Ghent University Academic Bibliography

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Expanding the TDP-43 proteinopathy pathway from neurons to muscle : physiological and pathophysiological functions

Lauren Versluys (UGent) , Pedro Ervilha Pereira (UGent) , Nika Schuermans (UGent) , Boel De Paepe (UGent) , Jan De Bleecker (UGent) , Elke Bogaert (UGent) and Bart Dermaut (UGent)

(2022) FRONTIERS IN NEUROSCIENCE. 16.
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No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers

Cemile Koçoğlu, Helena Gossye, Lubina Dillen, Sara Van Mossevelde, Jan De Bleecker (UGent) , Rik Vandenberghe, Peter P. De Deyn, Kristel Sleegers, Patrick Cras, Sebastiaan Engelborghs, et al.

(2021) NEUROBIOLOGY OF AGING. 97. p.145.e1-145.e4
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Genetic insights in canine degenerative myelopathy

Fréderique Boeykens (UGent) , Luc Peelman (UGent) , Sofie Bhatti (UGent) and Bart Broeckx (UGent)

(2020) VLAAMS DIERGENEESKUNDIG TIJDSCHRIFT. 89(5). p.253-261
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Network approach identifies Pacer as an autophagy protein involved in ALS pathogenesis

S. Beltran, M. Nassif, E. Vicencio, J. Arcos, L. Labrador, B. I. Cortes, C. Cortez, C. A. Bergmann, S. Espinoza, M. F. Hernandez, et al.

(2019) MOLECULAR NEURODEGENERATION. 14.
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Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion

Jelle van den Ameele (UGent) , Ivana Jedlickova, Anna Pristoupilova, Anne Sieben (UGent) , Sara Van Mossevelde, Chantal Ceuterick-de Groote, Helena Hůlková, Radoslav Matej, Alfred Meurs, Christine Van Broeckhoven, et al.

(2018) NEUROLOGY. 90(8). p.e658-e663
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TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis

Julie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, Federica Perrone, Lubina Dillen, Bavo Heeman, Veerle Bäumer, Sebastiaan Engelborghs, Jan De Bleecker (UGent) , Jonathan Baets, et al.

(2017) HUMAN MUTATION. 38(3). p.297-309
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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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Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion

Sara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, Kristel Sleegers, Jan De Bleecker (UGent) , Anne Sieben (UGent) , Rik Vandenberghe, Tim Van Langenhove (UGent) , Jonathan Baets, Olivier Deryck, et al.

(2017) JAMA NEUROLOGY. 74(4). p.445-452
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Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis

Qiang Gang, Conceicão Bettencourt, Pedro M Machado, Stefen Brady, Janice L Holton, Alan M Pittman, Deborah Hughes, Estelle Healy, Matthew Parton, David Hilton-Jones, et al.

(2016) NEUROBIOLOGY OF AGING. 47. p.218.e1-218.e9
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Pixel versus object : a comparison of strategies for the semi-automated mapping of archaeological features using airborne laser scanning data

Christopher Sevara, Michael Pregesbauer, Michael Done, Geert Verhoeven (UGent) and Immo Trinks

(2016) JOURNAL OF ARCHAEOLOGICAL SCIENCE-REPORTS. 5. p.485-498
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Functional complementation in Drosophila to predict the pathogenicity of TARDBP variants: evidence for a loss-of-function mechanism.

Lies Vanden Broeck, Gernot Kleinberger, Julien Chapuis, Marc Gistelinck, Philippe Amouyel, Christine Van Broeckhoven, Jean-Charles Lambert, Patrick Callaerts and Bart Dermaut (UGent)

(2015) NEUROBIOLOGY OF AGING. 36(2). p.1121-1129
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Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort

Ilse Gijselinck, Sara Van Mossevelde, Julie van der Zee, Anne Sieben (UGent) , Stephanie Philtjens, Bavo Heeman, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Greet De Baets, Veerle Baumer, et al.

(2015) NEUROLOGY. 85(24). p.2116-2125
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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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A pan-European study of the C9orf72 repeat associated with FTLD : geographic prevalence, genomic instability, and intermediate repeats

Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove (UGent) , Jessie Theuns, Sebastiaan Engelborghs, Stéphanie Philtjens, Mathieu Vandenbulcke, Kristel Sleegers, Anne Sieben (UGent) , et al.

(2013) HUMAN MUTATION. 34(2). p.363-373
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Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients

Lubina Dillen, Tim Van Langenhove (UGent) , Sebastiaan Engelborghs, Mathieu Vandenbulcke, Stayko Sarafov, Ivailo Tournev, Celine Merlin, Patrick Cras, Rik Vandenberghe, Peter P De Deyn, et al.

(2013) NEUROBIOLOGY OF AGING. 34(6).
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Loss and gain of Drosophila TDP-43 impair synaptic efficacy and motor control leading to age-related neurodegeneration by loss-of-function phenotypes

Danielle C Diaper, Yoshitsugu Adachi, Ben Sutcliffe, Dickon M Humphrey, Christopher JH Elliott, Alan Stepto, Zoe N Ludlow, Lies Vanden Broeck, Patrick Callaerts, Bart Dermaut (UGent) , et al.

(2013) HUMAN MOLECULAR GENETICS. 22(8). p.1539-1557
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TDP-43 loss-of-function causes neuronal loss due to defective steroid receptor-mediated gene program switching in Drosophila

Lies Vanden Broeck, Marina Naval-Sánchez, Yoshitsugu Adachi, Danielle Diaper, Pierre Dourlen, Julien Chapuis, Gernot Kleinberger, Marc Gistelinck, Christine Van Broeckhoven, Jean-Charles Lambert, et al.

(2013) CELL REPORTS. 3(1). p.160-172
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TDP-43-mediated neurodegeneration : towards a loss-of-function hypothesis?

Lies Vanden Broeck, Patrick Callaerts and Bart Dermaut (UGent)

(2013) TRENDS IN MOLECULAR MEDICINE. 20(2). p.66-71
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Dexpramipexole versus placebo for patients with amyotrophic lateral sclerosis (EMPOWER): a randomised, double-blind, phase 3 trial

Merit E Cudkowicz, Leonard H van den Berg, Jeremy M Shefner, Hiroshi Mitsumoto, Jesus S Mora, Albert Ludolph, Orla Hardiman, Michael E Bozik, Evan W Ingersoll, Donald Archibald, et al.

(2013) LANCET NEUROLOGY. 12(11). p.1059-1067
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Vascular insult accompanied by overexpressed heme oxygenase-1 as a pathophysiological mechanism in experimental neurolathyrism with hind-leg paraparesis

Kimino Kawaguchi, Fernand Lambein and Kuniko Kusama-Eguchi

(2012) BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS. 428(1). p.160-166
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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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Right hemisphere dysfunction and emotional processing in ALS: an fMRI study

A Palmieri, M Naccarato, S Abrahams, Mario Bonato (UGent) , C D'Ascenzo, S Balestreri, V Cima, G Querin, R Dal Borgo, L Barachino, et al.

(2010) JOURNAL OF NEUROLOGY. 257(12). p.1970-1978

Academic Bibliography

Expanding the TDP-43 proteinopathy pathway from neurons to muscle : physiological and pathophysiological functions

No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers

Genetic insights in canine degenerative myelopathy

Network approach identifies Pacer as an autophagy protein involved in ALS pathogenesis

Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion

TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis

Phase separation of C9orf72 dipeptide repeats perturbs stress granule dynamics

Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion

Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis

Pixel versus object : a comparison of strategies for the semi-automated mapping of archaeological features using airborne laser scanning data

Functional complementation in Drosophila to predict the pathogenicity of TARDBP variants: evidence for a loss-of-function mechanism.

Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

A pan-European study of the C9orf72 repeat associated with FTLD : geographic prevalence, genomic instability, and intermediate repeats

Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients

Loss and gain of Drosophila TDP-43 impair synaptic efficacy and motor control leading to age-related neurodegeneration by loss-of-function phenotypes

TDP-43 loss-of-function causes neuronal loss due to defective steroid receptor-mediated gene program switching in Drosophila

TDP-43-mediated neurodegeneration : towards a loss-of-function hypothesis?

Dexpramipexole versus placebo for patients with amyotrophic lateral sclerosis (EMPOWER): a randomised, double-blind, phase 3 trial

Vascular insult accompanied by overexpressed heme oxygenase-1 as a pathophysiological mechanism in experimental neurolathyrism with hind-leg paraparesis

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

Right hemisphere dysfunction and emotional processing in ALS: an fMRI study

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