Murri L - Search Results

1

Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene.

Siciliano G, Tessa A, Petrini S, Mancuso M, Bruno C, Grieco GS, Malandrini A, DeFlorio L, Martini B, Federico A, Nappi G, Santorelli FM, Murri L. Siciliano G, et al. Among authors: murri l. Neuromuscul Disord. 2003 Feb;13(2):162-5. doi: 10.1016/s0960-8966(02)00221-3. Neuromuscul Disord. 2003. PMID: 12565915

2

Autosomal dominant psychiatric disorders and mitochondrial DNA multiple deletions: report of a family.

Mancuso M, Ricci G, Choub A, Filosto M, DiMauro S, Davidzon G, Tessa A, Santorelli FM, Murri L, Siciliano G. Mancuso M, et al. Among authors: murri l. J Affect Disord. 2008 Feb;106(1-2):173-7. doi: 10.1016/j.jad.2007.05.016. Epub 2007 Jun 22. J Affect Disord. 2008. PMID: 17588675

3

Mitochondrial tRNA(Cys) gene mutation (A5814G): a second family with mitochondrial encephalopathy.

Santorelli FM, Siciliano G, Casali C, Basirico MG, Carrozzo R, Calvosa F, Sartucci F, Bonfiglio L, Murri L, DiMauro S. Santorelli FM, et al. Among authors: murri l. Neuromuscul Disord. 1997 May;7(3):156-9. doi: 10.1016/s0960-8966(97)00444-6. Neuromuscul Disord. 1997. PMID: 9185178 Free article.

4

Abnormal H-Tfam in a patient harboring a single mtDNA deletion.

Tessa A, Manca ML, Mancuso M, Renna MR, Murri L, Martini B, Santorelli FM, Siciliano G. Tessa A, et al. Among authors: murri l. Funct Neurol. 2000 Oct-Dec;15(4):211-4. Funct Neurol. 2000. PMID: 11213524

5

A non-syndromic hearing loss caused by very low levels of the mtDNA A3243G mutation.

Mancuso M, Filosto M, Forli F, Rocchi A, Berrettini S, Siciliano G, Murri L. Mancuso M, et al. Among authors: murri l. Acta Neurol Scand. 2004 Jul;110(1):72-4. doi: 10.1111/j.1600-0404.2004.00254.x. Acta Neurol Scand. 2004. PMID: 15180810

6

Human mitochondrial transcription factor A reduction and mitochondrial dysfunction in Hashimoto's hypothyroid myopathy.

Siciliano G, Monzani F, Manca ML, Tessa A, Caraccio N, Tozzi G, Piemonte F, Mancuso M, Santorelli FM, Ferrannini E, Murri L. Siciliano G, et al. Among authors: murri l. Mol Med. 2002 Jun;8(6):326-33. Mol Med. 2002. PMID: 12428064 Free PMC article.

7

Mitochondrial dysfunction and Alzheimer's disease: new developments.

Mancuso M, Siciliano G, Filosto M, Murri L. Mancuso M, et al. Among authors: murri l. J Alzheimers Dis. 2006 Jul;9(2):111-7. doi: 10.3233/jad-2006-9203. J Alzheimers Dis. 2006. PMID: 16873958 Review.

8

Genes and the environment in neurodegeneration.

Coppedè F, Mancuso M, Siciliano G, Migliore L, Murri L. Coppedè F, et al. Among authors: murri l. Biosci Rep. 2006 Oct;26(5):341-67. doi: 10.1007/s10540-006-9028-6. Biosci Rep. 2006. PMID: 17029001 Review.

9

Mitochondrial cascade hypothesis of Alzheimer's disease: myth or reality?

Mancuso M, Coppedè F, Murri L, Siciliano G. Mancuso M, et al. Among authors: murri l. Antioxid Redox Signal. 2007 Oct;9(10):1631-46. doi: 10.1089/ars.2007.1761. Antioxid Redox Signal. 2007. PMID: 17887917 Review.

10

Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitation.

Siciliano G, Tessa A, Renna M, Manca ML, Mancuso M, Murri L. Siciliano G, et al. Among authors: murri l. Clin Genet. 1999 Jul;56(1):51-8. doi: 10.1034/j.1399-0004.1999.560107.x. Clin Genet. 1999. PMID: 10466417

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