Failla P - Search Results

1

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

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

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.

6

How microsatellite analysis can be exploited for subtelomeric chromosomal rearrangement analysis in mental retardation.

Borgione E, Giudice ML, Galesi O, Castiglia L, Failla P, Romano C, Ragusa A, Fichera M. Borgione E, et al. Among authors: failla p. J Med Genet. 2001 Jan;38(1):E1. doi: 10.1136/jmg.38.1.e1. J Med Genet. 2001. PMID: 11134240 Free PMC article. No abstract available.

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

Medial telangiectatic sacral nevi and MCA/MR syndromes.

Schepis C, Greco D, Failla P, Siragusa M, Romano C, Scaffidi M, Sindoni A. Schepis C, et al. Among authors: failla p. Pediatr Dermatol. 2003 Jul-Aug;20(4):370-1. doi: 10.1046/j.1525-1470.2003.20326_2.x. Pediatr Dermatol. 2003. PMID: 12869167 No abstract available.

9

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, Failla P. Castiglia L, et al. Among authors: failla p. Am J Hum Genet. 2005 Nov;77(5):892-4; author reply 894-5. doi: 10.1086/497082. Am J Hum Genet. 2005. PMID: 16252246 Free PMC article. No abstract available.

10

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.

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