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PubPharm (42)
1
Effect of RNS60 in amyotrophic lateral sclerosis : a phase II multicentre, randomized, double-blind, placebo-controlled trial
enthalten in:
European journal of neurology
| 2023
von
Beghi, E.
|
Pupillo, E.
|
Bianchi, E.
| +112
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2
A Single mtDNA Deletion in Association with a LMNA Gene New Frameshift Variant : A Case Report
enthalten in:
Journal of neuromuscular diseases
| 2022
von
Montano, V.
|
Mancuso, M.
|
Simoncini, C.
| +12
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3
Movement Disorders in Children with a Mitochondrial Disease : A Cross-Sectional Survey from the Nationwide Italian Collaborative Network of Mitochondrial Diseases
enthalten in:
Journal of clinical medicine
| 2021
von
Ticci, C.
|
Orsucci, D.
|
Ardissone, A.
| +38
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4
Therapeutical Management and Drug Safety in Mitochondrial Diseases-Update 2020
enthalten in:
Journal of clinical medicine
| 2020
von
Gruosso, F.
|
Montano, V.
|
Simoncini, C.
| +2
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5
Fibroblast growth factor 21 and grow differentiation factor 15 are sensitive biomarkers of mitochondrial diseases due to mitochondrial transfer-RNA mutations and mitochondrial DNA deletions
enthalten in:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
| 2020
von
Formichi, P.
|
Cardone, N.
|
Taglia, I.
| +10
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6
Fibroblast growth factor 21 and grow differentiation factor 15 are sensitive biomarkers of mitochondrial diseases due to mitochondrial transfer-RNA mutations and mitochondrial DNA deletions
enthalten in:
Neurological sciences
| 2020
von
Formichi, P.
|
Cardone, N.
|
Taglia, I.
| +10
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7
Fibroblast growth factor 21 and grow differentiation factor 15 are sensitive biomarkers of mitochondrial diseases due to mitochondrial transfer-RNA mutations and mitochondrial DNA deletions
enthalten in:
Neurological sciences
| 2020
von
Formichi, P.
|
Cardone, N.
|
Taglia, I.
| +10
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8
Fibroblast growth factor 21 and grow differentiation factor 15 are sensitive biomarkers of mitochondrial diseases due to mitochondrial transfer-RNA mutations and mitochondrial DNA deletions
enthalten in:
Neurological sciences
| 2020
von
Formichi, P.
|
Cardone, N.
|
Taglia, I.
| +10
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9
Mitochondrial epilepsy : a cross-sectional nationwide Italian survey
enthalten in:
Neurogenetics
| 2020
von
Ticci, C.
|
Sicca, F.
|
Ardissone, A.
| +22
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10
Neuromuscular tetanic hyperexcitability syndrome associated to a heterozygous Kv1.1 N255D mutation with normal serum magnesium levels
enthalten in:
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
| 2020
von
Bianchi, F.
|
Simoncini, C.
|
Brugnoni, R.
| +2
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Genotype-phenotype correlations
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Erscheinungszeitraum
15
2020-
27
2010-2019
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Sprache
39
Englisch
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