Failla P - Search Results

1

Identification of novel mutations in patients with Coffin-Lowry syndrome by a denaturing HPLC-based assay.

Falco M, Romano C, Alberti A, Greco D, Scuderi C, Avola E, Failla P, Belli S, Tolmie JL, Amata S, Fichera M. Falco M, et al. Among authors: failla p. Clin Chem. 2005 Dec;51(12):2356-8. doi: 10.1373/clinchem.2005.056036. Clin Chem. 2005. PMID: 16306095 No abstract available.

2

Skin-picking: the best cutaneous feature in the recognization of Prader-Willi syndrome.

Schepis C, Failla P, Siragusa M, Romano C. Schepis C, et al. Among authors: failla p. Int J Dermatol. 1994 Dec;33(12):866-7. doi: 10.1111/j.1365-4362.1994.tb01024.x. Int J Dermatol. 1994. PMID: 7883413 No abstract available.

3

Celiac disease in Down's syndrome with HLA serological and molecular studies.

Failla P, Ruberto C, Pagano MC, Lombardo M, Bottaro G, Perichon B, Krishnamoorthy R, Romano C, Ragusa A. Failla P, et al. J Pediatr Gastroenterol Nutr. 1996 Oct;23(3):303-6. doi: 10.1097/00005176-199610000-00016. J Pediatr Gastroenterol Nutr. 1996. PMID: 8890082

4

Hypomelanosis of Ito: a syndrome requiring a multisystem approach.

Failla P, Romano C, Schepis C. Failla P, et al. Australas J Dermatol. 1997 May;38(2):65-70. doi: 10.1111/j.1440-0960.1997.tb01108.x. Australas J Dermatol. 1997. PMID: 9159959

5

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, Greco D, Cardoso C, Fontés M, Ragusa A. Fichera M, et al. Among authors: failla p. Hum Mutat. 1998;12(3):214. Hum Mutat. 1998. PMID: 10660327

6

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, Romano C. Barone C, et al. Among authors: failla p. Minerva Pediatr. 2000 Mar;52(3):161-5. Minerva Pediatr. 2000. PMID: 10879009 English, Italian.

7

Is there a relationship between zinc and the peculiar comorbidities of Down syndrome?

Romano C, Pettinato R, Ragusa L, Barone C, Alberti A, Failla P. Romano C, et al. Among authors: failla p. Downs Syndr Res Pract. 2002 Mar;8(1):25-8. doi: 10.3104/reports.126. Downs Syndr Res Pract. 2002. PMID: 11915434 Free article.

8

Schizophrenia in a patient with subtelomeric duplication of chromosome 22q.

Failla P, Romano C, Alberti A, Vasta A, Buono S, Castiglia L, Luciano D, Di Benedetto D, Fichera M, Galesi O. Failla P, et al. Clin Genet. 2007 Jun;71(6):599-601. doi: 10.1111/j.1399-0004.2007.00819.x. Clin Genet. 2007. PMID: 17539913 No abstract available.

9

12q12 deletion: a new patient contributing to genotype-phenotype correlation.

Failla P, Romano C, Reitano S, Di Benedetto D, Grillo L, Fichera M, Castiglia L. Failla P, et al. Am J Med Genet A. 2008 May 15;146A(10):1354-7. doi: 10.1002/ajmg.a.32280. Am J Med Genet A. 2008. PMID: 18412123 No abstract available.

10

Complex segmental duplications mediate a recurrent dup(X)(p11.22-p11.23) associated with mental retardation, speech delay, and EEG anomalies in males and females.

Giorda R, Bonaglia MC, Beri S, Fichera M, Novara F, Magini P, Urquhart J, Sharkey FH, Zucca C, Grasso R, Marelli S, Castiglia L, Di Benedetto D, Musumeci SA, Vitello GA, Failla P, Reitano S, Avola E, Bisulli F, Tinuper P, Mastrangelo M, Fiocchi I, Spaccini L, Torniero C, Fontana E, Lynch SA, Clayton-Smith J, Black G, Jonveaux P, Leheup B, Seri M, Romano C, dalla Bernardina B, Zuffardi O. Giorda R, et al. Among authors: failla p. Am J Hum Genet. 2009 Sep;85(3):394-400. doi: 10.1016/j.ajhg.2009.08.001. Epub 2009 Aug 27. Am J Hum Genet. 2009. PMID: 19716111 Free PMC article.

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