Ghent University Academic Bibliography

Show Sort by

Your filters: cql: author="Cras, Patrick" or (type any "bookEditor journalEditor issueEditor" and editor="Cras, Patr...

Add to list
- Journal Article
- A1
- open access
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
Add to list
- Journal Article
- A1
Processing of laser-evoked potentials in patients with chronic whiplash-associated disorders, chronic fatigue syndrome, and healthy controls : a case–control study

Lisa Goudman, Liesbeth Daenen, Andre Mouraux, Jo Nijs, Patrick Cras, Nathalie Roussel, Maarten Moens, Iris Coppieters (UGent) , Eva Huysmans and Margot De Kooning

(2020) PAIN MEDICINE. 21(10). p.2553-2563
Add to list
- Journal Article
- A1
- open access
Does motor cortex engagement during movement preparation differentially inhibit nociceptive processing in patients with chronic whiplash associated disorders, chronic fatigue syndrome and healthy controls? An experimental study

Lisa Goudman, André Mouraux, Liesbeth Daenen, Jo Nijs, Patrick Cras, Nathalie Roussel, Maarten Moens, Dorine Lenoir (UGent) , Iris Coppieters (UGent) , Eva Huysmans, et al.

(2020) JOURNAL OF CLINICAL MEDICINE. 9(5).
Add to list
- Journal Article
- A1
Practices and opinions about disclosure of the diagnosis of Alzheimer’s disease to patients with MCI or dementia : a survey among Belgian medical experts in the field of dementia

Eric Mormont, Jean-Christophe Bier, Rose Bruffaerts, Patrick Cras, Peter De Deyn, Olivier Deryck, Sebastiaan Engelborghs, Mirko Petrovic (UGent) , Gaëtane Picard, Kurt Segers, et al.

(2020) ACTA NEUROLOGICA BELGICA. 120(5). p.1157-1163
Add to list
- Miscellaneous
- open access
Homozygous and compound heterozygous rare variants in VPS13C contribute to Lewy body diseases

Stefanie Smolders, Stéphanie Philtjens, David Crosiers, Anne Sieben, Elisabeth Hens, Bavo Heeman, Sara Van Mossevelde, Philippe Pals, Bob Asselbergh, Roberto Dos Santos Dias, et al.

(2020) Research Square.
Add to list
- Journal Article
- A1
- open access
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export

Shaun Martin, Stefanie Smolders, Chris Van den Haute, Bavo Heeman, Sarah van Veen, David Crosiers, Igor Beletchi, Aline Verstraeten, Helena Gossye, Geraldine Gelders, et al.

(2020) ACTA NEUROPATHOLOGICA. 139(6). p.1001-1024
Add to list
- Journal Article
- A1
- open access
Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability

Rita Cacace, Bavo Heeman, Sara Van Mossevelde, Arne De Roeck, Julie Hoogmartens, Peter De Rijk, Helena Gossye, Kristof De Vos, Wouter De Coster, Mojca Strazisar, et al.

(2019) ACTA NEUROPATHOLOGICA. 137(6). p.901-918
Add to list
- Journal Article
- A2
Medische zorg toegediend door de arts in verband met toxicomanie : risico’s, gevolgen en mogelijke oplossingen

Jean Colin, Nick van Gelder, Patrick Cras, Marc De Hert and Freya Vander Laenen (UGent)

(2018) TIJDSCHRIFT VOOR GENEESKUNDE. 74(19). p.1274-1279
Add to list
- Journal Article
- A1
- open access
An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease

Arne De Roeck, Lena Duchateau, Jasper Van Dongen, Rita Cacace, Maria Bjerke, Tobi Van den Bossche, Patrick Cras, Rik Vandenberghe, Peter P De Deyn, Sebastiaan Engelborghs, et al.

(2018) ACTA NEUROPATHOLOGICA. 135(6). p.827-837
Add to list
- Journal Article
- A1
- open access
Extended FTLD pedigree segregating a Belgian GRN-null mutation : neuropathological heterogeneity in one family

Anne Sieben (UGent) , Sara Van Mossevelde, Eline Wauters, Sebastiaan Engelborghs, Julie van der Zee, Tim Van Langenhove (UGent) , Patrick Santens (UGent) , Marleen Praet, Paul Boon (UGent) , Marijke Miatton (UGent) , et al.

(2018) ALZHEIMERS RESEARCH & THERAPY. 10.
Add to list
- Journal Article
- A1
- open access
Clinical variability and onset age modifiers in an extended Belgian GRN founder family

Eline Wauters, Sara Van Mossevelde, Kristel Sleegers, Julie van der Zee, Sebastiaan Engelborghs, Anne Sieben (UGent) , Rik Vandenberghe, Stephanie Philtjens, Marleen Van den Broeck, Karin Peeters, et al.

(2018) NEUROBIOLOGY OF AGING. 67. p.84-94
Add to list
- Journal Article
- A1
- open access
No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

Yalda Baradaran-Heravi, Lubina Dillen, Hung Phuoc Nguyen, Sara Van Mossevelde, Jonathan Baets, Peter De Jonghe, Sebastiaan Engelborghs, Peter P De Deyn, Mathieu Vandenbulcke, Rik Vandenberghe, et al.

(2018) NEUROBIOLOGY OF AGING. 69.
Add to list
- Journal Article
- A1
Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients

Federica Perrone, Hung Phuoc Nguyen, Sara Van Mossevelde, Matthieu Moisse, Anne Sieben (UGent) , Patrick Santens (UGent) , Jan De Bleecker (UGent) , Mathieu Vandenbulcke, Sebastiaan Engelborghs, Jonathan Baets, et al.

(2017) NEUROBIOLOGY OF AGING. 51. p.177.e9-177.e16
Add to list
- Journal Article
- A1
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
Add to list
- Journal Article
- A1
Alzheimer’s disease and driving : review of the literature and consensus guideline from Belgian dementia experts and the Belgian road safety institute endorsed by the Belgian Medical Association

Jan Versijpt, Mark Tant, Ingo Beyer, Jean-Christophe Bier, Patrick Cras, Peter P. De Deyn, Patrick De Wit, Olivier Deryck, Bernard Hanseeuw, Margareta Lambert, et al.

(2017) ACTA NEUROLOGICA BELGICA. 117(4). p.811-819
Add to list
- Journal Article
- A1
- open access
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
Add to list
- Journal Article
- A1
What is in a name? : comparing diagnostic criteria for chronic fatigue syndrome with or without fibromyalgia

Mira Meeus (UGent) , Kelly Ickmans, Filip Struyf, Daphne Kos (UGent) , Luc Lambrecht, Barbara Willekens, Patrick Cras and Jo Nijs

(2016) CLINICAL RHEUMATOLOGY. 35(1). p.191-203
Add to list
- Conference Paper
- C3
PSP and small vessel disease : more than occasional co-occurence?

Anne Sieben (UGent) , Patrick Santens (UGent) , Dimitri Hemelsoet (UGent) , Sebastiaan Engelborghs, Peter De Jonghe, Jan De Bleecker (UGent) , Jen Maes, Christina Jadoul, Patrick Cras, Peter-Paul De Deyn, et al.

(2016) NEUROBIOLOGY OF AGING. In Neurobiology of Aging 39(Supplement 1). p.S9-S10
Add to list
- Journal Article
- A2
- open access
Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD

Julie van der Zee, Peter Marien, Roeland Crols, Sara Van Mossevelde, Lubina Dillen, Federica Perrone, Sebastiaan Engelborghs, Jo Verhoeven, Tine D'aes, Chantal Ceuterick-De Groote, et al.

(2016) NEUROLOGY-GENETICS. 2(5).
Add to list
- Journal Article
- A1
- open access
Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

Tobi Van den Bossche, Kristel Sleegers, Elise Cuyvers, Sebastiaan Engelborghs, Anne Sieben (UGent) , Arne De Roeck, Caroline Van Cauwenberghe, Steven Vermeulen, Marleen Van den Broeck, Annelies Laureys, et al.

(2016) NEUROLOGY. 86(23). p.2126-2133
Add to list
- Journal Article
- A1
- open access
Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

Sara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, Sebastiaan Engelborghs, Anne Sieben (UGent) , Tim Van Langenhove (UGent) , Jan De Bleecker (UGent) , Jonathan Baets, Mathieu Vandenbulcke, Koen Van Laere, et al.

(2016) BRAIN. 139. p.452-467
Add to list
- Journal Article
- A1
- open access
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease

Jan Verheijen, Tobi Van den Bossche, Julie van der Zee, Sebastiaan Engelborghs, Raquel Sanchez-Valle, Albert Llado, Caroline Graff, Hakan Thonberg, Pau Pastor, Sara Ortega-Cubero, et al.

(2016) ACTA NEUROPATHOLOGICA. 132(2). p.213-224
Add to list
- Journal Article
- A1
- open access
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
Add to list
- Journal Article
- A1
- open access
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains

Jonathan Janssens, Stephanie Philtjens, Gernot Kleinberger, Sara Van Mossevelde, Julie van der Zee, Rita Cacace, Sebastiaan Engelborghs, Anne Sieben (UGent) , Julia Banzhaf-Strathmann, Lubina Dillen, et al.

(2015) ACTA NEUROPATHOLOGICA COMMUNICATIONS. 3.
Add to list
- Journal Article
- A1
Recovery of peripheral muscle function from fatiguing exercise and daily physical activity level in patients with multiple sclerosis: a case-control study

Kelly Ickmans, Fauve Simoens, Jo Nijs, Daphne Kos (UGent) , Patrick Cras, Barbara Willekens and Mira Meeus (UGent)

(2014) CLINICAL NEUROLOGY AND NEUROSURGERY. 122. p.97-105
Add to list
- Journal Article
- A1
Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia

Elise Cuyvers, Karolien Bettens, Stéphanie Philtjens, Tim Van Langenhove (UGent) , Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Jasper Van Dongen, Nathalie Geerts, et al.

(2014) NEUROBIOLOGY OF AGING. 35(3). p.726.e11-726.e19
Add to list
- Journal Article
- A1
- open access
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
Add to list
- Conference Paper
- C3
Management of chronic sensitization, from drugs to physical therapy

Nathalie Roussel, Mira Meeus (UGent) , Liesbeth Daenen, Jessica Van Oosterwijck (UGent) , Patrick Cras and Jo Nijs

(2013) JOURNAL OF HEADACHE AND PAIN. 14(suppl. 1).
Add to list
- Journal Article
- A1
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).
Add to list
- Journal Article
- A1
Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort

Tim Van Langenhove (UGent) , Julie van der Zee, Ilse Gijselinck, Sebastiaan Engelborghs, Rik Vandenberghe, Mathieu Vandenbulcke, Jan De Bleecker (UGent) , Anne Sieben (UGent) , Jan Versijpt, Adrian Ivanoiu, et al.

(2013) JAMA NEUROLOGY. 70(3). p.365-373
Add to list
- Journal Article
- A1
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
Add to list
- Journal Article
- A1
- open access
The genetics and neuropathology of frontotemporal lobar degeneration

Anne Sieben (UGent) , Tim Van Langenhove (UGent) , Sebastiaan Engelborghs, Jean-Jacques Martin, Paul Boon (UGent) , Patrick Cras, Peter-Paul De Deyn, Patrick Santens (UGent) , Christine Van Broeckhoven and Marc Cruts

(2012) ACTA NEUROPATHOLOGICA. 124(3). p.353-372
Add to list
- Journal Article
- A1
Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts

Tim Van Langenhove (UGent) , Julie van der Zee, Sebastiaan Engelborghs, Rik Vandenberghe, Patrick Santens (UGent) , Marleen Van den Broeck, Maria Mattheijssens, Karin Peeters, Dirk Nuytten, Patrick Cras, et al.

(2012) NEUROBIOLOGY OF AGING. 33(5).
Add to list
- Conference Paper
- C3
Distinct clinical characteristics of C9orf72 expansion carriers compared to GRN, MAPT and non-mutation carries in a Flanders-Belgian FTLD cohort

Tim Van Langenhove (UGent) , Julie van der Zee, Ilse Gijselinck, Sebastiaan Engelborghs, Rik Vandenberghe, Mathieu Vandenbulcke, Jan De Bleecker (UGent) , Anne Sieben (UGent) , Adrian Ivanoiu, Oliver Deryck, et al.

(2012) DEMENTIA AND GERIATRIC COGNITIVE DISORDERS. 33(suppl. 1). p.226-226
Add to list
- Journal Article
- A1
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
Add to list
- Book Chapter
Evaluatie en behandeling van patiënten met chronische whiplashgeassocieerde aandoeningen: recente ontwikkelingen

Liesbeth Daenen, Jessica Van Oosterwijck (UGent) , Mira Meeus (UGent) , Nathalie Roussel, Patrick Cras and Jo Nijs

(2011) Jaarboek Fysiotherapie/Kinesitherapie 2012. In Jaarboek Fysiotherapie/Kinesitherapie p.146-156
Add to list
- Journal Article
- A1
Neoplastic meningitis: a rare presentation of bronchial adenocarcinoma

Emke Marechal, Patrick Cras, Paul M Parizel, David Creytens (UGent) , Sofie Verbeke and Gregory Helsen

(2011) ACTA NEUROLOGICA BELGICA. 111(4). p.337-339
Add to list
- Journal Article
- A1
- open access
Assessment of prosodic communicative efficiency in Parkinson's disease as judged by professional listeners

Heidi Martens, Gwen Van Nuffelen, Patrick Cras, Barbara Pickut, Miet De Letter (UGent) and Marc De Bodt (UGent)

(2011) PARKINSON'S DISEASE.
Add to list
- Journal Article
- A1
Long-term functioning following whiplash injury : the role of social support and personality traits

Jo Nijs, Els Inghelbrecht, Liesbeth Daenen, Saïd Hachimi Idrissi (UGent) , Luc Hens, Bert Willems, Nathalie Roussel, Patrick Cras and Jan Bernheim

(2011) CLINICAL RHEUMATOLOGY. 30(7). p.927-935
Add to list
- Journal Article
- A1
Recruitment bias in chronic pain research : whiplash as a model

Jo Nijs, Els Inghelbrecht, Liesbeth Daenen, Saïd Hachimi Idrissi (UGent) , Luc Hens, Bert Willems, Nathalie Roussel, Patrick Cras, Kristien Wouters and Jan Bernheim

(2011) CLINICAL RHEUMATOLOGY. 30(11). p.1481-1489
Add to list
- Journal Article
- A1
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort

Julie van der Zee, Tim Van Langenhove (UGent) , Gernot Kleinberger, Kristel Sleegers, Sebastiaan Engelborghs, Rik Vandenberghe, Patrick Santens (UGent) , Marleen Van Den Broeck, Geert Joris, Jolien Brys, et al.

(2011) BRAIN. 134(3). p.808-815
Add to list
- Journal Article
- A1
Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family

Nathalie Brouwers, Karen Nuytemans, Julie van der Zee, Ilse Gijselinck, Sebastiaan Engelborghs, Jessie Theuns, Samir Kumar-Singh, Barbara A Pickut, Philippe Pals, Bart Dermaut (UGent) , et al.

(2007) ARCHIVES OF NEUROLOGY. 64(10). p.1436-1446
Add to list
- Journal Article
- A1
A novel presenilin 1 mutation associated with Pick's disease but not β-amyloid plaques

Bart Dermaut (UGent) , Samir Kumar-Singh, Sebastian Engelborghs, Jessie Theuns, Rosa Rademakers, Jos Saerens, Barbara A Pickut, Karin Peeters, Marleen van den Broeck, Krist'l Vennekens, et al.

(2004) ANNALS OF NEUROLOGY. 55(5). p.617-626
Add to list
- Journal Article
- A1
Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob disease phenotype

Bart Van Everbroeck, Esther A Croes, Philippe Pals, Bart Dermaut (UGent) , Gerard Jansen, Cornelia M van Duijn, Marc Cruts, Christine Van Broeckhoven, Jean-Jacques Martin and Patrick Cras

(2001) NEUROSCIENCE LETTERS. 313(1-2). p.69-72
Add to list
- Journal Article
- A1
Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertion

Bart Dermaut (UGent) , Marc Cruts, Hubert Backhovens, Ursula Lubke, Bart Van Everbroeck, Raf Sciot, René Dom, Jean-Jacques Martin, Christine Van Broeckhoven and Patrick Cras

(2000) JOURNAL OF NEUROLOGY. 247(5). p.364-368

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

Processing of laser-evoked potentials in patients with chronic whiplash-associated disorders, chronic fatigue syndrome, and healthy controls : a case–control study

Does motor cortex engagement during movement preparation differentially inhibit nociceptive processing in patients with chronic whiplash associated disorders, chronic fatigue syndrome and healthy controls? An experimental study

Practices and opinions about disclosure of the diagnosis of Alzheimer’s disease to patients with MCI or dementia : a survey among Belgian medical experts in the field of dementia

Homozygous and compound heterozygous rare variants in VPS13C contribute to Lewy body diseases

Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export

Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability

Medische zorg toegediend door de arts in verband met toxicomanie : risico’s, gevolgen en mogelijke oplossingen

An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease

Extended FTLD pedigree segregating a Belgian GRN-null mutation : neuropathological heterogeneity in one family

Clinical variability and onset age modifiers in an extended Belgian GRN founder family

No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients

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

Alzheimer’s disease and driving : review of the literature and consensus guideline from Belgian dementia experts and the Belgian road safety institute endorsed by the Belgian Medical Association

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

What is in a name? : comparing diagnostic criteria for chronic fatigue syndrome with or without fibromyalgia

PSP and small vessel disease : more than occasional co-occurence?

Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD

Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation

Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort

A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease

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

Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains

Recovery of peripheral muscle function from fatiguing exercise and daily physical activity level in patients with multiple sclerosis: a case-control study

Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Management of chronic sensitization, from drugs to physical therapy

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

Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort

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

The genetics and neuropathology of frontotemporal lobar degeneration

Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts

Distinct clinical characteristics of C9orf72 expansion carriers compared to GRN, MAPT and non-mutation carries in a Flanders-Belgian FTLD cohort

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

Evaluatie en behandeling van patiënten met chronische whiplashgeassocieerde aandoeningen: recente ontwikkelingen

Neoplastic meningitis: a rare presentation of bronchial adenocarcinoma

Assessment of prosodic communicative efficiency in Parkinson's disease as judged by professional listeners

Long-term functioning following whiplash injury : the role of social support and personality traits

Recruitment bias in chronic pain research : whiplash as a model

TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort

Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family

A novel presenilin 1 mutation associated with Pick's disease but not β-amyloid plaques

Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob disease phenotype

Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertion