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Tuan Vu

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Catarina M Quinzii; Tuan H Vu; K Christopher Min; Kurenai Tanji; Sandra Barral; Raji P Grewal; Andrea Kattah; Pilir Camaño; David Otaegui; Teruhito Kunimatsu; David M Blake; Kirk Wilhelmsen; Lewis P Rowland; Arthur P Hays; Eduardo Bonilla; Michio Hirano
X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1.
Charalampos L Karadimas; Tuan H Vu; STEPHEN HOLVE; Penelope Chronopoulou; Catarina M Quinzii; Stanley D Johnsen; Janice Kurth; Elizabeth Eggers; Lluis Palenzuela; Kurenai Tanji; Eduardo Bonilla; Darryl C De Vivo; Salvatore DiMauro; Michio Hirano
Navajo neurohepatopathy is caused by a mutation in the MPV17 gene.
Kurenai Tanji; Govind Bhagat; Tuan H Vu; Lailani Monzon; Eduardo Bonilla; Jay H Lefkowitch
Mitochondrial DNA dysfunction in oncocytic hepatocytes.

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All Publications

2008: Catarina M Quinzii; Tuan H Vu; K Christopher Min; Kurenai Tanji; Sandra Barral; Raji P Grewal; Andrea Kattah; Pilir Camaño; David Otaegui; Teruhito Kunimatsu; David M Blake; Kirk Wilhelmsen; Lewis P Rowland; Arthur P Hays; Eduardo Bonilla; Michio Hirano
X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1.
American journal of human genetics 2008;82(1):208-13.
2006: Charalampos L Karadimas; Tuan H Vu; STEPHEN HOLVE; Penelope Chronopoulou; Catarina M Quinzii; Stanley D Johnsen; Janice Kurth; Elizabeth Eggers; Lluis Palenzuela; Kurenai Tanji; Eduardo Bonilla; Darryl C De Vivo; Salvatore DiMauro; Michio Hirano
Navajo neurohepatopathy is caused by a mutation in the MPV17 gene.
American journal of human genetics 2006;79(3):544-8.
2003: Kurenai Tanji; Govind Bhagat; Tuan H Vu; Lailani Monzon; Eduardo Bonilla; Jay H Lefkowitch
Mitochondrial DNA dysfunction in oncocytic hepatocytes.
Liver international : official journal of the International Association for the Study of the Liver 2003;23(5):397-403.
2003: Michelangelo Mancuso; Massimiliano Filosto; Eduardo Bonilla; Michio Hirano; Sara Shanske; Tuan H Vu; Salvatore DiMauro
Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene.
Archives of neurology 2003;60(7):1007-9.
2002: Michelangelo Mancuso; Leonardo Salviati; Sabrina Sacconi; David Otaegui; Pilar Camaño; Alberto Marina; Sandra R Bacman; Carlos T Moraes; Jose R Carlo; M Garcia; M Garcia-Alvarez; L Monzon; Ali Naini; Michio Hirano; Eduardo Bonilla; A L Taratuto; Salvatore DiMauro; Tuan H Vu
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA.
Neurology 2002;59(8):1197-202.
2002: Leonardo Salviati; Sabrina Sacconi; Michelangelo Mancuso; David Otaegui; Pilar Camaño; Alberto Marina; Simon Rabinowitz; Rebecca Shiffman; Karen Thompson; Claire M Wilson; Annette Feigenbaum; Ali Naini; Michio Hirano; Eduardo Bonilla; Salvatore DiMauro; Tuan H Vu
Mitochondrial DNA depletion and dGK gene mutations.
Annals of neurology 2002;52(3):311-7.
2002: Tuan H Vu; Michio Hirano; Salvatore DiMauro
Mitochondrial diseases.
Neurologic clinics 2002;20(3):809-39, vii-viii.
2001: Kurenai Tanji; T Kunimatsu; Tuan H Vu; Eduardo Bonilla
Neuropathological features of mitochondrial disorders.
Seminars in cell & developmental biology 2001;12(6):429-39.
2001: Michio Hirano; Ramon Marti; C Ferreiro-Barros; Maya R Vilà; Saba Tadesse; Yutaka Nishigaki; Ichizo Nishino; Tuan H Vu
Defects of intergenomic communication: autosomal disorders that cause multiple deletions and depletion of mitochondrial DNA.
Seminars in cell & developmental biology 2001;12(6):417-27.
2001: Tuan H Vu; Arthur P Hays; Kurenai Tanji; DS Younger; Gregg G Gundersen; A Eastwood; C W Braun; Salvatore DiMauro; Eduardo Bonilla
Myopathy with tubulin-reactive crystalline inclusions.
Neurology 2001;57(1):149-52.
2001: Tuan H Vu; Kurenai Tanji; STEPHEN HOLVE; Eduardo Bonilla; Ronald Sokol; R D Snyder; S Fiore; G H Deutsch; Salvatore DiMauro; Darryl C De Vivo
Navajo neurohepatopathy: a mitochondrial DNA depletion syndrome?
Hepatology (Baltimore, Md.) 2001;34(1):116-20.
2000: Michio Hirano; Tuan H Vu
Defects of intergenomic communication: where do we stand?
Brain pathology (Zurich, Switzerland) 2000;10(3):451-61.
2000: Ichizo Nishino; antonella spinazzola; A Papadimitriou; S Hammans; I Steiner; C D Hahn; A M Connolly; Alain Verloes; J Guimarães; Ivan P Maillard; H Hamano; Maria Alice Donati; Carol E Semrad; J A Russell; Antoni L Andreu; Georgios M Hadjigeorgiou; Tuan H Vu; Saba Tadesse; TG Nygaard; I Nonaka; I Hirano; Eduardo Bonilla; Lewis P Rowland; Salvatore DiMauro; Michio Hirano
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations.
Annals of neurology 2000;47(6):792-800.
2000: Tuan H Vu; Kurenai Tanji; Francesco Pallotti; V Golzi; Michio Hirano; Salvatore DiMauro; Eduardo Bonilla
Analysis of mtDNA deletions in muscle by in situ hybridization.
Muscle & nerve 2000;23(1):80-5.
1999: Kurenai Tanji; Tuan H Vu; Eric A Schon; Salvatore DiMauro; Eduardo Bonilla
Kearns-Sayre syndrome: unusual pattern of expression of subunits of the respiratory chain in the cerebellar system.
Annals of neurology 1999;45(3):377-83.
1998: M Sciacco; P Gasparo-Rippa; Tuan H Vu; Kurenai Tanji; Sara Shanske; Jerry R Mendell; Eric A Schon; Salvatore DiMauro; Eduardo Bonilla
Study of mitochondrial DNA depletion in muscle by single-fiber polymerase chain reaction.
Muscle & nerve 1998;21(11):1374-81.
1998: Tuan H Vu; Kurenai Tanji; H Valsamis; Salvatore DiMauro; Eduardo Bonilla
Mitochondrial DNA depletion in a patient with long survival.
Neurology 1998;51(4):1190-3.
1998: Tuan H Vu; M Sciacco; Kurenai Tanji; C Nichter; Eduardo Bonilla; S Chatkupt; P Maertens; Sara Shanske; Jerry R Mendell; MR Koenigsberger; Leroy R Sharer; Eric A Schon; Salvatore DiMauro; Darryl C DeVivo
Clinical manifestations of mitochondrial DNA depletion.
Neurology 1998;50(6):1783-90.
1996: Filippo M Santorelli; M Sciacco; Kurenai Tanji; Sara Shanske; Tuan H Vu; V Golzi; R C Griggs; J R Mendell; Arthur P Hays; T E Bertorini; A Pestronk; Eduardo Bonilla; Salvatore DiMauro
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients.
Annals of neurology 1996;39(6):789-95.