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Creutzfeldt-Jakob
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Publications (1007)
- Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease Patients. (2018/11/20) ♡
- Review of diffuse cortical injury on diffusion-weighted imaging in acutely encephalopathic patients with an acronym: "CRUMPLED". (2018/11/09) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Creutzfeldt-Jakob Disease Presenting as Nonconvulsive Status Epilepticus. (2018/11/04) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Prion Diseases. (2018/11/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Unravelling the glial response in the pathogenesis of Alzheimer's disease. (2018/11/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Lenalidomide induced reversible parkinsonism, dystonia, and dementia in subclinical Creutzfeldt-Jakob disease. (2018/10/15) ♡
- Overexpression of quality control proteins reduces prion conversion in prion-infected cells. (2018/10/12) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Clinical Reasoning: Rapidly progressive dementia in a patient with HIV after an exotic journey. (2018/10/02) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Oligodendrogliopathy in neurodegenerative diseases with abnormal protein aggregates: The forgotten partner. (2018/10/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Autopsied case of non-plaque-type dura mater graft-associated Creutzfeldt-Jakob disease presenting with extensive amyloid-β deposition. (2018/10/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Sporadic Creutzfeldt-Jakob disease with glial PrP(Res) nuclear and perinuclear immunoreactivity. (2018/10/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Diagnostic challenges in rapidly progressive dementia. (2018/10/01) ♡
- Rapidly Progressive Dementia in the Outpatient Clinic: More Than Prions. (2018/10/01) ♡
- Analysis of 22 Years of Surveillance for Prion Diseases in Slovenia, 1996 to 2017. (2018/10/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Creutzfeldt-Jakob disease with unusual presentation of peripheral neuropathy and ophthalmoplegia. (2018/10/01) ♡
- Effect of Urea, Arginine, and Ethanol Concentration on Aggregation of (179)CVNITV(184) Fragment of Sheep Prion Protein. (2018/09/30) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. An Evaluation of Rapidly Progressive Dementia Culminating in a Diagnosis of Creutzfeldt-Jakob Disease. (2018/09/23) ♡
- A Bioluminescent Cell Assay to Quantify Prion Protein Dimerization. (2018/09/21) ♡
- Muskelin Coordinates PrP(C) Lysosome versus Exosome Targeting and Impacts Prion Disease Progression. (2018/09/19) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Rapidly Progressing Sporadic Creutzfeldt-Jakob Disease Presenting as a Stroke. (2018/09/13) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Sporadic MM-1 Type Creutzfeldt-Jakob Disease With Hemiballic Presentation and No Cognitive Impairment Until Death: How New NCJDRSU Diagnostic Criteria May Allow Early Diagnosis. (2018/09/05) ♡
- Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges. (2018/09/01) ♡
- Chorea in Sporadic Creutzfeldt-Jakob Disease. (2018/09/01) ♡
- Systematic reviewiAll research on one question is searched according to fixed rules and compared side by side, so that no studies with poor outcomes are missed. A systematic review comparing the diagnostic value of 14-3-3 protein in the cerebrospinal fluid, RT-QuIC and RT-QuIC on nasal brushing in sporadic Creutzfeldt-Jakob disease. (2018/09/01) ♡
- Extending the functional characteristics of naturally occurring autoantibodies against β-amyloid, prion protein and α-synuclein. (2018/08/29) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Genetic Predisposition to Infectious Disease. (2018/08/27) ♡
- Susceptibility to Creutzfeldt-Jakob disease after human growth hormone treatment in France. (2018/08/21) ♡
- Unexpected prion phenotypes in experimentally transfused animals: predictive models for humans? (2018/08/16) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Characterization of mutations in PRNP (prion) gene and their possible roles in neurodegenerative diseases. (2018/08/14) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. PrP(res) deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD). (2018/08/10) ♡
- Post-mortem magnetic resonance imaging in patients with suspected prion disease: Pathological confirmation, sensitivity, specificity and observer reliability. A national registry. (2018/08/07) ♡
- Impaired transmissibility of atypical prions from genetic CJD(G114V). (2018/08/07) ♡
- RFAmyloid: A Web Server for Predicting Amyloid Proteins. (2018/07/16) ♡
- Interlaboratory validation of cerebrospinal fluid α-synuclein quantification in the diagnosis of sporadic Creutzfeldt-Jakob disease. (2018/07/07) ♡
- Predictive Factors for Early Initiation of Artificial Feeding in Patients With Sporadic Creutzfeldt-Jakob Disease. (2018/07/03) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. A critical review of the prion hypothesis of human synucleinopathies. (2018/07/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Primary Central Nervous System Lymphoma with Associated Demyelination and Creutzfeldt Astrocytes. (2018/07/01) ♡
- CSF nonphosphorylated Tau as a biomarker for the discrimination of AD from CJD. (2018/05/26) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Intravascular large B-cell lymphoma presenting clinically as rapidly progressive dementia. (2018/05/01) ♡
- Brain biopsies requiring Creutzfeldt-Jakob disease precautions in the Republic of Ireland 2005-2016. (2018/05/01) ♡
- Brains with sporadic Creutzfeldt-Jakob disease and copathology showed a prolonged end-stage of disease. (2018/05/01) ♡
- Imaging and CSF analyses effectively distinguish CJD from its mimics. (2018/05/01) ♡
- Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein. (2018/03/15) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Diagnostic challenge of non-specific visual symptoms: consideration of Heidenhain variant of Creutzfeldt-Jakob disease. (2018/03/01) ♡
- Chitotriosidase (CHIT1) is increased in microglia and macrophages in spinal cord of amyotrophic lateral sclerosis and cerebrospinal fluid levels correlate with disease severity and progression. (2018/03/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. The function of the cellular prion protein in health and disease. (2018/02/01) ♡
- Neuropathology of iatrogenic Creutzfeldt-Jakob disease and immunoassay of French cadaver-sourced growth hormone batches suggest possible transmission of tauopathy and long incubation periods for the transmission of Abeta pathology. (2018/02/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Toward Therapy of Human Prion Diseases. (2018/01/06) ♡
- MSA prions exhibit remarkable stability and resistance to inactivation. (2018/01/01) ♡
- The Translational Science Benefits Model: A New Framework for Assessing the Health and Societal Benefits of Clinical and Translational Sciences. (2018/01/01) ♡
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