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Items: 19

1.

The Autophagy Signaling Pathway: A Potential Multifunctional Therapeutic Target of Curcumin in Neurological and Neuromuscular Diseases.

Perrone L, Squillaro T, Napolitano F, Terracciano C, Sampaolo S, Melone MAB.

Nutrients. 2019 Aug 13;11(8). pii: E1881. doi: 10.3390/nu11081881. Review.

2.

Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders.

Giugliano T, Santoro C, Torella A, Del Vecchio Blanco F, Grandone A, Onore ME, Melone MAB, Straccia G, Melis D, Piccolo V, Limongelli G, Buono S, Perrotta S, Nigro V, Piluso G.

Genes (Basel). 2019 Jul 31;10(8). pii: E580. doi: 10.3390/genes10080580.

3.

Senescence Phenomena and Metabolic Alteration in Mesenchymal Stromal Cells from a Mouse Model of Rett Syndrome.

Squillaro T, Alessio N, Capasso S, Di Bernardo G, Melone MAB, Peluso G, Galderisi U.

Int J Mol Sci. 2019 May 21;20(10). pii: E2508. doi: 10.3390/ijms20102508.

4.

A rapid, safe, and quantitative in vitro assay for measurement of uracil-DNA glycosylase activity.

Squillaro T, Finicelli M, Alessio N, Del Gaudio S, Di Bernardo G, Melone MAB, Peluso G, Galderisi U.

J Mol Med (Berl). 2019 Jul;97(7):991-1001. doi: 10.1007/s00109-019-01788-8. Epub 2019 May 1.

PMID:
31041464
5.

Early posterior vitreous detachment is associated with LAMA5 dominant mutation.

Napolitano F, Di Iorio V, Di Iorio G, Melone MAB, Gianfrancesco F, Simonelli F, Esposito T, Testa F, Sampaolo S.

Ophthalmic Genet. 2019 Feb;40(1):39-42. doi: 10.1080/13816810.2018.1558261. Epub 2018 Dec 27.

PMID:
30589377
6.

Neuro-Behçet's disease presenting as an isolated progressive cognitive and behavioral syndrome.

Saracino D, Allegorico L, Barbarulo AM, Pollo B, Giaccone G, D'Amico A, D'Incerti L, Bugiani O, Di Iorio G, Sampaolo S, Melone MAB.

Neurocase. 2018 Oct - Dec;24(5-6):238-241. doi: 10.1080/13554794.2018.1561898. Epub 2018 Dec 25.

PMID:
30583716
7.

Meldonium improves Huntington's disease mitochondrial dysfunction by restoring peroxisome proliferator-activated receptor γ coactivator 1α expression.

Di Cristo F, Finicelli M, Digilio FA, Paladino S, Valentino A, Scialò F, D'Apolito M, Saturnino C, Galderisi U, Giordano A, Melone MAB, Peluso G.

J Cell Physiol. 2019 Jun;234(6):9233-9246. doi: 10.1002/jcp.27602. Epub 2018 Oct 26.

PMID:
30362565
8.

Metabolic syndrome, Mediterranean diet, and polyphenols: Evidence and perspectives.

Finicelli M, Squillaro T, Di Cristo F, Di Salle A, Melone MAB, Galderisi U, Peluso G.

J Cell Physiol. 2019 May;234(5):5807-5826. doi: 10.1002/jcp.27506. Epub 2018 Oct 14. Review.

PMID:
30317573
9.

Neurofibromatous neuropathy: An ultrastructural study.

Terracciano C, Pachatz C, Rastelli E, Pastore FS, Melone MAB, Massa R.

Ultrastruct Pathol. 2018 May-Jun;42(3):312-316. doi: 10.1080/01913123.2018.1454562. Epub 2018 Mar 27.

PMID:
29583067
10.

Successful long-term therapy with flecainide in a family with paramyotonia congenita.

Terracciano C, Farina O, Esposito T, Lombardi L, Napolitano F, Blasiis P, Ciccone G, Todisco V, Tuccillo F, Bernardini S, Di Iorio G, Melone MAB, Sampaolo S.

J Neurol Neurosurg Psychiatry. 2018 Nov;89(11):1232-1234. doi: 10.1136/jnnp-2017-317615. Epub 2018 Feb 27. No abstract available.

PMID:
29487168
11.

The carnitine system and cancer metabolic plasticity.

Melone MAB, Valentino A, Margarucci S, Galderisi U, Giordano A, Peluso G.

Cell Death Dis. 2018 Feb 14;9(2):228. doi: 10.1038/s41419-018-0313-7. Review.

12.

Verapamil Inhibits Ser202/Thr205 Phosphorylation of Tau by Blocking TXNIP/ROS/p38 MAPK Pathway.

Melone MAB, Dato C, Paladino S, Coppola C, Trebini C, Giordana MT, Perrone L.

Pharm Res. 2018 Feb 5;35(2):44. doi: 10.1007/s11095-017-2276-2.

PMID:
29404777
13.

Synergistic Interplay between Curcumin and Polyphenol-Rich Foods in the Mediterranean Diet: Therapeutic Prospects for Neurofibromatosis 1 Patients.

Esposito T, Schettino C, Polverino P, Allocca S, Adelfi L, D'Amico A, Capaldo G, Varriale B, Di Salle A, Peluso G, Sorrentino G, Lus G, Sampaolo S, Di Iorio G, Melone MAB.

Nutrients. 2017 Jul 21;9(7). pii: E783. doi: 10.3390/nu9070783.

14.

Identification of the first dominant mutation of LAMA5 gene causing a complex multisystem syndrome due to dysfunction of the extracellular matrix.

Sampaolo S, Napolitano F, Tirozzi A, Reccia MG, Lombardi L, Farina O, Barra A, Cirillo F, Melone MAB, Gianfrancesco F, Iorio GD, Esposito T.

J Med Genet. 2017 Oct;54(10):710-720. doi: 10.1136/jmedgenet-2017-104555. Epub 2017 Jul 22.

PMID:
28735299
15.

First study on the peptidergic innervation of the brain superior sagittal sinus in humans.

Sampaolo S, Liguori G, Vittoria A, Napolitano F, Lombardi L, Figols J, Melone MAB, Esposito T, Di Iorio G.

Neuropeptides. 2017 Oct;65:45-55. doi: 10.1016/j.npep.2017.04.008. Epub 2017 Apr 24.

16.

Impact of lysosomal storage disorders on biology of mesenchymal stem cells: Evidences from in vitro silencing of glucocerebrosidase (GBA) and alpha-galactosidase A (GLA) enzymes.

Squillaro T, Antonucci I, Alessio N, Esposito A, Cipollaro M, Melone MAB, Peluso G, Stuppia L, Galderisi U.

J Cell Physiol. 2017 Dec;232(12):3454-3467. doi: 10.1002/jcp.25807. Epub 2017 Feb 7.

PMID:
28098348
17.

Reduced expression of MECP2 affects cell commitment and maintenance in neurons by triggering senescence: new perspective for Rett syndrome.

Squillaro T, Alessio N, Cipollaro M, Melone MA, Hayek G, Renieri A, Giordano A, Galderisi U.

Mol Biol Cell. 2012 Apr;23(8):1435-45. doi: 10.1091/mbc.E11-09-0784. Epub 2012 Feb 22.

18.

Differential carnitine/acylcarnitine translocase expression defines distinct metabolic signatures in skeletal muscle cells.

Peluso G, Petillo O, Margarucci S, Grippo P, Melone MA, Tuccillo F, Calvani M.

J Cell Physiol. 2005 May;203(2):439-46.

PMID:
15515015
19.

Decreased mitochondrial carnitine translocase in skeletal muscles impairs utilization of fatty acids in insulin-resistant patients.

Peluso G, Petillo O, Margarucci S, Mingrone G, Greco AV, Indiveri C, Palmieri F, Melone MA, Reda E, Calvani M.

Front Biosci. 2002 May 1;7:a109-16.

PMID:
11991847

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