Publicaties

In de afgelopen 12 maanden werden de volgende artikels gepubliceerd, waaraan onze dienst meewerkte:

Augustus 2010
	Dystonic drop foot gait in a patient with manganism. Janssens J, Vandenberghe W Neurology; 2010 Aug 31;75(9):835
	Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. Shatunov A, Mok K, Newhouse S, Weale ME, Smith B, Vance C, Johnson L, Veldink JH, van Es MA, van den Berg LH, Robberecht W, Van Damme P, Hardiman O, Farmer AE, Lewis CM, Butler AW, Abel O, Andersen PM, Fogh I, Silani V, Chiò A, Traynor BJ, Melki J, Meini Lancet Neurol; 2010 Aug 27;
	Defective membrane expression of the Na+-HCO3- cotransporter NBCe1 is associated with familial migraine. Suzuki M, Van Paesschen W, Stalmans I, Horita S, Yamada H, Bergmans BA, Legius E, Riant F, De Jonghe P, Li Y, Sekine T, Igarashi T, Fujimoto I, Mikoshiba K, Shimadzu M, Shiohara M, Braverman N, Al-Gazali L, Fujita T, Seki G Proc Natl Acad Sci U S A; 2010 Aug 23;
	Widespread Decrease of Type 1 Cannabinoid Receptor Availability in Huntington Disease In Vivo. Van Laere K, Casteels C, Dhollander I, Goffin K, Grachev I, Bormans G, Vandenberghe W J Nucl Med; 2010 Aug 18;
	Intracranial hypertension following intrathecal administration of liposomal cytarabine. Lunskens S, Lammertijn L, Deeren D, Bergmans B, Maertens J, Vandenberghe R J Neurol; 2010 Aug 13;
	(18)F-flutemetamol amyloid imaging in Alzheimer disease and mild cognitive impairment: A phase 2 trial. Vandenberghe R, Van Laere K, Ivanoiu A, Salmon E, Bastin C, Triau E, Hasselbalch S, Law I, Andersen A, Korner A, Minthon L, Garraux G, Nelissen N, Bormans G, Buckley C, Owenius R, Thurfjell L, Farrar G, Brooks DJ Ann Neurol; 2010 Aug 4;
	A large genome scan for rare CNVs in amyotrophic lateral sclerosis. Blauw HM, Al-Chalabi A, Andersen PM, van Vught PW, Diekstra FP, van Es MA, Saris CG, Groen EJ, van Rheenen W, Koppers M, van 't Slot R, Strengman E, Estrada K, Rivadeneira F, Hofman A, Uitterlinden AG, Kiemeney LA, Vermeulen SH, Birve A, Waibel S, Meyer T Hum Mol Genet; 2010 Aug 4;
	Mutations in PEX10 are a cause of autosomal recessive ataxia. Régal L, Ebberink MS, Goemans N, Wanders RJ, De Meirleir L, Jaeken J, Schrooten M, Van Coster R, Waterham HR Ann Neurol; 2010 Aug;68(2):259-63
Juli 2010
	The Association of the 4q25 Susceptibility Variant for Atrial Fibrillation With Stroke Is Limited to Stroke of Cardioembolic Etiology. Lemmens R, Buysschaert I, Geelen V, Fernandez I, Montaner J, Schmidt H, Schmidt R, Attia J, Maguire J, Levi C, Jood K, Blomstrand C, Jern C, Wnuk M, Slowik A, Lambrechts D, Thijs V Stroke; 2010 Jul 29;
	In vivo amyloid imaging in cortical superficial siderosis. Dhollander I, Nelissen N, Van Laere K, Peeters D, Demaerel P, Van Paesschen W, Thijs V, Vandenberghe R J Neurol Neurosurg Psychiatry; 2010 Jul 28;
	Microbleeds and the Risk of Recurrent Stroke. Thijs V, Lemmens R, Schoofs C, Görner A, Van Damme P, Schrooten M, Demaerel P Stroke; 2010 Jul 22;
	Freezing of gait in Parkinson's disease: The impact of dual-tasking and turning. Spildooren J, Vercruysse S, Desloovere K, Vandenberghe W, Kerckhofs E, Nieuwboer A Mov Disord; 2010 Jul 14;
	Subclinical GvHD in non-irradiated F1 hybrids: severe lymphoid-tissue GvHD causing prolonged immune dysfunction. Sprangers B, Van Wijmeersch B, Luyckx A, Sagaert X, Verbinnen B, Rutgeerts O, Lenaerts C, Tousseyn T, Dubois B, Waer M, Billiau AD Bone Marrow Transplant; 2010 Jul 5;
	Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy. Kovacs GG, Seguin J, Quadrio I, Höftberger R, Kapás I, Streichenberger N, Biacabe AG, Meyronet D, Sciot R, Vandenberghe R, Majtenyi K, László L, Ströbel T, Budka H, Perret-Liaudet A Acta Neuropathol; 2010 Jul 1;
	Cerebral distribution of white matter lesions in migraine with aura patients. Rossato G, Adami A, Thijs V, Cerini R, Pozzi-Mucelli R, Mazzucco S, Anzola G, Sette MD, Dinia L, Meneghetti G, Zanferrari C Cephalalgia; 2010 Jul;30(7):855-859
Juni 2010
	Replication of KIF21B as a susceptibility locus for multiple sclerosis. Goris A, Boonen S, D'hooghe MB, Dubois B J Med Genet; 2010 Jun 28;
	Mutant HSPB8 causes motor neuron specific neurite degeneration. Irobi J, Almeida-Souza L, Asselbergh B, De Winter V, Goethals S, Dierick I, Krishnan J, Timmermans JP, Robberecht W, De Jonghe P, Van Den Bosch L, Janssens S, Timmerman V Hum Mol Genet; 2010 Jun 10;
	The neurobiology of amyotrophic lateral sclerosis. Bento-Abreu A, Van Damme P, Van Den Bosch L, Robberecht W Eur J Neurosci; 2010 Jun 7;
	Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis. Booth DR, Heard RN, Stewart GJ, Cox M, Scott RJ, Lechner-Scott J, Goris A, Dobosi R, Dubois B, Saarela J, Leppä V, Peltonen L, Pirttila T, Cournu-Rebeix I, Fontaine B, Bergamaschi L, D'Alfonso S, Leone M, Lorentzen AR, Harbo HF, Celius EG, Spurkland A, L Nat Genet; 2010 Jun;42(6):469-70; author reply 470-1
Mei 2010
	Chemotherapy-induced structural changes in cerebral white matter and its correlation with impaired cognitive functioning in breast cancer patients. Deprez S, Amant F, Yigit R, Porke K, Verhoeven J, Van den Stock J, Smeets A, Christiaens MR, Leemans A, Van Hecke W, Vandenberghe J, Vandenbulcke M, Sunaert S Hum Brain Mapp; 2010 May 13;
	Gesture discrimination in primary progressive aphasia: the intersection between gesture and language processing pathways. Nelissen N, Pazzaglia M, Vandenbulcke M, Sunaert S, Fannes K, Dupont P, Aglioti SM, Vandenberghe R J Neurosci; 2010 May 5;30(18):6334-41
	An unusual presentation of Guillain-Barré syndrome associated with monospecific anti-GD1b antibodies. Dewil M, Robberecht W, Van Damme P J Neurol Neurosurg Psychiatry; 2010 May;81(5):587-8
April 2010
	Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis. Bogaert E, Goris A, Van Damme P, Geelen V, Lemmens R, van Es MA, van den Berg LH, Sleegers K, Verpoorten N, Timmerman V, Jonghe PD, Van Broeckhoven C, Traynor BJ, Landers JE, Brown RH Jr, Glass JD, Al-Chalabi A, Shaw CE, Birve A, Andersen PM, Slowik A, To Neurobiol Aging; 2010 Apr 19;
	Belgian Fabry Study. Prevalence of Fabry Disease in a Cohort of 1000 Young Patients With Cerebrovascular Disease. Brouns R, Thijs V, Eyskens F, Van den Broeck M, Belachew S, Van Broeckhoven C, Redondo P, Hemelsoet D, Fumal A, Jeangette S, Verslegers W, Baker R, Hughes D, De Deyn PP Stroke; 2010 Apr 1;
Maart 2010
	Anatomy-based reconstruction of FDG-PET images with implicit partial volume correction improves detection of hypometabolic regions in patients with epilepsy due to focal cortical dysplasia diagnosed on MRI. Goffin K, Van Paesschen W, Dupont P, Baete K, Palmini A, Nuyts J, Van Laere K Eur J Nucl Med Mol Imaging; 2010 Mar 20;
	Combined Striatal Binding and Cerebral Influx Analysis of Dynamic 11C-Raclopride PET Improves Early Differentiation Between Multiple-System Atrophy and Parkinson Disease. Van Laere K, Clerinx K, D'Hondt E, de Groot T, Vandenberghe W J Nucl Med; 2010 Mar 17;
	RNA metabolism and the pathogenesis of motor neuron diseases. Lemmens R, Moore MJ, Al-Chalabi A, Brown RH Jr, Robberecht W Trends Neurosci; 2010 Mar 11;
	Quality control of vital capacity as a primary outcome measure during phase lll therapeutic clinical trial in amyotrophic lateral sclerosis. Sanjak M, Salachas F, Frija-Orvoen E, Theys P, Hutchinson D, Verheijde J, Pianta T, Stewart H, Brooks BR, Meininger V, Douillet P Amyotroph Lateral Scler; 2010 Mar 2;
	Fear conditioning following a unilateral anterior temporal lobectomy: reduced autonomic responding and stimulus contingency knowledge. Coppens E, van Paesschen W, Vandenbulcke M, Vansteenwegen D Acta Neurol Belg; 2010 Mar;110(1):36-48
Februari 2010
	Genetic contribution of FUS to frontotemporal lobar degeneration. Van Langenhove T, van der Zee J, Sleegers K, Engelborghs S, Vandenberghe R, Gijselinck I, Van den Broeck M, Mattheijssens M, Peeters K, De Deyn PP, Cruts M, Van Broeckhoven C Neurology; 2010 Feb 2;74(5):366-71
Januari 2010
	Follow-up study of susceptibility Loci for Alzheimer's disease and onset age identified by genome-wide association. Bettens K, Brouwers N, Van Miegroet H, Gil A, Engelborghs S, De Deyn PP, Vandenberghe R, Van Broeckhoven C, Sleegers K J Alzheimers Dis; 2010 Jan;19(4):1169-75
	Guidelines for preclinical animal research in ALS/MND: A consensus meeting. Ludolph AC, Bendotti C, Blaugrund E, Chio A, Greensmith L, Loeffler JP, Mead R, Niessen HG, Petri S, Pradat PF, Robberecht W, Ruegg M, Schwalenstöcker B, Stiller D, van den Berg L, Vieira F, von Horsten S Amyotroph Lateral Scler; 2010;11(1-2):38-45
	Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C. Dermaut B, Seneca S, Dom L, Smets K, Ceulemans L, Smet J, De Paepe B, Tousseyn S, Weckhuysen S, Gewillig M, Pals P, Parizel P, De Bleecker JL, Boon P, De Meirleir L, De Jonghe P, Van Coster R, Van Paesschen W, Santens P J Neurol Neurosurg Psychiatry; 2010 Jan;81(1):90-3
December 2009
	Imaging techniques for acute ischemic stroke: nice gadgets or essential tools for effective treatment? Thijs V Neuroradiology; 2009 Dec 17;
	Pathogenic Cysteine Mutations Affect Progranulin Function and Production of Mature Granulins. Wang J, Van Damme P, Cruchaga C, Gitcho MA, Vidal JM, Seijo-Martínez M, Wang L, Wu JY, Robberecht W, Goate A J Neurochem; 2009 Dec 17;
	Follow-Up Study of Susceptibility Loci for Alzheimer's Disease and Onset Age Identified by Genome-Wide Association. Bettens K, Brouwers N, Van Miegroet H, Gil A, Engelborghs S, De Deyn PP, Vandenberghe R, Van Broeckhoven C, Sleegers K J Alzheimers Dis; 2009 Dec 14;
	The amodal system for conscious word and picture identification in the absence of a semantic task. Van Doren L, Dupont P, De Grauwe S, Peeters R, Vandenberghe R Neuroimage; 2009 Dec 8;
	Organisation of inhospital acute stroke care and minimum criteria for stroke care units. Recommendations of the Belgian Stroke Council. Thijs V, Peeters A, Dewindt A, Hemelsoet D, De Klippel N, Laloux P, Redondo P, Cras P, De Deyn PP, Desfontaines P, Brouns R, De Raedt S, Van Landegem W, Vandermeeren Y, Vanhooren G Acta Neurol Belg; 2009 Dec;109(4):247-51
November 2009
	Expression of mutant but not wild-type SOD1 in intact neuronal cells induces alterations in mitochondrial complex I activity, calcium signaling, ATP production, and morphology. Coussee E, Bogaert E, De Smet P, Faes L, D'hooge P, Gomes P, Elens I, Van Damme P, Willems P, Koopman W, Van Den Bosh L, Callewaert G FASEB J; 2009 Nov 25;
	Improvement of health-related quality of life in relapsing remitting multiple sclerosis patients after 2 years of treatment with intramuscular interferon-beta-1a. Jongen PJ, Sindic C, Carton H, Zwanikken C, Lemmens W, Borm G J Neurol; 2009 Nov 18;
	The occurrence of mutations in FUS in a Belgian cohort of patients with familial ALS. Damme PV, Goris A, Race V, Hersmus N, Dubois B, Bosch LV, Matthijs G, Robberecht W Eur J Neurol; 2009 Nov 13;
Oktober 2009
	Randomized, Placebo-Controlled, Dose-Ranging Clinical Trial of Intravenous Microplasmin in Patients With Acute Ischemic Stroke. Thijs VN, Peeters A, Vosko M, Aichner F, Schellinger PD, Schneider D, Neumann-Haefelin T, Röther J, Davalos A, Wahlgren N, Verhamme P Stroke; 2009 Oct 15;
	Glatiramer acetate has no impact on disease progression in ALS at 40 mg/day: a double- blind, randomized, multicentre, placebo-controlled trial. Meininger V, Drory VE, Leigh PN, Ludolph A, Robberecht W, Silani V Amyotroph Lateral Scler; 2009 Oct-Dec;10(5-6):378-83
	Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis. Van Es MA, Van Vught PW, Veldink JH, Andersen PM, Birve A, Lemmens R, Cronin S, Van Der Kooi AJ, De Visser M, Schelhaas HJ, Hardiman O, Ragoussis I, Lambrechts D, Robberecht W, Wokke JH, Ophoff RA, Van Den Berg LH Amyotroph Lateral Scler; 2009 Oct-Dec;10(5-6):441-7