about
May "mitochondrial eve" and mitochondrial haplogroups play a role in neurodegeneration and Alzheimer's disease?Alzheimer's pathogenesis and its link to the mitochondrionLack of association between nuclear factor erythroid-derived 2-like 2 promoter gene polymorphisms and oxidative stress biomarkers in amyotrophic lateral sclerosis patients.POLG1-related and other "mitochondrial Parkinsonisms": an overview.Oxidative stress treatment for clinical trials in neurodegenerative diseases.Myopathic involvement and mitochondrial pathology in Kennedy disease and in other motor neuron diseases.Redefining phenotypes associated with mitochondrial DNA single deletion."Mitochondrial neuropathies": A survey from the large cohort of the Italian Network.High-Resolution 7T MR Imaging of the Motor Cortex in Amyotrophic Lateral Sclerosis.The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?Semiautomated Evaluation of the Primary Motor Cortex in Patients with Amyotrophic Lateral Sclerosis at 3T.Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation.Myoclonus in mitochondrial disorders.An "inflammatory" mitochondrial myopathy. A case report.A new truncating MPZ mutation associated with a very mild CMT1 B phenotype.Erratum to: Redefining phenotypes associated with mitochondrial DNA single deletionNerve and muscle involvement in mitochondrial disorders: an electrophysiological study
P50
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P50
description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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name
Elena Caldarazzo Ienco
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Elena Caldarazzo Ienco
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Elena Caldarazzo Ienco
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Elena Caldarazzo Ienco
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Elena Caldarazzo Ienco
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type
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Elena Caldarazzo Ienco
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Elena Caldarazzo Ienco
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Elena Caldarazzo Ienco
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Elena Caldarazzo Ienco
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Elena Caldarazzo Ienco
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Elena Caldarazzo Ienco
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Elena Caldarazzo Ienco
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Elena Caldarazzo Ienco
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Elena Caldarazzo Ienco
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Elena Caldarazzo Ienco
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P106
P1153
36470385800
P21
P31
P496
0000-0003-0134-5062