Mancuso M - Search Results

1

TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations.

Del Bo R, Ghezzi S, Corti S, Pandolfo M, Ranieri M, Santoro D, Ghione I, Prelle A, Orsetti V, Mancuso M, Sorarù G, Briani C, Angelini C, Siciliano G, Bresolin N, Comi GP. Del Bo R, et al. Among authors: mancuso m. Eur J Neurol. 2009 Jun;16(6):727-32. doi: 10.1111/j.1468-1331.2009.02574.x. Epub 2009 Feb 19. Eur J Neurol. 2009. PMID: 19236453

2

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: mancuso m. Clin Genet. 1999 Jul;56(1):51-8. doi: 10.1034/j.1399-0004.1999.560107.x. Clin Genet. 1999. PMID: 10466417

3

Encephalomyopathy with multiple mitochondrial DNA deletions and multiple symmetric lipomatosis: further evidence of a possible association.

Mancuso M, Bianchi MC, Santorelli FM, Tessa A, Casali C, Murri L, Siciliano G. Mancuso M, et al. J Neurol. 1999 Dec;246(12):1197-8. doi: 10.1007/s004150050543. J Neurol. 1999. PMID: 10653316 No abstract available.

4

Sudden bilateral hearing loss and sporadic mitochondrial DNA deletion.

Berrettini S, Forli F, Siciliano G, Mancuso M. Berrettini S, et al. Among authors: mancuso m. J Laryngol Otol. 2001 Feb;115(2):128-31. doi: 10.1258/0022215011907514. J Laryngol Otol. 2001. PMID: 11320830

5

Cytogenetic damage in peripheral lymphocytes of mitochondrial disease patients.

Naccarati A, Molinu S, Mancuso M, Siciliano G, Migliore L. Naccarati A, et al. Among authors: mancuso m. Neurol Sci. 2000;21(5 Suppl):S963-5. doi: 10.1007/s100720070010. Neurol Sci. 2000. PMID: 11382196

6

Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathies.

Siciliano G, Mancuso M, Pasquali L, Manca ML, Tessa A, Iudice A. Siciliano G, et al. Among authors: mancuso m. Neurol Sci. 2000;21(5 Suppl):S985-7. doi: 10.1007/s100720070017. Neurol Sci. 2000. PMID: 11382203

7

Mitochondrial DNA rearrangements in young onset parkinsonism: two case reports.

Siciliano G, Mancuso M, Ceravolo R, Lombardi V, Iudice A, Bonuccelli U. Siciliano G, et al. Among authors: mancuso m. J Neurol Neurosurg Psychiatry. 2001 Nov;71(5):685-7. doi: 10.1136/jnnp.71.5.685. J Neurol Neurosurg Psychiatry. 2001. PMID: 11606686 Free PMC article.

8

Dissection and atherosclerosis of carotid arteries in the young: role of the apolipoprotein E polymorphism.

Orlandi G, Fanucchi S, Mancuso M, Gelli A, Rocchi A, Siciliano G, Murri L. Orlandi G, et al. Among authors: mancuso m. Eur J Neurol. 2002 Jan;9(1):19-21. doi: 10.1046/j.1468-1331.2002.00340.x. Eur J Neurol. 2002. PMID: 11784371

9

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: mancuso m. Neuromuscul Disord. 2003 Feb;13(2):162-5. doi: 10.1016/s0960-8966(02)00221-3. Neuromuscul Disord. 2003. PMID: 12565915

10

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. Acta Neurol Scand. 2004 Jul;110(1):72-4. doi: 10.1111/j.1600-0404.2004.00254.x. Acta Neurol Scand. 2004. PMID: 15180810

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