Silvia Vannelli

Turin, Italy

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 13 publications

Real-life long-term efficacy and safety of recombinant human growth hormone therapy in children with short stature homeobox-containing deficiency.

Real-life long-term efficacy and safety of recombinant human growth hormone therapy in children with short stature homeobox-containing deficiency.

Journal: Endocrine connections

Published: March 12, 2023

Growth in Children With Noonan Syndrome and Effects of Growth Hormone Treatment on Adult Height.

Growth in Children With Noonan Syndrome and Effects of Growth Hormone Treatment on Adult Height.

Journal: Frontiers in endocrinology

Published: August 19, 2021

Copy number variations residing outside the SHOX enhancer region are involved in Short Stature and Léri-Weill dyschondrosteosis.

Copy number variations residing outside the SHOX enhancer region are involved in Short Stature and Léri-Weill dyschondrosteosis.

Journal: Molecular genetics & genomic medicine

Published: November 16, 2020

SHOX deficiency in children with growth impairment: evaluation of known and new auxological and radiological indicators.

SHOX deficiency in children with growth impairment: evaluation of known and new auxological and radiological indicators.

Journal: Italian journal of pediatrics

Published: July 10, 2020

Growth Assessment in Preterm Children from Birth to Preschool Age.

Growth Assessment in Preterm Children from Birth to Preschool Age.

Journal: Nutrients

Published: May 29, 2020

Variants in the 5'UTR reduce SHOX expression and contribute to SHOX haploinsufficiency.

Variants in the 5'UTR reduce SHOX expression and contribute to SHOX haploinsufficiency.

Journal: European journal of human genetics : EJHG

Published: January 14, 2020

Pretreatment Endocrine Disorders Due to Optic Pathway Gliomas in Pediatric Neurofibromatosis Type 1: Multicenter Study.

Pretreatment Endocrine Disorders Due to Optic Pathway Gliomas in Pediatric Neurofibromatosis Type 1: Multicenter Study.

Journal: The Journal of clinical endocrinology and metabolism

Published: November 21, 2019

Jaffe-Campanacci syndrome or neurofibromatosis type 1: a case report of phenotypic overlap with detection of NF1 gene mutation in non-ossifying fibroma.

Jaffe-Campanacci syndrome or neurofibromatosis type 1: a case report of phenotypic overlap with detection of NF1 gene mutation in non-ossifying fibroma.

Journal: Italian journal of pediatrics

Published: July 23, 2019

Long-term response to recombinant human growth hormone treatment: a new predictive mathematical method.

Long-term response to recombinant human growth hormone treatment: a new predictive mathematical method.

Journal: Journal of endocrinological investigation

Published: June 28, 2017

Duplications upstream and downstream of SHOX identified as novel causes of Leri-Weill dyschondrosteosis or idiopathic short stature.

Duplications upstream and downstream of SHOX identified as novel causes of Leri-Weill dyschondrosteosis or idiopathic short stature.

Journal: American journal of medical genetics. Part A

Published: September 10, 2015

Unidentified bright objects and neuropsychiatric disturbances

Unidentified bright objects and neuropsychiatric disturbances

Journal: Minerva pediatrica

Published: September 21, 2013

Combined therapy with insulin and growth hormone in 17 patients with type-1 diabetes and growth disorders.

Combined therapy with insulin and growth hormone in 17 patients with type-1 diabetes and growth disorders.

Journal: Hormone research in paediatrics

Published: August 14, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026