Tuan Vu

1.   Vu TH, Hamill GS: Prenatal and Postnatal Development of Substance P Immunocytochemistry Within Subnuclei of the Rat Interpeduncular Nucleus.  Brain Res Bull 1988;20:59-74.

2.   Vu TH, Weissman AD, London ED:  Pharmacological Characteristics and Distributions of Sigma and Phencyclidine Binding Sites in the Animal Kingdom.  J Neurochem 1990;54(2):598-604.

3.   Majewska MD, Parameswaram S, Vu TH, London ED:  Divergent Ontogeny of Sigma and Phencyclidine Binding Sites in the Rat Brain. Dev Brain Res 1989;47:13-18.

4.     Santorelli FM, Sciacco M, Shanske S, Vu TH, Golzi V, Griggs RC, Mendell JR, Bonilla E, DiMauro S:  Multiple Mitochondrial DNA Deletions in Inclusion-Body Myositis.  Clinical, Morphological, Biochemical, and Molecular Genetic Studies in 56 Patients.  Ann Neurol 1996;39:789-795.

5.     Pons R, Andreeta F, Wang C, Vu TH, Bonilla E, DiMauro S, DeVivo DC: Mitochondrial Myopathy Simulating Spinal Muscular Atrophy.   Pediatr Neurol 1996;15:153-158.

6.     Manfredi G, Vu TH, Bonilla E, Schon EA, DiMauro S, Arnaudo E, Zhang L, Rowland LP, Hirano M:  Association of Myopathy with Large-Scale Mitochondrial DNA Duplications and Deletions:  Which is Pathogenic?  Ann Neurol 1997;42:180-188.

7.     Vu TH, Sciacco M, Tanji K, Nichter C, Bonilla E, Chatkupt S, Maertens P, Shanske S, Mendell J, Koenigsberger MR, Sharer L., DiMauro S, DeVivo D: Clinical Manifestations of Mitochondrial DNA Depletion.  Neurology 1998;50:1783-1790.

8.     Sciacco M, Gasparo-Rippa P, Vu TH, Tanji K, Shanske S, Mendell JR, Schon EA, DiMauro S, Bonilla E: Study of Mitochondrial DNA Depletion in Muscle by Single-Fiber Polymerase Chain Reaction.  Muscle & Nerve 1998;21:1374-1381.

9.     Vu TH, Tanji K, Valsamis H, DiMauro S, Bonilla E:  Mitochondrial DNA Depletion in a Patient with Long Survival.  Neurology, 1998;51:1190-1193.

10.  Tanji K, Vu TH, Schon EA, DiMauro S, Bonilla E:  Kearns-Sayre Syndrome:  Unusual Pattern of Expression of Subunits of the Respiratory Chain in the Cerebellar System.  Ann Neurol 1999;45:377-383.

11.  Bonilla E, Tanji K, Hirano M, Vu TH, DiMauro S, Schon EA:  Mitochondrial involvement in Alzheimer’s disease.  Biochim et Biophys Acta 1999;1410:171-182.

12.  Vu TH, Tanji K, Pallotti F, Golzi V, Hirano M, DiMauro S, Bonilla E:  Analysis of Muscle from patients with multiple mtDNA deletions by in situ hybridization.  Muscle Nerve 2000;23(1):80-85.

13.  Nishino I, Spinazzola A, Papadimitriou A, Hammans S, Steiner I, Hahn CD, Connolly AM, Verloes A, Guimarâes, Maillard I, Hamano H, Donati MA, Semrad CE, Russell JA, Andreu AL, Hadjigeorgiou, Vu TH, Tadesse S, Nygaard TG, Nonaka I, Hirano I, Bonilla E, Rowland LP, DiMauro S, Hirano M:  Mitochondrial neurogastrointestinal encephalomyopathy:  an autosomal recessive disorder due to thymidine phosphorylase mutations.  Ann Neurol 2000;47:792-800.

14.  Hirano M, Vu TH:  Defects of intergenomic communication: Where do we stand?  Brain Pathol 2000;10:451-461.

15.  Church J, Mitchell W, Gonzalez-Gomez I, Christensen J, Vu TH, DiMauro S, Boles RG:  Mitochondrial DNA depletion, near-fatal metabolic acidosis and liver failure in an HIV-infected child treated with combination antiretroviral therapy.  J Pediatr 2001;138:748-751.

16.  Vu TH, Tanji K, Holve SA, Bonilla E, Sokol RJ, Snyder RD, Fiore S, DiMauro S, De Vivo D:  Navajo neurohepatopathy:  A mitochondrial DNA depletion syndrome?  Hepatology 2001;34:116-120.

17.  Vu TH, Hays AP, Tanji K, Younger D, Gundersen GG, Eastwood A, Braun CW, DiMauro S, Bonilla E:  Myopathy with tubulin-reactive crystalline inclusions.  Neurology 2001;57:149-152.

18.  Hirano M, Marti R, Ferreiro C, Vila M, Tadesse S, Vu TH:  Defects of intergenomic communication:  Autosomal disorders causing multiple deletions and depletion of mitochondrial DNA.  Seminars Cell & Devel Biology, 2001;12:417-427.

19.  Tanji K, Kunimatsu T, Vu TH, Bonilla E:  Neuropathological features of mitochondrial disorders.  Seminars Cell & Devel Biology, 2001;12:429-439.

20.  Mancuso M, Salviati M, Sacconi S, Otaegui D, Camano P, Marina A, Garcia-Alvarez M, Garcia M, Carlo J, Monzon L, Naini AB, Hirano M, Bonilla E, DiMauro S, and Vu, TH: New thymidine kinase mutations in myopathy associated with mtDNA depletion.  Neurology 2002;59:1197-1202.

21.  Salviati L, Sacconi S, Mancuso M, Otaegui D, Camano P, Marina A, Rabinowitz S, Schiffman R, Thompson K, Wilson CM, Feigenbaum A, Monzon L, Naini AB, Hirano M, Bonilla E, DiMauro S, and Vu, TH:  Mitochondrial DNA depletion and dGK gene mutations.  Ann Neurol 2002;52:311-316.

22.  Vu TH:  Myotonic Dystrophies.  Encyclopedia of Neurological Sciences, 2003.

23.  Vu TH:  Myotonic Disorders.  Encyclopedia of Neurological Sciences, 2003.

24.  Vu TH, Hirano M, DiMauro S:  Mitochondrial Diseases.  Neurol Clinics of North America, August, 2002.

25.  Mancuso M, Filosto M, Bonilla E, Hirano M, Vu TH, DiMauro S:  Mitochondrial myopathy of childhood associated with mtDNA depletion and a homozygous mutation (T77M) in the TK2 gene.  Arch Neurology 2003;60(7):1007-9.

26.  Tanji K, Bhagat G, Vu TH, Monzon L, Bonilla E, Lefkowitch JH.  Mitochondrial DNA dysfunction in oncocytic hepatocytes.  Liver Int. 2003;23(5):397-403.

27.  Bedlack RS, Vu TH, Sparr SA, Hammans S, Myers B, Morgenlander J, Hirano M:  MNGIE neuropathy:  5 cases confused with CIDP.  Musc Nerve 2004;29: 364–368.

28.  Karadimas CL, Vu TH, Holve SA, Chronopoulou P, Quinzii C, Johnsen SD, Kurth J, Eggers E, Palenzuela L, Tanji K, Bonilla E, De Vivo DC, DiMauro S, Hirano M:  Navajo Neurohepatopathy is caused by a mutation in the MPV17 gene.  American J of Human Genetics 2006;79:544-548.

29.  Quinzii CM, Vu TH, Min KC, Tanji K, Barral S, Grewal RP, Kattah A, Camano P, Otaegui D, Kunimatsu T, Blake DM, Wilhelmsen KC, Rowland LP, Hays AP, Bonilla E, and Hirano, M:  X-linked dominant Scupuloperoneal Myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1.  American J of Human Genetics 2008:82:208-213.

30.  Vu TH:  Myotonic Dystrophies.  Encyclopedia of Neurological Sciences, 2011 (submitted).