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Neurobiology of Disease, ISSN 0969-9961, 2014, Volume 81, pp. 119 - 133
Journal Article
Frontiers in neuroscience, ISSN 1662-4548, 2019, Volume 13, p. 1195
Cellular growth, function, and protection require proper iron management, and ferritin plays a crucial role as the major iron sequestration and storage... 
ferroptosis | LIPID-PEROXIDATION | JAPANESE FAMILY | MUTANT FORM | neurodegeneration | ferritinophagy | NEUROFERRITINOPATHY | mutant ferritin | CLINICAL-FEATURES | ALPHA-SYNUCLEIN | NEUROSCIENCES | hereditary ferritinopathy | PROTEIN NANOCAGES | ROS | IN-VIVO | CHAIN GENE MUTATION
Journal Article
Revista de Neurologia, ISSN 0210-0010, 10/2012, Volume 54, pp. S99 - S106
Journal Article
Journal Article
NEUROBIOLOGY OF DISEASE, ISSN 0969-9961, 01/2010, Volume 37, Issue 1, pp. 77 - 85
Neuroferritinopathies are dominantly inherited movement disorders associated with nucleotide insertions in the L-ferritin gene that modify the protein's... 
Oxidative stress | JAPANESE FAMILY | Ferritin | LIGHT-CHAIN GENE | Iron | CLINICAL-FEATURES | Neuroferritinopathy | NEUROSCIENCES | Hereditary ferritinopathy | POLYPEPTIDE GENE | ALPHA-INDUCED APOPTOSIS | IRON-METABOLISM | HELA-CELLS | HUNTINGTONS-DISEASE | PARKINSONS-DISEASE
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 01/2014, Volume 336, Issue 1-2, pp. 254 - 256
We report a healthy adult male, who underwent, as a control subject, part of a Huntington's disease study, extensive testing during three visits in a two year... 
NBIA | Iron | Eye-of-the-tiger sign | PKAN | Neuroferritinopathy | Movement disorder | Analysis | Adults | Tigers
Journal Article
Parkinsonism and Related Disorders, ISSN 1353-8020, 2015, Volume 22, pp. S21 - S25
Journal Article
Clinical Neurology, ISSN 0009-918X, 2012, Volume 52, Issue 11, pp. 951 - 954
Journal Article
Current Neurology and Neuroscience Reports, ISSN 1528-4042, 6/2011, Volume 11, Issue 3, pp. 254 - 261
Journal Article
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, ISSN 0925-4439, 04/2011, Volume 1812, Issue 4, pp. 544 - 548
Hereditary ferritinopathy (HF) is a neurodegenerative disease characterized by intracellular ferritin inclusion bodies (IBs) and iron accumulation throughout... 
JAPANESE FAMILY | STABILITY | BIOCHEMISTRY & MOLECULAR BIOLOGY | Ferritin | Iron | NEUROFERRITINOPATHY | Hereditary ferritinopathy | POLYPEPTIDE GENE | BIOPHYSICS | Pore | Neurodegeneration | MUTATION | DISEASE | MICE | ACCUMULATION
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 2013, Volume 336, Issue 1, pp. 254 - 256
Abstract We report a healthy adult male, who underwent, as a control subject, part of a Huntington's disease study, extensive testing during three visits in a... 
Neurology | NBIA | Iron | Eye-of-the-tiger sign | Neuroferritinopathy | PKAN | Movement disorder | HALLERVORDEN-SPATZ-SYNDROME | BRAIN IRON ACCUMULATION | KINASE-ASSOCIATED NEURODEGENERATION | NEUROSCIENCES | CLINICAL NEUROLOGY | Magnetic Resonance Imaging - methods | Male | Health Status Indicators | Globus Pallidus - pathology | Humans | Middle Aged
Journal Article
Journal Article
Free Radical Biology and Medicine, ISSN 0891-5849, 05/2012, Volume 52, Issue 9, pp. 1692 - 1697
Intracellular inclusion bodies (IBs) containing ferritin and iron are hallmarks of hereditary ferritinopathy (HF). This neurodegenerative disease is caused by... 
Iron | Free radicals | Neurodegeneration | Oxidative damage | Ferritin | JAPANESE FAMILY |