Concolino P - Search Results

1

Functional effect of Saffron supplementation and risk genotypes in early age-related macular degeneration: a preliminary report.

Marangoni D, Falsini B, Piccardi M, Ambrosio L, Minnella AM, Savastano MC, Bisti S, Maccarone R, Fadda A, Mello E, Concolino P, Capoluongo E. Marangoni D, et al. Among authors: concolino p. J Transl Med. 2013 Sep 25;11:228. doi: 10.1186/1479-5876-11-228. J Transl Med. 2013. PMID: 24067115 Free PMC article. Clinical Trial.

2

Genetic Characterization of a Cohort of Italian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.

Concolino P, Perrucci A, Carrozza C, Urbani A. Concolino P, et al. Mol Diagn Ther. 2023 Sep;27(5):621-630. doi: 10.1007/s40291-023-00666-x. Epub 2023 Aug 7. Mol Diagn Ther. 2023. PMID: 37548905

3

Serum levels of seven cytokines in premature ventilated newborns: correlations with old and new forms of bronchopulmonary dysplasia.

Vento G, Capoluongo E, Matassa PG, Concolino P, Vendettuoli V, Vaccarella C, Frezza S, Zuppi C, Romagnoli C, Ameglio F. Vento G, et al. Among authors: concolino p. Intensive Care Med. 2006 May;32(5):723-30. doi: 10.1007/s00134-006-0138-1. Epub 2006 Mar 21. Intensive Care Med. 2006. PMID: 16550369 Clinical Trial.

4

GSTT1 and GSTM1 allelic polymorphisms in head and neck cancer patients from Italian Lazio Region.

Capoluongo E, Almadori G, Concolino P, Bussu F, Santonocito C, Vendittelli F, Galli J, Zuppi C, Ameglio F, Paludetti G, Giardina B. Capoluongo E, et al. Among authors: concolino p. Clin Chim Acta. 2007 Feb;376(1-2):174-8. doi: 10.1016/j.cca.2006.08.017. Epub 2006 Aug 17. Clin Chim Acta. 2007. PMID: 17005168

5

Genetic analysis of the dystroglycan gene in bronchopulmonary dysplasia affected premature newborns.

Concolino P, Capoluongo E, Santonocito C, Vento G, Tana M, Romagnoli C, Zuppi C, Ameglio F, Brancaccio A, Sciandra F. Concolino P, et al. Clin Chim Acta. 2007 Mar;378(1-2):164-7. doi: 10.1016/j.cca.2006.11.016. Epub 2006 Nov 25. Clin Chim Acta. 2007. PMID: 17196572

6

Association of periodontitis with GSTM1/GSTT1-null variants--a pilot study.

Concolino P, Cecchetti F, D'Autilia C, Santonocito C, Di Stasio E, Zuppi C, Arcuri C, Deli G, Giardina B, Capoluongo E, Ameglio F. Concolino P, et al. Clin Biochem. 2007 Sep;40(13-14):939-45. doi: 10.1016/j.clinbiochem.2007.04.012. Epub 2007 Apr 27. Clin Biochem. 2007. PMID: 17524385

7

Description of a novel missense mutation of glucose-6-phosphate dehydrogenase gene associated with asymptomatic high enzyme deficiency.

Minucci A, Concolino P, Antenucci M, Santonocito C, Ameglio F, Zuppi C, Giardina B, Capoluongo E. Minucci A, et al. Among authors: concolino p. Clin Biochem. 2007 Aug;40(12):856-8. doi: 10.1016/j.clinbiochem.2007.03.025. Epub 2007 Apr 20. Clin Biochem. 2007. PMID: 17524386

8

Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study.

Capoluongo E, Vento G, Rocchetti S, Giardina E, Concolino P, Sinibaldi C, Santonocito C, Vendettuoli V, Tana M, Tirone C, Zuppi C, Romagnoli C, Novelli G, Giardina B, Ameglio F. Capoluongo E, et al. Among authors: concolino p. Intensive Care Med. 2007 Oct;33(10):1787-94. doi: 10.1007/s00134-007-0793-x. Epub 2007 Jul 26. Intensive Care Med. 2007. PMID: 17653692

9

First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy.

Concolino P, Corsello S, Carrozza C, Minucci A, Santonocito C, Lovicu RM, Santini SA, Ameglio F, Zuppi C, Capoluongo E. Concolino P, et al. Clin Biochem. 2007 Dec;40(18):1435-6. doi: 10.1016/j.clinbiochem.2007.09.002. Epub 2007 Sep 26. Clin Biochem. 2007. PMID: 18028896

10

Novel human pathological mutations. Gene symbol: COL4A5. Disease: Alport syndrome.

Minucci A, Capoluongo E, Concolino P, Concetta S, Zuppi C, Giardina B. Minucci A, et al. Among authors: concolino p. Hum Genet. 2007 Nov;122(3-4):414. Hum Genet. 2007. PMID: 18350645 No abstract available.

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