Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

Piero Parchi, Armin Giese, Sabina Capellari, +15

Annals of Neurology

Phenotypic AnalysisNeurobiology Of DiseaseSporadic Creutzfeldt-jakob DiseaseCreutzfeldt-jakob DiseaseNeurological Disorder +13

Detection of 14‐3‐3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt‐Jakob disease

Inga Zerr, Monika Bodemer, Olaf Gefeller, +6

Annals of Neurology

Evidence of Presynaptic Location and Function of the Prion Protein

Jochen Herms, Tobias Tings, Stefan Gall, +7

Journal of Neuroscience

Prion Protein Binds Copper within the Physiological Concentration Range

M. Kramer, Hartmut Kratzin, Bernhard Schmidt, +5

Journal of Biological Chemistry

Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene

Otto Windl, Maureen Dempster, J. Peter Estibeiro, +9

Human Genetics

Mendelian DisorderCreutzfeldt-jakob DiseaseGenetic DisorderGeneticsGenetic Epidemiology +7

The Heidenhain Variant of Creutzfeldt-Jakob Disease

Stefan Kropp, Walter Schulz‐Schaeffer, Michael Finkenstaedt, +6

Archives of Neurology

Efficacy of flupirtine on cognitive function in patients with CJD

Markus Otto, Lukas Cepek, Peter Ratzka, +10

Neurology

Current clinical diagnosis in Creutzfeldt-Jakob disease: Identification of uncommon variants

Inga Zerr, Walter Schulz‐Schaeffer, Armin Giese, +10

Annals of Neurology

Sporadic Creutzfeldt-jakob DiseaseCreutzfeldt-jakob DiseaseNeurological DisorderGenetic EpidemiologyDiagnosis +15

Decreased β-amyloid _1-42 in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease

Markus Otto, Hermann Esselmann, Walter Schulz‐Schaeffer, +11

Neurology

Molecular genetics of human prion diseases in Germany

Otto Windl, Armin Giese, Walter Schulz‐Schaeffer, +7

Human Genetics

Creutzfeldt-jakob DiseaseGenetic DisorderGeneticsPathogenesisPathology +5