Concolino P - Search Results

1

Pregnancy and Prenatal Management of Congenital Adrenal Hyperplasia.

Cera G, Locantore P, Novizio R, Maggio E, Ramunno V, Corsello A, Policola C, Concolino P, Paragliola RM, Pontecorvi A. Cera G, et al. Among authors: concolino p. J Clin Med. 2022 Oct 19;11(20):6156. doi: 10.3390/jcm11206156. J Clin Med. 2022. PMID: 36294476 Free PMC article. Review.

2

Reverse-hybridization assay for rapid detection of common CYP21A2 mutations in dried blood spots from newborns with elevated 17-OH progesterone.

Németh S, Riedl S, Kriegshäuser G, Baumgartner-Parzer S, Concolino P, Neocleous V, Phylactou LA, Borucka-Mankiewicz M, Onay H, Tukun A, Oberkanins C. Németh S, et al. Among authors: concolino p. Clin Chim Acta. 2012 Dec 24;414:211-4. doi: 10.1016/j.cca.2012.09.013. Epub 2012 Sep 14. Clin Chim Acta. 2012. PMID: 22985688

3

Is there a relationship between ELF free-IGF-1 levels and fibrotic process enhancement characterizing CLD development in neutropenic premature babies?

Capoluongo E, Concolino P, Giardina B, Zuppi C, Ameglio F, Vento G, Romagnoli C. Capoluongo E, et al. Among authors: concolino p. Pediatr Pulmonol. 2006 Mar;41(3):286-7; author reply 288. doi: 10.1002/ppul.20323. Pediatr Pulmonol. 2006. PMID: 16429428 No abstract available.

4

Identification of twenty-nine novel germline unclassified variants of BRCA1 and BRCA2 genes in 1400 Italian individuals.

Santonocito C, Scapaticci M, Guarino D, Bartolini A, Minucci A, Concolino P, Scambia G, Paris I, Capoluongo E. Santonocito C, et al. Among authors: concolino p. Breast. 2017 Dec;36:74-78. doi: 10.1016/j.breast.2017.09.007. Epub 2017 Oct 8. Breast. 2017. PMID: 29020660

5

High Resolution Melting Analysis (HRMA) for the identification of a rare UGT1A1 promoter polymorphism.

Minucci A, Mello E, Tripodi D, Concolino P, Zuppi C, Capoluongo E. Minucci A, et al. Among authors: concolino p. Clin Biochem. 2011 Nov;44(16):1359-60. doi: 10.1016/j.clinbiochem.2011.08.1130. Epub 2011 Aug 25. Clin Biochem. 2011. PMID: 21889933 No abstract available.

6

Association between serum free IGF-I and IGFBP-3 levels in type-I diabetes patients affected with associated autoimmune diseases or diabetic complications.

Capoluongo E, Pitocco D, Santonocito C, Concolino P, Santini SA, Manto A, Lulli P, Ghirlanda G, Zuppi C, Ameglio F. Capoluongo E, et al. Among authors: concolino p. Eur Cytokine Netw. 2006 Sep;17(3):167-74. Eur Cytokine Netw. 2006. PMID: 17194636 Free article.

7

A case of patient affected by hirsutism carrying the P482S CYP21 gene mutation associated with loss of heterozygosity (LOH).

Concolino P, Carrozza C, Minucci A, Santonocito C, Ameglio F, Zuppi C, Capoluongo E. Concolino P, et al. Clin Chim Acta. 2006 Aug;370(1-2):201-2. doi: 10.1016/j.cca.2006.01.013. Epub 2006 Feb 28. Clin Chim Acta. 2006. PMID: 16500637 No abstract available.

8

First genetic analysis of lattice corneal dystrophy type I in a family from Bulgaria.

Capoluongo E, De Benedetti G, Concolino P, Sepe M, Ambu R, Faa G, Sciandra F, Santonocito C, D'Alberto A, Caselli M, Brancaccio A. Capoluongo E, et al. Among authors: concolino p. Eur J Ophthalmol. 2005 Nov-Dec;15(6):804-8. doi: 10.1177/112067210501500624. Eur J Ophthalmol. 2005. PMID: 16329070

9

Characterization of a new BRCA1 rearrangement in an Italian woman with hereditary breast and ovarian cancer syndrome.

Concolino P, Rizza R, Hackmann K, Paris I, Minucci A, De Paolis E, Scambia G, Zuppi C, Schrock E, Capoluongo E. Concolino P, et al. Breast Cancer Res Treat. 2017 Jul;164(2):497-503. doi: 10.1007/s10549-017-4275-8. Epub 2017 May 9. Breast Cancer Res Treat. 2017. PMID: 28488140

10

Preliminary molecular evidence associating a novel BRCA1 synonymous variant with hereditary ovarian cancer syndrome.

Minucci A, Concolino P, De Bonis M, Costella A, Paris I, Scambia G, Capoluongo E. Minucci A, et al. Among authors: concolino p. Hum Genome Var. 2018 Apr 20;5:2. doi: 10.1038/s41439-018-0003-0. eCollection 2018. Hum Genome Var. 2018. PMID: 29760936 Free PMC article.

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