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Can Digital Technologies Be Useful for Weight Loss in Individuals with Overweight or Obesity? A Systematic Review.
Protano C, De Giorgi A, Valeriani F, Mazzeo E, Zanni S, Cofone L, D'Ancona G, Hasnaoui A, Pindinello I, Sabato M, Ubaldi F, Volpini V, Romano Spica V, Vitali M, Gallè F. Protano C, et al. Among authors: volpini v. Healthcare (Basel). 2024 Mar 16;12(6):670. doi: 10.3390/healthcare12060670. Healthcare (Basel). 2024. PMID: 38540634 Free PMC article. Review.
New spinocerebellar ataxia subtype caused by SAMD9L mutation triggering mitochondrial dysregulation (SCA49).
Corral-Juan M, Casquero P, Giraldo-Restrepo N, Laurie S, Martinez-Piñeiro A, Mateo-Montero RC, Ispierto L, Vilas D, Tolosa E, Volpini V, Alvarez-Ramo R, Sánchez I, Matilla-Dueñas A. Corral-Juan M, et al. Among authors: volpini v. Brain Commun. 2022 Feb 10;4(2):fcac030. doi: 10.1093/braincomms/fcac030. eCollection 2022. Brain Commun. 2022. PMID: 35310830 Free PMC article.
A clinical report of the massive CAG repeat expansion in spinocerebellar ataxia type 2: Severe onset in a Mexican child and review previous cases.
Sánchez-Corona J, Ramirez-Garcia SA, Castañeda-Cisneros G, Gutiérrez-Rubio SA, Volpini V, Sánchez-Garcia DM, García-Ortiz JE, García-Cruz D. Sánchez-Corona J, et al. Among authors: volpini v. Genet Mol Biol. 2020 Aug 21;43(3):e20190325. doi: 10.1590/1678-4685-gmb-2019-0325. Genet Mol Biol. 2020. PMID: 32870233 Free PMC article.
Spinocerebellar Ataxia Type 37.
Matilla-Dueñas A, Volpini V. Matilla-Dueñas A, et al. Among authors: volpini v. 2019 May 30. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2019 May 30. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 31145571 Free Books & Documents. Review.
Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48).
Genis D, Ortega-Cubero S, San Nicolás H, Corral J, Gardenyes J, de Jorge L, López E, Campos B, Lorenzo E, Tonda R, Beltran S, Negre M, Obón M, Beltran B, Fàbregas L, Alemany B, Márquez F, Ramió-Torrentà L, Gich J, Volpini V, Pastor P. Genis D, et al. Among authors: volpini v. Neurology. 2018 Nov 20;91(21):e1988-e1998. doi: 10.1212/WNL.0000000000006550. Epub 2018 Oct 31. Neurology. 2018. PMID: 30381368
Clinical, genetic and neuropathological characterization of spinocerebellar ataxia type 37.
Corral-Juan M, Serrano-Munuera C, Rábano A, Cota-González D, Segarra-Roca A, Ispierto L, Cano-Orgaz AT, Adarmes AD, Méndez-Del-Barrio C, Jesús S, Mir P, Volpini V, Alvarez-Ramo R, Sánchez I, Matilla-Dueñas A. Corral-Juan M, et al. Among authors: volpini v. Brain. 2018 Jul 1;141(7):1981-1997. doi: 10.1093/brain/awy137. Brain. 2018. PMID: 29939198 Free article.
Treatment with escitalopram modulates cardiovascular function in rats.
Veríssimo LF, Volpini VL, Estrada VB, Matsubara NK, Gomes MV, Resstel LBM, Correa FMA, Pelosi GG. Veríssimo LF, et al. Among authors: volpini vl. Eur J Pharmacol. 2018 Apr 5;824:120-127. doi: 10.1016/j.ejphar.2018.02.003. Epub 2018 Feb 8. Eur J Pharmacol. 2018. PMID: 29428469
107 results