Mancuso M - Search Results

1

A Multisystem Mitochondrial Disease Caused by a Novel MT-TL1 mtDNA Variant: A Case Report.

Giannese D, Montano V, Lopriore P, Nesti C, LoGerfo A, Caligo MA, Dal Canto F, Pasquinelli G, Bonadio AG, Moriconi D, Siciliano G, Mancuso M. Giannese D, et al. Among authors: mancuso m. J Neuromuscul Dis. 2023;10(1):119-123. doi: 10.3233/JND-221526. J Neuromuscul Dis. 2023. PMID: 36404555 Free PMC article.

2

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: mancuso m. Funct Neurol. 2000 Oct-Dec;15(4):211-4. Funct Neurol. 2000. PMID: 11213524

3

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

4

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

5

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

6

Coenzyme Q10, exercise lactate and CTG trinucleotide expansion in myotonic dystrophy.

Siciliano G, Mancuso M, Tedeschi D, Manca ML, Renna MR, Lombardi V, Rocchi A, Martelli F, Murri L. Siciliano G, et al. Among authors: mancuso m. Brain Res Bull. 2001 Oct-Nov 1;56(3-4):405-10. doi: 10.1016/s0361-9230(01)00653-0. Brain Res Bull. 2001. PMID: 11719279

7

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

8

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

9

Auditory neuropathy in a patient with mitochondrial myopathy and multiple mtDNA deletions.

Forli F, Mancuso M, Santoro A, Dotti MT, Siciliano G, Berrettini S. Forli F, et al. Among authors: mancuso m. J Laryngol Otol. 2006 Oct;120(10):888-91. doi: 10.1017/S0022215106001472. Epub 2006 May 24. J Laryngol Otol. 2006. PMID: 16719954

10

No evidence for allelic association of serotonin 2A receptor and transporter gene polymorphisms with depression in Alzheimer disease.

Micheli D, Bonvicini C, Rocchi A, Ceravolo R, Mancuso M, Tognoni G, Gennarelli M, Siciliano G, Murri L. Micheli D, et al. Among authors: mancuso m. J Alzheimers Dis. 2006 Dec;10(4):371-8. doi: 10.3233/jad-2006-10405. J Alzheimers Dis. 2006. PMID: 17183148

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