Autor(en): Warnecke T, Duning T, Schwan A, Lohmann H, Epplen JT, Young P
A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation
Publiziert: NEUROLOGY 69 (2007); S. 368-375
Autor(en): Nareyeck G., Zeschnigk M., Prescher G., Lohmann D.R., Anastassiou G.
Establishment and characterization of two uveal melanoma cell lines derived from tumors with loss of one chromosome
Publiziert: 3. Exp Eye Res. 2006 Oct; 83(4);Epub 2006 Jun 5. Review. PMID: 16750193; S. 858-64;
Autor(en): Schwan A, JT Epplen
Predictive testing and genetic counselling
Publiziert: Encyclopedic Reference of Genomics and Proteomics in Molecular Medicine, D Ganten, K Ruckpaul (ea); 2006, S. 1453-1456
Autor(en): U. Demme, J. Becker, H. Bussemas, F. Erdmann, M. Erkens, P.X. Iten, H. Käferstein, J.K. Lusthoff, H.J. Magerl, L.v.Meyer, A. Reiter, A. Schmoldt, E. Schneider, H.W. Schütz, Th. Stimpfl, F. Tarbah, J. Teske, W. Vycudilik, J.P. Weller and W. Wei
Systematic evaluation of 1-chlorobutane for liquid-liquid extraction of drugs
Publiziert: TIAFT "43 International Meeting (Seoul Korea) 29. August (2005)
Autor(en): Alber B, M Pernauer, A Schwan, G Rothmund, KT Hoffmann, D Brummer, AD Sperfeld, I Uttner, H Binder, JT Epplen, J Dullinger, AC Ludolph, T Meyer
Spastin related hereditary spastic paraplegia with dysplastic corpus callosum
Publiziert: J NEUROL SCI 236 (2005), S. 9-12
Autor(en): Meyer T, A Schwan, JS Dullinger, J Brocke, KT Hoffmann, CH Nolte, A Hopt, U Kopp, P Andersen, JT Epplen, P Linke
Early-onset ALS with long-term survival associated with spastin gene mutation
Publiziert: NEUROLOGY 65 (2005); S. 141-143
Autor(en): Norbert Ostendorf, Thomas Glosemeyer-Allhoff, Katrin Schauerte, Raina Yamamoto
Hemoglobin (Hb) Stanleyville II Causes Gross Overestimation of the Hb A1c Proportion in Routine HPLC.
Publiziert: Clinical Chemistry 51, No 9 (2005); S. 1752-1754
Autor(en): J. R. Novotny, U. Schmücker, B. Staats, U. Dührsen
Failed or inadequate bone marrow aspiration: a fast, simple and cost-effective method to produce a cell suspension from a core biopsy specimen
Publiziert: Clinical and Laboratory Haematology (2005) 27 (1); S. 33-40
Autor(en): Schwan A, JT Epplen
Prädiktive Beratung bei Risikopersonen für Chorea Huntington
Publiziert: PATIENTENAUFKLÄRUNG BEI GENETISCHEM RISIKO, v H-M Sass, P Schröder (eds) Lit, Münster 2; 2004; S. 139-146
Autor(en): Léon von Brasch, Chuanbing Zang, Thomas Haverkamp, Horst Schlechte, Herbert Heckers, Petro E. Petrides
Molecular analysis of acute intermittent porphyria: mutation screening in 20 patients in Germany reveals 11 novel mutations.
Publiziert: Blood Cells, Molecules and Diseases 32 (2004); S. 309-314