Works by Dong-Kyu Jin

Results: 116

Prevalence and risk factors for type 2 diabetes mellitus with Prader-Willi syndrome: a single center experience.

Published in:

2017

By:

Aram Yang;
Jinsup Kim;
Sung Yoon Cho;
Dong-Kyu Jin;
Yang, Aram;
Kim, Jinsup;
Cho, Sung Yoon;
Jin, Dong-Kyu

Publication type:

journal article

Clinical and endocrine characteristics and genetic analysis of Korean children with McCune-Albright syndrome: a retrospective cohort study.

Published in:

2016

By:

Eun-Kyung Cho;
Jinsup Kim;
Aram Yang;
Chang-Seok Ki;
Ji-Eun Lee;
Sung Yoon Cho;
Dong-Kyu Jin;
Cho, Eun-Kyung;
Kim, Jinsup;
Yang, Aram;
Ki, Chang-Seok;
Lee, Ji-Eun;
Cho, Sung Yoon;
Jin, Dong-Kyu

Publication type:

journal article

Decreased performance in IDUA knockout mouse mimic limitations of joint function and locomotion in patients with Hurler syndrome.

Published in:

2015

By:

Chihwa Kim;
Min Jung Kwak;
Sung Yoon Cho;
Ah-ra Ko;
Rheey, Jinguen;
Jeong-Yi Kwon;
Yokyung Chung;
Dong-Kyu Jin;
Kim, Chihwa;
Kwak, Min Jung;
Cho, Sung Yoon;
Ko, Ah-Ra;
Kwon, Jeong-Yi;
Chung, Yokyung;
Jin, Dong-Kyu

Publication type:

journal article

Impaired generation of reactive oxygen species in leprechaunism through downregulation of Nox4.

Published in:

2005

By:

Park, Hye Sun;
Dong Kyu Jin;
Sang Min Shin;
Mi Kyung Jang;
Longo, Nicholas;
Ji Won Park;
Duk Soo Bae;
Yun Soo Bae;
Jin, Dong Kyu;
Shin, Sang Min;
Jang, Mi Kyung;
Park, Ji Won;
Bae, Duk Soo;
Bae, Yun Soo

Publication type:

journal article

Identification and In Vivo Functional Characterization of Novel Compound Heterozygous BMP1 Variants in Osteogenesis Imperfecta.

Published in:

Human Mutation, 2015, v. 36, n. 2, p. 191, doi. 10.1002/humu.22731

By:

Cho, Sung Yoon;
Asharani, P.V.;
Kim, Ok‐Hwa;
Iida, Aritoshi;
Miyake, Noriko;
Matsumoto, Naomichi;
Nishimura, Gen;
Ki, Chang‐Seok;
Hong, Geehay;
Kim, Su Jin;
Sohn, Young Bae;
Park, Sung Won;
Lee, Jieun;
Kwun, Younghee;
Carney, Thomas J.;
Huh, Rimm;
Ikegawa, Shiro;
Jin, Dong‐Kyu

Publication type:

Article

Identification of mutations in the GNPTA (MGC4170) gene coding for GlcNAc-phosphotransferase α/β subunits in Korean patients with mucolipidosis type II or type IIIA.

Published in:

Human Mutation, 2005, v. 26, n. 4, p. 308, doi. 10.1002/humu.20205

By:

Paik, Kyung Hoon;
Song, Seng Mi;
Ki, Chang Seok;
Yu, Han-Wook;
Kim, Jung Sim;
Min, Ki Hoon;
Chang, Soo Hee;
Yoo, Eun Jae;
Lee, In Jung;
Kwan, Eun Kyung;
Han, Sun Joo;
Jin, Dong-Kyu

Publication type:

Article

Mutational spectrum of the iduronate 2 sulfatase gene in 25 unrelated Korean Hunter syndrome patients: Identification of 13 novel mutationsCommunicated by Mark H. PaalmanOnline Citation: Human Mutation, Mutation in Brief #599 (2002) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/599.pdf

Published in:

Human Mutation, 2003, v. 21, n. 4, p. 449, doi. 10.1002/humu.9128

By:

Chi Hwa Kim;
Hye Zin Hwang;
Seng Mi Song;
Kyung Hoon Paik;
Eun Kyung Kwon;
Kwang Bin Moon;
Jeong Hyeok Yoon;
Cheol Kyu Han;
Dong?Kyu Jin

Publication type:

Article

Otologic Manifestations of Hunter Syndrome and Their Relationship with Speech Development.

Published in:

Audiology & Neurotology, 2008, v. 13, n. 3, p. 206, doi. 10.1159/000113511

By:

Cho, Yang-Sun;
Kim, Joon Ho;
Kim, Tae Wook;
Chung, Soo Chan;
Chang, Son-A;
Jin, Dong-Kyu

Publication type:

Article

Appropriate Age for Height Control Treatment in Patients With Marfan Syndrome.

Published in:

Frontiers in Endocrinology, 2021, v. 12, p. 1, doi. 10.3389/fendo.2021.708931

By:

Kim, Sung Eun;
Lee, Dong-Yun;
Kim, Min-Sun;
Cho, Sung Yoon;
Jin, Dong-Kyu;
Choi, DooSeok

Publication type:

Article

Long-Term Antithyroid Drug Treatment of Graves' Disease in Children and Adolescents: A 20-Year Single-Center Experience.

Published in:

Frontiers in Endocrinology, 2021, v. 12, p. 1, doi. 10.3389/fendo.2021.687834

By:

Song, Ari;
Kim, Su Jin;
Kim, Min-Sun;
Kim, Jiyeon;
Kim, Insung;
Bae, Ga Young;
Seo, Eunseop;
Cho, Young Seok;
Choi, Joon Young;
Cho, Sung Yoon;
Jin, Dong-Kyu

Publication type:

Article

Clinical Presentation and Treatment Outcomes of Children and Adolescents With Pheochromocytoma and Paraganglioma in a Single Center in Korea.

Published in:

Frontiers in Endocrinology, 2021, v. 11, p. N.PAG, doi. 10.3389/fendo.2020.610746

By:

Park, Hyojung;
Kim, Min-Sun;
Lee, Jiwon;
Kim, Jung-Han;
Jeong, Byong Chang;
Lee, Sanghoon;
Lee, Suk-Koo;
Cho, Sung Yoon;
Jin, Dong-Kyu

Publication type:

Article

The Youngest Infant to Be Diagnosed with Autosomal Dominant Hypocalcemia Type 2 Harboring a Novel Variant of GNA11: A Case Study and Literature Review.

Published in:

Annals of Clinical & Laboratory Science, 2022, v. 52, n. 3, p. 494

By:

Eun-Jung Kwon;
Min-Sun Kim;
Eu-seon Noh;
Chi-woo Kim;
Jahyun Jang;
Jin-Ho Choi;
Sung Yoon Cho;
Dong-Kyu Jin

Publication type:

Article

The First Korean Family with Aarskog-Scott Syndrome Harboring a Novel Mutation in FGD1 Diagnosed via Targeted Gene Panel Sequencing.

Published in:

Annals of Clinical & Laboratory Science, 2020, v. 50, n. 5, p. 691

By:

Ga young Bae;
Min Sun Kim;
Ji-yeon Kim;
Ja-Hyun Jang;
Sae-Mi Lee;
Sung Yoon Cho;
Dong-Kyu Jin

Publication type:

Article

Oculodentodigital Dysplasia with a Novel Mutation in GJA1 Diagnosed by Targeted Gene Panel Sequencing: A Case Report and Literature Review.

Published in:

Annals of Clinical & Laboratory Science, 2018, v. 48, n. 6, p. 776

By:

Jaeyoung Choi;
Aram Yang;
Ari Song;
Minji Lim;
Jinsup Kim;
Ja-Hyun Jang;
Ki-Tae Park;
Sung Yoon Cho;
Dong-Kyu Jin

Publication type:

Article

Rare Association of Mucolipidosis III alpha/beta with Dilated Cardiomyopathy.

Published in:

Annals of Clinical & Laboratory Science, 2018, v. 48, n. 6, p. 785

By:

Min Jung Kwak;
Hye Won Lee;
Young Mi Kim;
Sung Yoon Cho;
Hyung-Doo Park;
Dong-Kyu Jin

Publication type:

Article

First Korean Case of Renpenning Syndrome with Novel Mutation in PQBP1 Diagnosed by Targeted Exome Sequencing, and Literature Review.

Published in:

Annals of Clinical & Laboratory Science, 2018, v. 48, n. 4, p. 522

By:

Hye-In Jeong;
Aram Yang;
Jinsup Kim;
Ja-Hyun Jang;
Sung Yoon Cho;
Dong-Kyu Jin

Publication type:

Article

First Korean Case of Infantile Hypophosphatasia with Novel Mutation in ALPL and Literature Review.

Published in:

Annals of Clinical & Laboratory Science, 2016, v. 46, n. 3, p. 302

By:

Eu Gene Park;
Sung Yoon Cho;
Jeehun Lee;
Jihyun Kim;
Heeyeon Cho;
Jinsup Kim;
Rimm Huh;
Chang-Seok Ki;
Ok-Hwa Kim;
Dong-Kyu Jin

Publication type:

Article

Letter to the Editor: A Novel Mutation in the CREBBP Gene of a Korean Girl with Rubinstein-Taybi syndrome.

Published in:

Annals of Clinical & Laboratory Science, 2015, v. 45, n. 4, p. 458

By:

Rimm Huh;
Sung Yoon Cho;
Jinsup Kim;
Chang-Seok Ki;
Dong-Kyu Jin

Publication type:

Article

Spinal Stenosis with Paraparesis in a Korean Boy with Albright's Hereditary Osteodystrophy: Identification of a Novel Nonsense Mutation in the GNAS.

Published in:

Annals of Clinical & Laboratory Science, 2015, v. 45, n. 3, p. 344

By:

Sang Heon Lee;
Seung Hyeon Mun;
Sung Yoon Cho;
Yeo Ju Kim;
Dong-Kyu Jin;
Chang-Seok Ki;
Ji-Eun Lee

Publication type:

Article

Hypoparathyroidism in a 3-year-old Korean Boy with Sotos Syndrome and a Novel Mutation in NSD1.

Published in:

Annals of Clinical & Laboratory Science, 2015, v. 45, n. 2, p. 215

By:

Karn Wejaphikul;
Sung Yoon Cho;
Rimm Huh;
Younghee Kwun;
Jieun Lee;
Chang-Seok Ki;
Dong-Kyu Jin

Publication type:

Article

Osteogenesis Imperfecta Type I Caused by a Novel Mutation in the Start Codon of the COL1A1 Gene in a Korean Family.

Published in:

Annals of Clinical & Laboratory Science, 2015, v. 45, n. 1, p. 100

By:

Sung Yoon Cho;
Ji-Ho Lee;
Chang-Seok Ki;
Mi Sun Chang;
Dong-Kyu Jin;
Heon-Seok Han

Publication type:

Article

A Novel Splice Site Mutation in the PAX6 Gene in a Korean Family with Isolated Aniridia.

Published in:

Annals of Clinical & Laboratory Science, 2015, v. 45, n. 1, p. 90

By:

Mi Sun Chang;
Jong Chul Han;
Jieun Lee;
Younghee Kwun;
Rimm Huh;
Chang-Seok Ki;
Changwon Kee;
Sung Yoon Cho;
Dong-Kyu Jin

Publication type:

Article

A Korean Patient with Glutaric Aciduria Type 1 with a Novel Mutation in the Glutaryl CoA Dehydrogenase Gene.

Published in:

Annals of Clinical & Laboratory Science, 2014, v. 44, n. 2, p. 213

By:

Hee Su Kim;
Hee Joon Yu;
Jeehun Lee;
Hyung-Doo Park;
Ji Hye Kim;
Hyung-Jin Shin;
Dong kyu Jin;
Munhyang Lee

Publication type:

Article

Effects of recombinant human growth hormone treatment on growth, body composition, and safety in infants or toddlers with Prader-Willi syndrome: a randomized, active-controlled trial.

Published in:

2019

By:

Yang, Aram;
Choi, Jin-Ho;
Sohn, Young Bae;
Eom, Yunae;
Lee, Jiyoon;
Yoo, Han-Wook;
Jin, Dong-Kyu

Publication type:

journal article

Obestatin Is Not Elevated or Correlated with Insulin in Children with Prader-Willi Syndrome.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 1, p. 229, doi. 10.1210/jc.2006-0754

By:

Won Hah Park;
Yoo Joung Oh;
Gae Young Kim;
Sang Eun Kim;
Kyung-Hoon Paik;
Sun Ju Han;
An Hee Kim;
Su Hyun Chu;
Eun Kyung Kwon;
Seon Woo Kim;
Dong-Kyu Jin

Publication type:

Article

Suppression of Acylated Ghrelin during Oral Glucose Tolerance Test Is Correlated with Whole-Body Insulin Sensitivity in Children with Prader-Willi Syndrome.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 5, p. 1876, doi. 10.1210/jc.2005-2168

By:

Kyung Hoon Paik;
Yon Ho Choe;
Won Hah Park;
Yoo Joung Oh;
An Hee Kim;
Su Hyun Chu;
Seon Woo Kim;
Eun Kyung Kwon;
Sun Ju Han;
Woo Yun Shon;
Dong-Kyu Jin

Publication type:

Article

Increased Density of Ghrelin-Expressing Cells in the Gastric Fundus and Body in Prader-Willi Syndrome.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 9, p. 5441, doi. 10.1210/jc.2004-1935

By:

Yon Ho Choe;
Sang Yong Song;
Kyung-Hoon Paik;
Yoo Joung Oh;
Su-Hyun Chu;
Sung Hee Yeo;
Eun Kyung Kwon;
Eun Mee Kim;
Mee Yong Rha;
Dong-Kyu Jin

Publication type:

Article

Hyperghrelinemia Does Not Accelerate Gastric Emptying in Prader-Willi Syndrome Patients.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 6, p. 3367, doi. 10.1210/jc.2004-1651

By:

Yon Ho Choe;
Dong-Kyu Jin;
Sang Eun Kim;
Sang Yong Song;
Kyung Hoon Paik;
Hwa Young Park;
Yoo Joung Oh;
An Hee Kim;
Jung Sim Kim;
Chi Wha Kim;
Su-Hyun Chu;
Eun Kyung Kwon;
Kyung Han Lee

Publication type:

Article

Correlation between Fasting Plasma Ghrelin Levels and Age, Body Mass Index (BMI), BMI Percentiles, and 24- Hour Plasma Ghrelin Profiles in Prader-Willi Syndrome.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 8, p. 3885, doi. 10.1210/jc.2003-032137

By:

KYUNG HOON PAIK;
DONG-KYU JIN;
SANG YONG SONG;
JI EUN LEE;
SI HWAN KO;
SENG MI SONG;
JUNG SIM KIM;
YOO JOUNG OH;
SUN WOO KIM;
SOO HYUN LEE;
SUNG HYE KIM;
EUN KYUNG KWON;
YON HO CHOE

Publication type:

Article

Molecular cloning and characterization of thermostable DNA ligase from Aquifex pyrophilus, a hyperthermophilic bacterium.

Published in:

Extremophiles, 2001, v. 5, n. 3, p. 161, doi. 10.1007/s007920100187

By:

Jae-Hwan Lim;
Juhyun Choi;
Soo-Jin Han;
Sung Kim;
Hye-Zin Hwang;
Dong-Kyu Jin;
Byung-Yoon Ahn;
Ye Han

Publication type:

Article

Genetic investigation of patients with undetectable peaks of growth hormone after two provocation tests.

Published in:

Clinical Endocrinology, 2013, v. 78, n. 2, p. 317, doi. 10.1111/j.1365-2265.2012.04514.x

By:

Cho, Sung Y.;
Ki, Chang‐Seok;
Park, Hyung‐Doo;
Kim, Su J.;
Sohn, Young B.;
Maeng, Se H.;
Jung, Yu J.;
Jin, Dong‐Kyu

Publication type:

Article

High-dose enzyme replacement therapy attenuates cerebroventriculomegaly in a mouse model of mucopolysaccharidosis type II.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 11, p. 728, doi. 10.1038/jhg.2013.92

By:

Ahn, So Yoon;
Chang, Yun Sil;
Sung, Dong Kyung;
Ko, Ah-ra;
Kim, Chi Hwa;
Yoo, Dong Kyeom;
Lim, Keun Ho;
Sohn, Young Bae;
Jin, Dong Kyu;
Park, Won Soon

Publication type:

Article

The proportion of uniparental disomy is increased in Prader-Willi syndrome due to an advanced maternal childbearing age in Korea.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 3, p. 150, doi. 10.1038/jhg.2012.148

By:

Yoon Cho, Sung;
Ki, Chang-Seok;
Bae Sohn, Young;
Hyun Maeng, Se;
Jin Jung, You;
Jin Kim, Su;
Jin, Dong-Kyu

Publication type:

Article

Genetic variations on the Y chromosome in the Japanese population and implications for modern human Y chromosome lineage.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 4, p. 240, doi. 10.1007/s100380050151

By:

Shinka, Toshikatsu;
Tomita, Keiko;
Toda, Tatsushi;
Kotliarova, Svetlana E.;
Lee, Juwon;
Kuroki, Yoko;
Jin, Dong Kyu;
Tokunaga, Katsushi;
Nakamura, Hideki;
Nakahori, Y.

Publication type:

Article

Clinical, biochemical, and genetic analysis of two Korean patients with Trichorhinophalangeal syndrome type I and growth hormone deficiency.

Published in:

2013

By:

Young Bae Sohn;
Chang-Seok Ki;
Sung Won Park;
Sung-Yoon Cho;
Ah-Ra Ko;
Min-Jung Kwon;
Ji-Youn Kim;
Hyung-Doo Park;
Ok-Hwa Kim;
Dong-Kyu Jin

Publication type:

Abstract

Serum levels of FGF21 are reduced and negatively correlated with adiponectin in children with Prader-Willi syndrome.

Published in:

2013

By:

Su Jin Kim;
Young Bae Sohn;
Sung-Yoon Cho;
Young Ok Choi;
Chi Hwa Kim;
Dong-Kyu Jin

Publication type:

Abstract

Identification of a novel TGFBR2 gene mutation in a Korean patient with Loeys–Dietz aortic aneurysm syndrome; no mutation in TGFBR2 gene in 30 patients with classic Marfan's syndrome.

Published in:

2005

By:

Jin, Dong-Kyu

Publication type:

Letter

Acromesomelic dysplasia, type maroteaux caused by novel loss-of-function mutations of the NPR2 gene: Three case reports.

Published in:

American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 2, p. 426, doi. 10.1002/ajmg.a.37463

By:

Wang, Wei;
Song, Mi Hyun;
Miura, Kohji;
Fujiwara, Makoto;
Nawa, Nobutoshi;
Ohata, Yasuhisa;
Kitaoka, Taichi;
Kubota, Takuo;
Namba, Noriyuki;
Jin, Dong Kyu;
Kim, Ok Hwa;
Ozono, Keiichi;
Cho, Tae‐Joon

Publication type:

Article

Disease-specific growth charts for Korean infants with Prader-Willi syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 1, p. 86, doi. 10.1002/ajmg.a.36816

By:

Lee, Jieun;
Isojima, Tsuyoshi;
Chang, Mi Sun;
Kwun, Young Hee;
Huh, Rimm;
Cho, Sung Yoon;
Sohn, Young Bae;
Jin, Dong‐Kyu

Publication type:

Article

Acroscyphodysplasia as a phenotypic variation of pseudohypoparathyroidism and acrodysostosis type 2.

Published in:

American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 10, p. 2529, doi. 10.1002/ajmg.a.36669

By:

Mitsui, Toshikatsu;
Kim, Ok‐Hwa;
Hall, Christine M.;
Offiah, Amaka;
Johnson, Diana;
Jin, Dong‐Kyu;
Toh, Teck‐Hock;
Soneda, Shun;
Keino, Dai;
Matsubayashi, Shohei;
Ishii, Tomohiro;
Nishimura, Gen;
Hasegawa, Tomonobu

Publication type:

Article

Osteogenesis imperfecta type V: Clinical and radiographic manifestations in mutation confirmed patients.

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 8, p. 1972, doi. 10.1002/ajmg.a.36024

By:

Kim, Ok ‐ Hwa;
Jin, Dong ‐ Kyu;
Kosaki, Keisuke;
Kim, Jung ‐ Wook;
Cho, Sung Yoon;
Yoo, Won Joon;
Choi, In Ho;
Nishimura, GEN;
Ikegawa, Shiro;
Cho, Tae ‐ Joon

Publication type:

Article

Improvement of CNS Defects Via Continuous Intrathecal Enzyme Replacement by Osmotic Pump in Mucopolysaccharidosis Type II Mice.

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 5, p. 1036, doi. 10.1002/ajmg.a.35869

By:

Sohn, Young Bae;
Lee, Jeehun;
Cho, Sung Yoon;
Kim, Su Jin;
Ko, Ah‐Ra;
Nam, Mi Hyun;
Jin, Dong‐Kyu

Publication type:

Article

Five novel mutations of GALNS in Korean patients with mucopolysaccharidosis IVA.

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 3, p. 509, doi. 10.1002/ajmg.a.35298

By:

Park, Hyung‐Doo;
Ko, Ah‐Ra;
Ki, Chang‐Seok;
Lee, Soo‐Youn;
Kim, Jong‐Won;
Cho, Sung Yoon;
Kim, Se Hwa;
Park, Sung Won;
Sohn, Young Bae;
Jin, Dong‐Kyu

Publication type:

Article

Auditory characteristics and therapeutic effects of enzyme replacement in mouse model of the mucopolysaccharidosis (MPS) II.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 9, p. 2131, doi. 10.1002/ajmg.a.35498

By:

Hong, Sung Hwa;
Chu, Hosuk;
Kim, Ki Ryung;
Ko, Moon Hee;
Kwon, See Youn;
Moon, Il Joon;
Chung, Won-Ho;
Cho, Yang-Sun;
Kim, Chi-Hwa;
Suh, Myung-Whan;
Choi, Eun Wha;
Sohn, Young Bae;
Park, Sung Won;
Kim, Se-Hwa;
Cho, Sung-Yoon;
Ko, Ah-Ra;
Jin, Dong-Kyu

Publication type:

Article

Familial Xp22.33-Xp22.12 deletion delineated by chromosomal microarray analysis causes proportionate short stature.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 6, p. 1462, doi. 10.1002/ajmg.a.35357

By:

Cho, Sung Yoon;
Ki, Chang-Seok;
Jang, Ja-Hyun;
Sohn, Young Bae;
Park, Sung Won;
Kim, Se Hwa;
Kim, Su Jin;
Jin, Dong-Kyu

Publication type:

Article

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.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 5, p. 1158, doi. 10.1002/ajmg.a.35263

By:

Sohn, Young Bae;
Park, Sung Won;
Kim, Se-Hwa;
Cho, Sung-Yoon;
Ji, Sun-Tae;
Kwon, Eun Kyung;
Han, Sun Ju;
Oh, Se Jung;
Park, Yong Jae;
Ko, Ah-Ra;
Paik, Kyung-Hoon;
Lee, Jeehun;
Lee, Dong Hwan;
Jin, Dong-Kyu

Publication type:

Article

Retrospective analysis of the clinical manifestations and survival of Korean patients with mucopolysaccharidosis type II: Emphasis on the cardiovascular complication and mortality cases.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 1, p. 90, doi. 10.1002/ajmg.a.34371

By:

Sohn, Young Bae;
Choi, Eun Wha;
Kim, Su Jin;
Park, Sung Won;
Kim, Se-Hwa;
Cho, Sung-Yoon;
Jeong, Soo In;
Huh, June;
Kang, I-Seok;
Lee, Heung Jae;
Paik, Kyung-Hoon;
Jin, Dong-Kyu

Publication type:

Article

Efficacy and safety of LB03002, a once-weekly sustained-release human GH for 12-month treatment in Korean children with GH deficiency.

Published in:

European Journal of Endocrinology, 2013, v. 169, n. 2, p. 179, doi. 10.1530/EJE-13-0148

By:

Jin Soon Hwang;
Hae Sang Lee;
Woo Yeong Chung;
Heon-Seok Han;
Dong-Kyu Jin;
Cheol-Woo Ko;
Byung-Churl Lee;
Dae-Yeol Lee;
Kee-Hyoung Lee;
Jeh-Hoon Shin;
Byung-Kyu Suh;
Han-Wook Yoo;
Hyi-Jeong Ji;
Jin-Hwa Lee;
Yoon Ju Bae;
Duk-Hee Kim;
Sei Won Yang

Publication type:

Article

Correlation between Hyperghrelinemia and Carotid Artery Intima-Media Thickness in Children with Prader-Willi Syndrome.

Published in:

Yonsei Medical Journal, 2010, v. 51, n. 3, p. 339, doi. 10.3349/ymj.2010.51.3.339

By:

Su Jin Kim;
Kyung Hoon Paik;
Dong-Ik Kim;
Yon Ho Choe;
Seon Woo Kim;
Dong-Kyu Jin

Publication type:

Article

A biochemical and physicochemical comparison of two recombinant enzymes used for enzyme replacement therapies of hunter syndrome.

Published in:

Glycoconjugate Journal, 2014, v. 31, n. 4, p. 309, doi. 10.1007/s10719-014-9523-0

By:

Chung, Yo;
Sohn, Young;
Sohn, Jong;
Lee, Jieun;
Chang, Mi;
Kwun, Younghee;
Kim, Chi;
Lee, Jin;
Yook, Yeon;
Ko, Ah-Ra;
Jin, Dong-Kyu

Publication type:

Article