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Frontiers in neuroscience, ISSN 1662-4548, 2019, Volume 13, p. 575
Iron homeostasis is an essential prerequisite for metabolic and neurological functions throughout the healthy human life, with a dynamic interplay between... 
Nervous system diseases | divalent metal transporter 1 up-regulation | neurodegenerative diseases | aging | non-transferrin bound iron transport | transport of iron and heavy metals | iron homoeostasis
Journal Article
Energy and Environmental Science, ISSN 1754-5692, 2008, Volume 1, Issue 4, pp. 417 - 429
In less than a decade the levels of performance of microbial fuel cells (MFCs) in terms of current output, voltage, and power density have grown tremendously... 
WASTE-WATER TREATMENT | ENERGY & FUELS | POLYETHER ETHER KETONE | ANAEROBIC RESPIRATION | CHEMISTRY, MULTIDISCIPLINARY | OF-THE-ART | ENGINEERING, CHEMICAL | ENVIRONMENTAL SCIENCES | CATHODIC OXYGEN REDUCTION | BIOELECTRICITY PRODUCTION | PROTON-EXCHANGE MEMBRANE | ELECTRICITY-GENERATION | POWER-GENERATION | EXTRACELLULAR ELECTRON-TRANSFER
Journal Article
Journal of Neurology, ISSN 0340-5354, 8/2017, Volume 264, Issue 8, pp. 1583 - 1607
Since the official and systematic inclusion of sex and gender in biomedical research, gender differences have been acknowledged as important determinants of... 
Neurosciences | Biomarker | Motor | Sex | Genetic | Gender | Neuroradiology | Parkinson | Neurology | Treatment | Medicine & Public Health | Surgery | Non-motor
Journal Article
Frontiers in Genetics, ISSN 1664-8021, 2015, Volume 5, p. 78
Mutations in PARK2, encoding Parkin, cause an autosomal recessive form of juvenile Parkinson Disease (JPD). The aim of the present study was to investigate the... 
oxygen consumption | PARK2 | mitochondrial membrane potential | mitochondrial dynamics | Parkin | Oxygen consumption | Mitochondrial dynamics | Mitochondrial membrane potential | Parkinson Disease | parkin
Journal Article
Frontiers in genetics, ISSN 1664-8021, 2017, Volume 8, p. 18
Mutations in gene, coding for a beta-propeller protein, have been found in patients affected by Neurodegeneration with Brain Iron Accumulation, NBIA5 (also... 
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2017, Volume 12, Issue 3, p. e0174560
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2013, Volume 8, Issue 1, p. 19
Background: To review the descriptive epidemiological data on neuronal ceroid lipofuscinoses (NCLs) in Italy, identify the spectrum of mutations in the... 
NCL Genes | Italy | Childhood NCL | Epidemiology | MEDICINE, RESEARCH & EXPERIMENTAL | CLN1 GENE | WEST | BATTEN-DISEASE | PATIENT | MUTATIONS | Molecular Epidemiology | Humans | Female | Italy - epidemiology | Male | Child | Neuronal Ceroid-Lipofuscinoses - epidemiology | Cohort Studies
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 10/2018, Volume 26, Issue 10, pp. 1462 - 1477
Journal Article
Journal of Neurology, ISSN 0340-5354, 3/2017, Volume 264, Issue 3, pp. 586 - 588
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s00415-017-8393-3 
Neurology | Neurosciences | Medicine & Public Health | Neuroradiology | PHENOTYPE | RARE CAUSES | MUTATIONS | CYP2U1 | SPG56 | CLINICAL NEUROLOGY
Journal Article
Journal Article
European Journal of Paediatric Neurology, ISSN 1090-3798, 2016, Volume 20, Issue 4, pp. 604 - 610
Journal Article