Hasil Pencarian - SungYoon Cho

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  1. 1
    Guidelines for genetic skeletal dysplasias for pediatricians

    Guidelines for genetic skeletal dysplasias for pediatricians oleh Sung Yoon Cho, Dong-Kyu Jin

    Diterbitkan 2015-12-01
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  2. 2
    A Korean boy with a mutation who presented with overgrowth, intellectual disability, and autism

    A Korean boy with a mutation who presented with overgrowth, intellectual disability, and autism oleh Chiwoo Kim, Eu-seon Noh, Sung Yoon Cho

    Diterbitkan 2023-02-01
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  3. 3
    Mixed diabetic ketoacidosis and hyperglycemic hyperosmolarity in a girl with nephronophthisis 4 presenting with rhabdomyolysis and pancreatitis

    Mixed diabetic ketoacidosis and hyperglycemic hyperosmolarity in a girl with nephronophthisis 4 presenting with rhabdomyolysis and pancreatitis oleh Eu-Seon Noh, Chiwoo Kim, Sung Yoon Cho

    Diterbitkan 2023-12-01
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  4. 4
    Prader-Willi syndrome: an update on obesity and endocrine problems

    Prader-Willi syndrome: an update on obesity and endocrine problems oleh Su Jin Kim, Sung Yoon Cho, Dong-Kyu Jin

    Diterbitkan 2021-12-01
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  5. 5
    Prevalence and risk factors for type 2 diabetes mellitus with Prader–Willi syndrome: a single center experience

    Prevalence and risk factors for type 2 diabetes mellitus with Prader–Willi syndrome: a single center experience oleh Aram Yang, Jinsup Kim, Sung Yoon Cho, Dong-Kyu Jin

    Diterbitkan 2017-08-01
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  6. 6
    A Case of Mitochondrial Trifunctional Protein Deficiency with Variants Diagnosed Using Whole-Exome Sequencing

    A Case of Mitochondrial Trifunctional Protein Deficiency with Variants Diagnosed Using Whole-Exome Sequencing oleh Chan Kim, Dajeong Lee, Jiwon Lee, Sung Yoon Cho, Jeehun Lee

    Diterbitkan 2021-10-01
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  7. 7
    Etiological trends in male central precocious puberty

    Etiological trends in male central precocious puberty oleh Jisun Lee, Jinsup Kim, Aram Yang, Sung Yoon Cho, Dong-Kyu Jin

    Diterbitkan 2018-06-01
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  8. 8
    Elevation of serum creatine kinase during methimazole treatment of Graves disease in a 13-year-old girl and a literature review of similar cases

    Elevation of serum creatine kinase during methimazole treatment of Graves disease in a 13-year-old girl and a literature review of similar cases oleh Hyeseon Kim, Jinsup Kim, Rimm Huh, Sung Yoon Cho, Dong-Kyu Jin

    Diterbitkan 2015-06-01
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  9. 9
    2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis

    2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis oleh Eun-Kyung Cho, Jinsup Kim, Aram Yang, Sung Yoon Cho, Dong-Kyu Jin

    Diterbitkan 2017-06-01
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  10. 10
    Tailored management of life-threatening complications related to severe obesity in a young adult with Prader-Willi syndrome

    Tailored management of life-threatening complications related to severe obesity in a young adult with Prader-Willi syndrome oleh Min-Sun Kim, Jiyeon Kim, Joongbum Cho, Sung Yoon Cho, Dong-Kyu Jin

    Diterbitkan 2021-10-01
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  11. 11
    A case of 18p deletion syndrome with panhypopituitarism

    A case of 18p deletion syndrome with panhypopituitarism oleh Aram Yang, Jinsup Kim, Sung Yoon Cho, Ji-Eun Lee, Hee-Jin Kim, Dong-Kyu Jin

    Diterbitkan 2019-03-01
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  12. 12
    657 A combination treatment of bone marrow-derived CD141+dendritic cells and PD1/PD-L1 inhibitors for effective immunotherapy for solid tumors

    657 A combination treatment of bone marrow-derived CD141+dendritic cells and PD1/PD-L1 inhibitors for effective immunotherapy for solid tumors oleh Jeong Seong Mun, SungYoon Cho, Youngjoo Jeon, Jisun Lim, Gawhan Lee, Sungeun Yun, Hyunsoo Kim

    Diterbitkan 2023-11-01
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  13. 13
    HDR syndrome with a novel mutation in GATA3 mimicking a congenital X-linked stapes gusher: a case report

    HDR syndrome with a novel mutation in GATA3 mimicking a congenital X-linked stapes gusher: a case report oleh Aram Yang, Jinsup Kim, Chang-Seok Ki, Sung Hwa Hong, Sung Yoon Cho, Dong-Kyu Jin

    Diterbitkan 2017-10-01
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  14. 14
    A novel mosaic mutation in in a Korean patient with hypophosphatemic rickets

    A novel mosaic mutation in in a Korean patient with hypophosphatemic rickets oleh Misun Yang, Jinsup Kim, Aram Yang, Jahyun Jang, Tae Yeon Jeon, Sung Yoon Cho, Dong-Kyu Jin

    Diterbitkan 2018-12-01
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  15. 15
    Resistance to thyroid hormone and nonfunctioning pituitary microadenoma in a 13-year-old boy with THRB mutation

    Resistance to thyroid hormone and nonfunctioning pituitary microadenoma in a 13-year-old boy with THRB mutation oleh Jiyeon Kim, Eu Seon Noh, Min-Sun Kim, Jong-Moon Choi, Sae-Mi Lee, Sung Yoon Cho

    Diterbitkan 2024-02-01
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  16. 16
    An atypical case of Noonan syndrome with mutation diagnosed by targeted exome sequencing

    An atypical case of Noonan syndrome with mutation diagnosed by targeted exome sequencing oleh Jinsup Kim, Sung Yoon Cho, Aram Yang, Ja-Hyun Jang, Youngbin Choi, Ji-Eun Lee, Dong-Kyu Jin

    Diterbitkan 2017-09-01
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  17. 17
    Appropriate Age for Height Control Treatment in Patients With Marfan Syndrome

    Appropriate Age for Height Control Treatment in Patients With Marfan Syndrome oleh Sung Eun Kim, Dong-Yun Lee, Min-Sun Kim, Sung Yoon Cho, Dong-Kyu Jin, DooSeok Choi

    Diterbitkan 2021-10-01
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  18. 18
    Development and validation of a distress measurement for insulin injections among patients with diabetes

    Development and validation of a distress measurement for insulin injections among patients with diabetes oleh Eujin Choi, Min-Sun Kim, Juhee Cho, Sooyeon Kim, Eun Kyung Kwon, Youngha Kim, Danbee Kang, Sung Yoon Cho

    Diterbitkan 2023-07-01
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  19. 19
    Clinical, Hormonal, and Neuroradiological Characteristics and Therapeutic Outcomes of Prolactinomas in Children and Adolescents at a Single Center

    Clinical, Hormonal, and Neuroradiological Characteristics and Therapeutic Outcomes of Prolactinomas in Children and Adolescents at a Single Center oleh Aram Yang, Sung Yoon Cho, Hyojung Park, Min Sun Kim, Doo-Sik Kong, Hyung-Jin Shin, Dong-Kyu Jin

    Diterbitkan 2020-08-01
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  20. 20
    Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center

    Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center oleh Yangho Yoo, Mi Sun Chang, Jieun Lee, Sung Yoon Cho, Sung Won Park, Dong-Kyu Jin, Hyung-Doo Park

    Diterbitkan 2013-09-01
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