Pathogenic cascades in lysosomal disease--Why so complex? von Walkley, S. U

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Secondary accumulation of gangliosides in lysosomal storage disorders von Walkley, Steven U

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Lysosomal dysfunction causes neurodegeneration in mucolipidosis II 'knock-in' mice von KOLLMANN, K, DAMME, M, KÄKELÄ, R, WALKLEY, S. U, BRAULKE, T, MARKMANN, S, MORELLE, W, SCHWEIZER, M, HERMANS-BORGMEYER, I, RÖCHERT, A. K, POHL, S, LÜBKE, T, MICHALSKI, J.-C

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Altered vitamin E status in Niemann-Pick type C disease von Ulatowski, L., Parker, R., Davidson, C., Yanjanin, N., Kelley, T.J., Corey, D., Atkinson, J., Porter, F., Arai, H., Walkley, S.U., Manor, D.

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Critical role for glycosphingolipids in Niemann-Pick disease type C von Zervas, Mark, Somers, Kyra L, Thrall, Mary Anna, Walkley, Steven U

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Neurons in Niemann-Pick Disease Type C Accumulate Gangliosides as Well as Unesterified Cholesterol and Undergo Dendritic and Axonal Alterations von ZERVAS, MARK, DOBRENIS, KOSTANTIN, WALKLEY, STEVEN U

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Gangliosides as Modulators of Dendritogenesis in Normal and Storage Disease-affected Pyramidal Neurons von Walkley, Steven U., Zervas, Mark, Wiseman, Samson

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A mouse model for mucopolysaccharidosis type III A (Sanfilippo syndrome) von Bhaumik, Mantu, Muller, Vivienne J., Rozaklis, Tina, Linda, Johnson, Dobrenis, Kostantin, Bhattacharyya, Riddhi, Wurzelmann, Sarah, Finamore, Peter, Hopwood, John J., Walkley, Steven U., Stanley, Pamela

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Bone Marrow Transplantation Corrects the Enzyme Defect in Neurons of the Central Nervous System in a Lysosomal Storage Disease von WALKLEY, S. U, THRALL, M. A, DOBRENIS, K, HUANG, M, MARCH, P. A, SIEGEL, D. A, WURZELMANN, S

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Lysosomal storage diseases of animals: an essay in comparative pathology von Jolly, R.D. (Massey University, Palmerston North, New Zealand.), Walkley, S.U

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Cellular Pathology of Lysosomal Storage Disorders von Walkley, Steven U.

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Abnormal neuronal metabolism and storage in mucopolysaccharidosis type VI (Maroteaux-Lamy) disease von Walkley, S. U., Thrall, M. A., Haskins, M. E., Mitchell, T. W., Wenger, D. A., Brown, D. E., Dial, S., Seim, H.

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Mitochondrial dysfunction in the neuronal ceroid-lipofuscinoses (Batten disease) von Jolly, R.D., Brown, S., Das, A.M., Walkley, S.U.

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GABAergic neuroaxonal dystrophy and other cytopathological alterations in feline Niemann-Pick disease type C von MARCH, P. A, THRALL, M. A, BROWN, D. E, MITCHELL, T. W, LOWENTHAL, A. C, WALKLEY, S. U

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Pyramidal neurons with ectopic dendrites in storage diseases exhibit increased GM2 ganglioside immunoreactivity von Walkley, S.U.

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Pathology of Mucopolysaccharidosis IIIA in Huntaway Dogs von Jolly, R.D, Johnstone, A.C, Norman, E.J, Hopwood, J.J, Walkley, S.U

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Lysosomal membrane permeability stimulates protein aggregate formation in neurons of a lysosomal disease von Micsenyi, Matthew C, Sikora, Jakub, Stephney, Gloria, Dobrenis, Kostantin, Walkley, Steven U

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Ferret pyramidal cell dendritogenesis: Changes in morphology and ganglioside expression during cortical development von Zervas, Mark, Walkley, Steven U.

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Clinical variants paired with phenotype: A rich resource for brain gene curation von Chopra, Maya, Savatt, Juliann M., Bingaman, Taylor I., Good, Molly E., Morgan, Alexis, Cooney, Caitlin, Rossel, Allison M., VanHoute, Bryanna, Cordova, Ineke, Mahida, Sonal, Lanzotti, Virginia, Baldridge, Dustin, Gurnett, Christina A., Piven, Joseph, Hazlett, Heather, Pomeroy, Scott L., Sahin, Mustafa, Payne, Philip R.O., Riggs, Erin Rooney, Constantino, John N., Gropman, A., Smith-Hicks, C.L., Neul, J., Agosto, J.A. Martinez, German, K., Izumi, K., Abbeduto, L., Dawalt, L., Wangler, M., Wasserstein, M., Storch, Eric A., Cohen, J.S., Samaco, R., Molholm, S., Shankar, S., Srivastava, S., Walkley, S., Sveden, A., Dies, K., Gupta, Aditi, Oh, Inez, Hauck, Rachel

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GM2 ganglioside and pyramidal neuron dendritogenesis von WALKLEY, S. U, SIEGEL, D. A, DOBRENIS, K

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