Siciliano G - Search Results

1

Progressive sensorineural hearing loss in childhood.

Berrettini S, Ravecca F, Sellari-Franceschini S, Matteucci F, Siciliano G, Ursino F. Berrettini S, et al. Among authors: siciliano g. Pediatr Neurol. 1999 Feb;20(2):130-6. doi: 10.1016/s0887-8994(98)00123-4. Pediatr Neurol. 1999. PMID: 10082342

2

The clinical spectrum of sarcoglycanopathies.

Angelini C, Fanin M, Freda MP, Duggan DJ, Siciliano G, Hoffman EP. Angelini C, et al. Among authors: siciliano g. Neurology. 1999 Jan 1;52(1):176-9. doi: 10.1212/wnl.52.1.176. Neurology. 1999. PMID: 9921870

3

Sudden bilateral hearing loss and sporadic mitochondrial DNA deletion.

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

4

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

5

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: siciliano g. J Laryngol Otol. 2006 Oct;120(10):888-91. doi: 10.1017/S0022215106001472. Epub 2006 May 24. J Laryngol Otol. 2006. PMID: 16719954

6

Mitochondrial syndromic sensorineural hearing loss.

Forli F, Passetti S, Mancuso M, Seccia V, Siciliano G, Nesti C, Berrettini S. Forli F, et al. Among authors: siciliano g. Biosci Rep. 2007 Jun;27(1-3):113-23. doi: 10.1007/s10540-007-9040-5. Biosci Rep. 2007. PMID: 17487579

7

Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions.

Trevisan CP, Pastorello E, Tomelleri G, Vercelli L, Bruno C, Scapolan S, Siciliano G, Comacchio F. Trevisan CP, et al. Among authors: siciliano g. Eur J Neurol. 2008 Dec;15(12):1353-8. doi: 10.1111/j.1468-1331.2008.02314.x. Eur J Neurol. 2008. PMID: 19049553

8

Mitochondrial DNA (mtDNA) haplotypes and dysfunctions in presbyacusis.

Mostafa H, Saad M, El-Attar A, Ahmed G, Berrettini S, Forli F, Siciliano G, Mancuso M. Mostafa H, et al. Among authors: siciliano g. Acta Otorhinolaryngol Ital. 2014 Feb;34(1):54-61. Acta Otorhinolaryngol Ital. 2014. PMID: 24711684 Free PMC article.

9

Revisiting mitochondrial ocular myopathies: a study from the Italian Network.

Orsucci D, Angelini C, Bertini E, Carelli V, Comi GP, Federico A, Minetti C, Moggio M, Mongini T, Santorelli FM, Servidei S, Tonin P, Ardissone A, Bello L, Bruno C, Ienco EC, Diodato D, Filosto M, Lamperti C, Moroni I, Musumeci O, Pegoraro E, Primiano G, Ronchi D, Rubegni A, Salvatore S, Sciacco M, Valentino ML, Vercelli L, Toscano A, Zeviani M, Siciliano G, Mancuso M. Orsucci D, et al. Among authors: siciliano g. J Neurol. 2017 Aug;264(8):1777-1784. doi: 10.1007/s00415-017-8567-z. Epub 2017 Jul 10. J Neurol. 2017. PMID: 28695364

10

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. 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.

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