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Items: 1 to 20 of 23

1.

The Endocannabinoid/Endovanilloid System in Bone: From Osteoporosis to Osteosarcoma.

Rossi F, Tortora C, Punzo F, Bellini G, Argenziano M, Di Paola A, Torella M, Perrotta S.

Int J Mol Sci. 2019 Apr 18;20(8). pii: E1919. doi: 10.3390/ijms20081919. Review.

2.

CB2 Receptor Stimulation and Dexamethasone Restore the Anti-Inflammatory and Immune-Regulatory Properties of Mesenchymal Stromal Cells of Children with Immune Thrombocytopenia.

Rossi F, Tortora C, Palumbo G, Punzo F, Argenziano M, Casale M, Di Paola A, Locatelli F, Perrotta S.

Int J Mol Sci. 2019 Feb 28;20(5). pii: E1049. doi: 10.3390/ijms20051049.

3.

Iron chelating properties of Eltrombopag: Investigating its role in thalassemia-induced osteoporosis.

Punzo F, Tortora C, Argenziano M, Casale M, Perrotta S, Rossi F.

PLoS One. 2018 Dec 3;13(12):e0208102. doi: 10.1371/journal.pone.0208102. eCollection 2018.

4.

Bortezomib and endocannabinoid/endovanilloid system: a synergism in osteosarcoma.

Punzo F, Tortora C, Di Pinto D, Pota E, Argenziano M, Di Paola A, Casale F, Rossi F.

Pharmacol Res. 2018 Nov;137:25-33. doi: 10.1016/j.phrs.2018.09.017. Epub 2018 Sep 26.

PMID:
30267762
5.

Association between 14 bp insertion/deletion HLA-G functional polymorphism and insulin resistance in a cohort of Italian children with obesity.

Marzuillo P, Bellini G, Punzo F, Di Sessa A, Guarino S, Umano GR, Toraldo R, Miraglia Del Giudice E, Rossi F.

Pediatr Diabetes. 2018 Dec;19(8):1357-1361. doi: 10.1111/pedi.12768. Epub 2018 Sep 25.

PMID:
30203576
6.

Role of Cannabinoids in Obesity.

Rossi F, Punzo F, Umano GR, Argenziano M, Miraglia Del Giudice E.

Int J Mol Sci. 2018 Sep 10;19(9). pii: E2690. doi: 10.3390/ijms19092690. Review.

7.

Effects of CB2 and TRPV1 receptors' stimulation in pediatric acute T-lymphoblastic leukemia.

Punzo F, Manzo I, Tortora C, Pota E, Angelo V, Bellini G, Di Paola A, Verace F, Casale F, Rossi F.

Oncotarget. 2018 Apr 20;9(30):21244-21258. doi: 10.18632/oncotarget.25052. eCollection 2018 Apr 20.

8.

The DMT1 IVS4+44C>A polymorphism and the risk of iron deficiency anemia in children with celiac disease.

Tolone C, Bellini G, Punzo F, Papparella A, Miele E, Vitale A, Nobili B, Strisciuglio C, Rossi F.

PLoS One. 2017 Oct 12;12(10):e0185822. doi: 10.1371/journal.pone.0185822. eCollection 2017.

9.

Anti-proliferative, pro-apoptotic and anti-invasive effect of EC/EV system in human osteosarcoma.

Punzo F, Tortora C, Di Pinto D, Manzo I, Bellini G, Casale F, Rossi F.

Oncotarget. 2017 Apr 13;8(33):54459-54471. doi: 10.18632/oncotarget.17089. eCollection 2017 Aug 15.

10.

Cannabinoid receptor 2-63 RR variant is independently associated with severe necroinflammation in HIV/HCV coinfected patients.

Sagnelli C, Uberti-Foppa C, Hasson H, Bellini G, Minichini C, Salpietro S, Messina E, Barbanotti D, Merli M, Punzo F, Coppola N, Lazzarin A, Sagnelli E, Rossi F.

PLoS One. 2017 Jul 31;12(7):e0181890. doi: 10.1371/journal.pone.0181890. eCollection 2017.

11.

The Role of Mifamurtide in Chemotherapy-induced Osteoporosis of Children with Osteosarcoma.

Bellini G, Di Pinto D, Tortora C, Manzo I, Punzo F, Casale F, Rossi F.

Curr Cancer Drug Targets. 2017;17(7):650-656. doi: 10.2174/1568009616666161215163426.

PMID:
27993113
12.

PKCβII-mediated cross-talk of TRPV1/CB2 modulates the glucocorticoid-induced osteoclast overactivity.

Bellini G, Torella M, Manzo I, Tortora C, Luongo L, Punzo F, Colacurci N, Nobili B, Maione S, Rossi F.

Pharmacol Res. 2017 Jan;115:267-274. doi: 10.1016/j.phrs.2016.11.039. Epub 2016 Dec 2.

PMID:
27919827
13.

Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range.

Perrotta S, Stiehl DP, Punzo F, Scianguetta S, Borriello A, Bencivenga D, Casale M, Nobili B, Fasoli S, Balduzzi A, Cro L, Nytko KJ, Wenger RH, Della Ragione F.

Haematologica. 2013 Oct;98(10):1624-32. doi: 10.3324/haematol.2013.088369. Epub 2013 May 28.

14.

Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease.

Quadri M, Federico A, Zhao T, Breedveld GJ, Battisti C, Delnooz C, Severijnen LA, Di Toro Mammarella L, Mignarri A, Monti L, Sanna A, Lu P, Punzo F, Cossu G, Willemsen R, Rasi F, Oostra BA, van de Warrenburg BP, Bonifati V.

Am J Hum Genet. 2012 Mar 9;90(3):467-77. doi: 10.1016/j.ajhg.2012.01.017. Epub 2012 Feb 16.

15.

Congenital dyserythropoietic anemia type II: molecular analysis and expression of the SEC23B gene.

Punzo F, Bertoli-Avella AM, Scianguetta S, Della Ragione F, Casale M, Ronzoni L, Cappellini MD, Forni G, Oostra BA, Perrotta S.

Orphanet J Rare Dis. 2011 Dec 30;6:89. doi: 10.1186/1750-1172-6-89.

16.

CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura.

Rossi F, Mancusi S, Bellini G, Roberti D, Punzo F, Vetrella S, Matarese SM, Nobili B, Maione S, Perrotta S.

Haematologica. 2011 Dec;96(12):1883-5. doi: 10.3324/haematol.2011.045732. Epub 2011 Aug 9.

17.

Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.

Noris P, Perrotta S, Seri M, Pecci A, Gnan C, Loffredo G, Pujol-Moix N, Zecca M, Scognamiglio F, De Rocco D, Punzo F, Melazzini F, Scianguetta S, Casale M, Marconi C, Pippucci T, Amendola G, Notarangelo LD, Klersy C, Civaschi E, Balduini CL, Savoia A.

Blood. 2011 Jun 16;117(24):6673-80. doi: 10.1182/blood-2011-02-336537. Epub 2011 Apr 5.

18.

Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2.

Pippucci T, Savoia A, Perrotta S, Pujol-Moix N, Noris P, Castegnaro G, Pecci A, Gnan C, Punzo F, Marconi C, Gherardi S, Loffredo G, De Rocco D, Scianguetta S, Barozzi S, Magini P, Bozzi V, Dezzani L, Di Stazio M, Ferraro M, Perini G, Seri M, Balduini CL.

Am J Hum Genet. 2011 Jan 7;88(1):115-20. doi: 10.1016/j.ajhg.2010.12.006.

19.

Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability.

Santoro L, Breedveld GJ, Manganelli F, Iodice R, Pisciotta C, Nolano M, Punzo F, Quarantelli M, Pappatà S, Di Fonzo A, Oostra BA, Bonifati V.

Neurogenetics. 2011 Feb;12(1):33-9. doi: 10.1007/s10048-010-0259-0. Epub 2010 Sep 21.

20.

Absence of CYCS mutations in a large Italian cohort of patients with inherited thrombocytopenias of unknown origin.

Savoia A, Noris P, Perrotta S, Punzo F, Rocco DD, Oostra BA, Balduini CL.

Platelets. 2009 Feb;20(1):72-3. doi: 10.1080/09537100802485129. No abstract available.

PMID:
19172527

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