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3-Hydroxy-3-methylglutaryl coenzyme A reductase inhibitor Atorvastatin mediated effects depend on the activation status of target cells in PLP-EAE.
Mix E, Ibrahim SM, Pahnke J, Glass A, Mazón-Peláez I, Lemcke S, Koczan D, Gimsa U, Bansemer S, Scheel T, Karopka T, Böttcher T, Müller J, Dazert E, Antipova V, Hoffrogge R, Wree A, Zschiesche M, Strauss U, Kundt G, Warzok R, Gierl L, Rolfs A. Mix E, et al. Among authors: zschiesche m. J Autoimmun. 2006 Dec;27(4):251-65. doi: 10.1016/j.jaut.2006.09.006. Epub 2006 Nov 3. J Autoimmun. 2006. PMID: 17085013
Niemann-Pick disease type A and B are clinically but also enzymatically heterogeneous: pitfall in the laboratory diagnosis of sphingomyelinase deficiency associated with the mutation Q292 K.
Harzer K, Rolfs A, Bauer P, Zschiesche M, Mengel E, Backes J, Kustermann-Kuhn B, Bruchelt G, van Diggelen OP, Mayrhofer H, Krägeloh-Mann I. Harzer K, et al. Among authors: zschiesche m. Neuropediatrics. 2003 Dec;34(6):301-6. doi: 10.1055/s-2003-44668. Neuropediatrics. 2003. PMID: 14681755
Severe clinical expression in X-linked Emery-Dreifuss muscular dystrophy.
Hoeltzenbein M, Karow T, Zeller JA, Warzok R, Wulff K, Zschiesche M, Herrmann FH, Grosse-Heitmeyer W, Wehnert MS. Hoeltzenbein M, et al. Among authors: zschiesche m. Neuromuscul Disord. 1999 May;9(3):166-70. doi: 10.1016/s0960-8966(98)00120-5. Neuromuscul Disord. 1999. PMID: 10382910
[Prenatal biochemical diagnosis in genetically-induced metabolic diseases].
Machill G, Seidlitz G, Grimm U, Zschiesche M, Petruschka L, Wehnert M, Knoll W, Schütz M, Knapp A, Herrmann FH. Machill G, et al. Among authors: zschiesche m. Z Arztl Fortbild (Jena). 1988;82(22):1133-7. Z Arztl Fortbild (Jena). 1988. PMID: 3150192 German. No abstract available.
73 results