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- [21] Functional dissection of the impact of KMT2D germline mutations in Kabuki syndromeHUMAN GENE THERAPY, 2016, 27 (11) : A77 - A77Gabriele, M.论文数: 0 引用数: 0 h-index: 0机构: European Inst Oncol, Milan, Italy Univ Milan, Milan, Italy European Inst Oncol, Milan, ItalyGermain, P. L.论文数: 0 引用数: 0 h-index: 0机构: European Inst Oncol, Milan, Italy European Inst Oncol, Milan, Italy论文数: 引用数: h-index:机构:Merla, G.论文数: 0 引用数: 0 h-index: 0机构: Fdn Casa Sollievo Sofferenza, Milan, Italy European Inst Oncol, Milan, Italy论文数: 引用数: h-index:机构:
- [22] Individual Clinically Diagnosed with CHARGE Syndrome but with a Mutation in KMT2D, a Gene Associated with Kabuki Syndrome: A Case ReportFRONTIERS IN GENETICS, 2017, 8Sakata, Sonoko论文数: 0 引用数: 0 h-index: 0机构: Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, Japan Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, JapanOkada, Satoshi论文数: 0 引用数: 0 h-index: 0机构: Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, Japan Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, Japan论文数: 引用数: h-index:机构:Hara, Keiichi论文数: 0 引用数: 0 h-index: 0机构: Natl Hosp Org, Dept Pediat, Kure Med Ctr, Kure, Japan Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, JapanTani, Chihiro论文数: 0 引用数: 0 h-index: 0机构: Hiroshima Univ, Dept Diagnost Radiol, Grad Sch Biomed & Hlth Sci, Hiroshima, Japan Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, JapanKagawa, Reiko论文数: 0 引用数: 0 h-index: 0机构: Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, Japan Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, JapanUtsunomiya-Nakamura, Akari论文数: 0 引用数: 0 h-index: 0机构: Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, Japan Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, JapanMiyagawa, Shinichiro论文数: 0 引用数: 0 h-index: 0机构: Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, Japan Miyagawa Kids Clin, Hiroshima, Japan Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, JapanOgata, Tsutomu论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Dept Pediat, Hamamatsu, Shizuoka, Japan Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, JapanMizuno, Haruo论文数: 0 引用数: 0 h-index: 0机构: Nagoya City Univ, Dept Pediat & Neonatol, Grad Sch Med Sci, Nagoya, Aichi, Japan Int Univ Hlth & Welf, Dept Pediat, Sch Med, Chiba, Japan Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, JapanKobayashi, Masao论文数: 0 引用数: 0 h-index: 0机构: Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, Japan Hiroshima Univ, Dept Pediat, Grad Sch Biomed & Hlth Sci, Hiroshima, Japan
- [23] Granulomatous and Lymphocytic Interstitial Lung Disease (GLILD) Associated with KMT2D Gene Mutation in Kabuki SyndromeJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2016, 137 (02) : AB118 - AB118Adams, Juan A.论文数: 0 引用数: 0 h-index: 0机构: Med Coll Wisconsin, Milwaukee, WI 53226 USA Med Coll Wisconsin, Milwaukee, WI 53226 USAGallagher, Joel L.论文数: 0 引用数: 0 h-index: 0机构: Med Coll Wisconsin, Milwaukee, WI 53226 USA Med Coll Wisconsin, Milwaukee, WI 53226 USAHintermeyer, Mary论文数: 0 引用数: 0 h-index: 0机构: Med Coll Wisconsin, Milwaukee, WI 53226 USA Med Coll Wisconsin, Milwaukee, WI 53226 USAVerbsky, James W.论文数: 0 引用数: 0 h-index: 0机构: Med Coll Wisconsin, Milwaukee, WI 53226 USA Med Coll Wisconsin, Milwaukee, WI 53226 USARoutes, John M.论文数: 0 引用数: 0 h-index: 0机构: Med Coll Wisconsin, Milwaukee, WI 53226 USA Med Coll Wisconsin, Milwaukee, WI 53226 USA
- [24] A de novo KMT2D mutation in a girl with Kabuki syndrome associated with endocrine symptoms: a case reportBMC MEDICAL GENETICS, 2018, 19Moon, Jung-Eun论文数: 0 引用数: 0 h-index: 0机构: Kyungpook Natl Univ, Childrens Hosp, Dept Pediat, Sch Med, 807 Hoguk Ro, Daegu 41404, South Korea Kyungpook Natl Univ, Childrens Hosp, Dept Pediat, Sch Med, 807 Hoguk Ro, Daegu 41404, South KoreaLee, Su-Jeong论文数: 0 引用数: 0 h-index: 0机构: Kyungpook Natl Univ, Childrens Hosp, Dept Pediat, Sch Med, 807 Hoguk Ro, Daegu 41404, South Korea Kyungpook Natl Univ, Childrens Hosp, Dept Pediat, Sch Med, 807 Hoguk Ro, Daegu 41404, South Korea论文数: 引用数: h-index:机构:
- [25] Haploinsufficiency of KMT2D is sufficient to cause Kabuki syndrome and is compatible with lifeMOLECULAR GENETICS & GENOMIC MEDICINE, 2020, 8 (02):Luperchio, Teresa Romeo论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, McKusick Nathans Dept Genet Med, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, McKusick Nathans Dept Genet Med, Baltimore, MD 21205 USAApplegate, Carolyn D.论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, McKusick Nathans Dept Genet Med, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, McKusick Nathans Dept Genet Med, Baltimore, MD 21205 USABodamer, Olaf论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Dept Pediat, Div Genet & Gen, Boston, MA 02115 USA Broad Inst MIT & Harvard Univ, Cambridge, MA USA Johns Hopkins Univ, Sch Med, McKusick Nathans Dept Genet Med, Baltimore, MD 21205 USABjornsson, Hans Tomas论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, McKusick Nathans Dept Genet Med, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA Univ Iceland, Sch Hlth Sci, Fac Med, Reykjavik, Iceland Landspitali Univ Hosp, Reykjavik, Iceland Johns Hopkins Univ, Sch Med, McKusick Nathans Dept Genet Med, Baltimore, MD 21205 USA
- [26] Diffuse Adenomatosis and Hepatocellular Carcinoma Treated with Liver Transplantation in an Adolescent Female with Kabuki Syndrome with a Novel KMT2D Gene MutationCASE REPORTS IN PEDIATRICS, 2019, 2019Timothy, Leander D.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Pediat & Adolescent Med, 200 First St SW, Rochester, MN 55905 USA Mayo Clin, Dept Pediat & Adolescent Med, 200 First St SW, Rochester, MN 55905 USALehrke, Heidi D.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Lab Med & Pathol, 200 First St SW, Rochester, MN 55905 USA Mayo Clin, Div Anat Pathol, 200 First St SW, Rochester, MN 55905 USA Mayo Clin, Dept Pediat & Adolescent Med, 200 First St SW, Rochester, MN 55905 USAChandan, Vishal S.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Lab Med & Pathol, 200 First St SW, Rochester, MN 55905 USA Mayo Clin, Div Anat Pathol, 200 First St SW, Rochester, MN 55905 USA Mayo Clin, Dept Pediat & Adolescent Med, 200 First St SW, Rochester, MN 55905 USAKolbe, Amy B.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Radiol, 200 First St SW, Rochester, MN 55905 USA Mayo Clin, Div Pediat Radiol, 200 First St SW, Rochester, MN 55905 USA Mayo Clin, Dept Pediat & Adolescent Med, 200 First St SW, Rochester, MN 55905 USAFuruya, Katryn N.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Pediat & Adolescent Med, 200 First St SW, Rochester, MN 55905 USA Mayo Clin, Div Pediat Gastroenterol & Hepatol, 200 First St SW, Rochester, MN 55905 USA Mayo Clin, Dept Pediat & Adolescent Med, 200 First St SW, Rochester, MN 55905 USA
- [27] Mutation Update for Kabuki Syndrome Genes KMT2D and KDM6A and Further Delineation of X-Linked Kabuki Syndrome Subtype 2HUMAN MUTATION, 2016, 37 (09) : 847 - 864Boegershausen, Nina论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, Germany Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, Germany论文数: 引用数: h-index:机构:Riehmer, Vera论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Inst Human Genet, Cologne, Germany Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyKayserili, Huelya论文数: 0 引用数: 0 h-index: 0机构: KUSOM, Dept Med Genet, Istanbul, Turkey Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyBecker, Jutta论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Inst Human Genet, Cologne, Germany Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyThoenes, Michaela论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Inst Human Genet, Cologne, Germany Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanySimsek-Kiper, Pelin OEzlem论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Dept Pediat, Fac Med, Pediat Genet Unit, Ankara, Turkey Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyBarat-Houari, Mouna论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Lab Rare & Autoinflammatory Dis, Montpellier, France INSERM, Montpellier, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyElcioglu, Nursel H.论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Dept Pediat Genet, Fac Med, Istanbul, Turkey Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyWieczorek, Dagmar论文数: 0 引用数: 0 h-index: 0机构: Univ Duesseldorf, Inst Human Genet, Dusseldorf, Germany Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyTinschert, Sigrid论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Dresden, Inst Clin Genet, Fac Med Carl Gustav Carus, Dresden, Germany Med Univ, Zentrum Humangenet, Innsbruck, Austria Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanySarrabay, Guillaume论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Lab Rare & Autoinflammatory Dis, Montpellier, France Univ Montpellier, Montpellier, France INSERM, Montpellier, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyStrom, Tim M.论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Inst Human Genet, Munich, Germany Helmholtz Zentrum Munchen, Inst Human Genet, Neuherberg, Germany Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyFabre, Aurelie论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Lab Rare & Autoinflammatory Dis, Montpellier, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyBaynam, Gareth论文数: 0 引用数: 0 h-index: 0机构: Princess Margaret & King Edward Mem Hosp, Genet Serv Western Australia, Perth, WA, Australia Western Australian Register Dev Anomalies, Perth, WA, Australia Telethon Kids Inst, Perth, WA, Australia Univ Western Australia, Sch Paediat & Child Hlth, Perth, WA, Australia Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanySanchez, Elodie论文数: 0 引用数: 0 h-index: 0机构: INSERM, Montpellier, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyNuernberg, Gudrun论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Cologne Ctr Genom, Cologne, Germany Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyAltunoglu, Umut论文数: 0 引用数: 0 h-index: 0机构: Istanbul Univ, Dept Med Genet, Istanbul Fac Med, Istanbul, Turkey Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyCapri, Yline论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 07, Denis Diderot Med Sch, Dept Genet, APHP Robert DEBRE Univ Hosp, Paris, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyIsidor, Bertrand论文数: 0 引用数: 0 h-index: 0机构: Nantes Univ Hosp, Dept Genet, Nantes, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyLacombe, Didier论文数: 0 引用数: 0 h-index: 0机构: Bordeaux Univ, Dept Med Genet, CHU Bordeaux, INSERM,U1211, Bordeaux, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyCorsini, Carole论文数: 0 引用数: 0 h-index: 0机构: Univ Montpellier, Montpellier, France INSERM, Montpellier, France CHU Montpellier, Dept Med Genet, Reference Ctr Dev Abnormal, Montpellier, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyCormier-Daire, Valerie论文数: 0 引用数: 0 h-index: 0机构: Paris Descartes Sorbonne Paris Cite Univ, Inst Imagine, INSERM, U1163, Paris, France Hop Univ Necker Enfants Malad, AP HP, Serv Genet, Paris, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanySanlaville, Damien论文数: 0 引用数: 0 h-index: 0机构: UCBL1, GENDEV Team, CRNL, HCL Genet Dept,INSERM,U1028,CNRS,UMR 5292, Lyon, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyGiuliano, Fabienne论文数: 0 引用数: 0 h-index: 0机构: Archet II Hosp, Dept Med Genet, Nice, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyLe Quan Sang, Kim-Hanh论文数: 0 引用数: 0 h-index: 0机构: Paris Descartes Sorbonne Paris Cite Univ, Inst Imagine, INSERM, U1163, Paris, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyKayirangwa, Honorine论文数: 0 引用数: 0 h-index: 0机构: Paris Descartes Sorbonne Paris Cite Univ, Inst Imagine, INSERM, U1163, Paris, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyNuernberg, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Cologne Ctr Genom, Cologne, Germany Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyMeitinger, Thomas论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Inst Human Genet, Munich, Germany Helmholtz Zentrum Munchen, Inst Human Genet, Neuherberg, Germany Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyBoduroglu, Koray论文数: 0 引用数: 0 h-index: 0机构: Hacettepe Univ, Dept Pediat, Fac Med, Pediat Genet Unit, Ankara, Turkey Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyZoll, Barbara论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, Germany Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyLyonnet, Stanislas论文数: 0 引用数: 0 h-index: 0机构: Paris Descartes Sorbonne Paris Cite Univ, Inst Imagine, INSERM, U1163, Paris, France Hop Univ Necker Enfants Malad, AP HP, Serv Genet, Paris, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, Germany论文数: 引用数: h-index:机构:Verloes, Alain论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 07, Denis Diderot Med Sch, Dept Genet, APHP Robert DEBRE Univ Hosp, Paris, France Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, Germany论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Netzer, Christian论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Inst Human Genet, Cologne, Germany Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyLi, Yun论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, Germany Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, Germany论文数: 引用数: h-index:机构:Yigit, Goekhan论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, Germany Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, GermanyWollnik, Bernd论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, Germany Univ Med Ctr Goettingen, Inst Human Genet, Gottingen, Germany
- [28] Treatment of immune thrombocytopenia with hetrombopag olamine tablets in a Kabuki syndrome patient with new KMT2D mutationsPLATELETS, 2023, 34 (01)Peng, Peng论文数: 0 引用数: 0 h-index: 0机构: Wannan Med Coll, Grad Sch, Wuhu, Anhui, Peoples R China Wannan Med Coll, Grad Sch, Wuhu, Anhui, Peoples R ChinaPan, Ying论文数: 0 引用数: 0 h-index: 0机构: Anhui Med Univ, Affiliated Hosp 2, Dept Hematol, Hefei, Anhui, Peoples R China Wannan Med Coll, Grad Sch, Wuhu, Anhui, Peoples R ChinaLu, Xueqing论文数: 0 引用数: 0 h-index: 0机构: Wannan Med Coll, Grad Sch, Wuhu, Anhui, Peoples R China Wannan Med Coll, Grad Sch, Wuhu, Anhui, Peoples R ChinaXu, Hui论文数: 0 引用数: 0 h-index: 0机构: Univ Sci & Technol China, Affiliated Hosp USTC 1, Dept Hematol, Div Life Sci & Med, Hefei, Anhui, Peoples R China Wannan Med Coll, Grad Sch, Wuhu, Anhui, Peoples R ChinaZhou, Ziwei论文数: 0 引用数: 0 h-index: 0机构: Univ Sci & Technol China, Affiliated Hosp USTC 1, Dept Hematol, Div Life Sci & Med, Hefei, Anhui, Peoples R China Wannan Med Coll, Grad Sch, Wuhu, Anhui, Peoples R ChinaHe, Yuanqing论文数: 0 引用数: 0 h-index: 0机构: Anhui Med Univ, Affiliated Hosp 2, Dept Hematol, Hefei, Anhui, Peoples R China Wannan Med Coll, Grad Sch, Wuhu, Anhui, Peoples R ChinaWang, Huiru论文数: 0 引用数: 0 h-index: 0机构: Univ Sci & Technol China, Affiliated Hosp USTC 1, Dept Transfus, Div Life Sci & Med, Hefei, Anhui, Peoples R China Wannan Med Coll, Grad Sch, Wuhu, Anhui, Peoples R ChinaZheng, Changcheng论文数: 0 引用数: 0 h-index: 0机构: Univ Sci & Technol China, Affiliated Hosp USTC 1, Dept Hematol, Div Life Sci & Med, Hefei, Anhui, Peoples R China Wannan Med Coll, Grad Sch, Wuhu, Anhui, Peoples R ChinaZhou, Li论文数: 0 引用数: 0 h-index: 0机构: Anhui Med Univ, Affiliated Hosp 2, Dept Hematol, Hefei, Anhui, Peoples R China Anhui Med Univ, Affiliated Hosp 2, Dept Hematol, Hefei 230601, Anhui, Peoples R China Wannan Med Coll, Grad Sch, Wuhu, Anhui, Peoples R China
- [29] Molecular insights of KMT2D and clinical aspects of Kabuki syndrome type 1BIRTH DEFECTS RESEARCH, 2023, 115 (19): : 1809 - 1824Golden, Carly S.论文数: 0 引用数: 0 h-index: 0机构: Boston Univ, Ctr Regenerat Med, Dept Med, Sect Vasc Biol, Boston, MA 02215 USA Boston Univ, Ctr Regenerat Med, Dept Med, Sect Vasc Biol, Boston, MA 02215 USA论文数: 引用数: h-index:机构:Serrano, Maria A.论文数: 0 引用数: 0 h-index: 0机构: Boston Univ, Ctr Regenerat Med, Dept Med, Sect Vasc Biol, Boston, MA 02215 USA Boston Univ, Ctr Regenerat Med, Dept Med, Sect Vasc Biol, Boston, MA 02215 USA
- [30] <it>KMT2D</it> Haploinsufficiency in Kabuki Syndrome Impairs Differentiation of Neural Crest CellsFASEB JOURNAL, 2020, 34Lavery, William论文数: 0 引用数: 0 h-index: 0机构: Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USAKotliar, Michael论文数: 0 引用数: 0 h-index: 0机构: Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USAChang, Ching论文数: 0 引用数: 0 h-index: 0机构: Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USABrugmann, Samantha论文数: 0 引用数: 0 h-index: 0机构: Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USABarski, Artem论文数: 0 引用数: 0 h-index: 0机构: Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USALindsley, Andrew论文数: 0 引用数: 0 h-index: 0机构: Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA