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1
Use of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob disease.
J Neurol Neurosurg Psychiatry. 2001 Jun;70(6):744-8. doi: 10.1136/jnnp.70.6.744.
2
Total tau protein in cerebrospinal fluid and diffusion-weighted MRI as an early diagnostic marker for Creutzfeldt-Jakob disease.
Dement Geriatr Cogn Disord. 2007;24(3):207-12. doi: 10.1159/000107082. Epub 2007 Aug 10.
3
Diagnostic value of CSF protein profile in a Portuguese population of sCJD patients.
J Neurol. 2009 Sep;256(9):1540-50. doi: 10.1007/s00415-009-5160-0. Epub 2009 May 6.
4
Influence of timing on CSF tests value for Creutzfeldt-Jakob disease diagnosis.
J Neurol. 2007 Jul;254(7):901-6. doi: 10.1007/s00415-006-0472-9. Epub 2007 Mar 25.
5
The role of cerebrospinal fluid 14-3-3 and other proteins in the diagnosis of sporadic Creutzfeldt-Jakob disease in the UK: a 10-year review.
J Neurol Neurosurg Psychiatry. 2010 Nov;81(11):1243-8. doi: 10.1136/jnnp.2009.197962. Epub 2010 Sep 20.
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Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies.
J Neurol. 2009 Oct;256(10):1620-8. doi: 10.1007/s00415-009-5163-x. Epub 2009 May 15.
9
Brain-derived proteins in the CSF: do they correlate with brain pathology in CJD?
BMC Neurol. 2006 Sep 21;6:35. doi: 10.1186/1471-2377-6-35.
10
Follow-up investigations of tau protein and S-100B levels in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease.
Dement Geriatr Cogn Disord. 2005;19(5-6):376-82. doi: 10.1159/000084708. Epub 2005 Mar 30.

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2
Variant CJD: Reflections a Quarter of a Century on.
Pathogens. 2021 Oct 30;10(11):1413. doi: 10.3390/pathogens10111413.
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The importance of ongoing international surveillance for Creutzfeldt-Jakob disease.
Nat Rev Neurol. 2021 Jun;17(6):362-379. doi: 10.1038/s41582-021-00488-7. Epub 2021 May 10.
6
Clinical Use of Improved Diagnostic Testing for Detection of Prion Disease.
Viruses. 2021 Apr 28;13(5):789. doi: 10.3390/v13050789.
7
Challenges and Advances in Antemortem Diagnosis of Human Transmissible Spongiform Encephalopathies.
Front Bioeng Biotechnol. 2020 Oct 20;8:585896. doi: 10.3389/fbioe.2020.585896. eCollection 2020.
8
Clinical Laboratory Tests Used To Aid in Diagnosis of Human Prion Disease.
J Clin Microbiol. 2019 Sep 24;57(10). doi: 10.1128/JCM.00769-19. Print 2019 Oct.
10
Detection of CSF 14-3-3 Protein in Sporadic Creutzfeldt-Jakob Disease Patients Using a New Automated Capillary Western Assay.
Mol Neurobiol. 2018 Apr;55(4):3537-3545. doi: 10.1007/s12035-017-0607-2. Epub 2017 May 16.

本文引用的文献

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14-3-3 testing in diagnosing Creutzfeldt-Jakob disease: a prospective study in 112 patients.
Neurology. 2000 Aug 22;55(4):514-6. doi: 10.1212/wnl.55.4.514.
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Diagnosis of new variant Creutzfeldt-Jakob disease.
Ann Neurol. 2000 May;47(5):575-82.
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14-3-3 protein in the cerebrospinal fluid of patients with acute transverse myelitis.
Lancet. 2000 Mar 11;355(9207):901. doi: 10.1016/S0140-6736(99)04745-5.
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Detection of 14-3-3 protein in the CSF of a patient with Hashimoto's encephalopathy.
Neurology. 2000 Apr 11;54(7):1539-40. doi: 10.1212/wnl.54.7.1539.
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Diagnosis of Creutzfeldt-Jakob disease: effect of clinical criteria on incidence estimates.
Neurology. 2000 Mar 14;54(5):1095-9. doi: 10.1212/wnl.54.5.1095.
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Increase of neuron-specific enolase in patients with Creutzfeldt-Jakob disease.
Neurosci Lett. 1999 Feb 12;261(1-2):124-6. doi: 10.1016/s0304-3940(98)00992-6.
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Neuropathological findings in new variant CJD and experimental transmission of BSE.
FEMS Immunol Med Microbiol. 1998 Jun;21(2):91-5. doi: 10.1111/j.1574-695X.1998.tb01153.x.

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