Concurrent Variably Protease-sensitive Prionopathy and Amyotrophic Lateral Sclerosis

Overview

Journal Acta Neuropathol

Specialty Neurology

Date 2014 Jun 15

PMID 24928712

Citations 6

Authors

Ashley Cannon

Kevin F Bieniek

Wen-Lang Lin

Silvio Notari

Wen-Quan Zou

Pierluigi Gambetti

Otto Pedraza

Neill R Graff-Radford

Tanis J Ferman

Dennis W Dickson

Affiliations

Soon will be listed here.

Citing Articles

Search for a genetic cause of variably protease-sensitive prionopathy.

Lian Y, Kotobelli K, Hall S, Talkowski M, ODonnell-Luria A, Vallabh S medRxiv. 2024; .

PMID: 39711705 PMC: 11661330. DOI: 10.1101/2024.12.12.24318867.

Characterization of variably protease-sensitive prionopathy by capillary electrophoresis.

Myskiw J, Bailey-Elkin B, Avery K, Barria M, Ritchie D, Cohen M Sci Rep. 2024; 14(1):27867.

PMID: 39537719 PMC: 11561330. DOI: 10.1038/s41598-024-79217-1.

Further Characterization of Glycoform-Selective Prions of Variably Protease-Sensitive Prionopathy.

Zhang W, Xiao X, Ding M, Yuan J, Foutz A, Moudjou M Pathogens. 2021; 10(5).

PMID: 33922765 PMC: 8146342. DOI: 10.3390/pathogens10050513.

Variably protease-sensitive prionopathy mimicking frontotemporal dementia.

Aizpurua M, Selvackadunco S, Yull H, Kipps C, Ironside J, Bodi I Neuropathology. 2019; 39(2):135-140.

PMID: 30847986 PMC: 6778052. DOI: 10.1111/neup.12538.

Co-occurrence of chronic traumatic encephalopathy and prion disease.

Nemani S, Notari S, Cali I, Alvarez V, Kofskey D, Cohen M Acta Neuropathol Commun. 2018; 6(1):140.

PMID: 30563563 PMC: 6299534. DOI: 10.1186/s40478-018-0643-9.

References

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Masters C, Harris J, Gajdusek D, Gibbs Jr C, BERNOULLI C, Asher D . Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering. Ann Neurol. 1979; 5(2):177-88. DOI: 10.1002/ana.410050212. View

Notari S, Strammiello R, Capellari S, Giese A, Cescatti M, Grassi J . Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease. J Biol Chem. 2008; 283(45):30557-65. PMC: 2662149. DOI: 10.1074/jbc.M801877200. View

Head M, Lowrie S, Chohan G, Knight R, Scoones D, Ironside J . Variably protease-sensitive prionopathy in a PRNP codon 129 heterozygous UK patient with co-existing tau, α synuclein and Aβ pathology. Acta Neuropathol. 2010; 120(6):821-3. DOI: 10.1007/s00401-010-0766-y. View

Gambetti P, Dong Z, Yuan J, Xiao X, Zheng M, Alshekhlee A . A novel human disease with abnormal prion protein sensitive to protease. Ann Neurol. 2008; 63(6):697-708. PMC: 2767200. DOI: 10.1002/ana.21420. View