Literature DB >> 4206122

Familial thyroxine-binding globulin deficiency. A study of three Danish families.

P Strunge.   

Abstract

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Year:  1974        PMID： 4206122

Source DB:  PubMed          Journal:  Acta Med Scand        ISSN： 0001-6101


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  3 in total

1.  Primary thyroid failure with concomitant thyroxine binding globulin deficiency.

Authors:  I R Wakefield; D A Hunter; S R Goodall; C J Hayter
Journal:  Br Med J (Clin Res Ed)       Date:  1985-04-06

2.  A NOVEL MUTATION CAUSING COMPLETE THYROID BINDING GLOBULIN DEFICIENCY (TBG-CD MIA) IN A MALE WITH COEXISTING GRAVES DISEASE.

Authors:  Hara Rosen Berger; Matthew K Creech; Zeina Hannoush; Yui Watanabe; Atil Kargi; Roy E Weiss
Journal:  AACE Clin Case Rep       Date:  2017

3.  [Familial coincidence of hypertrophic cardiomyopathies and thyroxine-binding globulin deficiency (athyropexinemia) (author's transl)].

Authors:  E Kallee; J Bohner; H Eichstädt; R Haasis; R Wahl; K Kochsiek
Journal:  Klin Wochenschr       Date:  1978-12-15
  3 in total

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