High Prevalence of Pituitary Magnetic Resonance Abnormalities and Gene Mutations in a Cohort of Brazilian Children with Growth Hormone Deficiency and Response to Treatment-Reference-Cited by-同舟云学术

High Prevalence of Pituitary Magnetic Resonance Abnormalities and Gene Mutations in a Cohort of Brazilian Children with Growth Hormone Deficiency and Response to Treatment

Published:2008-01 Issue:7 Volume:21 Page:
ISSN:2191-0251
Container-title:Journal of Pediatric Endocrinology and Metabolism
language:
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Author:

Rocha M.G.M.,Marchisotti F.G.,Osório M.G.F.,Marui S.,Carvalho L.R.S.,Jorge A.A.L.,Mendonca B.B.,Arnhold I.J.P.

Publisher

Walter de Gruyter GmbH

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Link

https://www.degruyter.com/document/doi/10.1515/JPEM.2008.21.7.673/pdf

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1. Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency: a long term follow-up of patients from a single center;Pituitary;2014-10-15

2. Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort;Growth Hormone & IGF Research;2014-10

3. Pituitary stalk interruption syndrome in 58 Chinese patients: clinical features and genetic analysis;Clinical Endocrinology;2013-04-27

4. Relatively high frequency of non-synonymousGLI2variants in patients with congenital hypopituitarism without holoprosencephaly;Clinical Endocrinology;2013-03-12

5. Growth hormone pharmacogenetics: the interactive effect of a microsatellite in the IGF1 promoter region with the GHR-exon 3 and −202 A/C IGFBP3 variants on treatment outcomes of children with severe GH deficiency;The Pharmacogenomics Journal;2011-04-05