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P Failla

Explore the profile of P Failla including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 32
Citations 155
Followers 0
Related Specialties
Pediatrics
Genetics
General Surgery
Top 10 Co-Authors
C Romano
G Bottaro
R Patane
C Schepis
N Castiglione
M Siragusa
M Fichera
A A Azad
L Castiglia
O Galesi
Published In
Pediatr Med Chir
Acta Paediatr
J Pediatr Gastroenterol Nutr
Minerva Pediatr
Australas J Dermatol
Affiliations
Soon will be listed here.
Recent Articles
1.
Multiplex ligation-dependent probe amplification detection of an unknown large deletion of the CREB-binding protein gene in a patient with Rubinstein-Taybi syndrome
Cali F, Failla P, Chiavetta V, Ragalmuto A, Ruggeri G, Schinocca P, et al.
Genet Mol Res . 2013 Jan; 12(3):2809-15. PMID: 23315884
Rubinstein-Taybi syndrome is a rare autosomal dominant congenital disorder characterized by postnatal growth retardation, psychomotor developmental delay, skeletal anomalies, peculiar facial morphology, and tumorigenesis. Mutations in the gene encoding the...
2.
Schizophrenia in a patient with subtelomeric duplication of chromosome 22q
Failla P, Romano C, Alberti A, Vasta A, Buono S, Castiglia L, et al.
Clin Genet . 2007 Jun; 71(6):599-601. PMID: 17539913
No abstract available.
3.
Narrowing the candidate region for congenital diaphragmatic hernia in chromosome 15q26: contradictory results
Castiglia L, Fichera M, Romano C, Galesi O, Grillo L, Sturnio M, et al.
Am J Hum Genet . 2005 Oct; 77(5):892-4. PMID: 16252246
No abstract available.
4.
Medial telangiectatic sacral nevi and MCA/MR syndromes
Schepis C, Greco D, Failla P, Siragusa M, Romano C, Scaffidi M, et al.
Pediatr Dermatol . 2003 Jul; 20(4):370-1. PMID: 12869167
No abstract available.
5.
Prevalence and clinical picture of celiac disease in italian down syndrome patients: a multicenter study
Bonamico M, Mariani P, Danesi H, Crisogianni M, Failla P, Gemme G, et al.
J Pediatr Gastroenterol Nutr . 2001 Sep; 33(2):139-43. PMID: 11568513
Background: A multicenter research study of Down syndrome patients was carried out to estimate the prevalence of celiac disease in patients with Down syndrome and to show clinical characteristics and...
6.
An additional case of macular phylloid mosaicism
Schepis C, Failla P, Siragusa M, Romano C
Dermatology . 2001 Mar; 202(1):73. PMID: 11244237
No abstract available.
7.
How microsatellite analysis can be exploited for subtelomeric chromosomal rearrangement analysis in mental retardation
Borgione E, Giudice M, Galesi O, Castiglia L, Failla P, Romano C, et al.
J Med Genet . 2001 Jan; 38(1):E1. PMID: 11134240
No abstract available.
8.
Comparison of three probiotics in the treatment of acute diarrhea in mentally retarded children
Barone C, Pettinato R, Avola E, Alberti A, Greco D, Failla P, et al.
Minerva Pediatr . 2000 Jul; 52(3):161-5. PMID: 10879009
Background: This article aims to compare the use of VIS-01 (Yovis) with two other probiotics (lactic acid bacteria), such as Lactogèrmine and Codex in the treatment of acute diarrhea in...
9.
New mutations in XNP/ATR-X gene: a further contribution to genotype/phenotype relationship in ATR/X syndrome. Mutations in brief no. 176. Online
Fichera M, Romano C, Castiglia L, Failla P, Ruberto C, Amata S, et al.
Hum Mutat . 2000 Feb; 12(3):214. PMID: 10660327
The molecular causes of ATR-X syndrome reside in mutations involving the XNP/ATR-X gene, which maps in the Xq13.3 region. Mutational analysis of this gene in two unrelated affected patients allowed...
10.
A prevalence study of celiac disease in persons with Down syndrome residing in the United States of America
Pueschel S, Romano C, Failla P, Barone C, Pettinato R, Castellano Chiodo A, et al.
Acta Paediatr . 1999 Oct; 88(9):953-6. PMID: 10519335
In order to estimate the prevalence of celiac disease in persons with Down syndrome, 105 patients with this chromosomal disorder residing on the East Coast of the United States of...