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1. A multicenter, open-label, phase III study of Abcertin in Gaucher disease. Issue 45 (November 2017)

2. Clinical characteristics and mutation spectrum of GLA in Korean patients with Fabry disease by a nationwide survey: Underdiagnosis of late-onset phenotype. Issue 29 (July 2017)

3. Comparative proteomic analysis in children with idiopathic short stature (ISS) before and after short‐term recombinant human growth hormone (rhGH) therapy. Issue 7 (4th March 2013)

4. Comparative proteomic analysis in children with idiopathic short stature (ISS) before and after short‐term recombinant human growth hormone (rhGH) therapy. Issue 7 (4th March 2013)

5. Diagnosis of Schaaf-Yang syndrome in Korean children with developmental delay and hypotonia. Issue 51 (18th December 2020)

7. Fabry disease: characterisation of the plasma proteome pre- and post-enzyme replacement therapy. Issue 11 (23rd August 2017)

8. Identification of a novel therapeutic target underlying atypical manifestation of Gaucher disease. Issue 5 (20th May 2022)

9. Pharmacologic properties of high-dose ambroxol in four patients with Gaucher disease and myoclonic epilepsy. Issue 2 (24th October 2019)