Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Michael K. Liem"'
Autor:
Julie W. Rutten, Gido Gravesteijn, Jeroen van der Grond, Saskia A J Lesnik Oberstein, Inge M.W. Verberk, Stefan Böhringer, Michael K. Liem, Annemieke Aartsma-Rus, Charlotte E. Teunissen
Publikováno v:
Annals of Clinical and Translational Neurology, 6(1), 46-56. John Wiley and Sons Ltd
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, 6(1), 46-56
Gravesteijn, G, Rutten, J W, Verberk, I M W, Böhringer, S, Liem, M K, van der Grond, J, Aartsma-Rus, A, Teunissen, C E & Lesnik Oberstein, S A J 2019, ' Serum Neurofilament light correlates with CADASIL disease severity and survival ', Annals of Clinical and Translational Neurology, vol. 6, no. 1, pp. 46-56 . https://doi.org/10.1002/acn3.678
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, 6(1), 46-56
Gravesteijn, G, Rutten, J W, Verberk, I M W, Böhringer, S, Liem, M K, van der Grond, J, Aartsma-Rus, A, Teunissen, C E & Lesnik Oberstein, S A J 2019, ' Serum Neurofilament light correlates with CADASIL disease severity and survival ', Annals of Clinical and Translational Neurology, vol. 6, no. 1, pp. 46-56 . https://doi.org/10.1002/acn3.678
Objective: To validate whether serum Neurofilament Light-chain (NfL) levels correlate with disease severity in CADASIL, and to determine whether serum NfL predicts disease progression and survival. Methods: Fourty-one (pre-) manifest individuals with
Autor:
Saskia A J Lesnik Oberstein, Michel D. Ferrari, Andrew G. Webb, Mark A. van Buchem, Maarten J. Versluis, Michael K. Liem, Jeroen van der Grond, Joost Haan
Publikováno v:
Stroke, 41(12), 2812-2816
Background and Purpose— Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary small vessel disease. Although postmortem studies have demonstrated mural thickening in leptomeningeal arte
Autor:
Joost Haan, Michel D. Ferrari, Jeroen van de Grond, S.A.M.J. Lesnik Oberstein, Michael K. Liem, Rivka van den Boom, Mark A. van Buchem
Publikováno v:
AJNR Am J Neuroradiol
BACKGROUND AND PURPOSE: Basal total cerebral blood flow (TCBF) and cerebrovascular reactivity (CVR) are assumed to play an important role in the pathophysiology of small-vessel disease. Cerebral autosomal dominant arteriopathy with subcortical infarc
Autor:
Harry J. de Koning, Ida J. Korfage, Ingrid W. van der Cruijsen, Michael K. Liem, Suzie J. Otto, Jan J. Lous, Fritz H. Schröder
Publikováno v:
International Journal of Cancer. 105:394-399
The extent of effective prostate-specific antigen (PSA) contamination in the Rotterdam section of the ongoing European Randomized Study of Screening for Prostate Cancer (ERSPC) trial was evaluated and defined as when opportunistic PSA testing of ≥
Autor:
Harry J. de Koning, Michael K. Liem, Caroline A. Baan, Rob Boer, Fritz H. Schröder, Freda E. Alexander on behalf of ERSPC
Publikováno v:
International Journal of Cancer. 98:268-273
From 1992-2001, 7 countries in Europe gradually recruited men for the European Randomised Screening for Prostate Cancer (ERSPC) trial. Centres recruit different age groups and have different designs for recruiting and countries have different underly
Autor:
M. J. Vollebregt, Huub A. M. Middelkoop, J. van der Grond, Michael K. Liem, A.T.J.M. Helderman-van den Enden, S. A. J. Lesnik Oberstein
Publikováno v:
Journal of Neurology. 255:1978-1980
Autor:
Michael K. Liem, Phillis Lakeman, Julie W. Rutten, Johannes G. Dauwerse, Anneke Maat-Kievit, Sjoerd G. van Duinen, Saskia A J Lesnik Oberstein, H.B. Ginjaar, Elles M. J. Boon, Gisela M. Terwindt, Margot J. Pont, Ellen Vollebregt
Publikováno v:
Human Mutation, 34(11), 1486-1489. Wiley-Liss Inc.
Human mutation, 34(11), 1486-1489. Wiley-Liss Inc.
Rutten, J W, Boon, E M J, Liem, M K, Dauwerse, J G, Pont, M J, Vollebregt, E, Maat-Kievit, A J, Ginjaar, H B, Lakeman, P, van Duinen, S G, Terwindt, G M & Oberstein, S A J L 2013, ' Hypomorphic NOTCH3 Alleles Do Not Cause CADASIL in Humans ', Human Mutation, vol. 34, no. 11, pp. 1486-1489 . https://doi.org/10.1002/humu.22432
Human Mutation, 34(11), 1486-1489
Human Mutation
Human mutation, 34(11), 1486-1489. Wiley-Liss Inc.
Rutten, J W, Boon, E M J, Liem, M K, Dauwerse, J G, Pont, M J, Vollebregt, E, Maat-Kievit, A J, Ginjaar, H B, Lakeman, P, van Duinen, S G, Terwindt, G M & Oberstein, S A J L 2013, ' Hypomorphic NOTCH3 Alleles Do Not Cause CADASIL in Humans ', Human Mutation, vol. 34, no. 11, pp. 1486-1489 . https://doi.org/10.1002/humu.22432
Human Mutation, 34(11), 1486-1489
Human Mutation
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is caused by stereotyped missense mutations in NOTCH3. Whether these mutations lead to the CADASIL phenotype via a neomorphic effect, or rather by a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3971b322fc5acc074446838e75ece9a3
https://hdl.handle.net/1887/101527
https://hdl.handle.net/1887/101527
Autor:
Jeroen van der Grond, Mark A. van Buchem, Andrea B. Maier, Michael K. Liem, Ania M. Oleksik, Andrew G. Webb, Julien Milles, Sanneke van Rooden, Maarten J. Versluis
Publikováno v:
Alzheimers & Dementia, 10(1), e19-e26. Elsevier
Alzheimers & Dementia, 10(1), e19-26. Elsevier Inc.
van Rooden, S, Versluis, M J, Liem, M K, Milles, J, Maier, A B, Oleksik, A M, Webb, A G, van Buchem, M A & van der Grond, J 2014, ' Cortical phase changes in Alzheimer's disease at 7T MRI : a novel imaging marker ', Alzheimers & Dementia, vol. 10, no. 1, pp. e19-26 . https://doi.org/10.1016/j.jalz.2013.02.002
van Rooden, S, Versluis, M J, Liem, M K, Milles, J, Maier, A B, Oleksik, A M, Webb, A G, van Buchem, M A & van der Grond, J 2014, ' Cortical phase changes in Alzheimer's disease at 7T MRI: a novel imaging marker ', Alzheimers & Dementia, vol. 10, no. 1, pp. e19-e26 . https://doi.org/10.1016/j.jalz.2013.02.002
Alzheimers & Dementia, 10(1), e19-26. Elsevier Inc.
van Rooden, S, Versluis, M J, Liem, M K, Milles, J, Maier, A B, Oleksik, A M, Webb, A G, van Buchem, M A & van der Grond, J 2014, ' Cortical phase changes in Alzheimer's disease at 7T MRI : a novel imaging marker ', Alzheimers & Dementia, vol. 10, no. 1, pp. e19-26 . https://doi.org/10.1016/j.jalz.2013.02.002
van Rooden, S, Versluis, M J, Liem, M K, Milles, J, Maier, A B, Oleksik, A M, Webb, A G, van Buchem, M A & van der Grond, J 2014, ' Cortical phase changes in Alzheimer's disease at 7T MRI: a novel imaging marker ', Alzheimers & Dementia, vol. 10, no. 1, pp. e19-e26 . https://doi.org/10.1016/j.jalz.2013.02.002
BACKGROUND: Postmortem studies have indicated the potential of high-field magnetic resonance imaging (MRI) to visualize amyloid depositions in the cerebral cortex. The aim of this study is to test this hypothesis in patients with Alzheimer's disease
Autor:
Joost Haan, Andrew G. Webb, Marion L.C. Maat-Schieman, Saskia A J Lesnik Oberstein, Maarten J. Versluis, Mark A. van Buchem, Jeroen van der Grond, Michael K. Liem, Michel D. Ferrari
Publikováno v:
Journal of Neurology, Neurosurgery and Psychiatry, 83(12), 1180-1185
Objective Diffuse iron deposition in the brain is commonly found in older people. One of the possible mechanisms that contribute to this iron deposition is cerebral small vessel disease. The aim of this study is to quantify diffuse iron deposition in
Autor:
Joost Haan, Jeroen van der Grond, Michel D. Ferrari, Michael K. Liem, Saskia A J Lesnik Oberstein
Publikováno v:
Cephalalgia, 30(11), 1284-9
Cephalalgia, 30(11), 1284-1289
Cephalalgia
Cephalalgia, 30(11), 1284-1289
Cephalalgia
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is caused by mutations in the NOTCH3 gene and is clinically characterized by recurrent stroke, cognitive decline, psychiatric disturbances and migrai