Search Results - Ja Hye Kim
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1
Pathophysiology and clinical characteristics of hypothalamic obesity in children and adolescents by Ja Hye Kim, Jin-Ho Choi
Published 2013Call Number: Loading…Connect to this object online.
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2
Applications of genomic research in pediatric endocrine diseases by Ja Hye Kim, Jin-Ho Choi
Published 2023Call Number: Loading…Connect to this object online.
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3
Efficacy of growth hormone therapy in adults with childhood-onset growth hormone deficiency by Ja Hye Kim, Ja Hyang Cho, Han-Wook Yoo, Jin-Ho Choi
Published 2014Call Number: Loading…Connect to this object online.
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4
Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndrome by Ja Hye Kim, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi
Published 2023Call Number: Loading…Connect to this object online.
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5
Bone Mineral Density According to Dual Energy X-ray Absorptiometry is Associated with Serial Serum Alkaline Phosphatase Level in Extremely Low Birth Weight Infants at Discharge by Jin Lee, Hyun-Kyung Park, Ja Hye Kim, Yun Young Choi, Hyun Ju Lee
Published 2017Call Number: Loading…Connect to this object online.
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6
Long-term clinical course of a patient with mucopolysaccharidosis type IIIB by Ja Hye Kim, Yang Hyun Chi, Gu-Hwan Kim, Han-Wook Yoo, Jun Hwa Lee
Published 2016Call Number: Loading…Connect to this object online.
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7
Etiologic distribution and clinical characteristics of pediatric diabetes in 276 children and adolescents with diabetes at a single academic center by Ja Hye Kim, Yena Lee, Yunha Choi, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi
Published 2021Call Number: Loading…Connect to this object online.
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8
Long-term follow-up on Cushing disease patient after transsphenoidal surgery by Insook Jeong, Moonyeon Oh, Ja Hye Kim, Ja Hyang Cho, Jin-Ho Choi, Han-Wook Yoo
Published 2014Call Number: Loading…Connect to this object online.
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9
Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene by Ji-Hee Yoon, Soojin Hwang, Ja Hye Kim, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi
Published 2024Call Number: Loading…Connect to this object online.
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10
Clinical outcomes and genotype-phenotype correlations in patients with complete and partial androgen insensitivity syndromes by Nae-yun Lee, Ja Hye Kim, Ji-Hee Yoon, Soojin Hwang, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi
Published 2023Call Number: Loading…Connect to this object online.
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11
Lowe syndrome: a single center's experience in Korea by Hyun-Kyung Kim, Ja Hye Kim, Yoo-Mi Kim, Gu-Hwan Kim, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo
Published 2014Call Number: Loading…Connect to this object online.
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12
Detection rate and clinical impact of respiratory viruses in children with Kawasaki disease by Ja Hye Kim, Jeong Jin Yu, Jina Lee, Mi-Na Kim, Hong Ki Ko, Hyung Soon Choi, Young-Hwue Kim, Jae-Kon Ko
Published 2012Call Number: Loading…Connect to this object online.
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13
Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience by Sun-Jeong Shin, Yeonah Sul, Ja Hye Kim, Ja Hyang Cho, Gu-Hwan Kim, Jae Hyun Kim, Jin-Ho Choi, Han-Wook Yoo
Published 2015Call Number: Loading…Connect to this object online.
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14
Long-term endocrine sequelae after hematopoietic stem cell transplantation in children and adolescents by Soojin Hwang, Yena Lee, Ji-Hee Yoon, Ja Hye Kim, Hyery Kim, Kyung-Nam Koh, Ho Joon Im, Han-Wook Yoo, Jin-Ho Choi
Published 2024Call Number: Loading…Connect to this object online.
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15
Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay by Go Hun Seo, Ja Hye Kim, Ja Hyang Cho, Gu-Hwan Kim, Eul-Ju Seo, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo
Published 2016Call Number: Loading…Connect to this object online.
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16
Phelan-McDermid syndrome presenting with developmental delays and facial dysmorphisms by Yoon-Myung Kim, In-Hee Choi, Jun Suk Kim, Ja Hye Kim, Ja Hyang Cho, Beom Hee Lee, Gu-Hwan Kim, Jin-Ho Choi, Eul-Ju Seo, Han-Wook Yoo
Published 2016Call Number: Loading…Connect to this object online.
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17
Determination of Autosomal Dominant or Recessive Methionine Adenosyltransferase I/III Deficiencies Based on Clinical and Molecular Studies by Yoo-Mi Kim, Ja Hye Kim, Jin-Ho Choi, Gu-Hwan Kim, Jae-Min Kim, Minji Kang, In-Hee Choi, Chong Kun Cheon, Young Bae Sohn, Marco Maccarana, Han-Wook Yoo, Beom Hee Lee
Published 2016Call Number: Loading…Connect to this object online.
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