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1Academic Journal
المؤلفون: Belén Pérez, Celia Angaroni, Rocio Sánchez-Alcudia, Begoña Merinero, Celia Pérez-Cerdá, N Specola, P Rodríguez-Pombo, Moacir Wajner, Raquel Dodelson De Kremer, Verónica Cornejo, Lourdes R Desviat, Magdalena Ugarte, B Pérez, R Sánchez-Alcudia, B Merinero, C Pérez-Cerdá, L R Desviat, M Ugarte, C Angaroni, R D De Kremer, M Wajner
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.1071.1671; http://www.metabolicaschile.cl/archivos/Publicaciones/AMM%20%20y%20mutaciones%20suplemento%20JIMD.pdf
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2
المؤلفون: R D, De Kremer, A, Paschini-Capra, S, Bacman, C, Argaraña, G, Civallero, R I, Kelley, N, Guelbert, A, Latini, I, Noher de Halac, A, Giner-Ayala, J, Johnston, R, Proujansky, I, Gonzalez, C, Depetris-Boldini, A, Oller-Ramírez, C, Angaroni, R A, Theaux, E, Hliba, E, Juaneda
المصدر: American journal of medical genetics. 99(2)
مصطلحات موضوعية: Male, 3-Hydroxybutyric Acid, Biopsy, Argentina, Syndrome, DNA, Mitochondrial, Mitochondria, Electron Transport, Phenotype, Child, Preschool, Lactates, MELAS Syndrome, Humans, Point Mutation, Muscle, Skeletal, Acids
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3Academic Journal
المؤلفون: LUIGI GALGANI, C. ANGARONI, L. FORTI, ANTONIO GIORGILLI, GUERRA, Francesco
المساهمون: Luigi, Galgani, C., Angaroni, L., Forti, Antonio, Giorgilli, Guerra, Francesco
Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:A1989AL20000007; volume:139; firstpage:221; lastpage:230; numberofpages:9; journal:PHYSICS LETTERS A; http://hdl.handle.net/11573/5691; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=A1989AL20000007&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a