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/vufind/Search/Results?lookfor=%22Curr%C3%B2%2C+Riccardo%22&type=Person&sort=year
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PubPharm (32)
1
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease
enthalten in:
bioRxiv.org
| 2024
von
Currò, R.
|
Dominik, N.
|
Facchini, S.
| +51
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2
Heterozygous APTX mutation associated with atypical multiple system atrophy-like phenotype : A case report
enthalten in:
Parkinsonism & related disorders
| 2024
von
Imarisio, A.
|
Pilotto, A.
|
Lupini, A.
| +8
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3
Intronic FGF14 GAA repeat expansions are a common cause of ataxia syndromes with neuropathy and bilateral vestibulopathy
enthalten in:
Journal of neurology, neurosurgery, and psychiatry
| 2024
von
Pellerin, D.
|
Wilke, C.
|
Traschütz, A.
| +19
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4
Can CANVAS due to RFC1 biallelic expansions present with pure ataxia?
enthalten in:
Journal of neurology, neurosurgery, and psychiatry
| 2024
von
Hadjivassiliou, M.
|
Currò, R.
|
Beauchamp, N.
| +6
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5
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease
enthalten in:
Brain : a journal of neurology
| 2024
von
Currò, R.
|
Dominik, N.
|
Facchini, S.
| +152
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6
Mutations in alpha-B-crystallin cause autosomal dominant axonal Charcot-Marie-Tooth disease with congenital cataracts
enthalten in:
European journal of neurology
| 2024
von
Cortese, A.
|
Currò, R.
|
Ronco, R.
| +14
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7
Serum Neurofilament Light Chain in Replication Factor Complex Subunit 1 CANVAS and Disease Spectrum
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2024
von
Quartesan, I.
|
Vegezzi, E.
|
Currò, R.
| +30
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8
Mutations in alpha‐B‐crystallin cause autosomal dominant axonal Charcot–Marie–Tooth disease with congenital cataracts
enthalten in:
European Journal of Neurology
| 2024
von
Cortese, A.
|
Currò, R.
|
Ronco, R.
| +14
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9
Serum Neurofilament Light Chain in Replication Factor Complex Subunit 1 CANVAS and Disease Spectrum
enthalten in:
Movement Disorders
| 2024
von
Quartesan, I.
|
Vegezzi, E.
|
Currò, R.
| +30
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10
Normal and pathogenic variation of RFC1 repeat expansions : implications for clinical diagnosis
enthalten in:
Brain : a journal of neurology
| 2023
von
Dominik, N.
|
Magri, S.
|
Currò, R.
| +116
ErratumIn: Brain. 2024 Feb 1;147(2):e23. - PMID 38181422
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4
Brain : a journal of neurology
4
Journal of neurology
4
Journal of neurology, neurosurgery, and psychiatry
3
Acta neurologica Belgica
2
Journal of the peripheral nervous system : JPNS
2
Multiple sclerosis and related disorders
2
bioRxiv.org
1
Biomolecules
1
European Journal of Neurology
1
European journal of neurology
1
Genetics in medicine : official journal of the ...
1
Journal of the Peripheral Nervous System
1
Movement Disorders
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Movement disorders : official journal of the Mo...
1
Neurology
1
Neurology(R) neuroimmunology & neuroinflammation
1
Parkinsonism & related disorders
1
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Thema
15
Journal Article
11
Research Support, Non-U.S. Gov't
8
CANVAS
6
Letter
6
RFC1
5
neuropathy
4
ATTR
4
Biomarker
4
Magnetic resonance imaging (MRI)
4
Outcome measure
4
Polyneuropathy
4
Research Support, N.I.H., Extramural
3
RFC1 protein, human
3
RFC1-related sensory neuropathy
3
Vestibular areflexia
3
Vestibular test
3
ataxia
2
570
2
Biology
2
Biomarkers
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Erscheinungszeitraum
9
2024
7
2023
11
2022
1
2021
4
2020
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