Vu TH - Search Results

1

Clinical manifestations of mitochondrial DNA depletion.

Vu TH, Sciacco M, Tanji K, Nichter C, Bonilla E, Chatkupt S, Maertens P, Shanske S, Mendell J, Koenigsberger MR, Sharer L, Schon EA, DiMauro S, DeVivo DC. Vu TH, et al. Neurology. 1998 Jun;50(6):1783-90. doi: 10.1212/wnl.50.6.1783. Neurology. 1998. PMID: 9633728

2

Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene.

Mancuso M, Filosto M, Bonilla E, Hirano M, Shanske S, Vu TH, DiMauro S. Mancuso M, et al. Among authors: vu th. Arch Neurol. 2003 Jul;60(7):1007-9. doi: 10.1001/archneur.60.7.1007. Arch Neurol. 2003. PMID: 12873860

3

Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?

Manfredi G, Vu T, Bonilla E, Schon EA, DiMauro S, Arnaudo E, Zhang L, Rowland LP, Hirano M. Manfredi G, et al. Ann Neurol. 1997 Aug;42(2):180-8. doi: 10.1002/ana.410420208. Ann Neurol. 1997. PMID: 9266727

4

A5814G mutation in mitochondrial DNA can cause mitochondrial myopathy and cardiomyopathy.

Karadimas C, Tanji K, Geremek M, Chronopoulou P, Vu T, Krishna S, Sue CM, Shanske S, Bonilla E, DiMauro S, Lipson M, Bachman R. Karadimas C, et al. J Child Neurol. 2001 Jul;16(7):531-3. doi: 10.1177/088307380101600715. J Child Neurol. 2001. PMID: 11453453

5

Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients.

Santorelli FM, Sciacco M, Tanji K, Shanske S, Vu TH, Golzi V, Griggs RC, Mendell JR, Hays AP, Bertorini TE, Pestronk A, Bonilla E, DiMauro S. Santorelli FM, et al. Among authors: vu th. Ann Neurol. 1996 Jun;39(6):789-95. doi: 10.1002/ana.410390615. Ann Neurol. 1996. PMID: 8651651

6

Mitochondrial myopathy simulating spinal muscular atrophy.

Pons R, Andreetta F, Wang CH, Vu TH, Bonilla E, DiMauro S, De Vivo DC. Pons R, et al. Among authors: vu th. Pediatr Neurol. 1996 Sep;15(2):153-8. doi: 10.1016/0887-8994(96)00118-x. Pediatr Neurol. 1996. PMID: 8888051 Free article.

7

Study of mitochondrial DNA depletion in muscle by single-fiber polymerase chain reaction.

Sciacco M, Gasparo-Rippa P, Vu TH, Tanji K, Shanske S, Mendell JR, Schon EA, DiMauro S, Bonilla E. Sciacco M, et al. Among authors: vu th. Muscle Nerve. 1998 Nov;21(11):1374-81. doi: 10.1002/(sici)1097-4598(199811)21:11<1374::aid-mus3>3.0.co;2-6. Muscle Nerve. 1998. PMID: 9771659

8

Mitochondrial DNA depletion in a patient with long survival.

Vu TH, Tanji K, Valsamis H, DiMauro S, Bonilla E. Vu TH, et al. Neurology. 1998 Oct;51(4):1190-3. doi: 10.1212/wnl.51.4.1190. Neurology. 1998. PMID: 9781557

9

Kearns-Sayre syndrome: unusual pattern of expression of subunits of the respiratory chain in the cerebellar system.

Tanji K, Vu TH, Schon EA, DiMauro S, Bonilla E. Tanji K, et al. Among authors: vu th. Ann Neurol. 1999 Mar;45(3):377-83. doi: 10.1002/1531-8249(199903)45:3<377::aid-ana14>3.0.co;2-m. Ann Neurol. 1999. PMID: 10072053

10

Mitochondrial involvement in Alzheimer's disease.

Bonilla E, Tanji K, Hirano M, Vu TH, DiMauro S, Schon EA. Bonilla E, et al. Among authors: vu th. Biochim Biophys Acta. 1999 Feb 9;1410(2):171-82. doi: 10.1016/s0005-2728(98)00165-0. Biochim Biophys Acta. 1999. PMID: 10076025 Free article. Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

397 results

Search Page

Filters