A Pilot Study of Discontinuous, Insulin-Like Growth Factor 1–Dosing Growth Hormone Treatment in Young Children with FGFR3 N540K-Mutated Hypochondroplasia
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference41 articles.
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2. A common FGFR3 gene mutation in hypochondroplasia;Prinos;Hum Mol Genet,1995
3. Clinical and genetic heterogeneity of hypochondroplasia;Rousseau;J Med Genet,1996
4. Novel FGFR3 mutations creating cysteine residues in the extracellular domain of the receptor cause achondroplasia or severe forms of hypochondroplasia;Heuertz;Eur J Hum Genet,2006
5. Analysis of the FGFR3 gene in Japanese patients with achondroplasia and hypochondroplasia;Katsumata;Endocr J,2000
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1. Growth reference charts for children with hypochondroplasia;American Journal of Medical Genetics Part A;2023-10-09
2. Clinical Manifestations and Outcomes of 20 Korean Hypochondroplasia Patients with the FGFR3 N540K variant;Experimental and Clinical Endocrinology & Diabetes;2022-11-28
3. Serum NT-proCNP levels increased after initiation of GH treatment in patients with achondroplasia/hypochondroplasia;Clinical Endocrinology;2016-02-25
4. FGFR3/fibroblast growth factor receptor 3 inhibits autophagy through decreasing the ATG12–ATG5 conjugate, leading to the delay of cartilage development in achondroplasia;Autophagy;2015-11-02
5. Height outcome of short children with hypochondroplasia after recombinant human growth hormone treatment: a meta-analysis;Pharmacogenomics;2015-11
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