Failla P - Search Results

1

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.

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

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

4

Failure of fluoxetine to modify the skin-picking behaviour of Prader-Willi syndrome.

Schepis C, Failla P, Siragusa M, Palazzo R, Romano C. Schepis C, et al. Among authors: failla p. Australas J Dermatol. 1998 Feb;39(1):57-8. doi: 10.1111/j.1440-0960.1998.tb01247.x. Australas J Dermatol. 1998. PMID: 9529694 No abstract available.

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

An additional case of macular phylloid mosaicism.

Schepis C, Failla P, Siragusa M, Romano C. Schepis C, et al. Among authors: failla p. Dermatology. 2001;202(1):73. doi: 10.1159/000051593. Dermatology. 2001. PMID: 11244237 No abstract available.

8

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.

9

An unusual presentation of Becker Nevus.

Schepis C, Lentini M, Failla P, Castiglia L, Fichera M, Romano C. Schepis C, et al. Among authors: failla p. Eur J Dermatol. 2010 Jul-Aug;20(4):522-3. doi: 10.1684/ejd.2010.0971. Epub 2010 Apr 20. Eur J Dermatol. 2010. PMID: 20406725 No abstract available.

10

Multiplex ligation-dependent probe amplification detection of an unknown large deletion of the CREB-binding protein gene in a patient with Rubinstein-Taybi syndrome.

Calì F, Failla P, Chiavetta V, Ragalmuto A, Ruggeri G, Schinocca P, Schepis C, Romano V, Romano C. Calì F, et al. Among authors: failla p. Genet Mol Res. 2013 Jan 7;12(3):2809-15. doi: 10.4238/2013.January.7.2. Genet Mol Res. 2013. PMID: 23315884 Free article.

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