Gallo O - Search Results

1

MALDI-ISD mass spectrometry analysis as a simple and reliable tool to detect post-translational modifications of hemoglobin variants: the case of Hb Raleigh.

De Benedittis S, Spadafora P, Gaspari M, Qualtieri G, Gallo O, Di Palma G, Cavalcanti F, Citrigno L, Qualtieri A. De Benedittis S, et al. Among authors: gallo o. Clin Chem Lab Med. 2023 Jun 12;61(12):e251-e254. doi: 10.1515/cclm-2023-0442. Print 2023 Nov 27. Clin Chem Lab Med. 2023. PMID: 37307396 No abstract available.

2

A Novel Homozygous Variant in DYSF Gene Is Associated with Autosomal Recessive Limb Girdle Muscular Dystrophy R2/2B.

Spadafora P, Qualtieri A, Cavalcanti F, Di Palma G, Gallo O, De Benedittis S, Cerantonio A, Citrigno L. Spadafora P, et al. Among authors: gallo o. Int J Mol Sci. 2022 Aug 11;23(16):8932. doi: 10.3390/ijms23168932. Int J Mol Sci. 2022. PMID: 36012197 Free PMC article.

3

Genomics landscape of mitochondrial DNA variations in patients from South Italy affected by mitochondriopathies.

Citrigno L, Qualtieri A, Cerantonio A, De Benedittis S, Gallo O, Di Palma G, Spadafora P, Cavalcanti F. Citrigno L, et al. Among authors: gallo o. J Neurol Sci. 2024 Feb 15;457:122869. doi: 10.1016/j.jns.2024.122869. Epub 2024 Jan 6. J Neurol Sci. 2024. PMID: 38215527 Free article.

4

Molecular Study of the Fukutin-Related Protein (FKRP) Gene in Patients from Southern Italy with Duchenne/Becker-like Phenotype.

Qualtieri A, De Benedittis S, Cerantonio A, Citrigno L, Di Palma G, Gallo O, Cavalcanti F, Spadafora P. Qualtieri A, et al. Among authors: gallo o. Int J Mol Sci. 2024 Sep 26;25(19):10356. doi: 10.3390/ijms251910356. Int J Mol Sci. 2024. PMID: 39408683 Free PMC article.

5

An magnetic resonance imaging T2*-weighted sequence at short echo time to detect putaminal hypointensity in Parkinsonisms.

Arabia G, Morelli M, Paglionico S, Novellino F, Salsone M, Giofrè L, Torchia G, Nicoletti G, Messina D, Condino F, Lanza P, Gallo O, Quattrone A. Arabia G, et al. Among authors: gallo o. Mov Disord. 2010 Dec 15;25(16):2728-34. doi: 10.1002/mds.23173. Mov Disord. 2010. PMID: 20925073

6

Accuracy of magnetic resonance parkinsonism index for differentiation of progressive supranuclear palsy from probable or possible Parkinson disease.

Morelli M, Arabia G, Salsone M, Novellino F, Giofrè L, Paletta R, Messina D, Nicoletti G, Condino F, Gallo O, Lanza P, Quattrone A. Morelli M, et al. Among authors: gallo o. Mov Disord. 2011 Feb 15;26(3):527-33. doi: 10.1002/mds.23529. Epub 2011 Feb 1. Mov Disord. 2011. PMID: 21287599

7

Cognitive deficits in multiple sclerosis patients with cerebellar symptoms.

Valentino P, Cerasa A, Chiriaco C, Nisticò R, Pirritano D, Gioia M, Lanza P, Canino M, Del Giudice F, Gallo O, Condino F, Torchia G, Quattrone A. Valentino P, et al. Among authors: gallo o. Mult Scler. 2009 Jul;15(7):854-9. doi: 10.1177/1352458509104589. Mult Scler. 2009. PMID: 19542264

8

Comparison of different MR venography techniques for detecting transverse sinus stenosis in idiopathic intracranial hypertension.

Fera F, Bono F, Messina D, Gallo O, Lanza PL, Auteri W, Nicoletti G, Santoro G, Quattrone A. Fera F, et al. Among authors: gallo o. J Neurol. 2005 Sep;252(9):1021-5. doi: 10.1007/s00415-005-0710-6. Epub 2005 Mar 7. J Neurol. 2005. PMID: 15742111

9

MR imaging of middle cerebellar peduncle width: differentiation of multiple system atrophy from Parkinson disease.

Nicoletti G, Fera F, Condino F, Auteri W, Gallo O, Pugliese P, Arabia G, Morgante L, Barone P, Zappia M, Quattrone A. Nicoletti G, et al. Among authors: gallo o. Radiology. 2006 Jun;239(3):825-30. doi: 10.1148/radiol.2393050459. Radiology. 2006. PMID: 16714464

10

Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man.

La Russa A, Cittadella R, Andreoli V, Valentino P, Trecroci F, Caracciolo M, Gallo O, Gambardella A, Quattrone A. La Russa A, et al. Among authors: gallo o. Mult Scler. 2011 Jun;17(6):763-6. doi: 10.1177/1352458511404033. Mult Scler. 2011. PMID: 21685233

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