Gentile M - Search Results

1

Genetic Associations of Alexithymia in Predicting Interferon-Induced Depression in Chronic Hepatitis C.

Porcelli P, Cozzolongo R, Cariola F, Giannuzzi V, Lanzilotta E, Gentile M, Sonnante G, Leandro G. Porcelli P, et al. Among authors: gentile m. Psychopathology. 2015;48(6):417-20. doi: 10.1159/000441682. Epub 2015 Nov 27. Psychopathology. 2015. PMID: 26609890

2

Serotonin gene polymorphisms and lifetime mood disorders in predicting interferon-induced depression in chronic hepatitis C.

Cozzolongo R, Porcelli P, Cariola F, Giannuzzi V, Lanzilotta E, Gentile M, Sonnante G, Leandro G. Cozzolongo R, et al. Among authors: gentile m. J Affect Disord. 2015 Sep 1;183:90-7. doi: 10.1016/j.jad.2015.04.056. Epub 2015 May 9. J Affect Disord. 2015. PMID: 26001668

3

Prenatal diagnosis of chromosome 4 mosaicism: prognostic role of cytogenetic, molecular, and ultrasound/MRI characterization.

Gentile M, Volpe P, Cariola F, Di Carlo A, Marotta V, Buonadonna AL, Boscia FM. Gentile M, et al. Am J Med Genet A. 2005 Jul 1;136(1):66-70. doi: 10.1002/ajmg.a.30506. Am J Med Genet A. 2005. PMID: 15940687 Review.

4

Low presence of p53 abnormalities in H pylori-infected gastric mucosa and in gastric adenocarcinoma.

Berloco P, Russo F, Cariola F, Gentile M, Giorgio P, Caruso ML, Valentini AM, Di Matteo G, Di Leo A. Berloco P, et al. Among authors: gentile m. J Gastroenterol. 2003;38(1):28-36. doi: 10.1007/s005350300003. J Gastroenterol. 2003. PMID: 12560919

5

Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).

Gentile M, Buonadonna AL, Cariola F, Fiorente P, Valenzano MC, Guanti G. Gentile M, et al. J Med Genet. 1999 Jan;36(1):77-82. J Med Genet. 1999. PMID: 9950374 Free PMC article.

6

Molecular and cytogenetic characterization of an azoospermic male with a de-novo Y;14 translocation and alternate centromere inactivation.

Buonadonna AL, Cariola F, Caroppo E, Di Carlo A, Fiorente P, Valenzano MC, D'Amato G, Gentile M. Buonadonna AL, et al. Among authors: gentile m. Hum Reprod. 2002 Mar;17(3):564-9. doi: 10.1093/humrep/17.3.564. Hum Reprod. 2002. PMID: 11870104

7

Oestrogen receptors and microsatellite instability in colorectal carcinoma patients.

Notarnicola M, Gristina R, Messa C, Cariola F, Fiorente P, Caruso ML, Gentile M, Di Leo A. Notarnicola M, et al. Among authors: gentile m. Cancer Lett. 2001 Jul 10;168(1):65-70. doi: 10.1016/s0304-3835(01)00494-3. Cancer Lett. 2001. PMID: 11368879

8

FISH approach to determine cat eye syndrome chromosome breakpoints of a patient with cat eye syndrome type II.

Gentile M, De Sanctis S, Cariola F, Spezzi T, Di Carlo A, Tontoli F, Lista F, Buonadonna AL. Gentile M, et al. Eur J Med Genet. 2005 Jan-Mar;48(1):33-9. doi: 10.1016/j.ejmg.2005.01.020. Epub 2005 Feb 1. Eur J Med Genet. 2005. PMID: 15953404

9

Clinical, cytogenetic, and molecular characterization of a patient with a de novo interstitial 22q12 duplication.

Gentile M, Wuyts W, Grittani S, Di Carlo A, Cariola F, Verdyck P, Margari L, Perniola T, Buonadonna AL. Gentile M, et al. Am J Med Genet A. 2004 Jun 1;127A(2):186-90. doi: 10.1002/ajmg.a.20672. Am J Med Genet A. 2004. PMID: 15108208

10

Molecular cytogenetic characterization and genotype/phenotype analysis in a patient with a de novo 8p23.2p23.3 deletion/12p13.31p13.33 duplication.

Margari L, Di Cosola ML, Buttiglione M, Pansini A, Buonadonna AL, Craig F, Cariola F, Petruzzelli MG, Gentile M. Margari L, et al. Among authors: gentile m. Am J Med Genet A. 2012 Jul;158A(7):1713-8. doi: 10.1002/ajmg.a.35400. Epub 2012 May 25. Am J Med Genet A. 2012. PMID: 22639464

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