Barone R - Search Results

1

CSF N-Glycoproteomics Using MALDI MS Techniques in Neurodegenerative Diseases.

Messina A, Palmigiano A, Bua RO, Romeo DA, Barone R, Sturiale L, Zappia M, Garozzo D. Messina A, et al. Among authors: barone r. Methods Mol Biol. 2019;2044:255-272. doi: 10.1007/978-1-4939-9706-0_16. Methods Mol Biol. 2019. PMID: 31432418

2

Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.

Sturiale L, Barone R, Fiumara A, Perez M, Zaffanello M, Sorge G, Pavone L, Tortorelli S, O'Brien JF, Jaeken J, Garozzo D. Sturiale L, et al. Among authors: barone r. Glycobiology. 2005 Dec;15(12):1268-76. doi: 10.1093/glycob/cwj021. Epub 2005 Jul 21. Glycobiology. 2005. PMID: 16037488

3

Borderline mental development in a congenital disorder of glycosylation (CDG) type Ia patient with multisystemic involvement (intermediate phenotype).

Barone R, Sturiale L, Fiumara A, Uziel G, Garozzo D, Jaeken J. Barone R, et al. J Inherit Metab Dis. 2007 Feb;30(1):107. doi: 10.1007/s10545-006-0486-6. Epub 2006 Dec 20. J Inherit Metab Dis. 2007. PMID: 17186415

4

Clinical phenotype correlates to glycoprotein phenotype in a sib pair with CDG-Ia.

Barone R, Sturiale L, Sofia V, Ignoto A, Fiumara A, Sorge G, Garozzo D, Zappia M. Barone R, et al. Am J Med Genet A. 2008 Aug 15;146A(16):2103-8. doi: 10.1002/ajmg.a.32446. Am J Med Genet A. 2008. PMID: 18629883

5

Multiplexed glycoproteomic analysis of glycosylation disorders by sequential yolk immunoglobulins immunoseparation and MALDI-TOF MS.

Sturiale L, Barone R, Palmigiano A, Ndosimao CN, Briones P, Adamowicz M, Jaeken J, Garozzo D. Sturiale L, et al. Among authors: barone r. Proteomics. 2008 Sep;8(18):3822-32. doi: 10.1002/pmic.200700496. Proteomics. 2008. PMID: 18712764

6

Mass spectrometry in the characterization of human genetic N-glycosylation defects.

Barone R, Sturiale L, Garozzo D. Barone R, et al. Mass Spectrom Rev. 2009 May-Jun;28(3):517-42. doi: 10.1002/mas.20201. Mass Spectrom Rev. 2009. PMID: 18844296

7

Secondary disorders of glycosylation in inborn errors of fructose metabolism.

Quintana E, Sturiale L, Montero R, Andrade F, Fernandez C, Couce ML, Barone R, Aldamiz-Echevarria L, Ribes A, Artuch R, Briones P. Quintana E, et al. Among authors: barone r. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S273-8. doi: 10.1007/s10545-009-1219-4. Epub 2009 Sep 20. J Inherit Metab Dis. 2009. PMID: 19768653

8

Outcome of psychiatric symptoms presenting at onset of multiple sclerosis: a retrospective study.

Lo Fermo S, Barone R, Patti F, Laisa P, Cavallaro TL, Nicoletti A, Zappia M. Lo Fermo S, et al. Among authors: barone r. Mult Scler. 2010 Jun;16(6):742-8. doi: 10.1177/1352458510365157. Epub 2010 Mar 29. Mult Scler. 2010. PMID: 20350959

9

The impact of mass spectrometry in the diagnosis of congenital disorders of glycosylation.

Sturiale L, Barone R, Garozzo D. Sturiale L, et al. Among authors: barone r. J Inherit Metab Dis. 2011 Aug;34(4):891-9. doi: 10.1007/s10545-011-9306-8. Epub 2011 Mar 8. J Inherit Metab Dis. 2011. PMID: 21384227 Review.

10

Sporadic motor neuron disease in a familial novel SOD1 mutation: incomplete penetrance or chance association?

Conforti FL, Barone R, Fermo SL, Giliberto C, Patti F, Gambardella A, Quattrone A, Zappia M. Conforti FL, et al. Among authors: barone r. Amyotroph Lateral Scler. 2011 May;12(3):220-2. doi: 10.3109/17482968.2010.545951. Amyotroph Lateral Scler. 2011. PMID: 21545237

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