The 20th European Study Group on Lysosomal Diseases Workshop "Lysosomal storage disorders: problems of neurodegeneration and new therapeutic avenues" (Napoli, Italy, 1-4 Oct. 2015)
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 116(5): 125-129
2016
ISSN/ISBN: 1997-7298 PMID: 27437549 Document Number: 688235
Document emailed within 1 workday
Related Documents
O'Brien, J.F. 1982: The lysosomal storage diseases Mayo Clinic Proceedings 57(3): 192-197Wraith, J.E. 2004: The clinical presentation of lysosomal storage disorders Acta Neurologica Taiwanica 13(3): 101-106
Kloska, A.; Tylki-Szymańska, A.; Wegrzyn, G. 2011: Lysosomal storage diseases--an overview Postepy Biochemii 57(2): 128-132
Jolly, R.D. 1982: Two model lysosomal storage diseases Progress in Clinical and Biological Research 94: 145-164
Wasant, P.; Wattanaweeradej, S.; Raksadawan, N.; Kolodny, E.H. 1995: Lysosomal storage disorders in Thailand: the Siriraj experience Southeast Asian Journal of Tropical Medicine and Public Health 26(Suppl 1): 54-58
Yano, T.; Ohno, K. 1995: Lysosomal membrane transport disorders--cystinosis and sialic acid storage disorders (Salla disease, ISSD) Nihon Rinsho. Japanese Journal of Clinical Medicine 53(12): 3068-3071
Bruni, S.; Loschi, L.; Incerti, C.; Gabrielli, O.; Coppa, G.V. 2007: Update on treatment of lysosomal storage diseases Acta Myologica: Myopathies and Cardiomyopathies: Official Journal of the Mediterranean Society of Myology 26(1): 87-92
Ohashi, T. 2010: Gene therapy for lysosomal storage diseases Nihon Rinsho. Japanese Journal of Clinical Medicine 68(Suppl 8): 665-669
Tylki-Szymańska, A. 1992: Treatment of patients with lysosomal storage diseases Polski Tygodnik Lekarski 47(20-21): 450-452
Lara-Aguilar, R.Alejandro.; Juárez-Vázquez, C.Ibet.; Medina-Lozano, C. 2011: Therapy of lysosomal storage diseases: update and perspectives Revista de Investigacion Clinica; Organo del Hospital de Enfermedades de la Nutricion 63(6): 651-658
Sly, W.S. 1981: Prospects for enzyme replacement for lysosomal storage diseases Birth Defects Original Article Series 17(1): 201-213
Weinreb, N.J. 2013: Oral small molecule therapy for lysosomal storage diseases Pediatric Endocrinology Reviews: Per 11(Suppl 1): 77-90
Wiesmann, U.N.; Spycher, M.A.; Gitzelmann, R. 1976: Lysosomal storage diseases: possibilities of the clinical-biochemical diagnostics Verhandlungen der Deutschen Gesellschaft für Pathologie 1976: 106-110
Libert, J.; Toussaint, D. 1982: Tortuosities of retinal and conjunctival vessels in lysosomal storage diseases Birth Defects Original Article Series 18(6): 347-358
De Falco, F.A.; Strisciuglio, P.; Sannolo, N.; Bartiromo, U.; Mundo, P.; Di Domenico, G. 1981: Usefulness and limits of a new method for biochemical screening of lysosomal storage diseases Acta Neurologica 3(6): 746-749
Ivleva, T.S.; Tint, I.S.; Bershadskiĭ, A.D.; Vidershaĭn, G.Ia. 1992: Changes in the organization of the intermediate filament system of human fibroblasts in lysosomal storage diseases and their modeling Biulleten' Eksperimental'noi Biologii i Meditsiny 113(3): 263-268
Tsuji, D.; Itoh, K. 2007: Molecular pathogenesis and therapeutic targets of lysosomal diseases Seikagaku. Journal of Japanese Biochemical Society 79(7): 678-682
Wilks, P.N. 1980: An optimized lead capture electronhistochemical technique for the demonstration of lysosomal and non lysosomal acid phosphatase activity in nervous tissue Medical Laboratory Sciences 37(2): 149-164
Dodelson de Kremer, R.; Paschini de Capra, A.; Angaroni, C.J.; Giner de Ayala, A. 1997: Plasma chitotriosidase activity in Argentinian patients with Gaucher disease, various lysosomal diseases and other inherited metabolic disorders Medicina 57(6): 677-684
Parini, R. 2007: How does the landscape change in lysosomal storage disease La Pediatria Medica e Chirurgica: Medical and Surgical Pediatrics 29(5): 275-278