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Recombinant growth hormone therapy for prepubertal children with idiopathic short stature in Korea: a phase III randomized trial

Journal of endocrinological investigation, 2018-04, Vol.41 (4), p.475-483

2018

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Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family

Journal of medical genetics, 2010-10, Vol.47 (10), p.704-709

2010

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IgE‐mediated anaphylaxis and allergic reactions to idursulfase in patients with Hunter syndrome

Allergy (Copenhagen), 2013-06, Vol.68 (6), p.796-802

2013

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Identification of 11 novel mutations in 49 Korean patients with mucopolysaccharidosis type II

Clinical genetics, 2012-02, Vol.81 (2), p.185-190

2012

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Clinical characterization and molecular classification of 12 Korean patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism

Experimental and clinical endocrinology & diabetes, 2013-10, Vol.121 (9), p.539-545

2013

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Mutational spectrum in eight Korean patients with 3-methylcrotonyl-CoA carboxylase deficiency

Clinical genetics, 2012-01, Vol.81 (1), p.96-98

2012

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A case report of rare XXY/XX mosaicism in a phenotypic male with Klinefelter syndrome and mediastinal germ cell tumor

Genetic counseling, 2014-01, Vol.25 (2), p.215

2014

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Structural Parameters Optimization for a Proportional Solenoid

International journal of simulation modelling, 2020-12, Vol.19 (4), p.689-700

2020

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Chemokine-mediated interaction of hematopoietic progenitors with the bone marrow vascular niche is required for thrombopoiesis

Nature medicine, 2004-01, Vol.10 (1), p.64-71

2004

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Primary headache in childhood associated with psychiatric disturbances: an update

European review for medical and pharmacological sciences, 2020-06, Vol.24 (12), p.6893

2020

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Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized?

Clinical genetics, 2004-10, Vol.66 (4), p.368-372

2004

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Late‐onset warfarin‐induced skin necrosis: case report and review of the literature

American journal of hematology, 1998-03, Vol.57 (3), p.233-237

1998

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17α-hydroxlyase/17, 20-lyase Deficiency in Three Siblings with Primary Amenorrhea and Absence of Secondary Sexual Development

Journal of pediatric & adolescent gynecology, 2012-10, Vol.25 (5), p.e103-e105

2012

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A simple method for the detection of neurologic disorders associated with CAG repeat expansion using PCR-microtiter plate hybridization

Journal of biotechnology, 2002-05, Vol.95 (3), p.215-223

2002

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A case of mitochondrial trifunctional protein deficiency diagnosed by acylcarnitine profile and DNA analysis in a dried blood spot of a 4‐day‐old boy

Journal of inherited metabolic disease, 2003-01, Vol.26 (4), p.403-406

2003

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Distribution of integrin subunits in human diabetic kidneys

Journal of the American Society of Nephrology, 1996-12, Vol.7 (12), p.2636-2645

1996

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Vascular effects of synthetic or natural progestagen combined with conjugated equine estrogen in healthy postmenopausal women

Circulation (New York, N.Y.), 2001-04, Vol.103 (15), p.1961-1966

2001

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Mutational analysis of the α-l-iduronidase gene in 10 unrelated Korean type I mucopolysaccharidosis patients: Identification of four novel mutations

Clinical genetics, 2004-12, Vol.66 (6), p.575-576

2004

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Comparative effects of diet and statin on NO bioactivity and matrix metalloproteinases in hypercholesterolemic patients with coronary artery disease

Arteriosclerosis, thrombosis, and vascular biology, 2002-09, Vol.22 (9), p.e19

2002

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

Journal of human genetics, 1999-01, Vol.44 (4), p.240-245

1999

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Simvastatin Combined With Ramipril Treatment in Hypercholesterolemic Patients

Hypertension (Dallas, Tex. 1979), 2004-08, Vol.44 (2), p.180-185

2004

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Significant differential effects of hormone therapy or tibolone on markers of cardiovascular disease in postmenopausal women: a randomized, double-blind, placebo-controlled, crossover study

Arteriosclerosis, thrombosis, and vascular biology, 2003-10, Vol.23 (10), p.1889-1894

2003

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Adenovirus E4 Gene Promotes Selective Endothelial Cell Survival and Angiogenesis via Activation of the Vascular Endothelial-Cadherin/Akt Signaling Pathway

The Journal of biological chemistry, 2004-03, Vol.279 (12), p.11760-11766

2004

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A Unique Origin and Multistep Process for the Generation of Expanded DRPLA Triplet Repeats

Human molecular genetics, 1996-03, Vol.5 (3), p.373-379

1996

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

The journal of clinical endocrinology and metabolism, 2004-08, Vol.89 (8), p.3885-3889

2004

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Recombinant growth hormone therapy for prepubertal children with idiopathic short stature in Korea: a phase III randomized trial

Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family

IgE‐mediated anaphylaxis and allergic reactions to idursulfase in patients with Hunter syndrome

Identification of 11 novel mutations in 49 Korean patients with mucopolysaccharidosis type II

Clinical characterization and molecular classification of 12 Korean patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism

Mutational spectrum in eight Korean patients with 3-methylcrotonyl-CoA carboxylase deficiency

A case report of rare XXY/XX mosaicism in a phenotypic male with Klinefelter syndrome and mediastinal germ cell tumor

Structural Parameters Optimization for a Proportional Solenoid

Chemokine-mediated interaction of hematopoietic progenitors with the bone marrow vascular niche is required for thrombopoiesis

Primary headache in childhood associated with psychiatric disturbances: an update

Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized?

Late‐onset warfarin‐induced skin necrosis: case report and review of the literature

17α-hydroxlyase/17, 20-lyase Deficiency in Three Siblings with Primary Amenorrhea and Absence of Secondary Sexual Development

A simple method for the detection of neurologic disorders associated with CAG repeat expansion using PCR-microtiter plate hybridization

A case of mitochondrial trifunctional protein deficiency diagnosed by acylcarnitine profile and DNA analysis in a dried blood spot of a 4‐day‐old boy

Distribution of integrin subunits in human diabetic kidneys

Vascular effects of synthetic or natural progestagen combined with conjugated equine estrogen in healthy postmenopausal women

Mutational analysis of the α-l-iduronidase gene in 10 unrelated Korean type I mucopolysaccharidosis patients: Identification of four novel mutations

Comparative effects of diet and statin on NO bioactivity and matrix metalloproteinases in hypercholesterolemic patients with coronary artery disease

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

Simvastatin Combined With Ramipril Treatment in Hypercholesterolemic Patients

Significant differential effects of hormone therapy or tibolone on markers of cardiovascular disease in postmenopausal women: a randomized, double-blind, placebo-controlled, crossover study

Adenovirus E4 Gene Promotes Selective Endothelial Cell Survival and Angiogenesis via Activation of the Vascular Endothelial-Cadherin/Akt Signaling Pathway

A Unique Origin and Multistep Process for the Generation of Expanded DRPLA Triplet Repeats

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

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