Letizia Straniero
Letizia Straniero
Humanitas University
Verified email at humanitasresearch.it
Title
Cited by
Cited by
Year
DNAJC12 and dopa‐responsive nonprogressive parkinsonism
L Straniero, I Guella, R Cilia, L Parkkinen, V Rimoldi, A Young, R Asselta, ...
Annals of Neurology 82 (4), 640-646, 2017
302017
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p
L Straniero, V Rimoldi, M Samarani, S Goldwurm, A Di Fonzo, R Krüger, ...
Scientific reports 7 (1), 1-13, 2017
292017
The LRRK2 variant E193K prevents mitochondrial fission upon MPP+ treatment by altering LRRK2 binding to DRP1
M Perez Carrion, F Pischedda, A Biosa, I Russo, L Straniero, L Civiero, ...
Frontiers in molecular neuroscience 11, 64, 2018
212018
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II
V Rimoldi, L Straniero, R Asselta, L Mauri, E Manfredini, S Penco, ...
Gene 537 (1), 79-84, 2014
182014
A lysosome‐plasma membrane‐sphingolipid axis linking lysosomal storage to cell growth arrest
M Samarani, N Loberto, G Soldà, L Straniero, R Asselta, S Duga, ...
The FASEB Journal 32 (10), 5685-5702, 2018
152018
2, 6‐Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ: Design, Synthesis, and Structure–Activity Relationships
V Straniero, C Zanotto, L Straniero, A Casiraghi, S Duga, A Radaelli, ...
ChemMedChem 12 (16), 1303-1318, 2017
112017
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis
L Straniero, G Soldà, L Costantino, M Seia, P Melotti, C Colombo, ...
Journal of human genetics 61 (12), 977-984, 2016
102016
First replication of the involvement of OTUD6B in intellectual disability syndrome with seizures and dysmorphic features
L Straniero, V Rimoldi, G Soldà, M Bellini, G Biasucci, R Asselta, S Duga
Frontiers in genetics 9, 464, 2018
62018
Identification of a novel large deletion in a patient with severe factor V deficiency using an in‐house F5 MLPA assay
F Nuzzo, EM Paraboschi, L Straniero, A Pavlova, S Duga, E Castoldi
Haemophilia 21 (1), 140-147, 2015
52015
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy
E Monfrini, L Straniero, S Bonato, GM Compagnoni, A Bordoni, R Dilena, ...
Parkinsonism & related disorders 63, 66-72, 2019
42019
Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites
L Straniero, V Rimoldi, G Soldà, L Mauri, E Manfredini, E Andreucci, ...
Journal of human genetics 60 (9), 467-471, 2015
32015
Chromosome Transplantation: A Possible Approach to Treat Human X-linked Disorders
M Paulis, L Susani, A Castelli, T Suzuki, T Hara, L Straniero, S Duga, ...
Molecular Therapy-Methods & Clinical Development 17, 369-377, 2020
22020
A rapid and low-cost test for screening the most common Parkinson's disease-related GBA variants
L Straniero, V Rimoldi, G Melistaccio, A Di Fonzo, G Pezzoli, S Duga, ...
Parkinsonism & Related Disorders 80, 138-141, 2020
12020
Saposin D variants are not a common cause of familial Parkinson’s disease among Italians
D Facchi, V Rimoldi, L Straniero, EM Paraboschi, G Soldà, AL Zecchinelli, ...
Brain 143 (9), e71-e71, 2020
12020
Late-onset leukoencephalopathy in a patient with recessive EARS2 mutations
E Monfrini, D Ronchi, G Franco, M Garbellini, L Straniero, E Scola, ...
Neurology: Genetics 6 (5), 2020
2020
SLC25A46 mutations in patients with Parkinson's Disease and optic atrophy
G Bitetto, MC Malaguti, R Ceravolo, E Monfrini, L Straniero, A Morini, ...
Parkinsonism & Related Disorders, 2020
2020
The SPID- GBA Study: The Largest Monocentric Study on Sex Distribution, Penetrance, Incidence, and Association with Dementia of GBA Mutations in Parkinson's …
L Straniero, R Asselta, S Bonvegna, V Rimoldi, G Soldà, M Aureli, ...
2020
Inside Cover: 2, 6‐Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ: Design, Synthesis, and Structure–Activity Relationships (ChemMedChem 16/2017)
V Straniero, C Zanotto, L Straniero, A Casiraghi, S Duga, A Radaelli, ...
ChemMedChem 12 (16), 1225-1225, 2017
2017
UNRAVELING THE MOLECULAR COMPLEXITY OF PARKINSON¿ S DISEASE: FROM GENETIC RISK FACTORS TO MENDELIAN CAUSATIVE GENES
L Straniero
Università degli Studi di Milano, 2017
2017
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Articles 1–19