Literature DB >> 6246137

Congenital hypothyroidism associated with thyrotropin unresponsiveness and thyroid cell membrane alterations.

J L Codaccioni, P Carayon, M Michel-Bechet, F Foucault, G Lefort, H Pierron.   

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Year:  1980        PMID： 6246137     DOI： 10.1210/jcem-50-5-932

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN： 0021-972X            Impact factor:   5.958


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  6 in total

Review 1.  Thyrotropin receptor mutations in thyroid diseases.

Authors:  P M Yen
Journal:  Rev Endocr Metab Disord       Date:  2000-01       Impact factor: 6.514

2.  Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland.

Authors:  M J Abramowicz; L Duprez; J Parma; G Vassart; C Heinrichs
Journal:  J Clin Invest       Date:  1997-06-15       Impact factor: 14.808

3.  Familial hypothyroidism with autosomal dominant inheritance.

Authors:  M Mimouni; A Mimouni-Bloch; J Schachter; M Shohat
Journal:  Arch Dis Child       Date:  1996-09       Impact factor: 3.791

Review 4.  Resistance to thyrotropin.

Authors:  S Refetoff
Journal:  J Endocrinol Invest       Date:  2003-08       Impact factor: 4.256

5.  Proceedings of the 2013 Joint JSTP/NTP Satellite Symposium.

Authors:  Susan A Elmore; Mark Hoenerhoff; Osamu Katsuta; Hiroko Kokoshima; Robert Maronpot; Hiroaki Nagai; Hiroshi Satoh; Yasuhiro Tanaka; Tomoaki Tochitani; Seiichiro Tsuchiya; Katsuhiko Yoshizawa
Journal:  J Toxicol Pathol       Date:  2013-07-10       Impact factor: 1.628

6.  Spontaneous vacuolar degeneration of the thyroid follicular epithelium in cynomolgus monkeys.

Authors:  Hirofumi Hatakeyama; Yoshihiro Takei; Yumiko Cruz; Seiji Miyoshi; Jun Watanabe; Haruko Koizumi; Akihito Shimoi; Hiroshi Satoh
Journal:  J Toxicol Pathol       Date:  2012-01-07       Impact factor: 1.628
  6 in total

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