Vitelli F - Search Results

1

FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation.

Piccini M, Vitelli F, Bruttini M, Pober BR, Jonsson JJ, Villanova M, Zollo M, Borsani G, Ballabio A, Renieri A. Piccini M, et al. Among authors: vitelli f. Genomics. 1998 Feb 1;47(3):350-8. doi: 10.1006/geno.1997.5104. Genomics. 1998. PMID: 9480748 Free article.

2

Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?

Jonsson JJ, Renieri A, Gallagher PG, Kashtan CE, Cherniske EM, Bruttini M, Piccini M, Vitelli F, Ballabio A, Pober BR. Jonsson JJ, et al. Among authors: vitelli f. J Med Genet. 1998 Apr;35(4):273-8. doi: 10.1136/jmg.35.4.273. J Med Genet. 1998. PMID: 9598718 Free PMC article.

3

Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME).

Vitelli F, Piccini M, Caroli F, Franco B, Malandrini A, Pober B, Jonsson J, Sorrentino V, Renieri A. Vitelli F, et al. Genomics. 1999 Feb 1;55(3):335-40. doi: 10.1006/geno.1998.5666. Genomics. 1999. PMID: 10049589

4

KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologs.

Piccini M, Vitelli F, Seri M, Galietta LJ, Moran O, Bulfone A, Banfi S, Pober B, Renieri A. Piccini M, et al. Among authors: vitelli f. Genomics. 1999 Sep 15;60(3):251-7. doi: 10.1006/geno.1999.5904. Genomics. 1999. PMID: 10493825

5

Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3.

Vitelli F, Meloni I, Fineschi S, Favara F, Tiziana Storlazzi C, Rocchi M, Renieri A. Vitelli F, et al. Cytogenet Cell Genet. 2000;88(3-4):259-63. doi: 10.1159/000015533. Cytogenet Cell Genet. 2000. PMID: 10828604

6

Inheritance of a 38-kb fragment in apparently sporadic facioscapulohumeral muscular dystrophy.

Vitelli F, Villanova M, Malandrini A, Bruttini M, Piccini M, Merlini L, Guazzi G, Renieri A. Vitelli F, et al. Muscle Nerve. 1999 Oct;22(10):1437-41. doi: 10.1002/(sici)1097-4598(199910)22:10<1437::aid-mus15>3.0.co;2-7. Muscle Nerve. 1999. PMID: 10487912

7

Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR).

Meloni I, Vitelli F, Pucci L, Lowry RB, Tonlorenzi R, Rossi E, Ventura M, Rizzoni G, Kashtan CE, Pober B, Renieri A. Meloni I, et al. Among authors: vitelli f. J Med Genet. 2002 May;39(5):359-65. doi: 10.1136/jmg.39.5.359. J Med Genet. 2002. PMID: 12011158 Free PMC article. No abstract available.

8

Preserved speech variant is allelic of classic Rett syndrome.

De Bona C, Zappella M, Hayek G, Meloni I, Vitelli F, Bruttini M, Cusano R, Loffredo P, Longo I, Renieri A. De Bona C, et al. Among authors: vitelli f. Eur J Hum Genet. 2000 May;8(5):325-30. doi: 10.1038/sj.ejhg.5200473. Eur J Hum Genet. 2000. PMID: 10854091 Free article.

9

Mosaicism in Alport syndrome with genetic counselling.

Bruttini M, Vitelli F, Meloni I, Rizzari G, Volpe MD, Mazzucco G, Marchi MD, Renieri A. Bruttini M, et al. Among authors: vitelli f. J Med Genet. 2000 Sep;37(9):717-9. doi: 10.1136/jmg.37.9.717. J Med Genet. 2000. PMID: 11182935 Free PMC article. No abstract available.

10

Somatic mutations in the neurofibromatosis type 2 gene in sporadic meningiomas.

Papi L, De Vitis LR, Vitelli F, Ammannati F, Mennonna P, Montali E, Bigozzi U. Papi L, et al. Among authors: vitelli f. Hum Genet. 1995 Mar;95(3):347-51. doi: 10.1007/BF00225206. Hum Genet. 1995. PMID: 7868131

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