Boellaard JW - Search Results

1

Tubulovesicular structures are a consistent (and unexplained) finding in the brains of humans with prion diseases.

Liberski PP, Sikorska B, Hauw JJ, Kopp N, Streichenberger N, Giraud P, Budka H, Boellaard JW, Brown P. Liberski PP, et al. Among authors: boellaard jw. Virus Res. 2008 Mar;132(1-2):226-8. doi: 10.1016/j.virusres.2007.11.008. Epub 2008 Jan 14. Virus Res. 2008. PMID: 18164506

2

Ultrastructural characteristics (or evaluation) of Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies or prion diseases.

Liberski PP, Sikorska B, Hauw JJ, Kopp N, Streichenberger N, Giraud P, Boellaard J, Budka H, Kovacs GG, Ironside J, Brown P. Liberski PP, et al. Ultrastruct Pathol. 2010 Dec;34(6):351-61. doi: 10.3109/01913123.2010.491175. Ultrastruct Pathol. 2010. PMID: 21070167

3

Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Sträussler-Scheinker syndrome.

Barcikowska M, Liberski PP, Boellaard JW, Brown P, Gajdusek DC, Budka H. Barcikowska M, et al. Among authors: boellaard jw. Acta Neuropathol. 1993;85(6):623-7. doi: 10.1007/BF00334672. Acta Neuropathol. 1993. PMID: 8337941

4

Gerstmann-Sträussler-Scheinker disease- the dilemma of molecular and clinical correlations.

Boellaard JW, Brown P, Tateishi J. Boellaard JW, et al. Clin Neuropathol. 1999 Nov-Dec;18(6):271-85. Clin Neuropathol. 1999. PMID: 10580553 Review.

5

Gerstmann-Sträussler-Scheinker disease with A117V mutation in a second French-Alsatian family.

Heldt N, Boellaard JW, Brown P, Cervenákova L, Doerr-Schott J, Thomas C, Scherer C, Rohmer F. Heldt N, et al. Among authors: boellaard jw. Clin Neuropathol. 1998 Jul-Aug;17(4):229-34. Clin Neuropathol. 1998. PMID: 9707339

6

Identification of a PRNP gene mutation in Jakob's original Creutzfeldt-Jakob disease family.

Brown P, Cervenáková L, Boellaard JW, Stavrou D, Goldfarb LG, Gajdusek DC. Brown P, et al. Among authors: boellaard jw. Lancet. 1994 Jul 9;344(8915):130-1. doi: 10.1016/s0140-6736(94)91318-8. Lancet. 1994. PMID: 7912367 No abstract available.

7

Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndrome.

Brown P, Goldfarb LG, Brown WT, Goldgaber D, Rubenstein R, Kascsak RJ, Guiroy DC, Piccardo P, Boellaard JW, Gajdusek DC. Brown P, et al. Among authors: boellaard jw. Neurology. 1991 Mar;41(3):375-9. doi: 10.1212/wnl.41.3.375. Neurology. 1991. PMID: 1672447

8

Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome.

Goldfarb LG, Brown P, Goldgaber D, Asher DM, Rubenstein R, Brown WT, Piccardo P, Kascsak RJ, Boellaard JW, Gajdusek DC. Goldfarb LG, et al. Among authors: boellaard jw. Exp Neurol. 1990 Jun;108(3):247-50. doi: 10.1016/0014-4886(90)90130-k. Exp Neurol. 1990. PMID: 2190844

9

Creutzfeldt-Jakob disease with amyloid angiopathy: diagnosis by immunological analyses and transmission experiments.

Tateishi J, Kitamoto T, Doh-ura K, Boellaard JW, Peiffer J. Tateishi J, et al. Among authors: boellaard jw. Acta Neuropathol. 1992;83(5):559-63. doi: 10.1007/BF00310037. Acta Neuropathol. 1992. PMID: 1621512

10

Miniplaques and shapeless cerebral amyloid deposits in a case of Gerstmann-Sträussler-Scheinker's syndrome.

Boellaard JW, Doerr-Schott J, Schlote W. Boellaard JW, et al. Acta Neuropathol. 1993;86(5):532-5. doi: 10.1007/BF00228593. Acta Neuropathol. 1993. PMID: 8310806

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

31 results

Search Page

Filters