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Items: 8

1.

Comment: Tau vs 14-3-3 protein--adjuncts for the diagnosis of CJD.

Drachman DA.

Neurology. 2012 Aug 7;79(6):551. doi: 10.1212/WNL.0b013e3182635834. Epub 2012 Jul 25. No abstract available.

PMID:
22843263
2.

Cerebrospinal fluid biomarkers in Creutzfeldt-Jakob disease.

Van Everbroeck B, Boons J, Cras P.

Clin Neurol Neurosurg. 2005 Aug;107(5):355-60. Epub 2005 Jan 12. Review.

PMID:
16023527
3.

[Clinical typing and diagnosis of sporadic human prion diseases (classic sproadic CJD, MM2-cortical form CJD, MM2-thalamic form CJD)].

Satoh K, Shirabe S, Eguchi K.

Nihon Rinsho. 2007 Aug;65(8):1423-32. Review. Japanese.

PMID:
17695279
4.
5.

Use of 14-3-3 in the diagnosis of Creutzfeldt-Jakob disease.

Green AJ.

Biochem Soc Trans. 2002 Aug;30(4):382-6. Review.

PMID:
12196099
6.

[Prion disease].

Mizusawa H.

Rinsho Shinkeigaku. 2010 Nov;50(11):797-802. Review. Japanese.

PMID:
21921445
7.

Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease.

Shiga Y, Miyazawa K, Sato S, Fukushima R, Shibuya S, Sato Y, Konno H, Doh-ura K, Mugikura S, Tamura H, Higano S, Takahashi S, Itoyama Y.

Neurology. 2004 Aug 10;63(3):443-9. Review.

PMID:
15304574
8.

Cerebrospinal fluid: when is it worthwhile to do a lumbar puncture?

Peskind ER.

CNS Spectr. 2008 Oct;13(10 Suppl 16):25-7. Review. No abstract available.

PMID:
18955957

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