2023 - Research.com Medicine in Germany Leader Award
Hans A. Kretzschmar mainly focuses on Pathology, Degenerative disease, Frontotemporal lobar degeneration, Amyotrophic lateral sclerosis and Frontotemporal dementia. His Pathology study is mostly concerned with Alzheimer's disease, Anatomical pathology, Tau protein, Neuropathology and Disease. His Degenerative disease research integrates issues from Creutzfeldt-Jakob Syndrome, Dementia, Pathogenesis and Virology.
His Frontotemporal lobar degeneration research is multidisciplinary, relying on both Genetics and Ubiquitin. His studies deal with areas such as Mutation and Progressive supranuclear palsy, Corticobasal degeneration as well as Amyotrophic lateral sclerosis. His studies in Frontotemporal dementia integrate themes in fields like Inclusion bodies, RNA-Binding Protein FUS and Tauopathy.
His primary areas of investigation include Pathology, Disease, Dementia, Degenerative disease and Biochemistry. Alzheimer's disease, Frontotemporal lobar degeneration, Cerebrospinal fluid, Tau protein and Differential diagnosis are the subjects of his Pathology studies. Hans A. Kretzschmar regularly links together related areas like Amyotrophic lateral sclerosis in his Frontotemporal lobar degeneration studies.
His research investigates the connection between Disease and topics such as Virology that intersect with issues in Gene. His Degenerative disease research is under the purview of Central nervous system disease. His study in Biochemistry is interdisciplinary in nature, drawing from both Oligomer and Amyloid.
Pathology, Neuroscience, Neurodegeneration, Disease and Internal medicine are his primary areas of study. His Pathology study integrates concerns from other disciplines, such as Mutation and Phenotype. His work deals with themes such as Syntaxin and Synaptotagmin 1, which intersect with Neuroscience.
His Neurodegeneration study also includes fields such as
Hans A. Kretzschmar mainly investigates Pathology, Genetics, Neurodegeneration, C9orf72 and C9orf72 Protein. In most of his Pathology studies, his work intersects topics such as Phenotype. He has included themes like Methylation, Epigenomics, DNA methylation, Mutation and Neuroscience in his Neurodegeneration study.
His biological study spans a wide range of topics, including DNA Repeat Expansion and Amyotrophic lateral sclerosis. His Amyotrophic lateral sclerosis research includes elements of Frontotemporal lobar degeneration, Frontotemporal dementia and Cell biology. The concepts of his Alzheimer's disease study are interwoven with issues in Preclinical imaging, Progressive supranuclear palsy, Retina, Intracellular and Human genetics.
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Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann;Deepak M. Sampathu;Linda K. Kwong;Adam C. Truax.
Staging of Alzheimer disease-associated neurofibrillary pathology using paraffin sections and immunocytochemistry.
Heiko Braak;Irina Alafuzoff;Thomas Arzberger;Hans Kretzschmar.
Acta Neuropathologica (2006)
The cellular prion protein binds copper in vivo
D R Brown;K Qin;J W Herms;A Madlung.
Classification of sporadic Creutzfeldt‐Jakob disease based on molecular and phenotypic analysis of 300 subjects
Piero Parchi;Armin Giese;Sabina Capellari;Paul Brown.
Annals of Neurology (1999)
The C9orf72 GGGGCC Repeat Is Translated into Aggregating Dipeptide-Repeat Proteins in FTLD/ALS
Kohji Mori;Shih-Ming Weng;Thomas Arzberger;Stephanie May.
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations
Ian R.A. Mackenzie;Eileen H. Bigio;Paul G. Ince;Felix Geser.
Annals of Neurology (2007)
Different Species of α-Synuclein Oligomers Induce Calcium Influx and Seeding
Karin M. Danzer;Dorothea Haasen;Anne R. Karow;Simon Moussaud.
The Journal of Neuroscience (2007)
Prion (PrPSc)-specific epitope defined by a monoclonal antibody.
Carsten Korth;Beat Stierli;Peter Streit;Markus Moser.
A new subtype of frontotemporal lobar degeneration with FUS pathology.
Manuela Neumann;Rosa Rademakers;Sigrun Roeber;Matt Baker.
Subcellular Localization of Wild-Type and Parkinson's Disease-Associated Mutant α-Synuclein in Human and Transgenic Mouse Brain
Philipp J. Kahle;Manuela Neumann;Laurence Ozmen;Veronika Müller.
The Journal of Neuroscience (2000)
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