Growth hormone excess in children with neurofibromatosis type-1 and optic glioma

Author:

Cambiaso Paola1,Galassi Stefania2,Palmiero Melania1,Mastronuzzi Angela3,Del Bufalo Francesca3,Capolino Rossella4,Cacchione Antonella3,Buonuomo Paola S.4,Gonfiantini Michaela V.4,Bartuli Andrea4,Cappa Marco1,Macchiaiolo Marina4ORCID

Affiliation:

1. Endocrinology and Diabetes Unit; Bambino Gesù Children Hospital; IRCCS; Rome Italy

2. Neuroradiology Unit; Bambino Gesù Children Hospital; Imaging Department; IRCCS; Rome Italy

3. Department of Paediatric Hematology Oncology; Bambino Gesù Children Hospital; IRCCS; Rome Italy

4. Rare Diseases and Medical Genetics Unit; Bambino Gesù Children Hospital; IRCCS; Rome Italy

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference34 articles.

1. Serum insulin-like growth factor-I (IGF-I) reference ranges for chemiluminescence assay in childhood and adolescence. Data from a population of in- and out-patients;Bedogni;Growth Hormone Research Society and the International IGF Research,2012

2. Outcomes of systematic screening for optic pathway tumours in children with Neurofibromatosis Type 1;Blazo;American Journal of Medical Genetics Part A,2004

3. Question 1: Should a child with neurofibromatosis type 1 be screened for Central Nervous System tumours with neuroimaging;Bodey;Archives of Disease in Childhood,2014

4. Reversible growth hormone excess in two girls with neurofibromatosis type 1 and optic pathway glioma;Bruzzi;Hormone Research in Paediatrics,2015

5. Characterization of IGFI receptor expression and localization in paediatric gliomas upon diagnosis according to WHO 2007 grading;Clément;Hormone Research in Paediatrics,2014

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