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Page 1
[Role of inflammation mediators in the pathogenesis of heart failure].
Boglioni FV, Metra M, Locati M, Nodari S, Bontempi L, Garbellini M, Doni A, Peri G, Mantovani A. Boglioni FV, et al. Among authors: garbellini m. Ital Heart J Suppl. 2001 Jun;2(6):628-33. Ital Heart J Suppl. 2001. PMID: 11460836 Review. Italian.
Maximal and submaximal exercise testing in heart failure.
Metra M, Nodari S, Raccagni D, Garbellini M, Boldi E, Bontempi L, Gaiti M, Dei Cas L. Metra M, et al. Among authors: garbellini m. J Cardiovasc Pharmacol. 1998;32 Suppl 1:S36-45. doi: 10.1097/00005344-199800003-00007. J Cardiovasc Pharmacol. 1998. PMID: 9731694 Review.
Cardiac resynchronisation therapy for advanced heart failure.
Oliva F, Frigerio M, Lunati M, Turazza FM, Cattafi G, Paolucci M, Garascia A, Garbellini M, Magenta G, Vicini I, Vitali E, Perego GB. Oliva F, et al. Among authors: garbellini m. J Heart Lung Transplant. 2001 Feb;20(2):216. doi: 10.1016/s1053-2498(00)00472-1. J Heart Lung Transplant. 2001. PMID: 11250399 No abstract available.
Mitochondrial Dysregulation and Impaired Autophagy in iPSC-Derived Dopaminergic Neurons of Multiple System Atrophy.
Monzio Compagnoni G, Kleiner G, Samarani M, Aureli M, Faustini G, Bellucci A, Ronchi D, Bordoni A, Garbellini M, Salani S, Fortunato F, Frattini E, Abati E, Bergamini C, Fato R, Tabano S, Miozzo M, Serratto G, Passafaro M, Deleidi M, Silipigni R, Nizzardo M, Bresolin N, Comi GP, Corti S, Quinzii CM, Di Fonzo A. Monzio Compagnoni G, et al. Among authors: garbellini m. Stem Cell Reports. 2018 Nov 13;11(5):1185-1198. doi: 10.1016/j.stemcr.2018.09.007. Epub 2018 Oct 18. Stem Cell Reports. 2018. PMID: 30344007 Free PMC article.
A Novel Homozygous VPS11 Variant May Cause Generalized Dystonia.
Monfrini E, Cogiamanian F, Salani S, Straniero L, Fagiolari G, Garbellini M, Carsana E, Borellini L, Biella F, Moggio M, Bresolin N, Corti S, Duga S, Comi GP, Aureli M, Di Fonzo A. Monfrini E, et al. Among authors: garbellini m. Ann Neurol. 2021 Apr;89(4):834-839. doi: 10.1002/ana.26021. Epub 2021 Feb 2. Ann Neurol. 2021. PMID: 33452836 Free PMC article.
Late-onset leukoencephalopathy in a patient with recessive EARS2 mutations.
Monfrini E, Ronchi D, Franco G, Garbellini M, Straniero L, Scola E, Arienti F, Duga S, Comi GP, Bresolin N, Di Fonzo A. Monfrini E, et al. Among authors: garbellini m. Neurol Genet. 2020 Jul 13;6(5):e488. doi: 10.1212/NXG.0000000000000488. eCollection 2020 Oct. Neurol Genet. 2020. PMID: 32802952 Free PMC article. No abstract available.
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