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Beom-Hee Lee

Showing results (31-40 of 197) with videos related to

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Annals of Pediatric Endocrinology & Metabolism|January 25, 2022
Genotype-phenotype correlations and long-term efficacy of pamidronate therapy in patients with osteogenesis imperfectaYunha Choi, Soojin Hwang, Gu-Hwan Kim, et al.
Medicine|March 31, 2021
Hematopoietic stem cell transplantation in an infant with dedicator of cytokinesis 8 (DOCK8) deficiency associated with systemic lupus erythematosus: A case reportEuri Seo, Beom Hee Lee, Joo Hoon Lee, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 11, 2017
Long-term Consequences of Congenital Adrenal Hyperplasia due to Classic 21-hydroxylase Deficiency in Adolescents and AdultsJa Hye Kim, Jin-Ho Choi, Eungu Kang, et al.
Medicine|December 29, 2021
Identification of FOXG1 mutations in infantile hypotonia and postnatal microcephalyHan Na Jang, Taeho Kim, Ah Young Jung, et al.
Journal of Korean Medical Science|May 9, 2017
DEND Syndrome with Heterozygous KCNJ11 Mutation Successfully Treated with SulfonylureaJa Hyang Cho, Eungu Kang, Beom Hee Lee, et al.
Medicine|April 6, 2018
Clinical characteristics and treatment outcomes in Camurati-Engelmann disease: A case seriesYoon-Myung Kim, Eungu Kang, Jin-Ho Choi, et al.
Annals of Pediatric Endocrinology & Metabolism|October 26, 2016
Long-term clinical outcome and the identification of homozygous <i>CYP27B1</i> gene mutations in a patient with vitamin D hydroxylation-deficient rickets type 1AJa Hyang Cho, Eungu Kang, Gu-Hwan Kim, et al.
Journal of Human Genetics|December 14, 2017
Characteristic dysmorphic features in congenital disorders of glycosylation type IIbYoon-Myung Kim, Go Hun Seo, Euiseok Jung, et al.
Annals of Pediatric Endocrinology & Metabolism|April 27, 2017
Diabetes mellitus caused by secondary hemochromatosis after multiple blood transfusions in 2 patients with severe aplastic anemiaHyun Jin Kim, Yoon-Myung Kim, Eungu Kang, et al.
Journal of Human Genetics|August 21, 2019
Lysinuric protein intolerance with homozygous SLC7A7 mutation caused by maternal uniparental isodisomy of chromosome 14Eungu Kang, Taeho Kim, Arum Oh, et al.
Pageof 20

Showing results (31-40 of 197) with videos related to

Sort By:
Pageof 20
Annals of Pediatric Endocrinology & Metabolism|January 25, 2022
Genotype-phenotype correlations and long-term efficacy of pamidronate therapy in patients with osteogenesis imperfectaYunha Choi, Soojin Hwang, Gu-Hwan Kim, et al.
Medicine|March 31, 2021
Hematopoietic stem cell transplantation in an infant with dedicator of cytokinesis 8 (DOCK8) deficiency associated with systemic lupus erythematosus: A case reportEuri Seo, Beom Hee Lee, Joo Hoon Lee, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 11, 2017
Long-term Consequences of Congenital Adrenal Hyperplasia due to Classic 21-hydroxylase Deficiency in Adolescents and AdultsJa Hye Kim, Jin-Ho Choi, Eungu Kang, et al.
Medicine|December 29, 2021
Identification of FOXG1 mutations in infantile hypotonia and postnatal microcephalyHan Na Jang, Taeho Kim, Ah Young Jung, et al.
Journal of Korean Medical Science|May 9, 2017
DEND Syndrome with Heterozygous KCNJ11 Mutation Successfully Treated with SulfonylureaJa Hyang Cho, Eungu Kang, Beom Hee Lee, et al.
Medicine|April 6, 2018
Clinical characteristics and treatment outcomes in Camurati-Engelmann disease: A case seriesYoon-Myung Kim, Eungu Kang, Jin-Ho Choi, et al.
Annals of Pediatric Endocrinology & Metabolism|October 26, 2016
Long-term clinical outcome and the identification of homozygous <i>CYP27B1</i> gene mutations in a patient with vitamin D hydroxylation-deficient rickets type 1AJa Hyang Cho, Eungu Kang, Gu-Hwan Kim, et al.
Journal of Human Genetics|December 14, 2017
Characteristic dysmorphic features in congenital disorders of glycosylation type IIbYoon-Myung Kim, Go Hun Seo, Euiseok Jung, et al.
Annals of Pediatric Endocrinology & Metabolism|April 27, 2017
Diabetes mellitus caused by secondary hemochromatosis after multiple blood transfusions in 2 patients with severe aplastic anemiaHyun Jin Kim, Yoon-Myung Kim, Eungu Kang, et al.
Journal of Human Genetics|August 21, 2019
Lysinuric protein intolerance with homozygous SLC7A7 mutation caused by maternal uniparental isodisomy of chromosome 14Eungu Kang, Taeho Kim, Arum Oh, et al.
Pageof 20