DiMauro S - Search Results

1

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: dimauro s. 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

2

Mitochondrial DNA depletion and dGK gene mutations.

Salviati L, Sacconi S, Mancuso M, Otaegui D, Camaño P, Marina A, Rabinowitz S, Shiffman R, Thompson K, Wilson CM, Feigenbaum A, Naini AB, Hirano M, Bonilla E, DiMauro S, Vu TH. Salviati L, et al. Among authors: dimauro s. Ann Neurol. 2002 Sep;52(3):311-7. doi: 10.1002/ana.10284. Ann Neurol. 2002. PMID: 12205643

3

Mitochondrial abnormalities in muscle and other aging cells: classification, causes, and effects.

DiMauro S, Tanji K, Bonilla E, Pallotti F, Schon EA. DiMauro S, et al. Muscle Nerve. 2002 Nov;26(5):597-607. doi: 10.1002/mus.10194. Muscle Nerve. 2002. PMID: 12402281 Review.

4

Mitochondrial respiratory-chain diseases.

DiMauro S, Schon EA. DiMauro S, et al. N Engl J Med. 2003 Jun 26;348(26):2656-68. doi: 10.1056/NEJMra022567. N Engl J Med. 2003. PMID: 12826641 Review. No abstract available.

5

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: dimauro s. Arch Neurol. 2003 Jul;60(7):1007-9. doi: 10.1001/archneur.60.7.1007. Arch Neurol. 2003. PMID: 12873860

6

Medicinal and genetic approaches to the treatment of mitochondrial disease.

Schon EA, DiMauro S. Schon EA, et al. Among authors: dimauro s. Curr Med Chem. 2003 Dec;10(23):2523-33. doi: 10.2174/0929867033456503. Curr Med Chem. 2003. PMID: 14529468 Review.

7

Mitochondrial DNA deletion in a child with megaloblastic anemia and recurrent encephalopathy.

Akman CI, Sue CM, Shanske S, Tanji K, Bonilla E, Ojaimi J, Krishna S, Schubert R, DiMauro S. Akman CI, et al. Among authors: dimauro s. J Child Neurol. 2004 Apr;19(4):258-61. doi: 10.1177/088307380401900403. J Child Neurol. 2004. PMID: 15163090

8

Mitochondrial mutations: genotype to phenotype.

Schon EA, DiMauro S. Schon EA, et al. Among authors: dimauro s. Novartis Found Symp. 2007;287:214-25; discussion 226-33. doi: 10.1002/9780470725207.ch15. Novartis Found Symp. 2007. PMID: 18074641 Review.

9

The clinical maze of mitochondrial neurology.

DiMauro S, Schon EA, Carelli V, Hirano M. DiMauro S, et al. Nat Rev Neurol. 2013 Aug;9(8):429-44. doi: 10.1038/nrneurol.2013.126. Epub 2013 Jul 9. Nat Rev Neurol. 2013. PMID: 23835535 Free PMC article. Review.

10

Deletions of mitochondrial DNA in Kearns-Sayre syndrome.

Zeviani M, Moraes CT, DiMauro S, Nakase H, Bonilla E, Schon EA, Rowland LP. Zeviani M, et al. Among authors: dimauro s. Neurology. 1988 Sep;38(9):1339-46. doi: 10.1212/wnl.38.9.1339. Neurology. 1988. PMID: 3412580

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

735 results

Search Page