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Neurology|September 25, 2009
Normal and mutant HTT interact to affect clinical severity and progression in Huntington diseaseN A Aziz, C K Jurgens, G B Landwehrmeyer, et al.
Brain Pathology (Zurich, Switzerland)|December 6, 2003
Autosomal dominant adult neuronal ceroid lipofuscinosis: a novel form of NCL with granular osmiophilic deposits without palmitoyl protein thioesterase 1 deficiencyPeter C G Nijssen, Chantal Ceuterick, Otto P van Diggelen, et al.
Journal of Affective Disorders|July 24, 2013
Suicidal ideation in a European Huntington's disease populationAnna A M Hubers, Erik van Duijn, Raymund A C Roos, et al.
Neurology|September 28, 2005
Striatal dopamine D2 receptors, metabolism, and volume in preclinical Huntington diseaseJ C H van Oostrom, R P Maguire, C C Verschuuren-Bemelmans, et al.
Oral Oncology|August 4, 2004
Radioimmunodetection and radioimmunotherapy of head and neck cancerPontus K E Börjesson, Ernst J Postema, Remco de Bree, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|August 25, 2011
The impact of bone mineral density and disc degeneration on shear strength and stiffness of the lumbar spine following laminectomyArno Bisschop, Margriet G Mullender, Idsart Kingma, et al.
Parkinsonism & Related Disorders|October 30, 2012
The influence of gender on phenotype and disease progression in patients with Huntington's diseaseDaniel Zielonka, Johan Marinus, Raymund A C Roos, et al.
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