van Duinen SG - Search Results

1

Brain Transcriptomic Analysis of Hereditary Cerebral Hemorrhage With Amyloidosis-Dutch Type.

Grand Moursel L, van Roon-Mom WMC, Kiełbasa SM, Mei H, Buermans HPJ, van der Graaf LM, Hettne KM, de Meijer EJ, van Duinen SG, Laros JFJ, van Buchem MA, 't Hoen PAC, van der Maarel SM, van der Weerd L. Grand Moursel L, et al. Among authors: van buchem ma, van der maarel sm, van der weerd l, van roon mom wmc, van duinen sg, van der graaf lm. Front Aging Neurosci. 2018 Apr 13;10:102. doi: 10.3389/fnagi.2018.00102. eCollection 2018. Front Aging Neurosci. 2018. PMID: 29706885 Free PMC article.

2

Morphology of cerebral plaque-like lesions in hereditary cerebral hemorrhage with amyloidosis (Dutch).

Maat-Schieman ML, van Duinen SG, Haan J, Roos RA. Maat-Schieman ML, et al. Among authors: van duinen sg. Acta Neuropathol. 1992;84(6):674-9. doi: 10.1007/BF00227745. Acta Neuropathol. 1992. PMID: 1471474

3

Cortical tissue of patients with hereditary cerebral hemorrhage with amyloidosis (Dutch) contains various extracellular matrix deposits.

van Duinen SG, Maat-Schieman ML, Bruijn JA, Haan J, Roos RA. van Duinen SG, et al. Lab Invest. 1995 Aug;73(2):183-9. Lab Invest. 1995. PMID: 7637318

4

Hereditary cerebral hemorrhage with amyloidosis (Dutch): a model for congophilic plaque formation without neurofibrillary pathology.

Maat-Schieman ML, Radder CM, van Duinen SG, Haan J, Roos RA. Maat-Schieman ML, et al. Among authors: van duinen sg. Acta Neuropathol. 1994;88(4):371-8. doi: 10.1007/BF00310382. Acta Neuropathol. 1994. PMID: 7839831

5

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. Among authors: van duinen sg. Brain Pathol. 1996 Apr;6(2):111-4. doi: 10.1111/j.1750-3639.1996.tb00793.x. Brain Pathol. 1996. PMID: 8737926 Review.

6

Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): II--A review of histopathological aspects.

Maat-Schieman ML, van Duinen SG, Bornebroek M, Haan J, Roos RA. Maat-Schieman ML, et al. Among authors: van duinen sg. Brain Pathol. 1996 Apr;6(2):115-20. doi: 10.1111/j.1750-3639.1996.tb00794.x. Brain Pathol. 1996. PMID: 8737927 Review.

7

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. Among authors: van buchem ma, van duinen sg, van broeckhoven c. Ann Neurol. 1997 May;41(5):695-8. doi: 10.1002/ana.410410523. Ann Neurol. 1997. PMID: 9153536

8

Microvasculopathy is associated with the number of cerebrovascular lesions in hereditary cerebral hemorrhage with amyloidosis, Dutch type.

Natté R, Vinters HV, Maat-Schieman ML, Bornebroek M, Haan J, Roos RA, van Duinen SG. Natté R, et al. Among authors: van duinen sg. Stroke. 1998 Aug;29(8):1588-94. doi: 10.1161/01.str.29.8.1588. Stroke. 1998. PMID: 9707198

9

Subcortical lacunar lesions: an MR imaging finding in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

van Den Boom R, Lesnik Oberstein SA, van Duinen SG, Bornebroek M, Ferrari MD, Haan J, van Buchem MA. van Den Boom R, et al. Among authors: van buchem ma, van duinen sg. Radiology. 2002 Sep;224(3):791-6. doi: 10.1148/radiol.2243011123. Radiology. 2002. PMID: 12202716

10

Evaluation of diagnostic NOTCH3 immunostaining in CADASIL.

Lesnik Oberstein SA, van Duinen SG, van den Boom R, Maat-Schieman ML, van Buchem MA, van Houwelingen HC, Hegeman-Kleinn IM, Ferrari MD, Breuning MH, Haan J. Lesnik Oberstein SA, et al. Among authors: van den boom r, van buchem ma, van houwelingen hc, van duinen sg. Acta Neuropathol. 2003 Aug;106(2):107-11. doi: 10.1007/s00401-003-0701-6. Epub 2003 May 17. Acta Neuropathol. 2003. PMID: 12756589

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