D'Andrea G - Search Results

1

Associations Between Personality Traits, Perceived Stress and Depressive Symptoms in Gynecological Cancer Patients Characterized by the Short and Long Allele Variant of the 5-HTTLPR Genotype: Preliminary Results.

Iuso S, Monacis L, Nappi L, Malerba S, D'Andrea G, Altamura M, Margaglione M, Bellomo A, Petito A. Iuso S, et al. Clin Neuropsychiatry. 2022 Jun;19(3):156-162. doi: 10.36131/cnfioritieditore20220304. Clin Neuropsychiatry. 2022. PMID: 35821869 Free PMC article.

2

Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism.

D'Andrea G, Margaglione M; Glansmann's Thrombasthemia Italian Team (GLATIT). D'Andrea G, et al. Haematologica. 2003 Dec;88(12):1378-82. Haematologica. 2003. PMID: 14687991

3

Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes.

Zefferino R, Piccaluga S, Lasalvia M, D' Andrea G, Margaglione M, Ambrosi L. Zefferino R, et al. Int J Immunopathol Pharmacol. 2006 Oct-Dec;19(4 Suppl):15-20. Int J Immunopathol Pharmacol. 2006. PMID: 17291401

4

Oral anticoagulants: Pharmacogenetics Relationship between genetic and non-genetic factors.

D'Andrea G, D'Ambrosio R, Margaglione M. D'Andrea G, et al. Blood Rev. 2008 May;22(3):127-40. doi: 10.1016/j.blre.2007.11.004. Epub 2008 Jan 30. Blood Rev. 2008. PMID: 18234403 Review.

5

A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions.

D'Andrea G, Bafunno V, Del Vecchio L, Amoriello A, Morabito P, Vecchione G, Grandone E, Margaglione M. D'Andrea G, et al. Blood Coagul Fibrinolysis. 2008 Oct;19(7):657-62. doi: 10.1097/MBC.0b013e3283048e42. Blood Coagul Fibrinolysis. 2008. PMID: 18832906

6

Inherited platelet disorders: thrombocytopenias and thrombocytopathies.

D'Andrea G, Chetta M, Margaglione M. D'Andrea G, et al. Blood Transfus. 2009 Oct;7(4):278-92. doi: 10.2450/2009.0078-08. Blood Transfus. 2009. PMID: 20011639 Free PMC article. Review. No abstract available.

7

Mutation analysis in hyperphenylalaninemia patients from South Italy.

Trunzo R, Santacroce R, D'Andrea G, Longo V, De Girolamo G, Dimatteo C, Leccese A, Lillo V, Papadia F, Margaglione M. Trunzo R, et al. Clin Biochem. 2013 Dec;46(18):1896-8. doi: 10.1016/j.clinbiochem.2013.06.009. Epub 2013 Jun 18. Clin Biochem. 2013. PMID: 23792259

8

Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees.

Trunzo R, Santacroce R, D'Andrea G, Longo V, De Girolamo G, Dimatteo C, Leccese A, Lillo V, Papadia F, Margaglione M. Trunzo R, et al. Clin Biochem. 2014 Feb;47(3):233-5. doi: 10.1016/j.clinbiochem.2013.11.015. Epub 2013 Dec 1. Clin Biochem. 2014. PMID: 24296287

9

Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia.

D'Andrea G, Schiavulli M, Dimatteo C, Santacroce R, Guerra E, Longo VA, Grandone E, Margaglione M. D'Andrea G, et al. Blood. 2013 Dec 19;122(26):4289-91. doi: 10.1182/blood-2013-09-528943. Blood. 2013. PMID: 24357714 Free article. No abstract available.

10

Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene.

Leccese A, Longo V, Dimatteo C, De Girolamo G, Trunzo R, D'Andrea G, Bafunno V, Margaglione M, Santacroce R. Leccese A, et al. Clin Chim Acta. 2014 Nov 1;437:48-51. doi: 10.1016/j.cca.2014.07.009. Epub 2014 Jul 12. Clin Chim Acta. 2014. PMID: 25025300

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