syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8227%2802%2900004-9

7 January 2021

Human DCTN1: genomic structure and evaluation as a candidate for Alström syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8227%2802%2900004-9

7 January 2021

Alström syndrome: further evidence for linkage to human chromosome 2p13.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8227%2802%2900004-9

7 January 2021

Alstrom's syndrome: further evidence of autosomal recessive inheritance and endocrinological dysfunction

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8227%2802%2900004-9

7 January 2021

Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8227%2802%2900004-9

7 January 2021

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8227%2802%2900004-9

7 January 2021

Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: studies in four children

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8227%2802%2900004-9

7 January 2021

Alström syndrome. Report of 22 cases and literature review.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8227%2802%2900004-9

7 January 2021

10.1016/S0168-8227(02)00004-9

Identifiers

DOI

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28 November 2017

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