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Journal of Neuropathology & Experimental Neurology, ISSN 0022-3069, 02/2019, Volume 78, Issue 2, pp. 123 - 129
Abstract Selective neuronal death in neurodegenerative disorders represents the final step of a cascade of events, including neuroinflammation,... 
Parkinsonism | Mitochondrial dysfunction | MRI | Selective neuronal degeneration | 3-Nitropropionic acid | Bilateral striatal necrosis | Reactive astrocytosis | TOXIN 3-NITROPROPIONIC ACID | PATHOLOGY | ASTROCYTES | NEUROSCIENCES | CLINICAL NEUROLOGY | PATHOGENESIS | IN-VITRO | NEURONS | GLIA | HUNTINGTONS-DISEASE | EXPRESSION | BRAIN
Journal Article
British Journal of Dermatology, ISSN 0007-0963, 08/2018, Volume 179, Issue 2, pp. 509 - 511
Journal Article
NEUROPEDIATRICS, ISSN 0174-304X, 06/2018, Volume 49, Issue 3, pp. 209 - 212
Child bilateral striatal necrosis (BSN) is a rare and etiologically heterogeneous condition. An association with group A streptococcus (GAS) infection was... 
Sydenham's chorea | movement disorder | dystonia | BASAL GANGLIA | bilateral striatal necrosis | group A streptococcus | PEDIATRICS | CLINICAL NEUROLOGY
Journal Article
Neuropediatrics, ISSN 0174-304X, 06/2018, Volume 49, Issue 3, pp. 209 - 212
Abstract Child bilateral striatal necrosis (BSN) is a rare and etiologically heterogeneous condition. An association with group A streptococcus (GAS) infection... 
Short Communication | bilateral striatal necrosis | group A streptococcus | movement disorder | Sydenham's chorea | dystonia
Journal Article
Neuropediatrics, ISSN 0174-304X, 10/2019, Volume 50, Issue 5, pp. 313 - 317
Abstract Background   SLC25A19 gene mutations cause Amish congenital lethal microcephaly and bilateral striatal necrosis with polyneuropathy. We are reporting... 
Short Communication | bilateral striatal necrosis | PEDIATRICS | CLINICAL NEUROLOGY | polyneuropathy | BASAL GANGLIA DISEASE | India
Journal Article
Molecular Genetics & Genomic Medicine, ISSN 2324-9269, 03/2019, Volume 7, Issue 3, pp. e541 - n/a
Journal Article
Folia Neuropathologica, ISSN 1641-4640, 2016, Volume 54, Issue 4, pp. 405 - 409
Pathogenic molecular variants in the ADAR gene are a known cause of rare diseases, autosomal recessive Aicardi-Goutieres syndrome type 6, severe infantile... 
LS differentiation | Bilateral striatal necrosis | ADAR gene | Whole exome sequencing | GENE | AICARDI-GOUTIERES SYNDROME | I INTERFERON SIGNATURE | bilateral striatal necrosis | PATHOLOGY | NEUROSCIENCES | whole exome sequencing
Journal Article
Journal of Pediatric Neurology, ISSN 1304-2580, 12/2006, Volume 4, Issue 4, pp. 275 - 277
Abstract Acute bilateral striatal necrosis is considered to be a rare heterogeneous entity, in view of the variability of its clinical presentation. We report... 
Case Report | Infantile bilateral striatal necrosis | Measles | Hospitals | Infectious diseases | Herpes viruses | Vital signs | Neurological disorders | Children & youth
Journal Article
European Journal of Paediatric Neurology, ISSN 1090-3798, 03/2018, Volume 22, Issue 2, pp. 332 - 335
Encephalopathies with neostriatal involvement constitute a heterogeneous group of acquired and genetically inherited conditions that include Bilateral Striatal... 
SLC19A3 | Striatal lesions | Bilateral striatal necrosis | Dystonia | Thiamin | ENCEPHALOPATHY | GENE | PEDIATRICS | MUTATIONS | CLINICAL NEUROLOGY
Journal Article
Brain and Development, ISSN 0387-7604, 2005, Volume 27, Issue 1, pp. 62 - 65
Journal Article
by Crow, Y.J and Chase, D.S and Schmidt, J.L and Szynkiewicz, M and Forte, G.M.A and Gornall, H.L and Oojageer, A and Anderson, B and Pizzino, A and Helman, G and Abdel-Hamid, M.S and Abdel-Salam, G.M and Ackroyd, S and Aeby, A and Agosta, G and Albin, C and Allon-Shalev, S and Arellano, M and Ariaudo, G and Aswani, V and Babul-Hirji, R and Baildam, E.M and Bahi-Buisson, N and Bailey, K.M and Barnerias, C and Barth, M and Battini, R and Beresford, M.W and Bernard, G and Bianchi, M and de Villemeur, T.B and Blair, E.M and Bloom, M and Burlina, A.B and Carpanelli, M.L and Carvalho, D.R and Castro-Gago, M and Cavallini, A and Cereda, C and Chandler, K.E and Chitayat, D.A and Collins, A.E and Corcoles, C.S and Cordeiro, N.J.V and Crichiutti, G and Dabydeen, L and Dale, R.C and D'Arrigo, S and De Goede, C.G.E.L and de Laet, C and De Waele, L.M.H and Denzler, I and Desguerre, I and Devriendt, K and Di Rocco, M and Fahey, M.C and Fazzi, E and Ferrie, C.D and Figueiredo, A and Gener, B and Goizet, C and Gowrinathan, N.R and Gowrishankar, K and Hanrahan, D and Isidor, B and Kara, L and Khan, N and King, M.D and Kirk, E.P and Kumar, R and Lagae, L and Lanieu, P and Lauffer, H and Laugel, V and La Piana, R and Lim, M.J and Lin, J.P.S.M and Linnankivi, T and Mackay, M.T and Marom, D.R and Lourenco, C.M and McKee, S.A and Moroni, I and Morton, J.E.V and Moutard, M.L and Murray, K and Nabbout, R and Nampoothiri, S and Nunez-Enamorado, N and Oades, P.J and Olivieri, I and Ostergaard, J.R and Perez-Duenas, B and Prendiville, J.S and Ramesh, V and Rasmussen, M and Regal, L and Ricci, F and Rio, M and Knaap, M and ...
American Journal of Medical Genetics Part A, ISSN 1552-4825, 2015, Volume 167, Issue 2, pp. 296 - 312
Journal Article