Scarciolla O - Search Results

1

Holotranscobalamin is a useful marker of vitamin B12 deficiency in alcoholics.

Fragasso A, Mannarella C, Ciancio A, Scarciolla O, Nuzzolese N, Clemente R, Vitullo E, Sacco A. Fragasso A, et al. Among authors: scarciolla o. ScientificWorldJournal. 2012;2012:128182. doi: 10.1100/2012/128182. Epub 2012 Mar 12. ScientificWorldJournal. 2012. PMID: 22481895 Free PMC article.

2

Myocardial iron overload assessed by magnetic resonance imaging (MRI)T2* in multi-transfused patients with thalassemia and acquired anemias.

Fragasso A, Ciancio A, Mannarella C, Gaudiano C, Scarciolla O, Ottonello C, Francone M, Nardella M, Peluso A, Melpignano A, Veglio MR, Quarta G, Turchetti C. Fragasso A, et al. Among authors: scarciolla o. Eur J Intern Med. 2011 Feb;22(1):62-5. doi: 10.1016/j.ejim.2010.10.005. Epub 2010 Nov 24. Eur J Intern Med. 2011. PMID: 21238896

3

Peripheral blood hemophagocytosis in an unusual lymphoma.

Fragasso A, Mannarella C, Ciancio A, Scarciolla O. Fragasso A, et al. Among authors: scarciolla o. Clin Case Rep. 2015 Jan;3(1):11-3. doi: 10.1002/ccr3.124. Epub 2014 Dec 2. Clin Case Rep. 2015. PMID: 25678965 Free PMC article.

4

Multiplex ligation-dependent probe amplification and fluorescence in situ hybridization to detect chromosomal abnormalities in chronic lymphocytic leukemia: a comparative study.

Fabris S, Scarciolla O, Morabito F, Cifarelli RA, Dininno C, Cutrona G, Matis S, Recchia AG, Gentile M, Ciceri G, Ferrarini M, Ciancio A, Mannarella C, Neri A, Fragasso A. Fabris S, et al. Among authors: scarciolla o. Genes Chromosomes Cancer. 2011 Sep;50(9):726-34. doi: 10.1002/gcc.20894. Epub 2011 Jun 2. Genes Chromosomes Cancer. 2011. PMID: 21638517

5

Whorled hairless nevus of the scalp, linear hyperpigmentation, and telangiectatic nevi of the lower limbs: a novel variant of the "phacomatosis complex".

Castori M, Scarciolla O, Morlino S, Manente L, Biscaglia A, Fragasso A, Grammatico P. Castori M, et al. Among authors: scarciolla o. Am J Med Genet A. 2012 Feb;158A(2):445-9. doi: 10.1002/ajmg.a.34403. Epub 2012 Jan 13. Am J Med Genet A. 2012. PMID: 22247078

6

Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification.

Scarciolla O, Stuppia L, De Angelis MV, Murru S, Palka C, Giuliani R, Pace M, Di Muzio A, Torrente I, Morella A, Grammatico P, Giacanelli M, Rosatelli MC, Uncini A, Dallapiccola B. Scarciolla O, et al. Neurogenetics. 2006 Nov;7(4):269-76. doi: 10.1007/s10048-006-0051-3. Epub 2006 Jul 22. Neurogenetics. 2006. PMID: 16865356

7

Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA).

Gatta V, Scarciolla O, Gaspari AR, Palka C, De Angelis MV, Di Muzio A, Guanciali-Franchi P, Calabrese G, Uncini A, Stuppia L. Gatta V, et al. Among authors: scarciolla o. Hum Genet. 2005 Jun;117(1):92-8. doi: 10.1007/s00439-005-1270-7. Epub 2005 Apr 20. Hum Genet. 2005. PMID: 15841391

8

Multiplex ligation-dependent probe amplification assay for simultaneous detection of Parkinson's disease gene rearrangements.

Scarciolla O, Brancati F, Valente EM, Ferraris A, De Angelis MV, Valbonesi S, Garavaglia B, Uncini A, Palka G, Stuppia L, Dallapiccola B. Scarciolla O, et al. Mov Disord. 2007 Nov 15;22(15):2274-8. doi: 10.1002/mds.21532. Mov Disord. 2007. PMID: 17914726

9

A novel mutation of the IRF6 gene in an Italian family with Van der Woude syndrome.

Gatta V, Scarciolla O, Cupaioli M, Palka C, Chiesa PL, Stuppia L. Gatta V, et al. Among authors: scarciolla o. Mutat Res. 2004 Mar 22;547(1-2):49-53. doi: 10.1016/j.mrfmmm.2003.11.011. Mutat Res. 2004. PMID: 15013698

10

Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene.

Stuppia L, Gatta V, Scarciolla O, Antonucci I, Morizio E, Calabrese G, Palka G. Stuppia L, et al. Among authors: scarciolla o. Genomics. 2005 Feb;85(2):280-3. doi: 10.1016/j.ygeno.2004.10.015. Genomics. 2005. PMID: 15676287

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