E-LIB Suche - Ergebnisse für: Monzio-Compagnoni, Giacomo

1

Abnormalities of lipid metabolism in neuronal models of CoQ..:

Pesini, Alba ; Monzio-Compagnoni, Giacomo ; Barriocanal-Casado, Eliana...
Neurology. 100 (2023) 17_supplement_2 - p. , 2023

Link: https://doi.org/10.1212/..

2

The role of 123-I-MIBG cardiac scintigraphy in the differen..:

Monzio Compagnoni, Giacomo ; Appollonio, Ildebrando ; Ferrarese, Carlo
Neurological Sciences. , 2024

Link: https://doi.org/10.1007/..

3

The Role of Mitochondria in Neurodegenerative Diseases: the..:

Monzio Compagnoni, Giacomo ; Di Fonzo, Alessio ; Corti, Stefania...
Molecular Neurobiology. 57 (2020) 7 - p. 2959-2980 , 2020

Link: https://doi.org/10.1007/..

4

Understanding the pathogenesis of multiple system atrophy: ..:

Monzio Compagnoni, Giacomo ; Di Fonzo, Alessio
Acta Neuropathologica Communications. 7 (2019) 1 - p. , 2019

Link: https://doi.org/10.1186/..

5

Neurofascin (NFASC) gene mutation causes autosomal recessiv..:

Monfrini, Edoardo ; Straniero, Letizia ; Bonato, Sara...
Parkinsonism & Related Disorders. 63 (2019) - p. 66-72 , 2019

Link: https://doi.org/10.1016/..

6

Mitochondrial Dysregulation and Impaired Autophagy in iPSC-..:

Monzio Compagnoni, Giacomo ; Kleiner, Giulio ; Samarani, Maura...
Stem Cell Reports. 11 (2018) 5 - p. 1185-1198 , 2018

Link: https://doi.org/10.1016/..

7

Mitochondrial dysfunction in fibroblasts of Multiple System..:

Monzio Compagnoni, Giacomo ; Kleiner, Giulio ; Bordoni, Andreina...
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864 (2018) 12 - p. 3588-3597 , 2018

Link: https://doi.org/10.1016/..

8

Mutations in TMEM230 are rare in autosomal dominant Parkins..:

Buongarzone, Gabriele ; Monfrini, Edoardo ; Franco, Giulia...
Parkinsonism & Related Disorders. 39 (2017) - p. 87-88 , 2017

Link: https://doi.org/10.1016/..

9

Loss of the nucleoporin Aladin in central nervous system an..:

Bitetto, Giacomo ; Ronchi, Dario ; Bonato, Sara...
Human Molecular Genetics. 28 (2019) 23 - p. 3921-3927 , 2019

Link: https://doi.org/10.1093/..

10

Mutational analysis ofCOQ2in patients with MSA in Italy:

Ronchi, Dario ; Di Biase, Ernesto ; Franco, Giulia...
Neurobiology of Aging. 45 (2016) - p. 213.e1-213.e2 , 2016

Link: https://doi.org/10.1016/..

11

Generation and characterization of iPSC-derived cortical py..:

Compagnoni, Giacomo Monzio ; Frattini, Emanuele ; Salani, Sabrina...
Parkinsonism & Related Disorders. 22 (2016) - p. e119-e120 , 2016

Link: https://doi.org/10.1016/..

12

Understanding the pathogenesis of multiple system atrophy: ..:

Giacomo Monzio Compagnoni ; Alessio Di Fonzo
http://link.springer.com/article/10.1186/s40478-019-0730-6. , 2019

Link: https://doi.org/10.1186/..

13

Mitochondrial Dysregulation and Impaired Autophagy in iPSC-..:

Giacomo Monzio Compagnoni ; Giulio Kleiner ; Maura Samarani...
http://www.sciencedirect.com/science/article/pii/S2213671118303928. , 2018

Link: https://doi.org/10.1016/..

14

Neurofascin (NFASC) gene mutation causes autosomal recessiv..:

Monfrini, Edoardo ; Straniero, Letizia ; Bonato, Sara...
info:eu-repo/semantics/altIdentifier/pmid/30850329. , 2019

Link: http://hdl.handle.net/24..

15

Mitochondrial Dysregulation and Impaired Autophagy in iPSC-..:

Monzio Compagnoni, Giacomo ; Kleiner, Giulio ; Samarani, Maura...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6234905/. , 2018

Link: http://www.ncbi.nlm.nih...