D. Dolcetta

发表

Restoration of the GM2 Ganglioside Metabolism in Bone Marrow–Derived Stromal Cells from Tay-Sachs Disease Animal Model

M. G. Cusella De Angelis, A. Orlacchio, C. Emiliani, 2002, Neurochemical Research.

TFEB activation restores migration ability to Tsc1-deficient adult neural stem/progenitor cells

T. Cassano, C. Emiliani, S. Giovagnoli, 2017, Human molecular genetics.

Quantitative Evaluation of the Clinical Effects of S-Adenosylmethionine on Mood and Behavior in Lesch-Nyhan Patients

L. Salmaso, W. Nyhan, D. Dolcetta, 2013, Nucleosides, nucleotides & nucleic acids.

Analysis of the HPRT1 gene in 35 Italian Lesch-Nyhan families: 45 patients and 77 potential female carriers.

W. Nyhan, E. Fortunati, L. Fairbanks, 2010, Mutation research.

Specific treatment of Prader–Willi syndrome through cyclical rehabilitation programmes

D. Dolcetta, P. Parmigiani, Roberta Bernardelle, 2011, Disability and rehabilitation.

P. Gasparini, T. Nutile, M. Ciullo, 2009, International journal of audiology.

Myelin deterioration in Twitcher mice: Motor evoked potentials and magnetic resonance imaging as in vivo monitoring tools

E. Bongarzone, F. Galbiati, S. Amadio, 2005, Journal of neuroscience research.

A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood

N. Bresolin, C. Zucca, G. Casari, 2004, Journal of Medical Genetics.

The therapeutic potential of neural stem/progenitor cells in murine globoid cell leukodystrophy is conditioned by macrophage/microglia activation

G. Finocchiaro, S. Pellegatta, P. L. Poliani, 2006, Neurobiology of Disease.

In vitro treatment of congenital disorder of glycosylation type Ia using PLGA nanoparticles loaded with GDP‑Man.

B. Ruozi, G. Tosi, G. M. Severini, 2019, International journal of molecular medicine.

TO JMG A novel mutation in the ATP 1 A 2 gene causes alternating hemiplegia of childhood

N. Bresolin, C. Zucca, G. Casari, 2004 .

Metabolic correction in oligodendrocytes derived from metachromatic leukodystrophy mouse model by using encapsulated recombinant myoblasts

A. Consiglio, A. Orlacchio, N. Déglon, 2007, Journal of the Neurological Sciences.

Evaluation of a LC-MS method for everolimus preclinical determination in brain by using [(13)C2D4]RAD001 internal standard.

T. Cassano, C. Emiliani, M. Perluigi, 2015, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Potential use of polymeric nanoparticles for drug delivery across the blood-brain barrier.

M A Vandelli, F Forni, G Tosi, 2013, Current medicinal chemistry.

In vivo gene therapy of metachromatic leukodystrophy by lentiviral vectors: correction of neuropathology and protection against learning impairments in affected mice

A. Consiglio, V. Cestari, L. Naldini, 2001, Nature Medicine.

Analysis of galactocerebrosidase activity in the mouse brain by a new histological staining method

E. Bongarzone, A. Orlacchio, F. Galbiati, 2004, Journal of neuroscience research.

A direct gene transfer strategy via brain internal capsule reverses the biochemical defect in Tay-Sachs disease.

M. D. De Angelis, A. Orlacchio, C. Emiliani, 2005, Human molecular genetics.

An Italian Cohort Study Identifies Four New Pathologic Mutations in the ARSA Gene

D. Dolcetta, Paola de Gemmis, Daniela Galla, 2013, Journal of Molecular Neuroscience.

Robust in vivo gene transfer into adult mammalian neural stem cells by lentiviral vectors.

F. Gage, A. Consiglio, A. Gritti, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Early intrathecal infusion of everolimus restores cognitive function and mood in a murine model of Alzheimer's disease

A. Romano, T. Cassano, S. Gaetani, 2019, Experimental Neurology.

Design and optimization of lentiviral vectors for transfer of GALC expression in Twitcher brain

L Naldini, E. Bongarzone, G. Finocchiaro, 2006, The journal of gene medicine.

NIR-labeled nanoparticles engineered for brain targeting: in vivo optical imaging application and fluorescent microscopy evidences

A. De Vita, L. Badiali, B. Ruozi, 2010, Journal of Neural Transmission.

An Italian Cohort Study Identifies Four New Pathologic Mutations in the ARSA Gene

D. Dolcetta, Paola de Gemmis, Daniela Galla, 2013, Journal of Molecular Neuroscience.

Use of Polylactide-Co-Glycolide-Nanoparticles for Lysosomal Delivery of a Therapeutic Enzyme in Glycogenosis Type II Fibroblasts.

C. Emiliani, B. Ruozi, G. Tosi, 2015, Journal of nanoscience and nanotechnology.

The local mammalian target of rapamycin (mTOR) modulation: a promising strategy to counteract neurodegeneration

R. Dominici, D. Dolcetta, 2019, Neural regeneration research.

A direct gene transfer strategy via brain internal capsule reverses the biochemical defect in Tay-Sachs disease.

A. Orlacchio, S. Martino, P. Marconi, 2005, Human molecular genetics.