共 50 条
- [1] The first three years of screening for medium chain acyl-CoA dehydrogenase deficiency (MCADD) by newborn screening ontarioBMC PEDIATRICS, 2010, 10Kennedy, Shelley论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, Canada Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, CanadaPotter, Beth K.论文数: 0 引用数: 0 h-index: 0机构: Univ Ottawa, Dept Epidemiol & Community Med, Ottawa, ON, Canada Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, CanadaWilson, Kumanan论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, Canada Univ Ottawa, Dept Epidemiol & Community Med, Ottawa, ON, Canada Univ Ottawa, Dept Med, Ottawa Hosp, Res Inst, Ottawa, ON, Canada Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, CanadaFisher, Lawrence论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, Canada Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, CanadaGeraghty, Michael论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, Canada Univ Ottawa, Dept Pediat, Ottawa, ON K1N 6N5, Canada Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, CanadaMilburn, Jennifer论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, Canada Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, CanadaChakraborty, Pranesh论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, Canada Univ Ottawa, Dept Pediat, Ottawa, ON K1N 6N5, Canada Univ Ottawa, Dept Pathol & Lab Med, Ottawa, ON, Canada Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, Canada
- [2] Spectrum of medium-chain acyl-CoA dehydrogenase deficiency detected by newborn screeningPEDIATRICS, 2008, 121 (05) : E1108 - E1114Hsu, Ho-Wen论文数: 0 引用数: 0 h-index: 0机构: Univ Massachusetts, Sch Med, New England Newborn Screening Program, Dept Pediat, Boston, MA 02130 USA Univ Massachusetts, Sch Med, New England Newborn Screening Program, Dept Pediat, Boston, MA 02130 USAZytkovicz, Thomas H.论文数: 0 引用数: 0 h-index: 0机构: Univ Massachusetts, Sch Med, New England Newborn Screening Program, Dept Pediat, Boston, MA 02130 USA Univ Massachusetts, Sch Med, New England Newborn Screening Program, Dept Pediat, Boston, MA 02130 USAComeau, Anne Marie论文数: 0 引用数: 0 h-index: 0机构: Univ Massachusetts, Sch Med, New England Newborn Screening Program, Dept Pediat, Boston, MA 02130 USA Univ Massachusetts, Sch Med, New England Newborn Screening Program, Dept Pediat, Boston, MA 02130 USAStrauss, Arnold W.论文数: 0 引用数: 0 h-index: 0机构: Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH USA Univ Massachusetts, Sch Med, New England Newborn Screening Program, Dept Pediat, Boston, MA 02130 USAMarsden, Deborah论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Boston, Dept Pediat, Boston, MA USA Univ Massachusetts, Sch Med, New England Newborn Screening Program, Dept Pediat, Boston, MA 02130 USAShih, Vivian E.论文数: 0 引用数: 0 h-index: 0机构: Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA Univ Massachusetts, Sch Med, New England Newborn Screening Program, Dept Pediat, Boston, MA 02130 USAGrady, George F.论文数: 0 引用数: 0 h-index: 0机构: Univ Massachusetts, Sch Med, New England Newborn Screening Program, Dept Pediat, Boston, MA 02130 USA Univ Massachusetts, Sch Med, New England Newborn Screening Program, Dept Pediat, Boston, MA 02130 USAEaton, Roger B.论文数: 0 引用数: 0 h-index: 0机构: Univ Massachusetts, Sch Med, New England Newborn Screening Program, Dept Pediat, Boston, MA 02130 USA Univ Massachusetts, Sch Med, New England Newborn Screening Program, Dept Pediat, Boston, MA 02130 USA
- [3] Newborn screening and genetic variation of medium chain acyl-CoA dehydrogenase deficiency in the Chinese populationJOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2022, 35 (10): : 1264 - 1271Li, Yu-Yu论文数: 0 引用数: 0 h-index: 0机构: Zibo Maternal & Child Hlth Hosp, Med Genet, Zibo, Shandong, Peoples R China Zibo Maternal & Child Hlth Hosp, Med Genet, Zibo, Shandong, Peoples R ChinaXu, Jia论文数: 0 引用数: 0 h-index: 0机构: Zibo Maternal & Child Hlth Hosp, Med Genet, Zibo, Shandong, Peoples R China Zibo Maternal & Child Hlth Hosp, Med Genet, Zibo, Shandong, Peoples R ChinaSun, Xue-Cheng论文数: 0 引用数: 0 h-index: 0机构: Zibo Maternal & Child Hlth Hosp, Med Genet, Zibo, Shandong, Peoples R China Zibo Maternal & Child Hlth Hosp, Med Genet, Zibo, Shandong, Peoples R ChinaLi, Hong-Yu论文数: 0 引用数: 0 h-index: 0机构: Zibo Maternal & Child Hlth Hosp, Med Genet, Zibo, Shandong, Peoples R China Zibo Maternal & Child Hlth Hosp, Med Genet, Zibo, Shandong, Peoples R ChinaMu, Kai论文数: 0 引用数: 0 h-index: 0机构: Zibo Maternal & Child Hlth Hosp, Med Genet, Zibo, Shandong, Peoples R China Zibo Maternal & Child Hlth Hosp, Med Genet, Zibo, Shandong, Peoples R China
- [4] Newborn screening for medium chain acyl-CoA dehydrogenase deficiency: Performance improvement by monitoring a new ratioMOLECULAR GENETICS AND METABOLISM, 2014, 113 (04) : 274 - 277Hall, Patricia L.论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Human Genet, Emory Genet Lab, Decatur, GA 30033 USA Emory Univ, Dept Human Genet, Emory Genet Lab, Decatur, GA 30033 USAWittenauer, Angela论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Human Genet, Atlanta, GA 30322 USA Emory Univ, Dept Human Genet, Emory Genet Lab, Decatur, GA 30033 USAHagar, Arthur论文数: 0 引用数: 0 h-index: 0机构: Georgia Dept Publ Hlth, Newborn Screening Lab, Decatur, GA USA Emory Univ, Dept Human Genet, Emory Genet Lab, Decatur, GA 30033 USA
- [5] Medium Chain Acyl-CoA Dehydrogenase Deficiency Detected Among Hispanics by New Jersey Newborn ScreeningAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (09) : 2100 - 2105Anderson, Sharon论文数: 0 引用数: 0 h-index: 0机构: Univ Med & Dent New Jersey, Child Hlth Inst New Jersey, Robert Wood Johnson Med Sch, Div Med Genet,Dept Pediat, New Brunswick, NJ 08901 USA Univ Med & Dent New Jersey, Sch Nursing, Newark, NJ 07103 USA Univ Med & Dent New Jersey, Child Hlth Inst New Jersey, Robert Wood Johnson Med Sch, Div Med Genet,Dept Pediat, New Brunswick, NJ 08901 USABotti, Christina论文数: 0 引用数: 0 h-index: 0机构: Univ Med & Dent New Jersey, Child Hlth Inst New Jersey, Robert Wood Johnson Med Sch, Div Med Genet,Dept Pediat, New Brunswick, NJ 08901 USA Univ Med & Dent New Jersey, Child Hlth Inst New Jersey, Robert Wood Johnson Med Sch, Div Med Genet,Dept Pediat, New Brunswick, NJ 08901 USALi, Bo论文数: 0 引用数: 0 h-index: 0机构: Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Ctr Adv Biotechnol & Med, Piscataway, NJ 08854 USA Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Neurosci & Cell Biol, Piscataway, NJ 08854 USA Univ Med & Dent New Jersey, Child Hlth Inst New Jersey, Robert Wood Johnson Med Sch, Div Med Genet,Dept Pediat, New Brunswick, NJ 08901 USAMillonig, James H.论文数: 0 引用数: 0 h-index: 0机构: Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Ctr Adv Biotechnol & Med, Piscataway, NJ 08854 USA Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Neurosci & Cell Biol, Piscataway, NJ 08854 USA Univ Med & Dent New Jersey, Child Hlth Inst New Jersey, Robert Wood Johnson Med Sch, Div Med Genet,Dept Pediat, New Brunswick, NJ 08901 USALyon, Elaine论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Sch Med, Dept Pathol, Salt Lake City, UT USA ARUP Inst Clin & Expt Pathol, ARUP Labs, Salt Lake City, UT USA Univ Med & Dent New Jersey, Child Hlth Inst New Jersey, Robert Wood Johnson Med Sch, Div Med Genet,Dept Pediat, New Brunswick, NJ 08901 USAMillson, Alison论文数: 0 引用数: 0 h-index: 0机构: ARUP Inst Clin & Expt Pathol, ARUP Labs, Salt Lake City, UT USA Univ Med & Dent New Jersey, Child Hlth Inst New Jersey, Robert Wood Johnson Med Sch, Div Med Genet,Dept Pediat, New Brunswick, NJ 08901 USAKarabin, Suzanne S. M.论文数: 0 引用数: 0 h-index: 0机构: Dept Hlth & Senior Serv, Newborn Screening Serv, Trenton, NJ USA Dept Hlth & Senior Serv, Genet Serv, Trenton, NJ USA Univ Med & Dent New Jersey, Child Hlth Inst New Jersey, Robert Wood Johnson Med Sch, Div Med Genet,Dept Pediat, New Brunswick, NJ 08901 USABrooks, Susan Sklower论文数: 0 引用数: 0 h-index: 0机构: Univ Med & Dent New Jersey, Child Hlth Inst New Jersey, Robert Wood Johnson Med Sch, Div Med Genet,Dept Pediat, New Brunswick, NJ 08901 USA Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Div Maternal Fetal Med, Dept Obstet Gynecol & Reprod Med, New Brunswick, NJ 08901 USA Univ Med & Dent New Jersey, Child Hlth Inst New Jersey, Robert Wood Johnson Med Sch, Div Med Genet,Dept Pediat, New Brunswick, NJ 08901 USA
- [6] Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: regional experience and high incidence of carnitine deficiencyOrphanet Journal of Rare Diseases, 8Maria Luz Couce论文数: 0 引用数: 0 h-index: 0机构: Universidad de Santiago,Unidad de Diagnóstico y Tratamiento de Enfermedades Congénitas del Metabolismo, Departamento de PediatríaPaula Sánchez-Pintos论文数: 0 引用数: 0 h-index: 0机构: Universidad de Santiago,Unidad de Diagnóstico y Tratamiento de Enfermedades Congénitas del Metabolismo, Departamento de PediatríaLuisa Diogo论文数: 0 引用数: 0 h-index: 0机构: Universidad de Santiago,Unidad de Diagnóstico y Tratamiento de Enfermedades Congénitas del Metabolismo, Departamento de PediatríaElisa Leão-Teles论文数: 0 引用数: 0 h-index: 0机构: Universidad de Santiago,Unidad de Diagnóstico y Tratamiento de Enfermedades Congénitas del Metabolismo, Departamento de PediatríaEsmeralda Martins论文数: 0 引用数: 0 h-index: 0机构: Universidad de Santiago,Unidad de Diagnóstico y Tratamiento de Enfermedades Congénitas del Metabolismo, Departamento de PediatríaHelena Santos论文数: 0 引用数: 0 h-index: 0机构: Universidad de Santiago,Unidad de Diagnóstico y Tratamiento de Enfermedades Congénitas del Metabolismo, Departamento de PediatríaMaria Amor Bueno论文数: 0 引用数: 0 h-index: 0机构: Universidad de Santiago,Unidad de Diagnóstico y Tratamiento de Enfermedades Congénitas del Metabolismo, Departamento de PediatríaCarmen Delgado-Pecellín论文数: 0 引用数: 0 h-index: 0机构: Universidad de Santiago,Unidad de Diagnóstico y Tratamiento de Enfermedades Congénitas del Metabolismo, Departamento de PediatríaDaisy E Castiñeiras论文数: 0 引用数: 0 h-index: 0机构: Universidad de Santiago,Unidad de Diagnóstico y Tratamiento de Enfermedades Congénitas del Metabolismo, Departamento de PediatríaJosé A Cocho论文数: 0 引用数: 0 h-index: 0机构: Universidad de Santiago,Unidad de Diagnóstico y Tratamiento de Enfermedades Congénitas del Metabolismo, Departamento de PediatríaJudit García-Villoria论文数: 0 引用数: 0 h-index: 0机构: Universidad de Santiago,Unidad de Diagnóstico y Tratamiento de Enfermedades Congénitas del Metabolismo, Departamento de PediatríaAntonia Ribes论文数: 0 引用数: 0 h-index: 0机构: Universidad de Santiago,Unidad de Diagnóstico y Tratamiento de Enfermedades Congénitas del Metabolismo, Departamento de PediatríaJosé M Fraga论文数: 0 引用数: 0 h-index: 0机构: Universidad de Santiago,Unidad de Diagnóstico y Tratamiento de Enfermedades Congénitas del Metabolismo, Departamento de PediatríaHugo Rocha论文数: 0 引用数: 0 h-index: 0机构: Universidad de Santiago,Unidad de Diagnóstico y Tratamiento de Enfermedades Congénitas del Metabolismo, Departamento de Pediatría
- [7] Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: regional experience and high incidence of carnitine deficiencyORPHANET JOURNAL OF RARE DISEASES, 2013, 8论文数: 引用数: h-index:机构:Sanchez-Pintos, Paula论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, Spain Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, SpainDiogo, Luisa论文数: 0 引用数: 0 h-index: 0机构: Hosp Pediat Coimbra, Ctr Desenvolvimento Crianca Luis Borges, Coimbra, Portugal Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, SpainLeao-Teles, Elisa论文数: 0 引用数: 0 h-index: 0机构: EPE, Ctr Hosp S Joao, Hosp Pediat Integrado, Unidade Doencas Metab, Oporto, Portugal Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, SpainMartins, Esmeralda论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Porto, Hosp Criancas Maria Pia, Unidade Doencas Metab, Oporto, Portugal Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, SpainSantos, Helena论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Gaia Espinho, Dept Pediat, Gaia, Portugal Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, SpainAmor Bueno, Maria论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Virgen Rocio, Dept Pediat, Unidad Metabolopatias & Nutr Infantil, Seville, Spain Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, SpainDelgado-Pecellin, Carmen论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Virgen Rocio, Dept Bioquim Clin, Seville, Spain Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, SpainCastineiras, Daisy E.论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago, Hosp Clin Univ, Lab Metabolopatias, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, Spain Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, SpainCocho, Jose A.论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago, Hosp Clin Univ, Lab Metabolopatias, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, Spain Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, SpainGarcia-Villoria, Judit论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago, Hosp Clin Univ, Lab Metabolopatias, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, Spain Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, SpainRibes, Antonia论文数: 0 引用数: 0 h-index: 0机构: Hosp Clin & Ctr Invest Biomed Red Enfermedades Ra, Serv Bioquim & Genet Mol, Secc Errores Congenitos Metab IBC, Barcelona, Spain Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, SpainFraga, Jose M.论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, Spain Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, SpainRocha, Hugo论文数: 0 引用数: 0 h-index: 0机构: Inst Nacl Saude Doutor Ricardo Jorge, Unidade Rastreio Neonatal, Oporto, Portugal Univ Santiago, Hosp Clin Univ, Dept Pediat, Unidad Diagnost & Tratamiento Enfermedades Congen, Santiago De Compostela, Spain
- [8] Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screeningMOLECULAR GENETICS AND METABOLISM, 2010, 101 (01) : 33 - 39Yusupova, Roman论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp, Div Genet, Boston, MA 02115 USA Harvard Partners Ctr Genet & Genom, Boston, MA 02115 USA Childrens Hosp, Div Genet, Boston, MA 02115 USAFinegold, David N.论文数: 0 引用数: 0 h-index: 0机构: UPMC, Childrens Hosp Pittsburgh, Pittsburgh, PA 15224 USA Childrens Hosp, Div Genet, Boston, MA 02115 USANaylor, Edwin W.论文数: 0 引用数: 0 h-index: 0机构: Med Univ S Carolina, Charleston, SC 29425 USA Neo Gen Screening, Pittsburgh, PA USA Childrens Hosp, Div Genet, Boston, MA 02115 USASahai, Inderneel论文数: 0 引用数: 0 h-index: 0机构: New England Newborn Screening Program, Jamaica Plain, MA 02130 USA Univ Massachusetts, Sch Med, Dept Pediat, Worcester, MA 01655 USA Childrens Hosp, Div Genet, Boston, MA 02115 USAWaisbren, Susan论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp, Div Genet, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Psychiat, Boston, MA 02115 USA Childrens Hosp, Div Genet, Boston, MA 02115 USALevy, Harvey L.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp, Div Genet, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Childrens Hosp, Div Genet, Boston, MA 02115 USA
- [9] Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screeningBMC MEDICAL GENETICS, 2015, 16Gruenert, Sarah C.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, Germany Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, GermanyWehrle, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, Germany Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, GermanyVillavicencio-Lorini, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, Germany Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, GermanyLausch, E.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, Germany Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, GermanyVetter, B.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, GermanySchwab, K. O.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, Germany Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, GermanyTucci, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, Germany Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, GermanySpiekerkoetter, U.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, Germany Univ Hosp Freiburg, Ctr Pediat & Adolescent Med, D-79106 Freiburg, Germany
- [10] Maternal vitamin deficiency mimicking multiple acyl-CoA dehydrogenase deficiency on newborn screeningMOLECULAR GENETICS AND METABOLISM REPORTS, 2021, 27Gramer, Gwendolyn论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Heidelberg, Div Neuropediat & Metab Med, Ctr Pediat & Adolescent Med, Heidelberg, Germany Univ Hosp Heidelberg, Div Neuropediat & Metab Med, Ctr Pediat & Adolescent Med, Heidelberg, GermanyHoffmann, Georg F.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Heidelberg, Div Neuropediat & Metab Med, Ctr Pediat & Adolescent Med, Heidelberg, Germany Univ Hosp Heidelberg, Div Neuropediat & Metab Med, Ctr Pediat & Adolescent Med, Heidelberg, GermanyHennermann, Julia B.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Mainz, Dept Pediat & Adolescent Med, Villa Metabol, Mainz, Germany Univ Hosp Heidelberg, Div Neuropediat & Metab Med, Ctr Pediat & Adolescent Med, Heidelberg, Germany