Kyung‐Hoon Paik - Concepedia

Author

Kyung‐Hoon Paik

Samsung Medical Center

Also Known As

Ah-Ra Ko, K.S. Paik, KYUNG-HOON PAIK, Kyung-Hoon Paik, Kyung‐Hoon Paik

Publications

250

Citations

H-Index

Concepts

All Affiliations

Samsung Medical Center Sungkyunkwan University Samsung (South Korea)Ewha Womans University National Cancer Center

About

Kyung‐Hoon Paik is an author at Samsung Medical Center specializing in metabolism, physiology, and metabolic syndrome.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Health Sciences	3	3	49
2	Medicine	3	3	49
3	Diabetes	2	2	34
4	Endocrinology	2	2	34
5	Biochemistry	1	1	15

Kyung‐Hoon Paik

Publications

241

Citations

H-Index

Page 1

	Year	Citations
Obestatin Is Not Elevated or Correlated with Insulin in Children with Prader-Willi Syndrome Won Hah Park, Yoo Joung Oh, Gae Young Kim, The Journal of Clinical Endocrinology & Metabolism	2007	44
Increased Density of Ghrelin-Expressing Cells in the Gastric Fundus and Body in Prader-Willi Syndrome Yon Ho Choe, Sang Yong Song, Kyung‐Hoon Paik, The Journal of Clinical Endocrinology & Metabolism	2005	38
<i>LIN28B</i>polymorphisms are associated with central precocious puberty and early puberty in girls Sung Won Park, Seung‐Tae Lee, Young Bae Sohn, Korean Journal of Pediatrics	2012	27
Retrospective analysis of the clinical manifestations and survival of Korean patients with mucopolysaccharidosis type II: Emphasis on the cardiovascular complication and mortality cases Young Bae Sohn, Eun Wha Choi, Su Jin Kim, American Journal of Medical Genetics Part A	2011	23
Plasma adiponectin level and sleep structures in children with Prader-Willi syndrome Eun Yeon Joo, Seung Bong Hong, Young Bae Sohn, Journal of Sleep Research Sleep DisordersMetabolic DisorderAdipose Tissue-derived HormoneSleep-related Breathing DisorderObesity	2009	21
A mother and daughter with the p.R443X mutation of mucopolysaccharidosis type II: Genotype and phenotype analysis Young Bae Sohn, Su Jin Kim, Sung Won Park, American Journal of Medical Genetics Part A	2010	20
Mutations of ACADS gene associated with short-chain acyl-coenzyme A dehydrogenase deficiency. Se Hwa Kim, Hyung‐Doo Park, Young Bae Sohn, PubMed Acyl-coa DehydrogenaseMetabolic DisorderFirst Korean NeonateGeneticsMolecular Biology	2011	15
Enzyme replacement therapy improves joint motion and outcome of the 12‐min walk test in a mucopolysaccharidosis type VI patient previously treated with bone marrow transplantation Young Bae Sohn, Sung Won Park, Se‐Hwa Kim, American Journal of Medical Genetics Part A	2012	15
A polymorphism in the growth hormone receptor is associated with height in children with Prader–Willi syndrome Sung Won Park, Seung‐Tae Lee, Young Bae Sohn, American Journal of Medical Genetics Part A	2011	13
Marked Suppression of Ghrelin Concentration by Insulin in Prader-Willi Syndrome Kyung‐Hoon Paik, Moon‐Kyu Lee, Dong‐Kyu Jin, Journal of Korean Medical Science NutritionMetabolic DisorderInsulin SignalingObesityMetabolic Syndrome	2007	13

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