Literature DB >> 4176719

Congenital hypothyroidism with impaired thyroid response to thyrotropin.

J B Stanbury, P Rocmans, U K Buhler, Y Ochi.   

Abstract

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Year:  1968        PMID： 4176719     DOI： 10.1056/NEJM196811212792103

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


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  4 in total

1.  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

2.  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 3.  Resistance to thyrotropin.

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

4.  Frequency and effect on serum TSH of phosphodiesterase 8B (PDE8B) gene polymorphisms in patients with sporadic nonautoimmune subclinical hypothyroidism.

Authors:  P Agretti; G De Marco; C Di Cosmo; B Bagattini; E Ferrarini; L Montanelli; P Vitti; M Tonacchera
Journal:  J Endocrinol Invest       Date:  2014-01-09       Impact factor: 4.256
  4 in total

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