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Reduced rates of axonal and dendritic growth in embryonic hippocampal neurones cultured from a mouse model of Sandhoff diseasePELLED, D; RIEBELING, C; VAN ECHTEN-DECKERT, G et al.Neuropathology and applied neurobiology (Print). 2003, Vol 29, Num 4, pp 341-349, issn 0305-1846, 9 p.Article

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Diagnostic biologique des maladies lysosomales = Biological diagnosis of lysosomal diseasesBEKRI, S.Annales de biologie clinique (Paris). 2006, Vol 64, Num 6, pp 592-600, issn 0003-3898, 9 p.Conference Paper

Maladies lysosomales = Lysosomal disordersJournal de la Société de biologie. 2002, Vol 196, Num 2, issn 1295-0661, 65 p.Serial Issue

Screening patients referred to a metabolic clinic for lysosomal storage disordersFULLER, Maria; TUCKER, Justin N; LANG, Debbie L et al.Journal of medical genetics. 2011, Vol 48, Num 6, pp 422-425, issn 0022-2593, 4 p.Article

International Symposium on Lysosomal Storage DiseasesActa paediatrica. Supplement. 2007, Vol 96, Num 455, pp 93-112, issn 0803-5326, 19 p.Conference Paper

Combination therapies for lysosomal storage disease: is the whole greater than the sum of its parts?HAWKINS-SALSBURY, Jacqueline A; REDDY, Adarsh S; SANDS, Mark S et al.Human molecular genetics (Print). 2011, Vol 20, Num 1, issn 0964-6906, R54-R60, NSArticle

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New therapeutic options for lysosomal storage disorders : enzyme replacement, small molecules and gene therapyBECK, Michael.Human genetics. 2007, Vol 121, Num 1, pp 1-22, issn 0340-6717, 22 p.Article

Decreased T2 signal in the thalami may be a sign of lysosomal storage diseaseAUTTI, Taina; JOENSUU, Raimo; ABERG, Laura et al.Neuroradiology (Berlin. Print). 2007, Vol 49, Num 7, pp 571-578, issn 0028-3940, 8 p.Article

Newborn Bloodspot Screening for Lysosomal Storage DisordersHUI ZHOU; FERNHOFF, Paul; VOGT, Robert F et al.The Journal of pediatrics. 2011, Vol 159, Num 1, pp 7-13, issn 0022-3476, 7 p.Article

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Musculoskeletal manifestations of lysosomal storage disordersALDENHOVEN, M; SAKKERS, R. J. B; BOELENS, J et al.Annals of the rheumatic diseases. 2009, Vol 68, Num 11, pp 1659-1665, issn 0003-4967, 7 p.Article

The Role of Current Biomarkers in the Management of Lysosomal Storage DisordersMAIRE, Irène; GUFFON, Nathalie; PIRAUD, Monique et al.Clinical therapeutics. 2008, Vol 30, issn 0149-2918, S90-S91, SUPCConference Paper

Dysfunction of endocytic and autophagic pathways in a lysosomal storage diseaseFUKUDA, Tokiko; EWAN, Lindsay; BAUER, Martina et al.Annals of neurology. 2006, Vol 59, Num 4, pp 700-708, issn 0364-5134, 9 p.Article

Lysosomal storage disordersVELLODI, Ashok.British journal of haematology. 2005, Vol 128, Num 4, pp 413-431, issn 0007-1048, 19 p.Article

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ER and oxidative stresses are common mediators of apoptosis in both neurodegenerative and non-neurodegenerative lysosomal storage disorders and are alleviated by chemical chaperonesHUI WEI; KIM, Sung-Jo; ZHONGJIAN ZHANG et al.Human molecular genetics (Print). 2008, Vol 17, Num 4, pp 469-477, issn 0964-6906, 9 p.Article

Lysosomal storage disorders: The need for better pediatric recognition and comprehensive careWILCOX, William R.The Journal of pediatrics. 2004, Vol 144, Num 5, pp S3-S14, issn 0022-3476, SUPConference Paper

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Lysosomal storage diseases: cellular pathology, clinical and genetic heterogeneity, therapy = Les maladies lysosomiales: pathologie cellulaire, hétérogénéité clinique et génétique, thérapeutiqueREUSER, A. J. J; KROOS, M. A; VISSER, W. J et al.Annales de biologie clinique (Paris). 1994, Vol 52, Num 10, pp 721-728, issn 0003-3898Article