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1دورية أكاديمية
المؤلفون: Lee, Yuna, Lee, SeunghyunAff1, Aff2, IDs13023023027047_cor2, Hur, SaebeomAff1, Aff2, Jeong, Yun Soo, Suh, Dong In, Moon, Jangsup, Kim, Man Jin, Choi, Young HunAff1, Aff2, Cheon, Jung-EunAff1, Aff2, Aff6
المصدر: Orphanet Journal of Rare Diseases. 18(1)
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2دورية أكاديمية
المؤلفون: Yuna Lee, Seunghyun Lee, Saebeom Hur, Yun Soo Jeong, Dong In Suh, Jangsup Moon, Man Jin Kim, Young Hun Choi, Jung-Eun Cheon
المصدر: Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
مصطلحات موضوعية: Gorham–Stout disease, Osteolysis, Lymphatic malformation, Angiomatous lesion, Dynamic contrast-enhanced magnetic resonance lymphangiography, Medicine
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1750-1172
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3دورية أكاديمية
المؤلفون: Soo Yeon Kim, Seungbok Lee, Hyewon Woo, Jiyeon Han, Young Jun Ko, Youngkyu Shim, Soojin Park, Se Song Jang, Byung Chan Lim, Jung Min Ko, Ki Joong Kim, Anna Cho, Hunmin Kim, Hee Hwang, Ji Eun Choi, Man Jin Kim, Jangsup Moon, Moon-Woo Seong, Sung Sup Park, Sun Ah Choi, Ji Eun Lee, Young Se Kwon, Young Bae Sohn, Jon Soo Kim, Won Seop Kim, Yun Jeong Lee, Soonhak Kwon, Young Ok Kim, Hoon Kook, Yong Gon Cho, Chong Kun Cheon, Ki-Soo Kang, Mi-Ryoung Song, Young-Joon Kim, Hyuk-Jin Cha, Hee-Jung Choi, Yun Kee, Sung-Gyoo Park, Seung Tae Baek, Murim Choi, Dong-Sung Ryu, Jong-Hee Chae
المصدر: Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-11 (2022)
مصطلحات موضوعية: Rare disease, Undiagnosed disease program, Translational research, Data sharing, Medicine
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1750-1172
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4دورية أكاديمية
المؤلفون: Soo Yeon Kim, Saebom Ko, Hyunook Kang, Man Jin Kim, Jangsup Moon, Byung Chan Lim, Ki Joong Kim, Murim Choi, Hee-Jung Choi, Jong-Hee Chae
المصدر: Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-10 (2022)
مصطلحات موضوعية: FARSA, Phenylalanyl-tRNA synthetase, Aminoacyl-tRNA synthetase, Medicine
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1750-1172
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5دورية أكاديمية
المؤلفون: Kim, Soo Yeon, Lee, Seungbok, Woo, Hyewon, Han, Jiyeon, Ko, Young Jun, Shim, Youngkyu, Park, Soojin, Jang, Se Song, Lim, Byung Chan, Ko, Jung Min, Kim, Ki Joong, Cho, Anna, Kim, Hunmin, Hwang, Hee, Choi, Ji Eun, Kim, Man Jin, Moon, Jangsup, Seong, Moon-Woo, Park, Sung Sup, Choi, Sun Ah, Lee, Ji Eun, Kwon, Young Se, Sohn, Young Bae, Kim, Jon Soo, Kim, Won SeopAff11, Aff12, Lee, Yun Jeong, Kwon, Soonhak, Kim, Young Ok, Kook, Hoon, Cho, Yong Gon, Cheon, Chong Kun, Kang, Ki-Soo, Song, Mi-Ryoung, Kim, Young-Joon, Cha, Hyuk-Jin, Choi, Hee-Jung, Kee, Yun, Park, Sung-Gyoo, Baek, Seung Tae, Choi, Murim, Ryu, Dong-Sung, Chae, Jong-HeeAff1, Aff2, IDs13023022025205_cor42
المصدر: Orphanet Journal of Rare Diseases. 17(1)
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6دورية أكاديمية
المؤلفون: Kim, Soo Yeon, Ko, Saebom, Kang, Hyunook, Kim, Man Jin, Moon, Jangsup, Lim, Byung Chan, Kim, Ki Joong, Choi, Murim, Choi, Hee-JungAff2, IDs13023022024579_cor9, Chae, Jong-HeeAff1, Aff3, IDs13023022024579_cor10
المصدر: Orphanet Journal of Rare Diseases. 17(1)
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7دورية أكاديمية
المؤلفون: Hyun Jin Park, Chang Ho Shin, Won Joon Yoo, Tae-Joon Cho, Man Jin Kim, Moon-Woo Seong, Sung Sup Park, Jeong Ho Lee, Nam Suk Sim, Jung Min Ko
المصدر: Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
مصطلحات موضوعية: PIK3CA, Somatic overgrowth, Megalencephaly, Asymmetry, Cutaneous vascular malformation, Medicine
وصف الملف: electronic resource
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8دورية أكاديمية
المؤلفون: Park, Hyun Jin, Shin, Chang Ho, Yoo, Won Joon, Cho, Tae-Joon, Kim, Man JinAff3, Aff4, Seong, Moon-Woo, Park, Sung Sup, Lee, Jeong Ho, Sim, Nam Suk, Ko, Jung MinAff1, Aff4
المصدر: Orphanet Journal of Rare Diseases. 15(1)
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9
المؤلفون: Man Jin Kim, Moon Woo Seong, Chang Ho Shin, Tae Joon Cho, Hyun Jin Park, Jung Min Ko, Won Joon Yoo, Sung Sup Park, Jeong Ho Lee, Nam Suk Sim
المصدر: Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)مصطلحات موضوعية: 0301 basic medicine, Hemimegalencephaly, Pathology, medicine.medical_specialty, Cutaneous vascular malformation, Genotype, Class I Phosphatidylinositol 3-Kinases, Genetic counseling, lcsh:Medicine, 030105 genetics & heredity, 03 medical and health sciences, 0302 clinical medicine, Republic of Korea, medicine, Polymicrogyria, Humans, Pharmacology (medical), Megalencephaly, Genetics (clinical), Genetic testing, medicine.diagnostic_test, Mosaicism, business.industry, Research, lcsh:R, Vascular malformation, Macrocephaly, Asymmetry, PIK3CA, General Medicine, medicine.disease, Phenotype, Mutation, Somatic overgrowth, medicine.symptom, business, 030217 neurology & neurosurgery