Demonstration of McCune-Albright mutations in the liver of children with high γGT progressive cholestasis-Reference-Cited by-同舟云学术

Demonstration of McCune-Albright mutations in the liver of children with high γGT progressive cholestasis

Published:2000-01 Issue:1 Volume:32 Page:154-158
ISSN:0168-8278
Container-title:Journal of Hepatology
language:en
Short-container-title:Journal of Hepatology

Author:

Silva Ermelinda Santos,Lumbroso Serge,Medina Margarida,Gillerot Yves,Sultan Charles,Sokal Etienne Marc

Publisher

Elsevier BV

Subject

Hepatology

Reference18 articles.

1. Osteodystrophia fibrosa: report of a case in which the condition was combined with precocious puberty, pathologic pigmentation of the skin and hyperthyroidism, with a review of the literature;McCune;AJDC,1937

2. Syndrome characterised by osteitis fibrosa disseminata, areas of pigmentation and endocrine dysfunction, with precocious puberty in females;Albright;N Engl J Med,1937

3. McCune-Albright syndrome - long-term follow-up;Lee;JAMA,1986

4. Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein Gs;Shenker;J Pediatr,1993

5. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome;Weinstein;N Engl J Med,1991

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1. Developmental and Inherited Liver Disease;MacSween's Pathology of the Liver;2024

2. Neonatal cholestasis as the onset symptom of McCune–Albright syndrome: case reports and a literature review;Frontiers in Pediatrics;2023-10-11

3. Case Report: Severe McCune–Albright syndrome presenting with neonatal Cushing syndrome: navigating through clinical obstacles;Frontiers in Endocrinology;2023-07-25

4. Brain and eye involvement in McCune-Albright Syndrome: clinical and translational insights;Frontiers in Endocrinology;2023-05-19

5. A case report of McCune –Albright syndrome with hepatic manifestations;Clinical Case Reports;2022-07