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by Ross, Owen A, Dr and Soto-Ortolaza, Alexandra I, BSc and Heckman, Michael G, MS and Aasly, Jan O, Prof and Abahuni, Nadine, MD and Annesi, Grazia, Prof and Bacon, Justin A, BSc and Bardien, Soraya, PhD and Bozi, Maria, MD and Brice, Alexis, Prof and Brighina, Laura, MD and Van Broeckhoven, Christine, Prof and Carr, Jonathan, Prof and Chartier-Harlin, Marie-Christine, Prof and Dardiotis, Efthimios, MD and Dickson, Dennis W, Prof and Diehl, Nancy N, BS and Elbaz, Alexis, Prof and Ferrarese, Carlo, Prof and Ferraris, Alessandro, MD and Fiske, Brian, PhD and Gibson, J Mark, Prof and Gibson, Rachel, PhD and Hadjigeorgiou, Georgios M, MD and Hattori, Nobutaka, Prof and Ioannidis, John PA, Prof and Jasinska-Myga, Barbara, MD and Jeon, Beom S, Prof and Kim, Yun Joong, Prof and Klein, Christine, Prof and Kruger, Rejko, MD and Kyratzi, Elli, MD and Lesage, Suzanne, PhD and Lin, Chin-Hsien, MD and Lynch, Timothy, Prof and Maraganore, Demetrius M, Prof and Mellick, George D, PhD and Mutez, Eugénie, MD and Nilsson, Christer, Prof and Opala, Grzegorz, Prof and Park, Sung Sup, Prof and Puschmann, Andreas, MD and Quattrone, Aldo, Prof and Sharma, Manu, PhD and Silburn, Peter A, Prof and Sohn, Young Ho, Prof and Stefanis, Leonidas, MD and Tadic, Vera, MD and Theuns, Jessie, PhD and Tomiyama, Hiroyuki, MD and Uitti, Ryan J, Prof and Valente, Enza Maria, Prof and van de Loo, Simone, PhD and Vassilatis, Demetrios K, PhD and Vilariño-Güell, Carles, PhD and White, Linda R, Prof and Wirdefeldt, Karin, MD and Wszolek, Zbigniew K, Prof and Wu, Ruey-Meei, Prof and Farrer, Matthew J, Prof and Genetic Epidemiology Parkinson's D and Genetic Epidemiology Of Parkinson's Disease (GEO-PD) Consortium and Sektion IV and Lund University and Psychiatry (Lund) and Klinisk neurogenetik and MultiPark: Multidisciplinary research focused on Parkinson´s disease and Psykiatri, Lund and Division IV and Clinical Neurogenetics and Lunds universitet
Lancet Neurology, The, ISSN 1474-4422, 2011, Volume 10, Issue 10, pp. 898 - 908
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2017, Volume 16, Issue 5, pp. 351 - 359
Journal Article
Annals of Neurology, ISSN 0364-5134, 05/2011, Volume 69, Issue 5, pp. 778 - 792
Journal Article
European Journal of Neurology, ISSN 1351-5101, 01/2018, Volume 25, Issue 1, pp. 142 - 147
Background and purpose To establish and validate diagnostic criteria for adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) due to... 
diagnostic criteria | adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia | colony‐stimulating factor 1 receptor | alanyl‐transfer RNA synthetase 2 | leukoencephalopathy | pigmented orthochromatic leukodystrophy | hereditary diffuse leukoencephalopathy with spheroids | adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | colony-stimulating factor 1 receptor | alanyl-transfer RNA synthetase 2 | HDLS | LEUKODYSTROPHY | NEUROSCIENCES | CLINICAL NEUROLOGY | Leukoencephalopathies - pathology | Diagnosis, Differential | Leukoencephalopathies - genetics | Reproducibility of Results | CADASIL - pathology | Neuroglia - pathology | Humans | Middle Aged | Spheroids, Cellular - pathology | Male | Tomography, X-Ray Computed | CADASIL - genetics | Young Adult | Magnetic Resonance Imaging | Receptors, Granulocyte-Macrophage Colony-Stimulating Factor - genetics | Axons - pathology | Cognition Disorders - etiology | Leukoencephalopathies - diagnosis | Adolescent | CADASIL - diagnosis | Adult | Female | Receptor, Notch3 - genetics | Aged | Genetic aspects | Diagnosis | Ligases | Leukoencephalopathy | Analysis | Transfer RNA | Sensitivity | Macrophage colony-stimulating factor | Colony-stimulating factor | Diagnostic systems | Mutation | Criteria | Spheroids | Genetic screening | Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) | pigmented orthochromatic leukodystrophy (POLD) | colony stimulating factor 1 receptor (CSF1R) | alanyl-transfer (t)RNA synthetase 2 (AARS2) | hereditary diffuse leukoencephalopathy with spheroids (HDLS)
Journal Article
Neurodegenerative Diseases, ISSN 1660-2854, 02/2016, Volume 16, Issue 1-2, pp. 12 - 21
Background: Tauopathies are a group of neurodegenerative disorders characterized by the pathological accumulation of hyperphosphorylated and insoluble tau... 
Review | Tauopathies | Genetics | Tau pathology | Microtubule-associated protein tau gene | REPEAT EXPANSION | PARKINSONISM | DEMENTIA | DEPOSITION | CONSENSUS | FRONTOTEMPORAL LOBAR DEGENERATION | NEUROSCIENCES | CLINICAL NEUROLOGY | PRESENILIN-1 MUTATION | DISEASE | NEUROPATHOLOGY | BRAIN | Tauopathies - genetics | Pedigree | Humans | Fatal Outcome | Brain - pathology | Tauopathies - pathology | Family | Female | Male | Aged
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 01/2017, Volume 49, pp. 217.e1 - 217.e4
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2009, Volume 32, Issue 3, pp. 548.e9 - 548.e18
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2011, Volume 32, Issue 11, pp. 2108.e1 - 2108.e5
Journal Article
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