Works matching AU Dong-Kyu Jin

Results: 116

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

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

A Multi-Center, Prospective Observational Study to Investigate the Safety, Compliance, and Efficacy of Omethyl QTlet Soft Capsule.

Published in:

Journal of Clinical Medicine, 2022, v. 11, n. 23, p. 6949, doi. 10.3390/jcm11236949

By:

Ki, You-Jeong;
Han, Sang-Jin;
Cha, Tae-Joon;
Lee, Jae Hyuk;
Seo, Eui Kyo;
Yang, Jae Won;
Hwang, Won Min;
Jin, Dong Kyu;
Park, Joo-Hyun;
Ryu, Han Young;
Park, Chang Gyu;
Lee, Jun Hong;
Choi, Si Wan;
Cho, Eun Jeong;
Kim, Weon

Publication type:

Article

Efficacy and Safety of Dual-Drug-Eluting Stents for de Novo Coronary Lesions in South Korea—The Effect Trial.

Published in:

Journal of Clinical Medicine, 2021, v. 10, n. 1, p. 69, doi. 10.3390/jcm10010069

By:

Cha, Jung-Joon;
Kim, Gi Chang;
Hur, Seung Ho;
Bae, Jang Ho;
Choi, Jae Woong;
Jin, Dong-Kyu;
Woo, Seong Il;
Lee, Seung Uk;
Park, Jong Seon;
Cho, Yun-Hyeong;
Choi, Cheol Ung;
Lim, Do-Sun;
Ahn, Tae Hoon

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

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

Regional Cerebral Glucose Metabolic Abnormality in Prader--Willi Syndrome: A <sup>18</sup>F-FDG PET Study Under Sedation.

Published in:

Journal of Nuclear Medicine, 2006, v. 47, n. 7, p. 1088

By:

Sang Eun Kim;
Dong-Kyu Jin;
Sang Soo Cho;
Ji-Hae Kim;
Sungdo David Hong;
Kyung Hoon Paik;
Yoo Joung Oh;
An Hee Kim;
Eun Kyung Kwon;
Yon Ho Choe

Publication type:

Article

The longitudinal effect of oxcarbazepine on thyroid function in children and adolescents with epilepsy.

Published in:

Epilepsia (Series 4), 2022, v. 63, n. 12, p. 3148, doi. 10.1111/epi.17407

By:

Park, Hyunju;
Heo, Jung;
Kim, Min‐Ji;
Lee, Jee‐Hun;
Kim, Min‐Sun;
Jin, Dong‐Kyu;
Kim, Tae Hyuk;
Chung, Jae Hoon;
Cho, Sung Yoon;
Kim, Sun Wook

Publication type:

Article

Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability.

Published in:

Italian Journal of Pediatrics, 2022, v. 48, n. 1, p. 1, doi. 10.1186/s13052-021-01194-2

By:

Pavone, Piero;
Pappalardo, Xena Giada;
Mustafa, Naira;
Cho, Sung Yoon;
Jin, Dong Kyu;
Incorpora, Gemma;
Falsaperla, Raffaele;
Marino, Simona Domenica;
Corsello, Giovanni;
Parano, Enrico;
Ruggieri, Martino

Publication type:

Article

PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation?

Published in:

Italian Journal of Pediatrics, 2019, v. 45, n. 1, p. N.PAG, doi. 10.1186/s13052-019-0755-2

By:

Pavone, Piero;
Corsello, Giovanni.;
Cho, Sung Yoon;
Pappalardo, Xena Giada;
Ruggieri, Martino;
Marino, Simona Domenica;
Jin, Dong Kyu;
Marino, Silvia;
Falsaperla, Raffaele

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

Efficacy and safety of nebivolol in Korean patients with hypertension by age and sex: a subanalysis from the BENEFIT-KOREA study.

Published in:

Clinical Hypertension, 2021, v. 27, n. 1, p. 1, doi. 10.1186/s40885-021-00165-3

By:

Cho, Kyoung Im;
Jeon, Dong Woon;
Ahn, Hyo Seung;
Jin, Dong Kyu;
Lee, Hyun Sang;
Lee, Jong-Young;
Lim, Hong-Seok;
Manolis, Athanasios J.;
Rha, Seung-Woon;
Park, Sang Won

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

Development and validation of the Pediatric-Youth Hyperphagia Assessment for Prader-Willi syndrome.

Published in:

2022

By:

Sung Yoon Cho;
Danbee Kang;
Minji Im;
Aram Yang;
Min-Sun Kim;
Jiyeon Kim;
Eu-Seon Noh;
Eun Kyung Kwon;
Eujin Choi;
Sunju Han;
Young Ah Park;
Min Jung Kwak;
Youngha Kim;
Juhee Cho;
Dong-Kyu Jin;
Cho, Sung Yoon;
Kang, Danbee;
Im, Minji;
Yang, Aram;
Kim, Min-Sun

Publication type:

journal article

A Liquid Chromatography-Quadrupole-Time-of-Flight Mass Spectrometric Assay for the Quantification of Fabry Disease Biomarker Globotriaosylceramide (GB3) in Fabry Model Mouse.

Published in:

Pharmaceutics, 2018, v. 10, n. 2, p. 69, doi. 10.3390/pharmaceutics10020069

By:

Shin, Seok-Ho;
Park, Min-Ho;
Byeon, Jin-Ju;
Lee, Byeong Ill;
Park, Yuri;
Ko, Ah-Ra;
Seong, Mi-Ran;
Lee, Soyeon;
Kim, Mi Ra;
Seo, Jinwook;
Jung, Myung Eun;
Jin, Dong-Kyu;
Shin, Young G.

Publication type:

Article

Identification of a novel mutation in EXT2 in a fourth‐generation Korean family with multiple osteochondromas and overview of mutation spectrum.

Published in:

Annals of Human Genetics, 2019, v. 83, n. 3, p. 160, doi. 10.1111/ahg.12298

By:

Yang, Aram;
Kim, Jinsup;
Jang, Ja‐Hyun;
Lee, Chung;
Lee, Ji‐Eun;
Cho, Sung Yoon;
Jin, Dong‐Kyu

Publication type:

Article

Endocrine and Metabolic Illnesses in Young Adults with Prader–Willi Syndrome.

Published in:

Journal of Personalized Medicine, 2022, v. 12, n. 6, p. 858, doi. 10.3390/jpm12060858

By:

Noh, Eu-Seon;
Kim, Min-Sun;
Kim, Chiwoo;
Jeon, Kyeongman;
Kim, Seonwoo;
Cho, Sung Yoon;
Jin, Dong-Kyu

Publication type:

Article

Natural History and Molecular Characteristics of Korean Patients with Mucopolysaccharidosis Type III.

Published in:

Journal of Personalized Medicine, 2022, v. 12, n. 5, p. 665, doi. 10.3390/jpm12050665

By:

Kim, Min-Sun;
Yang, Aram;
Noh, Eu-seon;
Kim, Chiwoo;
Bae, Ga Young;
Lim, Han Hyuk;
Park, Hyung-Doo;
Cho, Sung Yoon;
Jin, Dong-Kyu

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

Effect of Growth Hormone Therapy on Height Velocity in Korean Children with Idiopathic Short Stature: A Phase III Randomised Controlled Trial.

Published in:

Hormone Research in Paediatrics, 2018, v. 90, n. 1, p. 44, doi. 10.1159/000491016

By:

Chung, Woo Yeong;
Yoo, Han-Wook;
Hwang, Jin Soon;
Ko, Cheol Woo;
Kim, Ho-Seong;
Jin, Dong-Kyu;
Lee, Kee-Hyoung;
Han, Heon-Seok;
Paranchothy, Premila;
Suh, Byung-Kyu

Publication type:

Article

Once-Weekly Administration of Sustained-Release Growth Hormone in Korean Prepubertal Children with Idiopathic Short Stature: A Randomized, Controlled Phase II Study.

Published in:

Hormone Research in Paediatrics, 2018, v. 90, n. 1, p. 54, doi. 10.1159/000489262

By:

Hwang, Jin Soon;
Lee, Hae Sang;
Lee, Kee-Hyoung;
Yoo, Han-Wook;
Lee, Dae-Yeol;
Suh, Byung-Kyu;
Ko, Cheol Woo;
Chung, Woo Yeong;
Jin, Dong-Kyu;
Shin, Choong Ho;
Han, Heon-Seok;
Han, Song;
Kim, Ho-Seong

Publication type:

Article

A Report of an Indian Boy with a Delayed Diagnosis of Pseudochondroplasia.

Published in:

Journal of Clinical & Diagnostic Research, 2013, v. 7, n. 7, p. 1479, doi. 10.7860/JCDR/2013/5410.3167

By:

SINGH, ANKUR;
ABIRAMALATHA, T.;
PRADHAN, GAURAV;
DONG- KYU JIN;
KAPOOR, SEEMA

Publication type:

Article

Efficacy of heparin-coated stent in early setting of acute myocardial infarction.

Published in:

Catheterization & Cardiovascular Interventions, 2001, v. 52, n. 3, p. 306, doi. 10.1002/ccd.1070

By:

Shin, Eak Kyun;
Son, Ji Won;
Sohn, Min Soo;
Jin, Dong Kyu;
Park, Gi Soo;
Koh, Kwang Kon;
Ahn, Tae Hoon;
Choi, In Suck

Publication type:

Article

Six novel mutations of the fibrillin-1 gene in Korean patients with Marfan syndrome.

Published in:

Pediatrics International, 2000, v. 42, n. 5, p. 488, doi. 10.1046/j.1442-200x.2000.01268.x

By:

Oh, Myung Ryurl;
Kim, Jung Sim;
Beck, Nam Seon;
Lee, Heung Jae;
Jin, Dong Kyu

Publication type:

Article

Human Leukocyte Antigens in Childhood Idiopathic Nephrotic Syndrome.

Published in:

Pediatrics International, 1991, v. 33, n. 6, p. 709, doi. 10.1111/j.1442-200X.1991.tb02595.x

By:

Jin, Dong Kyu;
Kohsaka, Takao;
Tanaka, Masahiro;
Abe, Jun;
Kobayashi, Noboru

Publication type:

Article

Worldwide distribution and broader clinical spectrum of muscle–eye–brain disease.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 5, p. 527, doi. 10.1093/hmg/ddg043

By:

Taniguchi, Kiyomi;
Kobayashi, Kazuhiro;
Saito, Kayoko;
Yamanouchi, Hideo;
Ohnuma, Akira;
Hayashi, Yukiko K.;
Manya, Hiroshi;
Jin, Dong Kyu;
Lee, Munhyang;
Parano, Enrico;
Falsaperla, Raffaele;
Pavone, Piero;
Van Coster, Rudy;
Talim, Beril;
Steinbrecher, Alice;
Straub, Volker;
Nishino, Ichizo;
Topaloglu, Haluk;
Voit, Thomas;
Endo, Tamao

Publication type:

Article

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

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

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

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 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

Identification of a cut-off for the macis score to predict the prognosis of differentiated thyroid carcinoma in children and young adults.

Published in:

Head & Neck, 2012, v. 34, n. 5, p. 696, doi. 10.1002/hed.21808

By:

Jang, Hye Won;
Lee, Ji In;
Kim, Hee Kyung;
Oh, Young Lyun;
Choi, Yoon-La;
Jin, Dong-Kyu;
Kim, Jung-Han;
Chung, Jae Hoon;
Kim, Sun Wook

Publication type:

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