Novel histotypes of sporadic Creutzfeldt–Jakob disease linked to 129MV genotype

[1]  B. Caughey,et al.  A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques , 2023, Acta Neuropathologica.

[2]  V. Redaelli,et al.  Defining the phenotypic spectrum of sporadic Creutzfeldt–Jakob disease MV2K: the kuru plaque type , 2023, Brain : a journal of neurology.

[3]  N. Bargalló,et al.  Sporadic Creutzfeldt-Jakob disease VM1: phenotypic and molecular characterization of a novel subtype of human prion disease , 2022, Acta Neuropathologica Communications.

[4]  N. Bargalló,et al.  Sporadic Creutzfeldt-Jakob disease VM1: phenotypic and molecular characterization of a novel subtype of human prion disease , 2022, Acta Neuropathologica Communications.

[5]  J. Torres,et al.  Two distinct conformers of PrPD type 1 of sporadic Creutzfeldt–Jakob disease with codon 129VV genotype faithfully propagate in vivo , 2021, Acta neuropathologica communications.

[6]  R. Occhipinti,et al.  Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion , 2020, Frontiers in Cellular Neuroscience.

[7]  W. Surewicz,et al.  A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease , 2020, Acta Neuropathologica Communications.

[8]  P. Péran,et al.  Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures , 2020, mBio.

[9]  A. Bizzi,et al.  Prion propagation estimated from brain diffusion MRI is subtype dependent in sporadic Creutzfeldt–Jakob disease , 2020, Acta Neuropathologica.

[10]  J. Hollister,et al.  Transmission characteristics of heterozygous cases of Creutzfeldt-Jakob disease with variable abnormal prion protein allotypes , 2020, Acta Neuropathologica Communications.

[11]  R. Occhipinti,et al.  Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics , 2020, Scientific Reports.

[12]  M. Bishop,et al.  Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes , 2019, Brain : a journal of neurology.

[13]  Piero Parchi,et al.  Understanding Prion Strains: Evidence from Studies of the Disease Forms Affecting Humans , 2019, Viruses.

[14]  C. Soto,et al.  PMCA-replicated PrPD in urine of vCJD patients maintains infectivity and strain characteristics of brain PrPD: Transmission study , 2019, Scientific Reports.

[15]  S. Capellari,et al.  Recent advances in the histo‐molecular pathology of human prion disease , 2019, Brain pathology.

[16]  John Hardy,et al.  Selective vulnerability in neurodegenerative diseases , 2018, Nature Neuroscience.

[17]  C. Duyckaerts,et al.  Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study , 2018, Acta Neuropathologica Communications.

[18]  M. D. Di Bari,et al.  Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature , 2017, Acta neuropathologica communications.

[19]  J. Bartz Prion Strain Diversity. , 2016, Cold Spring Harbor perspectives in medicine.

[20]  Roger A. Moore,et al.  The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients , 2016, PLoS pathogens.

[21]  T. Hortobágyi,et al.  Atypical sporadic CJD‐MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain disease , 2015, Neuropathology : official journal of the Japanese Society of Neuropathology.

[22]  J. Parisi,et al.  Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone , 2015, Acta neuropathologica communications.

[23]  J. Collinge,et al.  Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peaked , 2014, Nature Communications.

[24]  W. Jackson Selective vulnerability to neurodegenerative disease: the curious case of Prion Protein , 2014, Disease Models & Mechanisms.

[25]  Y. Matsuura,et al.  Deciphering the pathogenesis of sporadic Creutzfeldt-Jakob disease with codon 129 M/V and type 2 abnormal prion protein , 2013, Acta neuropathologica communications.

[26]  J. Yagüe,et al.  Atypical neuropathological sCJD‐MM phenotype with abundant white matter Kuru‐type plaques sparing the cerebellar cortex , 2013, Neuropathology : official journal of the Japanese Society of Neuropathology.

[27]  A. Bizzi,et al.  Sporadic human prion diseases: molecular insights and diagnosis , 2012, The Lancet Neurology.

[28]  B. Crain,et al.  Variably protease‐sensitive prionopathy: A new sporadic disease of the prion protein , 2010, Annals of neurology.

[29]  M. Bishop,et al.  Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties , 2010, Proceedings of the National Academy of Sciences.

[30]  J. Langeveld,et al.  Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics. , 2009, Brain : a journal of neurology.

[31]  K. Arima,et al.  Plaque-type deposition of prion protein in the damaged white matter of sporadic Creutzfeldt-Jakob disease MM1 patients , 2008, Acta Neuropathologica.

[32]  T. Montine,et al.  A novel human disease with abnormal prion protein sensitive to protease , 2008, Annals of neurology.

[33]  A. Giese,et al.  A refined method for molecular typing reveals that co-occurrence of PrPSc types in Creutzfeldt–Jakob disease is not the rule , 2007, Laboratory Investigation.

[34]  R. Castellani,et al.  Classification of sporadic Creutzfeldt-Jakob disease revisited. , 2006, Brain : a journal of neurology.

[35]  Shu G. Chen,et al.  Sporadic and familial CJD: classification and characterisation. , 2003, British medical bulletin.

[36]  B. Ghetti,et al.  Genetic influence on the structural variations of the abnormal prion protein. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[37]  L. Bour,et al.  Sporadic Creutzfeldt-Jakob disease: Co-occurrence of different types of PrPSc in the same brain , 1999, Neurology.

[38]  P Brown,et al.  Classification of sporadic Creutzfeldt‐Jakob disease based on molecular and phenotypic analysis of 300 subjects , 1999, Annals of neurology.

[39]  J Q Trojanowski,et al.  Molecular basis of phenotypic variability in sporadc creudeldt‐jakob disease , 1996, Annals of neurology.

[40]  R. Petersen,et al.  Fatal Familial Insomnia and Familial Creutzfeldt‐Jakob Disease: Clinical, Pathological and Molecular Features , 1995, Brain pathology.

[41]  P Brown,et al.  Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism. , 1992, Science.

[42]  John Collinge,et al.  Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease , 1991, Nature.

[43]  P. Gambetti,et al.  Human sporadic prion diseases , 2013 .

[44]  B. Ghetti,et al.  Effects of Different Experimental Conditions on the PrP Core Generated by Protease Digestion IMPLICATIONS FOR STRAIN TYPING AND MOLECULAR CLASSIFICATION OF CJD* , 2004 .

[45]  Hilde van der Togt,et al.  Publisher's Note , 2003, J. Netw. Comput. Appl..