Ghent University Academic Bibliography

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Your filters: cql: author="Robberecht, Wim" or (type exact bookEditor and editor="Robberecht, Wim")

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Efficacy and safety of IVIG in CIDP : combined data of the PRIMA and PATH studies

Ingemar SJ Merkies, Ivo N van Schaik, Jean-Marc Léger, Vera Bril, Nan van Geloven, Hans-Peter Hartung, Richard A Lewis, Gen Sobue, John-Philip Lawo, Billie L Durn, et al.

(2019) JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. 24(1). p.48-55
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Identification and characterization of nanobodies targeting the EphA4 receptor

Lies Schoonaert, Laura Rue, Bart Roucourt, Mieke Timmers, Susan Little, Lucia Chavez-Gutierrez, Maarten Dewilde, Peter Joyce, Adam Curnock, Peter Weber, et al.

(2017) JOURNAL OF BIOLOGICAL CHEMISTRY. 292(27). p.11452-11465
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Phase separation of C9orf72 dipeptide repeats perturbs stress granule dynamics

Steven Boeynaems, Elke Bogaert, Denes Kovacs, Albert Konijnenberg, Evy Timmerman (UGent) , Alex Volkov, Mainak Guharoy, Mathias De Decker, Tom Jaspers, Veronica H Ryan, et al.

(2017) MOLECULAR CELL. 65(6). p.1044-1055
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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Julie van der Zee, Tim Van Langenhove (UGent) , Gabor G Kovacs, Lubina Dillen, William Deschamps, Sebastiaan Engelborghs, Radoslav Matěj, Mathieu Vandenbulcke, Anne Sieben (UGent) , Bart Dermaut (UGent) , et al.

(2014) ACTA NEUROPATHOLOGICA. 128(3). p.397-410
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Efficacy and safety of Privigen® in patients with chronic inflammatory demyelinating polyneuropathy: results of a prospective, single-arm, open-label Phase III study (the PRIMA study)

Jean-Marc Léger, Jan De Bleecker (UGent) , Claudia Sommer, Wim Robberecht, Mika Saarela, Jerzy Kamienowski, Zbigniew Stelmasiak, Orell Mielke, Björn Tackenberg, Amgad Shebl, et al.

(2013) JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. 18(2). p.130-140
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A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum : a gene identification study

Ilse Gijselinck, Tim Van Langenhove (UGent) , Julie van der Zee, Kristel Sleegers, Stephanie Philtjens, Gernot Kleinberger, Jonathan Janssens, Karolien Bettens, Caroline Van Cauwenberghe, Sandra Pereson, et al.

(2012) LANCET NEUROLOGY. 11(1). p.54-65
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VEGF protects motor neurons against excitotoxicity by upregulation of GluR2

Elke Bogaert (UGent) , Philip Van Damme, Koen Poesen, Joke Dhondt (UGent) , Nicole Hersmus, Dora Kiraly, Wendy Scheveneels, Wim Robberecht and Ludo Van Den Bosch

(2010) NEUROBIOLOGY OF AGING. 31(12). p.2185-2191
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Mutant HSPB8 causes motor neuron-specific neurite degeneration

Joy Irobi, Leonardo Almeida-Souza, Bob Asselbergh, Vicky De Winter, Sofie Goethals, Ines Dierick, Jyothsna Krishnan, Jean-Pierre Timmermans, Wim Robberecht, Peter De Jonghe, et al.

(2010) HUMAN MOLECULAR GENETICS. 19(16). p.3254-3265
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Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS

Ilse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, Wim Robberecht, Jean-Jacques Martin, Rik Vandenberghe, Raf Sciot, Bart Dermaut (UGent) , Dirk Goossens, Julie van der Zee, et al.

(2009) NEUROBIOLOGY OF AGING. 30(8). p.1329-1331
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Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival

Philip Van Damme, Annelies Van Hoecke, Diether Lambrechts, Peter Vanacker, Elke Bogaert (UGent) , John van Swieten, Peter Carmeliet, Ludo Van Den Bosch and Wim Robberecht

(2008) JOURNAL OF CELL BIOLOGY. 181(1). p.37-41
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Genetic variant in the HSPB1 promoter region impairs the HSP27 stress response

Ines Dierick, Joy Irobi, Sophie Janssens (UGent) , Jessie Theuns, Robin Lemmens, An Jacobs, Ellen Corsmit, Nicole Hersmus, Ludo Van Den Bosch, Wim Robberecht, et al.

(2007) HUMAN MUTATION. 28(8). p.830-830
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Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS

Ilse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, Wim Robberecht, Jean-Jacques Martin, Rik Vandenberghe, Raf Sciot, Bart Dermaut (UGent) , Dirk Goossens, Julie van der Zee, et al.

(2007) New trends in Alzheimer and Parkinson related disorders : ADPD 2007. p.1-11
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Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration

Bert Oosthuyse, Lieve Moons, Erik Storkebaum, Heike Beck, Dieter Nuyens, Koen Brusselmans, Jo Van Dorpe (UGent) , Peter Hellings, Marchel Gorselink, Stéphane Heymans, et al.

(2001) NATURE GENETICS. 28(2). p.131-138

Academic Bibliography

Efficacy and safety of IVIG in CIDP : combined data of the PRIMA and PATH studies

Identification and characterization of nanobodies targeting the EphA4 receptor

Phase separation of C9orf72 dipeptide repeats perturbs stress granule dynamics

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Efficacy and safety of Privigen® in patients with chronic inflammatory demyelinating polyneuropathy: results of a prospective, single-arm, open-label Phase III study (the PRIMA study)

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum : a gene identification study

VEGF protects motor neurons against excitotoxicity by upregulation of GluR2

Mutant HSPB8 causes motor neuron-specific neurite degeneration

Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS

Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival

Genetic variant in the HSPB1 promoter region impairs the HSP27 stress response

Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS

Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration

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