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Alessio Di Fonzo
Alessio Di Fonzo
IRCCS Foundation Ca’ Granda Ospedale Maggiore Policlinico, Dino Ferrari Center
Verified email at policlinico.mi.it
Title
Cited by
Cited by
Year
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
106242021
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease
A Di Fonzo, CF Rohé, J Ferreira, HF Chien, L Vacca, F Stocchi, L Guedes, ...
The Lancet 365 (9457), 412-415, 2005
6652005
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome
AD Fonzo, MCJ Dekker, P Montagna, A Baruzzi, EH Yonova, LC Guedes, ...
Neurology 72 (3), 240-245, 2009
4462009
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease
A Di Fonzo, HF Chien, M Socal, S Giraudo, C Tassorelli, G Iliceto, ...
Neurology 68 (19), 1557-1562, 2007
4382007
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson’s disease risk in Taiwan
A Di Fonzo, YH Wu-Chou, CS Lu, M van Doeselaar, EJ Simons, CF Rohé, ...
neurogenetics 7, 133-138, 2006
2812006
GBA, Gaucher Disease, and Parkinson’s Disease: From Genetic to Clinic to New Therapeutic Approaches
GM Riboldi, AB Di Fonzo
Cells 8 (4), 364, 2019
2412019
The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson’s disease and originates from a common ancestor
S Goldwurm, A Di Fonzo, EJ Simons, CF Rohe, M Zini, M Canesi, S Tesei, ...
Journal of Medical Genetics 42 (11), e65-e65, 2005
2212005
Adaptive deep brain stimulation in a freely moving Parkinsonian patient
M Rosa, M Arlotti, G Ardolino, F Cogiamanian, S Marceglia, A Di Fonzo, ...
Movement Disorders 30 (7), 1003, 2015
2192015
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease
A Di Fonzo, C Tassorelli, M De Mari, HF Chien, J Ferreira, CF Rohé, ...
European journal of human genetics 14 (3), 322-331, 2006
2152006
The role of mitochondria in neurodegenerative diseases: the lesson from Alzheimer’s disease and Parkinson’s disease
G Monzio Compagnoni, A Di Fonzo, S Corti, GP Comi, N Bresolin, ...
Molecular neurobiology 57, 2959-2980, 2020
2072020
The LRRK2 Gly2385Arg variant is associated with Parkinson’s disease: genetic and functional evidence
EK Tan, Y Zhao, L Skipper, MG Tan, A Di Fonzo, L Sun, S Fook-Chong, ...
Human genetics 120, 857-863, 2007
1892007
The mitochondrial disulfide relay system protein GFER is mutated in autosomal-recessive myopathy with cataract and combined respiratory-chain deficiency
A Di Fonzo, D Ronchi, T Lodi, E Fassone, M Tigano, C Lamperti, S Corti, ...
The American Journal of Human Genetics 84 (5), 594-604, 2009
1522009
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability
D Ronchi, A Di Fonzo, W Lin, A Bordoni, C Liu, E Fassone, S Pagliarani, ...
The American Journal of Human Genetics 92 (2), 293-300, 2013
1472013
Cerebellar and motor cortical transcranial stimulation decrease levodopa-induced dyskinesias in Parkinson’s disease
R Ferrucci, F Cortese, M Bianchi, D Pittera, R Turrone, T Bocci, B Borroni, ...
The Cerebellum 15, 43-47, 2016
1322016
LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study
M Quadri, W Mandemakers, MM Grochowska, R Masius, H Geut, ...
The Lancet Neurology 17 (7), 597-608, 2018
1192018
LRRK2 G2019S mutation and Parkinson's disease: a clinical, neuropsychological and neuropsychiatric study in a large Italian sample
S Goldwurm, M Zini, A Di Fonzo, D De Gaspari, C Siri, EJ Simons, ...
Parkinsonism & related disorders 12 (7), 410-419, 2006
1192006
Adaptive deep brain stimulation controls levodopa‐induced side effects in Parkinsonian patients
M Rosa, M Arlotti, S Marceglia, F Cogiamanian, G Ardolino, A Di Fonzo, ...
Movement Disorders 32 (4), 628, 2017
1142017
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions
AD Fonzo, A Bordoni, M Crimi, G Sara, RD Bo, N Bresolin, GP Comi
Human mutation 22 (6), 498-499, 2003
1142003
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability
L Santoro, GJ Breedveld, F Manganelli, R Iodice, C Pisciotta, M Nolano, ...
Neurogenetics 12, 33-39, 2011
1122011
The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease
CS Lu, EJ Simons, YH Wu-Chou, A Di Fonzo, HC Chang, RS Chen, ...
Parkinsonism & related disorders 11 (8), 521-522, 2005
972005
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Articles 1–20