Potential disease-modifying therapies for Huntington's disease: lessons learned and future opportunities von Tabrizi, Sarah J, Estevez-Fraga, Carlos, van Roon-Mom, Willeke M C, Flower, Michael D, Scahill, Rachael I, Wild, Edward J, Muñoz-Sanjuan, Ignacio, Sampaio, Cristina, Rosser, Anne E, Leavitt, Blair R

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Iron loading is a prominent feature of activated microglia in Alzheimer's disease patients von Kenkhuis, Boyd, Somarakis, Antonios, de Haan, Lorraine, Dzyubachyk, Oleh, IJsselsteijn, Marieke E, de Miranda, Noel F C C, Lelieveldt, Boudewijn P F, Dijkstra, Jouke, van Roon-Mom, Willeke M C, Höllt, Thomas, van der Weerd, Louise

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Juvenile‐Onset Huntington Disease Pathophysiology and Neurodevelopment: A Review von Bakels, Hannah S., Roos, Raymund A.C., Roon‐Mom, Willeke M.C., Bot, Susanne T.

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Post‐mortem 7T MR imaging and neuropathology in middle stage juvenile‐onset Huntington disease: A case report von Bakels, Hannah S., Duinen, Sjoerd G., Bresser, Jeroen, Roon‐Mom, Willeke M. C., Weerd, Louise, Bot, Susanne T.

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Human Neuroblasts Migrate to the Olfactory Bulb via a Lateral Ventricular Extension von Curtis, Maurice A, Kam, Monica, Nannmark, Ulf, Anderson, Michelle F, Axell, Mathilda Zetterstrom, Wikkelso, Carsten, Holtås, Stig, van Roon-Mom, Willeke M.C, Björk-Eriksson, Thomas, Nordborg, Claes, Frisén, Jonas, Dragunow, Michael, Faull, Richard L.M, Eriksson, Peter S

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Genetics, Mechanisms, and Therapeutic Progress in Polyglutamine Spinocerebellar Ataxias von Buijsen, Ronald A.M., Toonen, Lodewijk J.A., Gardiner, Sarah L., van Roon-Mom, Willeke M.C.

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Peripheral mitochondrial function correlates with clinical severity in idiopathic Parkinson's disease von Milanese, Chiara, Payán‐Gómez, César, Galvani, Marta, Molano González, Nicolás, Tresini, Maria, Nait Abdellah, Soraya, van Roon‐Mom, Willeke M. C., Figini, Silvia, Marinus, Johan, van Hilten, Jacobus J., Mastroberardino, Pier G.

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Targeting several CAG expansion diseases by a single antisense oligonucleotide von Evers, Melvin M, Pepers, Barry A, van Deutekom, Judith C T, Mulders, Susan A M, den Dunnen, Johan T, Aartsma-Rus, Annemieke, van Ommen, Gert-Jan B, van Roon-Mom, Willeke M C

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Transcriptional profiling and biomarker identification reveal tissue specific effects of expanded ataxin-3 in a spinocerebellar ataxia type 3 mouse model von Toonen, Lodewijk J A, Overzier, Maurice, Evers, Melvin M, Leon, Leticia G, van der Zeeuw, Sander A J, Mei, Hailiang, Kielbasa, Szymon M, Goeman, Jelle J, Hettne, Kristina M, Magnusson, Olafur Th, Poirel, Marion, Seyer, Alexandre, 't Hoen, Peter A C, van Roon-Mom, Willeke M C

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Reduced acute myocardial ischemia–reperfusion injury in IL-6-deficient mice employing a closed-chest model von Jong, Willeke M. C., ten Cate, Hugo, Linnenbank, André C., de Boer, Onno J., Reitsma, Pieter H., de Winter, Robbert J., Zuurbier, Coert J.

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Deletion of the innate immune NLRP3 receptor abolishes cardiac ischemic preconditioning and is associated with decreased Il-6/STAT3 signaling von Zuurbier, Coert J, Jong, Willeke M C, Eerbeek, Otto, Koeman, Anneke, Pulskens, Wilco P, Butter, Loes M, Leemans, Jaklien C, Hollmann, Markus W

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Therapeutic Strategies for Spinocerebellar Ataxia Type 1 von Kerkhof, Laurie M C, van de Warrenburg, Bart P C, van Roon-Mom, Willeke M C, Buijsen, Ronald A M

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Ataxin-3 Protein and RNA Toxicity in Spinocerebellar Ataxia Type 3: Current Insights and Emerging Therapeutic Strategies von Evers, Melvin M., Toonen, Lodewijk J. A., van Roon-Mom, Willeke M. C.

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Machine learning in Huntington's disease: exploring the Enroll-HD dataset for prognosis and driving capability prediction von Ouwerkerk, Jasper, Feleus, Stephanie, van der Zwaan, Kasper F, Li, Yunlei, Roos, Marco, van Roon-Mom, Willeke M C, de Bot, Susanne T, Wolstencroft, Katherine J, Mina, Eleni

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Spinocerebellar Ataxia Type 1 Characteristics in Patient‐Derived Fibroblast and iPSC‐Derived Neuronal Cultures von Buijsen, Ronald A.M., Hu, Michel, Sáez‐González, Maria, Notopoulou, Sofia, Mina, Eleni, Koning, Winette, Gardiner, Sarah L., Graaf, Linda M., Daoutsali, Elena, Pepers, Barry A., Mei, Hailiang, Dis, Vera, Frimat, Jean‐Philippe, Maagdenberg, Arn M. J. M., Petrakis, Spyros, Roon‐Mom, Willeke M.C.

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The potential value of disease-modifying therapy in patients with spinocerebellar ataxia type 1: an early health economic modeling study von van Prooije, Teije, Ruigrok, Sanne, van den Berkmortel, Niels, Maas, Roderick P. P. W. M., Wijn, Stan, van Roon-Mom, Willeke M. C., van de Warrenburg, Bart, Grutters, Janneke P. C.

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Antisense Oligonucleotide-Mediated Removal of the Polyglutamine Repeat in Spinocerebellar Ataxia Type 3 Mice von Toonen, Lodewijk J.A., Rigo, Frank, van Attikum, Haico, van Roon-Mom, Willeke M.C.

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Frequency of nuclear mutant huntingtin inclusion formation in neurons and glia is cell‐type‐specific von Jansen, Anne H.P., van Hal, Maurik, op den Kelder, Ilse C., Meier, Romy T., de Ruiter, Anna‐Aster, Schut, Menno H., Smith, Donna L., Grit, Corien, Brouwer, Nieske, Kamphuis, Willem, Boddeke, H.W.G.M., den Dunnen, Wilfred F.A., van Roon, Willeke M.C., Bates, Gillian P., Hol, Elly M., Reits, Eric A.

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Exploring the transcriptome of ciliated cells using in silico dissection of human tissues von Ivliev, Alexander E, 't Hoen, Peter A C, van Roon-Mom, Willeke M C, Peters, Dorien J M, Sergeeva, Marina G

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TGFβ pathway deregulation and abnormal phospho‐SMAD2/3 staining in hereditary cerebral hemorrhage with amyloidosis‐Dutch type von Grand Moursel, Laure, Munting, Leon P., van der Graaf, Linda M., van Duinen, Sjoerd G., Goumans, Marie‐Jose T. H., Ueberham, Uwe, Natté, Remco, van Buchem, Mark A., van Roon‐Mom, Willeke M. C., van der Weerd, Louise

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