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For: Figgie MP Jr, Appleby BS. Clinical Use of Improved Diagnostic Testing for Detection of Prion Disease. Viruses 2021;13:789. [PMID: 33925126 DOI: 10.3390/v13050789] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 4.5] [Reference Citation Analysis]
Number Citing Articles
1 Mastrianni JA. Genetics of Prion Disease. Prions and Diseases 2023. [DOI: 10.1007/978-3-031-20565-1_19] [Reference Citation Analysis]
2 Nafría Jiménez B, Garrido Chércoles A. Biomarcadores diagnósticos de la enfermedad de Creutzfeld-Jakob. Med Lab 2023. [DOI: 10.20960/revmedlab.00125] [Reference Citation Analysis]
3 Appleby BS, Shetty S, Elkasaby M. Genetic aspects of human prion diseases. Front Neurol 2022;13:1003056. [DOI: 10.3389/fneur.2022.1003056] [Reference Citation Analysis]
4 Christenson PR, Li M, Rowden G, Schwabenlander MD, Wolf TM, Oh SH, Larsen PA. A field-deployable diagnostic assay for the visual detection of misfolded prions. Sci Rep 2022;12:12246. [PMID: 35851406 DOI: 10.1038/s41598-022-16323-y] [Reference Citation Analysis]
5 Goldman JS, Vallabh SM. Genetic counseling for prion disease: Updates and best practices. Genet Med 2022:S1098-3600(22)00812-7. [PMID: 35819418 DOI: 10.1016/j.gim.2022.06.003] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Carrasco AE, Appleby BS, Cali I, Okhravi HR. Atypical Case of VV1 Creutzfeldt–Jakob Disease Subtype: Case Report. Front Neurol 2022;13:875370. [DOI: 10.3389/fneur.2022.875370] [Reference Citation Analysis]
7 Ershova AA, Kotov AS. Creutzfeldt–Jakob disease: literature review and description of three clinical cases. Nevrol ž im L O Badalâna 2022;3:42-48. [DOI: 10.46563/2686-8997-2022-3-1-42-48] [Reference Citation Analysis]
8 Altuna M, Ruiz I, Zelaya MV, Mendioroz M. Role of Biomarkers for the Diagnosis of Prion Diseases: A Narrative Review. Medicina 2022;58:473. [DOI: 10.3390/medicina58040473] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Howlett WP. Rapidly progressive dementia: limitations in Africa. Pract Neurol. [DOI: 10.1136/practneurol-2022-003385] [Reference Citation Analysis]
10 Navarrete M, Zhou Y. The 14-3-3 Protein Family and Schizophrenia. Front Mol Neurosci 2022;15:857495. [DOI: 10.3389/fnmol.2022.857495] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
11 Christenson PR, Li M, Rowden G, Schwabenlander M, Wolf TM, Oh S, Larsen PA. A Field-Deployable Diagnostic Assay for the Visual Detection of Misfolded Prions.. [DOI: 10.1101/2021.11.22.469560] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Areškevičiūtė A, Lund EL, Capellari S, Parchi P, Pinkowsky CT. The First Sporadic Creutzfeldt-Jakob Disease Case with a Rare Molecular Subtype VV1 and 1-Octapeptide Repeat Deletion in PRNP. Viruses 2021;13:2061. [PMID: 34696491 DOI: 10.3390/v13102061] [Reference Citation Analysis]