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Journal of Neurology, ISSN 0340-5354, 12/2018, Volume 265, Issue 12, pp. 2934 - 2943
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 11/2015, Volume 86, Issue 11, pp. e4 - e4
IntroductionCerebral Autosomal Dominant Angoipathy with Subcortical Infarcts and Leucoencephalopathy is a disorder caused by mutations in the NOTCH 3 gene. It... 
SURGERY | PSYCHIATRY | CLINICAL NEUROLOGY | Complications and side effects | Hemiplegia | CADASIL | Diagnosis | Risk factors
Journal Article
Journal Article
Journal of Alzheimer's Disease, ISSN 1387-2877, 2009, Volume 17, Issue 4, pp. 787 - 794
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2016, Volume 11, Issue 6, pp. e0157613 - e0157613
Journal Article
Journal Article
Journal Article
Journal Article
Clinical Neurology, ISSN 0009-918X, 05/2012, Volume 52, Issue 5, pp. 303 - 313
Journal Article
European Journal of Neurology, ISSN 1351-5101, 01/2018, Volume 25, Issue 1, pp. 142 - 147
Background and purposeTo establish and validate diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) due to... 
alanyl‐transfer | diagnostic criteria | adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia | RNA | colony‐stimulating factor 1 receptor | leukoencephalopathy | pigmented orthochromatic leukodystrophy | hereditary diffuse leukoencephalopathy with spheroids | synthetase 2 | 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 | Index Medicus | 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