BASSI, MARIA TERESA

BASSI, MARIA TERESA  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Aberrant supracallosal longitudinal bundle : MR features, pathogenesis and associated clinical phenotype 2016 Arrigoni F.Bassi M. T.Triulzi F. + Article (author) -
Acid sphingomyelinase controls early phases of skeletal muscle regeneration by shaping the macrophage phenotype 2021 Roux-Biejat P.Coazzoli M.Zecchini S.Di Renzo I.Napoli A.Moscheni C.Giovarelli M.Bassi M. T.De Palma C.Clementi E.Perrotta C. + Article (author) -
Autophagy controls neonatal myogenesis by regulating the GH-IGF1 system through a NFE2L2- and DDIT3-mediated mechanism 2019 Zecchini SGiovarelli MPerrotta CMorisi FDi Renzo IMoscheni CBassi MTClementi EDe Palma C + Article (author) -
Case Reports: Novel Missense Variants in the Filamin C Actin Binding Domain Cause Variable Phenotypes 2022 D'Angelo, Maria GraziaNapoli, LauraCinnante, ClaudiaComi, Giacomo PietroRonchi, DarioBassi, Maria Teresa + Article (author) -
Cerebroretinal microangiopathy with calcifications and cysts associated with CTC1 and NDP mutations 2013 Arrigoni F.Citterio A.Tonelli A.Triulzi F.Bassi M. T. + Article (author) -
Clinical and genetic features of a cohort of patients with MFN2-related neuropathy 2022 Abati E.Manini A.Del Bo R.Rizzo F.Bresolin N.Bellone E.Bassi M. T.D'Angelo M. G.Comi G. P.Corti S. + Article (author) -
Deficient nitric oxide signalling impairs skeletal muscle growth and performance : involvement of mitochondrial dysregulation 2014 C. De PalmaF. MorisiS. PambiancoE. AssiS. RussoC. PerrottaV. CappelloP. PellegrinoC. MoscheniM.T. BassiE. Clementi + Article (author) -
The emerging role of acid sphingomyelinase in autophagy 2015 C. PerrottaC. De PalmaE. AssiP. PellegrinoM.T. BassiE. Clementi + Article (author) -
The Fine Tuning of Drp1-Dependent Mitochondrial Remodeling and Autophagy Controls Neuronal Differentiation 2019 Giovarelli, MatteoBassi, Maria TeresaClementi, EmilioDe Palma, Clara + Article (author) -
The role of clinical and neuroimaging features in the diagnosis of CADASIL 2018 Vitali, PaoloSasanelli, FrancescoComi, GiancarloSilani, VincenzoMeola, GiovanniComi, Giacomo PietroCorti, StefaniaRonchi, DarioBassi, Maria Teresa + Article (author) -
The spectrum of brainstem malformations associated to mutations of the tubulin genes family : MRI and DTI analysis 2019 Arrigoni F.Bassi M. T.Triulzi F. + Article (author) -
ZFYVE26/SPASTIZIN : a close link between complicated hereditary spastic paraparesis and autophagy 2014 E. ClementiM.T. Bassi + Article (author) -
ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis 2018 Scarlato MClementi EBassi MT + Article (author) -