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1 . Academic Journal
PEX7 Mutations Cause Congenital Cataract Retinopathy and Late-Onset Ataxia and Cognitive Impairment: Report of Two Siblings and Review of the Literature
저자
by
Lorenzo Nanetti
;
Viviana Pensato
;
Valerio Leoni
;
Manuela Rizzetto
;
Claudio Caccia
, et al.
소스
Journal of Clinical Neurology, 11(2), pp.197-199 Apr, 2015
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7 . Academic Journal
Analysis of miRNA rare variants in amyotrophic lateral sclerosis and in silico prediction of their biological effects
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by
Alberto Brusati
;
Antonia Ratti
;
Viviana Pensato
;
Silvia Peverelli
;
Davide Gentilini
, et al.
소스
Frontiers in Genetics, Vol 13 (2022)
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7 . Academic Journal
Identification of a cytokine profile in serum and cerebrospinal fluid of pediatric and adult spinal muscular atrophy patients and its modulation upon nusinersen treatment
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by
Silvia Bonanno
;
Paola Cavalcante
;
Erika Salvi
;
Eleonora Giagnorio
;
Claudia Malacarne
, et al.
소스
Frontiers in Cellular Neuroscience, Vol 16 (2022)
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7 . Academic Journal
MiR-146a in ALS: Contribution to Early Peripheral Nerve Degeneration and Relevance as Disease Biomarker
저자
by
Eleonora Giagnorio
;
Claudia Malacarne
;
Paola Cavalcante
;
Letizia Scandiffio
;
Marco Cattaneo
, et al.
소스
International Journal of Molecular Sciences, Vol 24, Iss 5, p 4610 (2023)
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7 . Academic Journal
Cortical markers of cognitive syndromes in amyotrophic lateral sclerosis
저자
by
Monica Consonni
;
Valeria E. Contarino
;
Eleonora Catricalà
;
Eleonora Dalla Bella
;
Viviana Pensato
, et al.
소스
NeuroImage: Clinical, Vol 19, Iss , Pp 675-682 (2018)
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7 . Academic Journal
Dysregulation of Muscle-Specific MicroRNAs as Common Pathogenic Feature Associated with Muscle Atrophy in ALS, SMA and SBMA: Evidence from Animal Models and Human Patients
저자
by
Claudia Malacarne
;
Mariarita Galbiati
;
Eleonora Giagnorio
;
Paola Cavalcante
;
Franco Salerno
, et al.
소스
International Journal of Molecular Sciences, Vol 22, Iss 11, p 5673 (2021)
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7 . Academic Journal
Cognitive Syndromes and C9orf72 Mutation Are Not Related to Cerebellar Degeneration in Amyotrophic Lateral Sclerosis
저자
by
Monica Consonni
;
Eleonora Dalla Bella
;
Anna Nigri
;
Chiara Pinardi
;
Greta Demichelis
, et al.
소스
Frontiers in Neuroscience, Vol 13 (2019)
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7 . Academic Journal
Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: OPTN, VCP, and SQSTM1 Variants Account for 3% of Rare Genetic Forms
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by
Viviana Pensato
;
Stefania Magri
;
Eleonora Dalla Bella
;
Pierpaola Tannorella
;
Enrica Bersano
, et al.
소스
Journal of Clinical Medicine, Vol 9, Iss 2, p 412 (2020)
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7 .
Behavioral and Cognitive Phenotypes of Patients With Amyotrophic Lateral Sclerosis Carrying SOD1 Variants
저자
by
Eleonora Dalla Bella
;
Enrica Bersano
;
Maria Grazia Bruzzone
;
Cinzia Gellera
;
Viviana Pensato
, et al.
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Neurology
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7 .
G507D mutation in FUS gene causes familial amyotrophic lateral sclerosis with a specific genotype-phenotype correlation
저자
by
Ilaria Martinelli
;
Elisabetta Zucchi
;
Viviana Pensato
;
Cinzia Gellera
;
Bryan J Traynor
, et al.
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