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F. Maltecca · SciRah

Researcher profile · Semantic Scholar

F. Maltecca

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F. Maltecca — researcher profile on SciRah

h-index: 17
Works: 30
Citations: 960

Most-cited papers

Intergenerational instability and marked anticipation in SCA-17
F. Maltecca, A. Filla, I. Castaldo, G. Coppola +7 more
2003Neurology109 citations
Semantic Scholar
The Mitochondrial Protease AFG3L2 Is Essential for Axonal Development
F. Maltecca, A. Aghaie, D. Schroeder, Laura Cassina +8 more
2008Journal of Neuroscience105 citations Open access
Semantic Scholar
Haploinsufficiency of AFG3L2, the Gene Responsible for Spinocerebellar Ataxia Type 28, Causes Mitochondria-Mediated Purkinje Cell Dark Degeneration
F. Maltecca, R. Magnoni, Federica Cerri, G. Cox +2 more
2009Journal of Neuroscience102 citations Open access
Semantic Scholar
Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutation.
A. Bruni, J. Takahashi‐Fujigasaki, F. Maltecca, J. Foncin +9 more
2004Archives of Neurology89 citations Open access
Semantic Scholar
Purkinje neuron Ca2+ influx reduction rescues ataxia in SCA28 model.
F. Maltecca, E. Baseggio, Francesco Consolato, D. Mazza +8 more
2015Journal of Clinical Investigation80 citations Open access
Semantic Scholar
Altered organization of the intermediate filament cytoskeleton and relocalization of proteostasis modulators in cells lacking the ataxia protein sacsin
Emma J. Duncan, R. Lariviére, Teisha Y. Bradshaw, Fabiana Longo +11 more
2017Human Molecular Genetics58 citations Open access
Semantic Scholar
Respiratory dysfunction by AFG3L2 deficiency causes decreased mitochondrial calcium uptake via organellar network fragmentation
F. Maltecca, Diego De Stefani, Laura Cassina, Francesco Consolato +4 more
2012Human Molecular Genetics54 citations Open access
Semantic Scholar
m-AAA and i-AAA complexes coordinate to regulate OMA1, the stress-activated supervisor of mitochondrial dynamics
Francesco Consolato, F. Maltecca, Susanna Tulli, Irene Sambri +1 more
2018Journal of Cell Science48 citations Open access
Semantic Scholar
Late onset motoneuron disorder caused by mitochondrial Hsp60 chaperone deficiency in mice.
R. Magnoni, J. Palmfeldt, J. Christensen, Majken Sand +5 more
2013Neurobiology of Disease46 citations Open access
Semantic Scholar
Impaired turnover of hyperfused mitochondria in severe axonal neuropathy due to a novel DRP1 mutation.
Fabiana Longo, S. Benedetti, A. Zambon, M. Sora +6 more
2019Human Molecular Genetics41 citations
Semantic Scholar
Restoring calcium homeostasis in Purkinje cells arrests neurodegeneration and neuroinflammation in the ARSACS mouse model
Andrea Del Bondio, Fabiana Longo, Daniele De Ritis, E. Spirito +5 more
2023JCI Insight29 citations Open access
Semantic Scholar
Mice harbouring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicity.
C. Mancini, Eriola Hoxha, L. Iommarini, A. Brussino +27 more
2019Neurobiology of Disease29 citations Open access
Semantic Scholar
Pathogenic variants in the AFG3L2 proteolytic domain cause SCA28 through haploinsufficiency and proteostatic stress-driven OMA1 activation
Susanna Tulli, Andrea Del Bondio, Valentina Baderna, D. Mazza +12 more
2019Journal of Medical Genetics25 citations Open access
Semantic Scholar
The WRB Subunit of the Get3 Receptor is Required for the Correct Integration of its Partner CAML into the ER
H. J. F. Carvalho, Andrea Del Bondio, F. Maltecca, S. Colombo +1 more
2019Scientific Reports24 citations Open access
Semantic Scholar
Assessment of Sacsin Turnover in Patients With ARSACS
Fabiana Longo, Daniele De Ritis, A. Miluzio, Davide Fraticelli +5 more
2021Neurology22 citations Open access
Semantic Scholar
A novel AFG3L2 mutation close to AAA domain leads to aberrant OMA1 and OPA1 processing in a family with optic atrophy
Valentina Baderna, Joshua Schultz, L. Kearns, M. Fahey +4 more
2020Acta Neuropathologica Communications22 citations Open access
Semantic Scholar
Sustained OMA1-mediated integrated stress response is beneficial for spastic ataxia type 5
C. A. Franchino, Martina Brughera, Valentina Baderna, Daniele De Ritis +9 more
2023Brain : a journal of neurology19 citations Open access
Semantic Scholar
Genome-wide expression profiling and functional characterization of SCA28 lymphoblastoid cell lines reveal impairment in cell growth and activation of apoptotic pathways
C. Mancini, P. Roncaglia, A. Brussino, G. Stevanin +19 more
2013BMC Medical Genomics15 citations Open access
Semantic Scholar
U-Fiber Leukoencephalopathy Due to a Novel Mutation in the TACO1 Gene
G. Sferruzza, Andrea Del Bondio, A. Citterio, P. Vezzulli +7 more
2021Neurology: Genetics10 citations Open access
Semantic Scholar
Upregulation of Peroxiredoxin 3 Protects Afg3l2-KO Cortical Neurons In Vitro from Oxidative Stress: A Paradigm for Neuronal Cell Survival under Neurodegenerative Conditions
Barbara Bettegazzi, I. Pelizzoni, Floramarida Salerno Scarzella, L. Restelli +5 more
2019Oxidative Medicine and Cellular Longevity10 citations Open access
Semantic Scholar
In vivo detection of oxidized proteins: a practical approach to tissue-derived mitochondria.
F. Maltecca, G. Casari
2010Methods in molecular biology10 citations
Semantic Scholar
Clinical-grade intranasal NGF fuels neurological and metabolic functions of Mecp2-deficient mice
D. Pozzer, M. Indrigo, M. Breccia, E. Florio +10 more
2024Brain : a journal of neurology7 citations Open access
Semantic Scholar
SETD5 haploinsufficiency affects mitochondrial compartment in neural cells
M. Zaghi, Fabiana Longo, Luca Massimino, Alicia Rubio +9 more
2023Molecular Autism4 citations Open access
Semantic Scholar
Reduction of sacsin levels in peripheral blood mononuclear cells as a diagnostic tool for spastic ataxia of Charlevoix–Saguenay
Daniele De Ritis, L. Ferrè, J. De Winter, Clémence Tremblay-Desbiens +6 more
2024Brain Communications3 citations Open access
Semantic Scholar
Longitudinal Imaging Biomarkers Correlate with Progressive Motor Deficit in the Mouse Model of Charlevoix‐Saguenay Ataxia
Valentina Gigliucci, Su-Chun Huang, Giorgio Boschetti, A. Scaravilli +6 more
2024Annals of Neurology2 citations
Semantic Scholar
Sacsin cotranslational degradation causes autosomal recessive spastic ataxia of Charlevoix-Saguenay
Fabiana Longo, Daniele De Ritis, A. Miluzio, Davide Fraticelli +5 more
2021bioRxiv0 citations Open access
Semantic Scholar
ROLE OF MITOCHONDRIA IN CORTICAL NEURONS FROM SPINOCEREBELLAR ATAXIA 28 (SCA28) MOUSE MODEL.
F. Codazzi, F. Salerno, F. Zucca, Barbara Bettegazzi +4 more
20150 citations
Semantic Scholar
Genome-wide expression analysis identified defects in cell growth, proliferation and viability in SCA28 lymphoblastoid cell lines.
C. Mancini, P. Roncaglia, A. Brussino, G. Stevanin +19 more
20130 citations
Semantic Scholar
A Genome-wide Expression profiling to unravel effect of missense mutations in SCA28 patients
C. Mancini, P. Roncaglia, N. L. Buono, A. Brussino +12 more
20110 citations
Semantic Scholar
[Modified Hanau technic. Setting up of teeth. Modified occlusal systematization (by the Lauritzen technic). 3].
F. Maltecca, M. Spirgi, J. Berta, J. Pouezat +2 more
1971Rassegna odontotecnica0 citations
Semantic Scholar

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