The lysosomal storage diseases
O'Brien, J.F.
Mayo Clinic Proceedings 57(3): 192-197
1982
ISSN/ISBN: 0025-6196 PMID: 7062784 Document Number: 195754
Document emailed within 1 workday
Related Documents
2016: 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): 125-129Kloska, 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
Tylki-Szymańska, A. 1992: Treatment of patients with lysosomal storage diseases Polski Tygodnik Lekarski 47(20-21): 450-452
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
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
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
Weinreb, N.J. 2013: Oral small molecule therapy for lysosomal storage diseases Pediatric Endocrinology Reviews: Per 11(Suppl 1): 77-90
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
Wraith, J.E. 2004: The clinical presentation of lysosomal storage disorders Acta Neurologica Taiwanica 13(3): 101-106
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
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
Pyvovar, S.M.; Rudyk, I.S.; Lozyk, T.V. 2021: Damage of the cardiovascular system in lysosomal storage disease - mucopolysaccharidosis Polski Merkuriusz Lekarski: Organ Polskiego Towarzystwa Lekarskiego 49(294): 448-452
Itoh, M.; Asano, Y.; Shimohira, M.; Iwakawa, Y.; Goto, Y.; Nonaka, I. 1993: A patient with lysosomal glycogen storage disease with normal acid maltase No to Hattatsu 25(5): 459-464
Yoshida, H.; Kuriyama, M. 1990: Genetic lipid storage disease with lysosomal acid lipase deficiency in rats Laboratory Animal Science 40(5): 486-489
Takenaka, T.; Tei, C. 2007: Fabry disease (cardiac lysosomal storage disease) associated with heart failure Nihon Rinsho. Japanese Journal of Clinical Medicine 65(Suppl 5): 460-464