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Items: 14

1.

Up-regulation of HIF-1α is associated with neuroprotective effects of agmatine against rotenone-induced toxicity in differentiated SH-SY5Y cells.

Ferlazzo N, Currò M, Giunta ML, Longo D, Rizzo V, Caccamo D, Ientile R.

Amino Acids. 2019 Jul 10. doi: 10.1007/s00726-019-02759-6. [Epub ahead of print]

PMID:
31292720
2.

Dysbiosis and Prematurity: Is There a Role for Probiotics?

Baldassarre ME, Di Mauro A, Capozza M, Rizzo V, Schettini F, Panza R, Laforgia N.

Nutrients. 2019 Jun 5;11(6). pii: E1273. doi: 10.3390/nu11061273.

3.

Weaning Time in Preterm Infants: An Audit of Italian Primary Care Paediatricians.

Baldassarre ME, Di Mauro A, Pedico A, Rizzo V, Capozza M, Meneghin F, Lista G, Laforgia N; Italian Society of Pediatrics (SIP), Italian Society of Neonatology (SIN), Italian Society of Pediatric Gastroenterology, Hepatology, and Nutrition (SIGENP) and Italian Federation of Paediatricians (FIMP).

Nutrients. 2018 May 15;10(5). pii: E616. doi: 10.3390/nu10050616.

4.

Dysautonomia as Onset Symptom of Myotonic Dystrophy Type 2.

Rossi S, Romano A, Modoni A, Perna F, Rizzo V, Santoro M, Monforte M, Pieroni M, Luigetti M, Pomponi MG, Silvestri G.

Eur Neurol. 2018;79(3-4):166-170. doi: 10.1159/000487508. Epub 2018 Mar 13.

PMID:
29533949
5.

Effectiveness and Safety of a Probiotic-Mixture for the Treatment of Infantile Colic: A Double-Blind, Randomized, Placebo-Controlled Clinical Trial with Fecal Real-Time PCR and NMR-Based Metabolomics Analysis.

Baldassarre ME, Di Mauro A, Tafuri S, Rizzo V, Gallone MS, Mastromarino P, Capobianco D, Laghi L, Zhu C, Capozza M, Laforgia N.

Nutrients. 2018 Feb 10;10(2). pii: E195. doi: 10.3390/nu10020195.

6.

Serial neuroimaging findings in a novel case of sporadic progressive ataxia and palatal tremor (PAPT).

Di Blasi C, Rizzo V, Di Lella G, Modoni A, Calcagni ML, Picciotti PM, Silvestri G.

J Neurol Sci. 2017 Aug 15;379:16-17. doi: 10.1016/j.jns.2017.05.031. Epub 2017 May 16. No abstract available.

PMID:
28716232
7.

Crude venom from nematocysts of Pelagia noctiluca (Cnidaria: Scyphozoa) elicits a sodium conductance in the plasma membrane of mammalian cells.

Morabito R, Costa R, Rizzo V, Remigante A, Nofziger C, La Spada G, Marino A, Paulmichl M, Dossena S.

Sci Rep. 2017 Jan 23;7:41065. doi: 10.1038/srep41065.

8.

Molecular Biology in Pediatric High-Grade Glioma: Impact on Prognosis and Treatment.

Rizzo D, Ruggiero A, Martini M, Rizzo V, Maurizi P, Riccardi R.

Biomed Res Int. 2015;2015:215135. doi: 10.1155/2015/215135. Epub 2015 Sep 13. Review.

9.

Aortic Intima-Media Thickness as an Early Marker of Atherosclerosis in Children With Inflammatory Bowel Disease.

Aloi M, Tromba L, Rizzo V, D'Arcangelo G, Dilillo A, Blasi S, Civitelli F, Kiltzanidi D, Redler A, Viola F.

J Pediatr Gastroenterol Nutr. 2015 Jul;61(1):41-6. doi: 10.1097/MPG.0000000000000771.

PMID:
26039941
10.

Presenting features and disease course of pediatric ulcerative colitis.

Aloi M, D'Arcangelo G, Pofi F, Vassallo F, Rizzo V, Nuti F, Di Nardo G, Pierdomenico M, Viola F, Cucchiara S.

J Crohns Colitis. 2013 Dec;7(11):e509-15. doi: 10.1016/j.crohns.2013.03.007. Epub 2013 Apr 11.

PMID:
23583691
11.

Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions.

Santoro M, Masciullo M, Pietrobono R, Conte G, Modoni A, Bianchi ML, Rizzo V, Pomponi MG, Tasca G, Neri G, Silvestri G.

J Neurol. 2013 May;260(5):1245-57. doi: 10.1007/s00415-012-6779-9. Epub 2012 Dec 23.

PMID:
23263591
12.

Somatic mosaicism in TPM2-related myopathy with nemaline rods and cap structures.

Tasca G, Fattori F, Ricci E, Monforte M, Rizzo V, Mercuri E, Bertini E, Silvestri G.

Acta Neuropathol. 2013 Jan;125(1):169-71. doi: 10.1007/s00401-012-1049-6. Epub 2012 Sep 27. No abstract available.

PMID:
23015096
13.

Lack of any cardiac involvement in a patient with Andersen-Tawil syndrome associated with the c.574A→G mutation in KCNJ2.

Modoni A, Bianchi ML, Vitulano N, Pagliarani S, Perna F, Sanna T, Rizzo V, Silvestri G.

Cardiology. 2011;120(4):200-3. doi: 10.1159/000335529. Epub 2012 Jan 26.

PMID:
22286118
14.

Loss of heterozygosity in acute leukemia: evidence of frequent submicroscopic deletions.

Agueli C, Basiricò R, Fabbiano F, Rizzo V, Cascio L, Cammarata G, Marfia A, La Rosa M, Mirto S, Santoro A.

Haematologica. 2007 May;92(5):678-81.

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