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F Vitelli

Explore the profile of F Vitelli including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 24
Citations 646
Followers 0
Related Specialties
Genetics
Endocrinology
Top 10 Co-Authors
A Renieri
M Bruttini
M Piccini
L Papi
L R De Vitis
I Meloni
F Ammannati
G Pagano
F Maneschi
P Mennonna
Published In
Genomics
Hum Genet
J Med Genet
Diabetologia
Radiol Med
Affiliations
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Recent Articles
1.
Randomized clinical trial "olfactory dysfunction after COVID-19: olfactory rehabilitation therapy vs. intervention treatment with Palmitoylethanolamide and Luteolin": preliminary results
DAscanio L, Vitelli F, Cingolani C, Maranzano M, Brenner M, Di Stadio A
Eur Rev Med Pharmacol Sci . 2021 Jun; 25(11):4156-4162. PMID: 34156697
Objective: Approximately 30% of patients with confirmed COVID-19 report persistent smell or taste disorders as long-term sequalae of infection. Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection is associated with...
2.
Genetic dissection of the DiGeorge syndrome phenotype
Vitelli F, Lindsay E, Baldini A
Cold Spring Harb Symp Quant Biol . 2003 Jul; 67:327-32. PMID: 12858556
No abstract available.
3.
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 R, Tonlorenzi R, Rossi E, et al.
J Med Genet . 2002 May; 39(5):359-65. PMID: 12011158
No abstract available.
4.
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice
Lindsay E, Vitelli F, Su H, Morishima M, Huynh T, Pramparo T, et al.
Nature . 2001 Mar; 410(6824):97-101. PMID: 11242049
DiGeorge syndrome is characterized by cardiovascular, thymus and parathyroid defects and craniofacial anomalies, and is usually caused by a heterozygous deletion of chromosomal region 22q11.2 (del22q11) (ref. 1). A targeted,...
5.
Mosaicism in Alport syndrome with genetic counselling
Bruttini M, Vitelli F, Meloni I, Rizzari G, Volpe M, Mazzucco G, et al.
J Med Genet . 2001 Feb; 37(9):717-9. PMID: 11182935
No abstract available.
6.
Preserved speech variant is allelic of classic Rett syndrome
De Bona C, Zappella M, Hayek G, Meloni I, Vitelli F, Bruttini M, et al.
Eur J Hum Genet . 2000 Jun; 8(5):325-30. PMID: 10854091
Rett syndrome is a neurological disorder affecting predominantly females with regression loss of speech and purposeful hand use, after a few months of almost normal development. Postnatal microcephaly, hand dispraxia,...
7.
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, et al.
Cytogenet Cell Genet . 2000 Jun; 88(3-4):259-63. PMID: 10828604
The contiguous gene deletion syndrome AMME is characterized by Alport syndrome, midface hypoplasia, mental retardation and elliptocytosis and is caused by a deletion in Xq22.3, comprising several genes including COL4A5,...
8.
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 L, Moran O, Bulfone A, et al.
Genomics . 1999 Sep; 60(3):251-7. PMID: 10493825
We describe the identification and characterization of a new gene deleted in the AMME contiguous gene syndrome. This gene is predominantly expressed in heart, skeletal muscle, spinal cord, and brain....
9.
Inheritance of a 38-kb fragment in apparently sporadic facioscapulohumeral muscular dystrophy
Vitelli F, Villanova M, Malandrini A, Bruttini M, Piccini M, Merlini L, et al.
Muscle Nerve . 1999 Sep; 22(10):1437-41. PMID: 10487912
Facioscapulohumeral dystrophy (FSHD) is an autosomal-dominant muscular disorder associated with a short (<35 kb) EcoRI/BlnI fragment resulting from deletion of an integral number of units of a 3.3-kb repeat located...
10.
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, et al.
Genomics . 1999 Mar; 55(3):335-40. PMID: 10049589
We recently described a novel contiguous gene deletion syndrome (AMME) in Xq22.3 that includes Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E). While the Alport syndrome...