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H W Yoo

Showing results (21-30 of 27) with videos related to

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Human Mutation|April 29, 1998
Identification of three novel mutations and a high frequency of the Arg778Leu mutation in Korean patients with Wilson diseaseE K Kim, O J Yoo, K Y Song, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|October 25, 2011
Clinical phenotype and mutation spectrum of the CYP21A2 gene in patients with steroid 21-hydroxylase deficiencyJ-H Choi, H-Y Jin, B H Lee, et al.
Transplantation Proceedings|April 18, 2012
Successful liver transplantation for a child with life-threatening recurrent bleeding episodes due to congenital factor X deficiency: a case reportS H Bang, S H Oh, K M Kim, et al.
European Journal of Endocrinology|June 14, 2013
A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndromeP Clayton, P Chatelain, L Tatò, et al.
The Pharmacogenomics Journal|April 10, 2013
Pharmacogenomics of insulin-like growth factor-I generation during GH treatment in children with GH deficiency or Turner syndromeA Stevens, P Clayton, L Tatò, et al.
Journal of Endocrinological Investigation|November 6, 2017
Recombinant growth hormone therapy for prepubertal children with idiopathic short stature in Korea: a phase III randomized trialJ Kim, B-K Suh, C W Ko, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|October 16, 2013
Clinical characterization and molecular classification of 12 Korean patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidismS Y Cho, Y A Yoon, C-S Ki, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Human Mutation|April 29, 1998
Identification of three novel mutations and a high frequency of the Arg778Leu mutation in Korean patients with Wilson diseaseE K Kim, O J Yoo, K Y Song, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|October 25, 2011
Clinical phenotype and mutation spectrum of the CYP21A2 gene in patients with steroid 21-hydroxylase deficiencyJ-H Choi, H-Y Jin, B H Lee, et al.
Transplantation Proceedings|April 18, 2012
Successful liver transplantation for a child with life-threatening recurrent bleeding episodes due to congenital factor X deficiency: a case reportS H Bang, S H Oh, K M Kim, et al.
European Journal of Endocrinology|June 14, 2013
A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndromeP Clayton, P Chatelain, L Tatò, et al.
The Pharmacogenomics Journal|April 10, 2013
Pharmacogenomics of insulin-like growth factor-I generation during GH treatment in children with GH deficiency or Turner syndromeA Stevens, P Clayton, L Tatò, et al.
Journal of Endocrinological Investigation|November 6, 2017
Recombinant growth hormone therapy for prepubertal children with idiopathic short stature in Korea: a phase III randomized trialJ Kim, B-K Suh, C W Ko, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|October 16, 2013
Clinical characterization and molecular classification of 12 Korean patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidismS Y Cho, Y A Yoon, C-S Ki, et al.
Pageof 3