J W Boellaard
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Explore the profile of J W Boellaard including associated specialties, affiliations and a list of published articles.
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213
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Recent Articles
1.
Liberski P, Sikorska B, Hauw J, Kopp N, Streichenberger N, Giraud P, et al.
Virus Res
. 2008 Jan;
132(1-2):226-8.
PMID: 18164506
Creutzfeldt-Jakob disease (CJD), Gerstmann-Sträussler-Scheinker disease (GSS) and Fatal Familial Insomnia (FFI) are slow neurodegenerative disorders classified as transmissible spongiform encephalopathies (TSEs) or prion diseases, which appear in sporadic, hereditary or...
2.
Boellaard J, Harzer K, Schlote W
Ultrastruct Pathol
. 2006 Nov;
30(5):387-91.
PMID: 17090518
The ultrastructure of lipofuscin (Lf) was studied in hippocampal and neocortical neurons of children and youngsters between 3 months and 24 years of age. As a standard, regions CA1 and...
3.
Boellaard J, Schlote W, Hofer W
Ultrastruct Pathol
. 2005 Mar;
28(5-6):341-51.
PMID: 15764582
Lipofuscin represents an integral part of neurons and glial cells in mammals and in submammalian species. It is a special lysosomal organelle, takes part of cellular metabolism, and is a...
4.
Boellaard J, Brown P, Tateishi J
Clin Neuropathol
. 1999 Dec;
18(6):271-85.
PMID: 10580553
Gerstmann-Sträussler-Scheinker disease (GSSD) is a hereditary as well as transmissible human prion disease, restricted to families carrying point mutations of the PRPN gene on chromosome 20. To date 7 different...
5.
Heldt N, Boellaard J, Brown P, Cervenakova L, DOERR-SCHOTT J, Thomas C, et al.
Clin Neuropathol
. 1998 Aug;
17(4):229-34.
PMID: 9707339
We report a kindred of French/Alsatian origin with symptoms of Gerstmann-Sträussler-Scheinker disease over 3 generations. In the propositus, cerebellar signs and memory disturbance were the presenting features, followed by other...
6.
Brown P, Cervenakova L, Boellaard J, Stavrou D, Goldfarb L, Gajdusek D
Lancet
. 1994 Jul;
344(8915):130-1.
PMID: 7912367
No abstract available.
7.
Barcikowska M, Liberski P, Boellaard J, Brown P, Gajdusek D, Budka H
Acta Neuropathol
. 1993 Jan;
85(6):623-7.
PMID: 8337941
The microglial cell has been demonstrated as component of the cerebral amyloid plaque of Alzheimer's disease. Involvement of microglia in plaques of another cerebral amyloidosis, the Gerstmann-Sträussler-Scheinker syndrome (GSS), has...
8.
Boellaard J, DOERR-SCHOTT J, Schlote W
Acta Neuropathol
. 1993 Jan;
86(5):532-5.
PMID: 8310806
Multicentric plaques of typical pathomorphology have been described in two members of the well-documented German family "Sch" with Gerstmann-Sträussler-Scheinker's syndrome (GSS). The case of a third affected member with a...
9.
Tateishi J, Kitamoto T, Doh-ura K, Boellaard J, PEIFFER J
Acta Neuropathol
. 1992 Jan;
83(5):559-63.
PMID: 1621512
It was difficult to make a definite pathological diagnosis in a 73-year-old man with Creutzfeldt-Jakob disease (CJD) due to extensive amyloid angiopathy which lacked any severe spongiform changes. Immunostaining using...
10.
Brown P, Goldfarb L, Brown W, Goldgaber D, Rubenstein R, Kascsak R, et al.
Neurology
. 1991 Mar;
41(3):375-9.
PMID: 1672447
We have verified, by full open reading frame sequencing, the presence of an amino-acid-altering mutation in codon 102 of the scrapie amyloid protein gene in three affected members of a...