Literature DB >> 5142935

Chronic hypoparathyroidism in two generations.

D G Barr, A Prader, U Esper, S Rampini, V J Marrian, J O Forfar.   

Abstract

Entities:  

Mesh：

Year:  1971        PMID： 5142935

Source DB:  PubMed          Journal:  Helv Paediatr Acta        ISSN： 0018-022X


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  6 in total

1.  Long-standing latent idiopathic hypoparathyroidism discovered during concurrent central nervous system disease.

Authors:  B E Wilson; S Tawney
Journal:  West J Med       Date:  1992-08

2.  Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27.

Authors:  D Trump; P H Dixon; S Mumm; C Wooding; K E Davies; D Schlessinger; M P Whyte; R V Thakker
Journal:  J Med Genet       Date:  1998-11       Impact factor: 6.318

3.  Familial DiGeorge syndrome with tetralogy of Fallot and prolonged survival.

Authors:  W E Winter; J H Silverstein; D J Barrett; E Kiel
Journal:  Eur J Pediatr       Date:  1984-01       Impact factor: 3.183

4.  Autosomal dominant idiopathic hypoparathyroidism and nervous system dysfunction: report of three cases and review of the literature.

Authors:  M Smits; F Gabreëls; P Froeling; H Thijssen; E Colon; B ter Haar; C Ruland; R Lam
Journal:  J Neurol       Date:  1982       Impact factor: 4.849

5.  Autosomal dominant hypoparathyroidism: a proband with concurrent nephrogenic diabetes insipidus.

Authors:  A G Hunter; H Heick; W J Poznanski; P N McLaine
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

6.  Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies.

Authors:  R V Thakker; K E Davies; M P Whyte; C Wooding; J L O'Riordan
Journal:  J Clin Invest       Date:  1990-07       Impact factor: 14.808
  6 in total

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