Características clínicas y moleculares de una familia con síndrome de neoplasia endocrina múltiple tipo 1-Reference-Cited by-同舟云学术

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Características clínicas y moleculares de una familia con síndrome de neoplasia endocrina múltiple tipo 1

Published:2008-12 Issue:10 Volume:31 Page:637-642
ISSN:0210-5705
Container-title:Gastroenterología y Hepatología
language:es
Short-container-title:Gastroenterología y Hepatología

Author:

Cosme Ángel,Álvarez Mariano,Beguiristain Adolfo,María Cobo Ana,Robledo Mercedes,Jesús Aranzadi María,Ojeda Evelia,Bujanda Luis,Goikoetxea Unai

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference31 articles.

1. Genetic aspects of adenomatosis of endocrine glands;Wermer;Am J Med,1954

2. Pluriglandular syndrome (II). Multiple endocrine adenomas in man: a report of five cases and a review of the literature;Berdjis;Oncologia,1962

3. Multiple endocrine neoplasia syndromes;Lips;CRC Crit Rev Oncol Hematol,1984

4. Guidelines for diagnosis and therapy of MEN type 1 and type 2;Brandi;J Clin Endocrinol Metab,2001

5. Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma;Larsson;Nature,1988

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features;PLOS ONE;2017-10-16

2. Clinical and Genetic Analysis of Multiple Endocrine Neoplasia Type 1-Related Primary Hyperparathyroidism in Chinese;PLOS ONE;2016-11-15

3. Deletion of exons 1–3 of the MEN1 gene in a large Italian family causes the loss of menin expression;Familial Cancer;2014-02-13

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