Samir Kumar-Singh
Samir Kumar-Singh
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Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
M Cruts, I Gijselinck, J Van Der Zee, S Engelborghs, H Wils, D Pirici, ...
Nature 442 (7105), 920-924, 2006
13422006
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
IRA Mackenzie, M Neumann, EH Bigio, NJ Cairns, I Alafuzoff, J Kril, ...
Acta neuropathologica 119 (1), 1, 2010
8332010
TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration
H Wils, G Kleinberger, J Janssens, S Pereson, G Joris, I Cuijt, V Smits, ...
Proceedings of the National Academy of Sciences 107 (8), 3858-3863, 2010
4972010
Identification of a novel plasmid-mediated colistin-resistance gene, mcr-2
BB Xavier, C Lammens, R Ruhal, S Kumar-Singh, P Butaye, H Goossens, ...
Escherichia coli 21 (27), 2016
4722016
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
VM Van Deerlin, PMA Sleiman, M Martinez-Lage, A Chen-Plotkin, ...
Nature genetics 42 (3), 234-239, 2010
3962010
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations
IRA Mackenzie, M Neumann, EH Bigio, NJ Cairns, I Alafuzoff, J Kril, ...
Acta neuropathologica 117 (1), 15-18, 2009
3812009
Mean age‐of‐onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40
S Kumar‐Singh, J Theuns, B Van Broeck, D Pirici, K Vennekens, ...
Human mutation 27 (7), 686-695, 2006
3642006
Identification of a novel plasmid-mediated colistin-resistance gene, mcr-2, in Escherichia coli, Belgium, June 2016
BB Xavier, C Lammens, R Ruhal, S Kumar-Singh, P Butaye, H Goossens, ...
Eurosurveillance 21 (27), 30280, 2016
3602016
FUS pathology defines the majority of tau-and TDP-43-negative frontotemporal lobar degeneration
H Urwin, KA Josephs, JD Rohrer, IR Mackenzie, M Neumann, A Authier, ...
Acta neuropathologica 120 (1), 33-41, 2010
2492010
Pathogenic APP mutations near the γ-secretase cleavage site differentially affect Aβ secretion and APP C-terminal fragment stability
C De Jonghe, C Esselens, S Kumar-Singh, K Craessaerts, S Serneels, ...
Human molecular genetics 10 (16), 1665-1671, 2001
2242001
A novel presenilin 1 mutation associated with Pick's disease but not β‐amyloid plaques
B Dermaut, S Kumar‐Singh, S Engelborghs, J Theuns, R Rademakers, ...
Annals of Neurology: Official Journal of the American Neurological …, 2004
2142004
Angiogenic cytokines in mesothelioma: a study of VEGF, FGF‐1 and‐2, and TGF β expression
S Kumar‐Singh, J Weyler, MJH Martin, PB Vermeulen, E Van Marck
The Journal of pathology 189 (1), 72-78, 1999
1931999
Dense-core plaques in Tg2576 and PSAPP mouse models of Alzheimer's disease are centered on vessel walls
S Kumar-Singh, D Pirici, E McGowan, S Serneels, C Ceuterick, J Hardy, ...
The American journal of pathology 167 (2), 527-543, 2005
1832005
Nonfibrillar diffuse amyloid deposition due to a γ 42‐secretase site mutation points to an essential role for N‐truncated A β 42 in Alzheimer’s disease
S Kumar-Singh, C De Jonghe, M Cruts, R Kleinert, R Wang, M Mercken, ...
Human molecular genetics 9 (18), 2589-2598, 2000
1662000
Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS‐1 mutations that lead to exceptionally high amyloid‐β concentrations
H Houlden, M Baker, E McGowan, P Lewis, M Hutton, R Crook, NW Wood, ...
Annals of neurology 48 (5), 806-808, 2000
1592000
Dense-core senile plaques in the Flemish variant of Alzheimer's disease are vasocentric
S Kumar-Singh, P Cras, R Wang, JM Kros, J van Swieten, U Lübke, ...
The American journal of pathology 161 (2), 507-520, 2002
1352002
Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
N Brouwers, K Nuytemans, J Van Der Zee, I Gijselinck, S Engelborghs, ...
Archives of neurology 64 (10), 1436-1446, 2007
1272007
WT1 MUTATION IN MALIGNANT MESOTHELIOMA AND WT1 IMMUNOREACTIVITY IN RELATION TO p53 AND GROWTH FACTOR RECEPTOR EXPRESSION …
S KUMAR‐SINGH, K SEGERS, U RODECK, H BACKHOVENS, ...
The Journal of Pathology: A Journal of the Pathological Society of Great …, 1997
1241997
Syndecan‐1 expression in malignant mesothelioma: correlation with cell differentiation, WT1 expression, and clinical outcome
S Kumar‐singh, W Jacobs, K Dhaene, B Weyn, J Bogers, J Weyler, ...
The Journal of Pathology: A Journal of the Pathological Society of Great …, 1998
1201998
Behavioral disturbances without amyloid deposits in mice overexpressing human amyloid precursor protein with Flemish (A692G) or Dutch (E693Q) mutation
S Kumar-Singh, I Dewachter, D Moechars, U Lübke, C De Jonghe, ...
Neurobiology of disease 7 (1), 9-22, 2000
1092000
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