Fogli A - Search Results

1

Clinical and genetic findings in a series of Italian children with pure hereditary spastic paraplegia.

Battini R, Fogli A, Borghetti D, Michelucci A, Perazza S, Baldinotti F, Conidi ME, Ferreri MI, Simi P, Cioni G. Battini R, et al. Among authors: fogli a. Eur J Neurol. 2011 Jan;18(1):150-7. doi: 10.1111/j.1468-1331.2010.03102.x. Eur J Neurol. 2011. PMID: 20550563

2

Alterations of Fas (APO-1/CD 95) gene and its relationship with p53 in non small cell lung cancer.

Boldrini L, Faviana P, Pistolesi F, Gisfredi S, Di Quirico D, Lucchi M, Mussi A, Angeletti CA, Baldinotti F, Fogli A, Simi P, Basolo F, Fontanini G. Boldrini L, et al. Among authors: fogli a. Oncogene. 2001 Oct 4;20(45):6632-7. doi: 10.1038/sj.onc.1204727. Oncogene. 2001. PMID: 11641789

3

Nonsense mutation in exon 2 of the alpha-galactosidase A gene in a patient with Fabry disease.

Manni E, Fogli A, Baldinotti F, Rossi S, Funel N, Barachini P, Simi P. Manni E, et al. Among authors: fogli a. Contrib Nephrol. 2001;(136):223-8. doi: 10.1159/000060192. Contrib Nephrol. 2001. PMID: 11688384 No abstract available.

4

Identification of Fas (APO-1/CD95) and p53 gene mutations in non-small cell lung cancer.

Boldrini L, Faviana P, Gisfredi S, Di Quirico D, Lucchi M, Mussi A, Angeletti CA, Baldinotti F, Fogli A, Simi P, Basolo F, Pingitore F, Fontanini G. Boldrini L, et al. Among authors: fogli a. Int J Oncol. 2002 Jan;20(1):155-9. doi: 10.3892/ijo.20.1.155. Int J Oncol. 2002. PMID: 11743657

5

Mutations of Fas (APO-1/CD95) and p53 genes in nonmelanoma skin cancer.

Boldrini L, Loggini B, Gisfredi S, Zucconi Y, Baldinotti F, Fogli A, Simi P, Cervadoro G, Barachini P, Basolo F, Pingitore R, Fontanini G. Boldrini L, et al. Among authors: fogli a. J Cutan Med Surg. 2003 Mar-Apr;7(2):112-8. doi: 10.1007/s10227-002-0105-6. Epub 2002 Nov 27. J Cutan Med Surg. 2003. PMID: 12447615

6

Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey.

Sensi A, Cavani S, Villa N, Pomponi MG, Fogli A, Gualandi F, Grasso M, Sala E, Pietrobono R, Baldinotti F, Savin E, Ferlini A, Cecconi M, Rossi S, Gallone S, Bellini C, Neri G, Martinoli E, Simi P, Dalprà L, Genuardi M, Dagna-Bricarelli F, Calzolari E. Sensi A, et al. Among authors: fogli a. Prenat Diagn. 2004 Aug;24(8):647-52. doi: 10.1002/pd.962. Prenat Diagn. 2004. PMID: 15305356

7

Cx26 gene mutations in idiopathic progressive hearing loss.

Ravecca F, Berrettini S, Forli F, Marcaccini M, Casani A, Baldinotti F, Fogli A, Siciliano G, Simi P. Ravecca F, et al. Among authors: fogli a. J Otolaryngol. 2005 Apr;34(2):126-34. doi: 10.2310/7070.2005.04017. J Otolaryngol. 2005. PMID: 16076412

8

Molecular characterization of 6 unrelated Italian patients with 5alpha-reductase type 2 deficiency.

Baldinotti F, Majore S, Fogli A, Marrocco G, Ghirri P, Vuerich M, Tumini S, Boscherini B, Vetri M, Scommegna S, Rinaldi R, Simi P, Grammatico P. Baldinotti F, et al. Among authors: fogli a. J Androl. 2008 Jan-Feb;29(1):20-8. doi: 10.2164/jandrol.107.002592. Epub 2007 Jul 3. J Androl. 2008. PMID: 17609295 Free article.

9

Novel human pathological mutations. Gene symbol: SPG4. Disease: spastic paraplegia, autosomal dominant.

Fogli A, Battini R, Baldinotti F, Conidi ME, Michelucci A, Simi P. Fogli A, et al. Hum Genet. 2009 Aug;126(2):340. Hum Genet. 2009. PMID: 19694022 No abstract available.

10

Novel human pathological mutations. Gene symbol: SPG4. Disease: spastic paraplegia, autosomal dominant.

Fogli A, Battini R, Baldinotti F, Angela M, Elena CM, Paolo S. Fogli A, et al. Hum Genet. 2009 Aug;126(2):341. Hum Genet. 2009. PMID: 19694023 No abstract available.

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