Literature DB >> 2913494

A child with phenotypic Laron dwarfism and normal somatomedin levels.

C Pintor1, S Loche, S G Cella, E E Müller, G Baumann.   

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Year:  1989        PMID： 2913494     DOI： 10.1056/NEJM198902093200607

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


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  5 in total

1.  A homozygous nonsense mutation of the human growth hormone receptor gene in a Sardinian boy with Laron-type dwarfism.

Authors:  M Putzolu; A Meloni; S Loche; C Pischedda; A Cao; P Moi
Journal:  J Endocrinol Invest       Date:  1997-05       Impact factor: 4.256

2.  Radiographic abnormalities in Laron dwarfism.

Authors:  M Vasil; A Baxova; K Kozlowski
Journal:  Pediatr Radiol       Date:  1994

Review 3.  Involvement of brain catecholamines and acetylcholine in growth hormone hypersecretory states. Pathophysiological, diagnostic and therapeutic implications.

Authors:  E E Müller; M Rolla; E Ghigo; D Belliti; E Arvat; A Andreoni; A Torsello; V Locatelli; F Camanni
Journal:  Drugs       Date:  1995-11       Impact factor: 9.546

Review 4.  Short stature with normal growth hormone and elevated IGF-I.

Authors:  T Momoi; C Yamanaka; M Kobayashi; T Haruta; H Sasaki; T Yorifuji; M Kaji; H Mikawa
Journal:  Eur J Pediatr       Date:  1992-05       Impact factor: 3.183

5.  Insulin-like growth factor 1 in relation to prostate cancer and benign prostatic hyperplasia.

Authors:  P Cohen; D M Peehl; R Rosenfeld
Journal:  Br J Cancer       Date:  1998-08       Impact factor: 7.640
  5 in total

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