(Q38315433)

2 September 2017

title

Demonstration of McCune-Albright mutations in the liver of children with high gammaGT progressive cholestasis (English)

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2 September 2017

Silva ES

1

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2 September 2017

Lumbroso S

2

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2 September 2017

Medina M

3

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2 September 2017

Gillerot Y

4

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2 September 2017

Sultan C

5

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2 September 2017

Sokal EM

6

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2 September 2017

publication date

1 January 2000

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2 September 2017

published in

Journal of Hepatology

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2 September 2017

volume

32

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2 September 2017

issue

1

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2 September 2017

page(s)

154-158

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Syndrome Characterized by Osteitis Fibrosa Disseminata, Areas of Pigmentation and Endocrine Dysfunction, with Precocious Puberty in Females

2 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980202-0

7 January 2021

McCune-Albright syndrome. Long-term follow-up.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980202-0

7 January 2021

Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein GS.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980202-0

7 January 2021

Activating mutations of the stimulatory G protein in the McCune-Albright syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980202-0

7 January 2021

Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980202-0

7 January 2021

Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980202-0

7 January 2021

Identification of a locus for progressive familial intrahepatic cholestasis PFIC2 on chromosome 2q24

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980202-0

7 January 2021

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980202-0

7 January 2021

Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980202-0

7 January 2021

Neonatal cholestasis. New approaches to diagnostic evaluation and therapy

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980202-0

7 January 2021

Melanotic macules following Blaschko's lines in McCune-Albright syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980202-0

7 January 2021

Ursodeoxycholic acid therapy in pediatric patients with progressive familial intrahepatic cholestasis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980202-0

7 January 2021

10.1016/S0168-8278(00)80202-0

Identifiers

DOI

1 reference

2 September 2017

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