Barone R - Search Results

1

Electroclinical features of a patient with GLUT1 deficiency syndrome and adult onset periodic weakness.

Giliberto C, Reggio E, Sofia V, Giuliano L, Lo Fermo S, Barone R, Zappia M. Giliberto C, et al. Among authors: barone r. Eur J Neurol. 2016 Jan;23(1):e1-3. doi: 10.1111/ene.12831. Eur J Neurol. 2016. PMID: 26768679 No abstract available.

2

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

3

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

4

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

5

Glycomics of pediatric and adulthood diseases of the central nervous system.

Barone R, Sturiale L, Palmigiano A, Zappia M, Garozzo D. Barone R, et al. J Proteomics. 2012 Sep 18;75(17):5123-39. doi: 10.1016/j.jprot.2012.07.007. Epub 2012 Jul 16. J Proteomics. 2012. PMID: 22813883 Review.

6

Report of two never treated adult sisters with aromatic L-amino Acid decarboxylase deficiency: a portrait of the natural history of the disease or an expanding phenotype?

Leuzzi V, Mastrangelo M, Polizzi A, Artiola C, van Kuilenburg AB, Carducci C, Ruggieri M, Barone R, Tavazzi B, Abeling NG, Zoetekouw L, Sofia V, Zappia M, Carducci C. Leuzzi V, et al. Among authors: barone r. JIMD Rep. 2015;15:39-45. doi: 10.1007/8904_2014_295. Epub 2014 May 1. JIMD Rep. 2015. PMID: 24788355 Free PMC article.

7

CSF N-glycan profile reveals sialylation deficiency in a patient with GM2 gangliosidosis presenting as childhood disintegrative disorder.

Barone R, Sturiale L, Fiumara A, Palmigiano A, Bua RO, Rizzo R, Zappia M, Garozzo D. Barone R, et al. Autism Res. 2016 Apr;9(4):423-8. doi: 10.1002/aur.1541. Epub 2015 Aug 19. Autism Res. 2016. PMID: 26286102

8

CSF N-glycoproteomics for early diagnosis in Alzheimer's disease.

Palmigiano A, Barone R, Sturiale L, Sanfilippo C, Bua RO, Romeo DA, Messina A, Capuana ML, Maci T, Le Pira F, Zappia M, Garozzo D. Palmigiano A, et al. Among authors: barone r. J Proteomics. 2016 Jan 10;131:29-37. doi: 10.1016/j.jprot.2015.10.006. Epub 2015 Oct 9. J Proteomics. 2016. PMID: 26455811

9

CSF N-Glycomics Using MALDI MS Techniques in Alzheimer's Disease.

Palmigiano A, Messina A, Bua RO, Barone R, Sturiale L, Zappia M, Garozzo D. Palmigiano A, et al. Among authors: barone r. Methods Mol Biol. 2018;1750:75-91. doi: 10.1007/978-1-4939-7704-8_5. Methods Mol Biol. 2018. PMID: 29512066

10

Hyperkinetic movement disorders in congenital disorders of glycosylation.

Mostile G, Barone R, Nicoletti A, Rizzo R, Martinelli D, Sturiale L, Fiumara A, Jankovic J, Zappia M. Mostile G, et al. Among authors: barone r. Eur J Neurol. 2019 Sep;26(9):1226-1234. doi: 10.1111/ene.14007. Epub 2019 Jun 21. Eur J Neurol. 2019. PMID: 31132195

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