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/vufind/Search/Results?lookfor=%22Bellone%2C+Emilia%22&type=Person&page=3
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PubPharm (127)
21
Validation of a new hand function outcome measure in individuals with Charcot‐Marie‐Tooth disease
enthalten in:
Journal of the Peripheral Nervous System
| 2020
von
Prada, V.
|
Robbiano, G.
|
Mennella, G.
| +5
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22
Expanding the spectrum of genes responsible for hereditary motor neuropathies
enthalten in:
Journal of neurology, neurosurgery, and psychiatry
| 2019
von
Previtali, S.
|
Zhao, E.
|
Lazarevic, D.
| +28
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23
Diagnostic Value of Sural Nerve Biopsy : Retrospective Analysis of Clinical Cases From 1981 to 2017
enthalten in:
Frontiers in neurology
| 2019
von
Prada, V.
|
Massucco, S.
|
Venturi, C.
| +8
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24
Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise"
enthalten in:
Orphanet journal of rare diseases
| 2018
von
Grandis, M.
|
Geroldi, A.
|
Gulli, R.
| +12
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25
Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy “in disguise”
enthalten in:
Orphanet journal of rare diseases
| 2018
von
Grandis, M.
|
Geroldi, A.
|
Gulli, R.
| +12
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26
Twenty years of molecular analyses in amyotrophic lateral sclerosis : genetic landscape of Italian patients
enthalten in:
Neurobiology of aging
| 2018
von
Lamp, M.
|
Origone, P.
|
Geroldi, A.
| +12
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27
Spinocerebellar ataxia 17: full phenotype in a 41 CAG/CAA repeats carrier
enthalten in:
Cerebellum & ataxias
| 2018
von
Origone, P.
|
Gotta, F.
|
Lamp, M.
| +11
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28
Spinocerebellar ataxia 17: full phenotype in a 41 CAG/CAA repeats carrier
enthalten in:
Cerebellum & ataxias
| 2018
von
Origone, P.
|
Gotta, F.
|
Lamp, M.
| +11
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29
Spinocerebellar ataxia 17 : full phenotype in a 41 CAG/CAA repeats carrier
enthalten in:
Cerebellum & ataxias
| 2018
von
Origone, P.
|
Gotta, F.
|
Lamp, M.
| +11
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30
Role of MAPT in Pure Motor Neuron Disease : Report of a Recurrent Mutation in Italian Patients
enthalten in:
Neuro-degenerative diseases
| 2018
von
Origone, P.
|
Geroldi, A.
|
Lamp, M.
| +9
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Human mutation
8
Journal of the peripheral nervous system : JPNS
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Amyotrophic lateral sclerosis : official public...
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26
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neuropathy
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5
DNA-Binding Proteins
5
Proteins
5
Transcription Factors
4
CMT1A
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Charcot-Marie-Tooth disease
4
Genetic counseling
4
HSP27 Heat-Shock Proteins
4
HSPB1 protein, human
4
Heat-Shock Proteins
4
Molecular Chaperones
4
Myelin P0 Protein
4
Myelin Proteins
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Nerve Tissue Proteins
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