Atypical sporadic CJD-MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain disease-Reference-Cited by-同舟云学术

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Atypical sporadic CJD-MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain disease

Published:2015-03-18 Issue:4 Volume:35 Page:336-342
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:Neuropathology

Author:

Berghoff Anna S.¹,Trummert Anita²,Unterberger Ursula¹,Ströbel Thomas¹,Hortobágyi Tibor³,Kovacs Gabor G.¹

Affiliation:

1. Institute of Neurology and Austrian Reference Center for Human Prion Diseases; Medical University of Vienna; Vienna Austria

2. Landesklinikum Weinviertel; Mistelbach-Gänserndorf Austria

3. Department of Neuropathology; Faculty of Medicine, University of Debrecen; Debrecen Hungary

Funder

Austrian Federal Ministry of Health (BMG)

Publisher

Wiley

Subject

Clinical Neurology,General Medicine,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/neup.12192/fullpdf

Reference24 articles.

1. Protein coding of neurodegenerative dementias: the neuropathological basis of biomarker diagnostics;Kovacs;Acta Neuropathol,2010

2. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects;Parchi;Ann Neurol,1999

3. Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA;Parchi;Acta Neuropathol,2012

4. Neuronal intranuclear hyaline inclusion disease;Takahashi-Fujigasaki;Neuropathology,2003

5. Ubiquitin-related proteins in neuronal and glial intranuclear inclusions in intranuclear inclusion body disease;Mori;Pathol Int,2012

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1. Novel histotypes of sporadic Creutzfeldt–Jakob disease linked to 129MV genotype;Acta Neuropathologica Communications;2023-08-31

2. A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques;Acta Neuropathologica;2023-05-08

3. Human Sporadic Prion Diseases;Prions and Diseases;2023

4. Degenerative dementias: a question of syndrome or disease?;Neurología (English Edition);2021-05

5. Neuronal intranuclear inclusion disease is genetically heterogeneous;Annals of Clinical and Translational Neurology;2020-08-10

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