Literature DB >> 10939901

Familial forms of thyroid dysgenesis among infants with congenital hypothyroidism.

M Castanet, S Lyonnet, C Bonaïti-Pellié, M Polak, P Czernichow, J Léger.   

Abstract

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Year:  2000        PMID： 10939901     DOI： 10.1056/NEJM200008103430614

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  16 in total

1.  Role for tissue-dependent methylation differences in the expression of FOXE1 in nontumoral thyroid glands.

Authors:  Rasha Abu-Khudir; Fabien Magne; Jean-Pierre Chanoine; Cheri Deal; Guy Van Vliet; Johnny Deladoëy
Journal:  J Clin Endocrinol Metab       Date:  2014-03-19       Impact factor: 5.958

2.  Congenital Hypothyroidism Due to Dyshormonogenesis in 2 Siblings.

Authors:  Sudha Rathna Prabhu; Shriraam Mahadevan
Journal:  Indian J Pediatr       Date:  2018-02-15       Impact factor: 1.967

Review 3.  Are lower TSH cutoffs in neonatal screening for congenital hypothyroidism warranted?

Authors:  Samantha Lain; Caroline Trumpff; Scott D Grosse; Antonella Olivieri; Guy Van Vliet
Journal:  Eur J Endocrinol       Date:  2017-07-10       Impact factor: 6.664

4.  TRANSCRIPTION FACTOR GLI-SIMILAR 3 (GLIS3): IMPLICATIONS FOR THE DEVELOPMENT OF CONGENITAL HYPOTHYROIDISM.

Authors:  Kristin Lichti-Kaiser; Gary ZeRuth; Anton M Jetten
Journal:  J Endocrinol Diabetes Obes       Date:  2014-04

5.  Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis.

Authors:  Aurore Carré; Mireille Castanet; Sylvia Sura-Trueba; Gabor Szinnai; Guy Van Vliet; Delphine Trochet; Jeanne Amiel; Juliane Léger; Paul Czernichow; Virginie Scotet; Michel Polak
Journal:  Hum Genet       Date:  2007-08-24       Impact factor: 4.132

Review 6.  Congenital hypothyroidism.

Authors:  Maynika V Rastogi; Stephen H LaFranchi
Journal:  Orphanet J Rare Dis       Date:  2010-06-10       Impact factor: 4.123

7.  Genetic deletion of sonic hedgehog causes hemiagenesis and ectopic development of the thyroid in mouse.

Authors:  Henrik Fagman; Mats Grände; Amel Gritli-Linde; Mikael Nilsson
Journal:  Am J Pathol       Date:  2004-05       Impact factor: 4.307

8.  High prevalence of congenital hypothyroidism in Isfahan: Do familial components have a role?

Authors:  Mahin Hashemipour; Silva Hovsepian; Roya Kelishadi
Journal:  Adv Biomed Res       Date:  2012-08-28

9.  Congenital hypothyroidism after assisted reproductive technology in Japan: comparison between multiples and singletons, 2005-2009.

Authors:  Syuichi Ooki
Journal:  Int J Pediatr Endocrinol       Date:  2013-02-12

10.  Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese.

Authors:  Keisuke Kanda; Haruo Mizuno; Yukari Sugiyama; Hiroki Imamine; Hajime Togari; Kazumichi Onigata
Journal:  Endocrine       Date:  2006-12       Impact factor: 3.925
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