Maat-Schieman ML - Search Results

1

The apolipoprotein E epsilon 4 allele does not influence the clinical expression of the amyloid precursor protein gene codon 693 or 692 mutations.

Haan J, Van Broeckhoven C, van Duijn CM, Voorhoeve E, van Harskamp F, van Swieten JC, Maat-Schieman ML, Roos RA, Bakker E. Haan J, et al. Ann Neurol. 1994 Sep;36(3):434-7. doi: 10.1002/ana.410360315. Ann Neurol. 1994. PMID: 8080251

2

Amyloid beta precursor protein-mRNA is expressed throughout cerebral vessel walls.

Natté R, de Boer WI, Maat-Schieman ML, Baelde HJ, Vinters HV, Roos RA, van Duinen SG. Natté R, et al. Brain Res. 1999 May 15;828(1-2):179-83. doi: 10.1016/s0006-8993(99)01361-x. Brain Res. 1999. PMID: 10320740

3

Dementia in hereditary cerebral hemorrhage with amyloidosis-Dutch type is associated with cerebral amyloid angiopathy but is independent of plaques and neurofibrillary tangles.

Natté R, Maat-Schieman ML, Haan J, Bornebroek M, Roos RA, van Duinen SG. Natté R, et al. Ann Neurol. 2001 Dec;50(6):765-72. doi: 10.1002/ana.10040. Ann Neurol. 2001. PMID: 11761474

4

Microglia in diffuse plaques in hereditary cerebral hemorrhage with amyloidosis (Dutch). An immunohistochemical study.

Maat-Schieman ML, Rozemuller AJ, van Duinen SG, Haan J, Eikelenboom P, Roos RA. Maat-Schieman ML, et al. J Neuropathol Exp Neurol. 1994 Sep;53(5):483-91. doi: 10.1097/00005072-199409000-00007. J Neuropathol Exp Neurol. 1994. PMID: 7521904

5

Co-localization of beta/A4 and cystatin C in cortical blood vessels in Dutch, but not in Icelandic hereditary cerebral hemorrhage with amyloidosis.

Haan J, Maat-Schieman ML, van Duinen SG, Jensson O, Thorsteinsson L, Roos RA. Haan J, et al. Acta Neurol Scand. 1994 May;89(5):367-71. doi: 10.1111/j.1600-0404.1994.tb02648.x. Acta Neurol Scand. 1994. PMID: 8085435

6

Clinical aspects of cerebral amyloid angiopathy.

Haan J, Maat-Schieman ML, Roos RA. Haan J, et al. Dementia. 1994 May-Aug;5(3-4):210-3. doi: 10.1159/000106725. Dementia. 1994. PMID: 8087182 Review.

7

Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): I--A review of clinical, radiologic and genetic aspects.

Bornebroek M, Haan J, Maat-Schieman ML, Van Duinen SG, Roos RA. Bornebroek M, et al. Brain Pathol. 1996 Apr;6(2):111-4. doi: 10.1111/j.1750-3639.1996.tb00793.x. Brain Pathol. 1996. PMID: 8737926 Review.

8

Association of vascular amyloid beta and cells of the mononuclear phagocyte system in hereditary cerebral hemorrhage with amyloidosis (Dutch) and Alzheimer disease.

Maat-Schieman ML, van Duinen SG, Rozemuller AJ, Haan J, Roos RA. Maat-Schieman ML, et al. J Neuropathol Exp Neurol. 1997 Mar;56(3):273-84. doi: 10.1097/00005072-199703000-00006. J Neuropathol Exp Neurol. 1997. PMID: 9056541

9

Dutch hereditary cerebral amyloid angiopathy: structural lesions and apolipoprotein E genotype.

Bornebroek M, Haan J, Van Duinen SG, Maat-Schieman ML, Van Buchem MA, Bakker E, Van Broeckhoven C, Roos RA. Bornebroek M, et al. Ann Neurol. 1997 May;41(5):695-8. doi: 10.1002/ana.410410523. Ann Neurol. 1997. PMID: 9153536

10

Hereditary cerebral hemorrhage with amyloidosis-Dutch type.

Maat-Schieman M, Roos R, van Duinen S. Maat-Schieman M, et al. Neuropathology. 2005 Dec;25(4):288-97. doi: 10.1111/j.1440-1789.2005.00631.x. Neuropathology. 2005. PMID: 16382777 Review.

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