Ghent University Academic Bibliography

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Your filters: cql: author="DE JONGHE, P*" or (type exact bookEditor and editor="DE JONGHE, P*")

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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
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Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders

JJT van Harssel, S Weckhuysen, MJA van Kempen, K Hardies, NE Verbeek, CGF de Kovel, WB Gunning, E van Daalen, MV de Jonge, AC Jansen, et al.

(2013) NEUROGENETICS. 14(1). p.23-34
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- Journal Article
- A1
- open access
Morphological spectrum and clinical features of myopathies with tubular aggregates

Fabian Funk, Chantal Ceuterick-de Groote, Jean-Jacques Martin, Axel Meinhardt, Ana Taratuto, Jan De Bleecker (UGent) , Rudy Van Coster (UGent) , Boel De Paepe (UGent) , Ulrike Schara, Matthias Vorgerd, et al.

(2013) HISTOLOGY AND HISTOPATHOLOGY. 28(8). p.1041-1054
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Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients

Sarah Weckhuysen, Vanja Ivanovic, Rik Hendrickx, Rudy Van Coster (UGent) , Helle Hjalgrim, Rikke S Møller, Sabine Grønborg, An-Sofie Schoonjans, Berten Ceulemans, Sinead B Heavin, et al.

(2013) NEUROLOGY. 81(19). p.1697-1703
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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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KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy

Sarah Weckhuysen, Simone Mandelstam, Arvid Suls, Dominique Audenaert (UGent) , Tine Deconinck, Lieve RF Claes, Liesbet Deprez, katrien Smets, Dimitrina Hristova, Iglika Yordanova, et al.

(2012) ANNALS OF NEUROLOGY. 71(1). p.15-25
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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).
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- 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
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Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patients

Joy Irobi, Anne Holmgren, Vicky De Winter, Bob Asselbergh, Jan Gettemans (UGent) , Dirk Adriaensen, Chantal Ceuterick-de Groote, Rudy Van Coster (UGent) , Peter De Jonghe and Vincent Timmerman

(2012) NEUROMUSCULAR DISORDERS. 22(8). p.699-711
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- Journal Article
- A1
Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis

Elke Bogaert (UGent) , A Goris, P Van Damme, V Geelen, R Lemmens, MA van Es, LH van den Berg, K Sleegers, N Verpoorten, V Timmerman, et al.

(2012) NEUROBIOLOGY OF AGING. 33(2). p.418-420

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Academic Bibliography

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

Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders

Morphological spectrum and clinical features of myopathies with tubular aggregates

Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients

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

KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy

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

Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patients

Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis

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