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Diagnostic Histopathology, ISSN 1756-2317, 01/2019, Volume 25, Issue 1, pp. 16 - 22
Prions are considered the prototype of transmissible proteopathies, and this property has for many decades been considered unique. More recently the... 
tauopathy | neurodegenerative disease | Parkinson's disease | prion disease | Creutzfeldt-Jakob disease | amyloid-β | neurodegeneration | tau | proteopathy | prions | CJD | Alzheimer's disease | α-synuclein
Journal Article
by Capper, David and Jones, David T. W and Sill, Martin and Hovestadt, Volker and Schrimpf, Daniel and Sturm, Dominik and Koelsche, Christian and Sahm, Felix and Chavez, Lukas and Reuss, David E and Kratz, Annekathrin and Wefers, Annika K and Huang, Kristin and Pajtler, Kristian W and Schweizer, Leonille and Stichel, Damian and Olar, Adriana and Engel, Nils W and Lindenberg, Kerstin and Harter, Patrick N and Braczynski, Anne K and Plate, Karl H and Dohmen, Hildegard and Garvalov, Boyan K and Coras, Roland and Hölsken, Annett and Hewer, Ekkehard and Bewerunge-Hudler, Melanie and Schick, Matthias and Fischer, Roger and Beschorner, Rudi and Schittenhelm, Jens and Staszewski, Ori and Wani, Khalida and Varlet, Pascale and Pages, Melanie and Temming, Petra and Lohmann, Dietmar and Selt, Florian and Witt, Hendrik and Milde, Till and Witt, Olaf and Aronica, Eleonora and Giangaspero, Felice and Rushing, Elisabeth and Scheurlen, Wolfram and Geisenberger, Christoph and Rodriguez, Fausto J and Becker, Albert and Preusser, Matthias and Haberler, Christine and Bjerkvig, Rolf and Cryan, Jane and Farrell, Michael and Deckert, Martina and Hench, Jürgen and Frank, Stephan and Serrano, Jonathan and Kannan, Kasthuri and Tsirigos, Aristotelis and Brück, Wolfgang and Hofer, Silvia and Brehmer, Stefanie and Seiz-Rosenhagen, Marcel and Hänggi, Daniel and Hans, Volkmar and Rozsnoki, Stephanie and Hansford, Jordan R and Kohlhof, Patricia and Kristensen, Bjarne W and Lechner, Matt and Lopes, Beatriz and Mawrin, Christian and Ketter, Ralf and Kulozik, Andreas and Khatib, Ziad and Heppner, Frank and Koch, Arend and Jouvet, Anne and Keohane, Catherine and Mühleisen, Helmut and Mueller, Wolf and Pohl, Ute and Prinz, Marco and Benner, Axel and Zapatka, Marc and Gottardo, Nicholas G and Driever, Pablo Hernáiz and Kramm, Christof M and Müller, Hermann L and Rutkowski, Stefan and Von Hoff, Katja and Frühwald, Michael C and Gnekow, Astrid and Fleischhack, Gudrun and Tippelt, Stephan and Calaminus, Gabriele and Monoranu, Camelia-Maria and Perry, Arie and Jones, Chris and ...
Nature, ISSN 0028-0836, 03/2018, Volume 555, Issue 7697, pp. 469 - 474
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 01/2017, Volume 376, Issue 3, pp. 292 - 294
In this case study, variant Creutzfeldt–Jakob disease (CJD) is shown to occur in a young man with heterozygosity, rather than homozygosity, at codon 129 of the... 
MEDICINE, GENERAL & INTERNAL | Magnetic Resonance Imaging | Brain - diagnostic imaging | Humans | Fatal Outcome | Brain - pathology | Adult | Heterozygote | Male | Creutzfeldt-Jakob Syndrome - genetics | Prion Proteins - genetics | Genotype & phenotype | Brain research | Disease | BSE | Creutzfeldt-Jakob disease | Prion protein | Heterozygosity
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 10/2018, Volume 89, Issue 10, pp. A32 - A32
Peripheral T-cell lymphomas (PTCLs) are rare and heterogeneous haematological malignancies that can rarely develop first in the peripheral nervous system, or... 
Journal Article
The Lancet Infectious Diseases, ISSN 1473-3099, 07/2019, Volume 19, Issue 7, pp. 788 - 788
A 46-year-old man with relapsed B-cell acute lymphoblastic leukaemia following allogeneic sibling haematopoietic stem cell transplantation presented with... 
INFECTIOUS DISEASES | Health care | Antigens | Therapy | Medical research | Acute lymphatic leukemia | Transplants & implants | Funding | Leukemia | Cognitive ability | Research facilities | Transplantation | Lymphocytes T | Blood | Neurotoxicity | Lymphocytes B | Toxoplasmosis | Neurological complications | Immunotherapy | Stem cells | Seizures | Cancer
Journal Article
Nature, ISSN 0028-0836, 09/2015, Volume 525, Issue 7568, pp. 247 - 250
Journal Article
Annals of Neurology, ISSN 0364-5134, 02/2019, Volume 85, Issue 2, pp. 284 - 290
Amyloid‐β transmission has been described in patients both with and without iatrogenic Creutzfeldt–Jakob disease; however, there is little information... 
TRIALS | TRANSMISSION | DEMENTIA | EMBOLIZATION | MATER | APP LOCUS DUPLICATION | GRAFT | CREUTZFELDT-JAKOB-DISEASE | ASSOCIATION | NEUROSCIENCES | CLINICAL NEUROLOGY | Neuroimaging | Medical imaging | Seeds | Exposure | Neurosurgery | Patients | Neurology | Cerebral amyloid angiopathy | Cadavers | Prions | Embolization | Diagnostic systems | Children | Prion protein | Brief Communication | Brief Communications
Journal Article
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 05/2016, Volume 87, Issue 5, pp. 512 - 519
Journal Article
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, ISSN 0022-3050, 10/2014, Volume 85, Issue 10, pp. e4.38 - e4
Gerstmann's syndrome is a rare disorder resulting from damage to the angular gyrus of the dominant parietal lobe leading to agraphia, acalculia, finger agnosia... 
SURGERY | PSYCHIATRY | CLINICAL NEUROLOGY
Conference Proceeding
PLoS ONE, ISSN 1932-6203, 01/2016, Volume 11, Issue 1, pp. e0145500 - e0145500
Mutations in the nuclear gene POLG (encoding the catalytic subunit of DNA polymerase gamma) are an important cause of mitochondrial disease. The most common... 
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA | DNA-POLYMERASE-GAMMA | MULTIDISCIPLINARY SCIENCES | PHENOTYPE | DOMINANT | MUTATIONS | SPECTRUM | EPILEPSY | MYOPATHY | ENCEPHALOMYOPATHY | FEATURES | DNA Polymerase gamma | Mitochondrial Diseases - genetics | Mitochondrial Diseases - pathology | Liver - pathology | Humans | Child, Preschool | Genotype | Male | Mitochondrial Myopathies - pathology | DNA-Directed DNA Polymerase - genetics | Diffuse Cerebral Sclerosis of Schilder - genetics | Homozygote | Mitochondrial Myopathies - genetics | Phenotype | DNA, Mitochondrial - genetics | Adolescent | Brain - pathology | Adult | Female | Polymorphism, Single Nucleotide | Diffuse Cerebral Sclerosis of Schilder - pathology | Muscle, Skeletal - pathology | Real-Time Polymerase Chain Reaction | DNA, Mitochondrial - chemistry | Complications and side effects | Prognosis | Gene mutations | Physiological aspects | Mitochondrial diseases | Genetic aspects | Research | Neurosciences | Nuclear magnetic resonance--NMR | DNA polymerase | Disease | Neuropathology | Downstream effects | Epilepsy | Childrens health | Electroencephalography | Mitochondrial DNA | Neurosurgery | Neuropathy | Genetics | Ataxia | Stroke-like episodes | Catalysis | Bioinformatics | Lactic acidosis | Deoxyribonucleic acid--DNA | Enzymes | Stroke | Neuromuscular diseases | Muscles | Patients | Environmental stress | Polymerase | Neurology | Brain research | Hospitals | Ophthalmoplegia | Mutation | MELAS syndrome | Acidosis | DNA-directed DNA polymerase | Myopathy | Index Medicus | Deoxyribonucleic acid | Nuclear magnetic resonance | NMR | DNA
Journal Article
Movement Disorders, ISSN 0885-3185, 01/2018, Volume 33, Issue 1, pp. 146 - 155
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 8/2018, Volume 136, Issue 2, pp. 273 - 291
Journal Article