Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Annals of Hematology|February 24, 2001
Complete remission of generalized relapsed extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue type of the gastrointestinal tract after high-dose chemotherapy and autologous peripheral stem cell transplantationP Neumeister, G Hoefler, C Beham-Schmid, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 31, 1993
Cyclooxygenase pathway in dermal fibroblasts from patients with metabolic disorders of peroxisomal originE Malle, H J Leis, A Steinmetz, et al.
The Journal of Clinical Investigation|December 1, 1991
Photosensitized killing of cultured fibroblasts from patients with peroxisomal disorders due to pyrene fatty acid-mediated ultraviolet damageG Hoefler, E Paschke, S Hoefler, et al.
British Journal of Plastic Surgery|May 13, 1998
Venous thrombosis in a replanted finger with underlying factor V Leiden mutationL Kenner, F Schwarzl, H Moshammer, et al.
Bone Marrow Transplantation|December 7, 2000
Extramedullary T cell lymphoblastic transformation of chronic myeloid leukaemia successfully treated with matched unrelated donor bone marrow transplantationU Apfelbeck, G Hoefler, P Neumeister, et al.
Arteriosclerosis (Dallas, Tex.)|July 1, 1988
Lipoprotein Lp(a). A risk factor for myocardial infarctionG Hoefler, F Harnoncourt, E Paschke, et al.
Virchows Archiv : an International Journal of Pathology|April 6, 1999
ABL amplification in a patient with lymphoid blast crisis of chronic myelogenous leukaemiaL Kenner, C Beham-Schmid, R Kerbl, et al.
British Journal of Cancer|May 3, 2012
Down-regulation of KRAS-interacting miRNA-143 predicts poor prognosis but not response to EGFR-targeted agents in colorectal cancerM Pichler, E Winter, M Stotz, et al.
Leukemia|April 10, 2009
Loss of RAF kinase inhibitor protein is a somatic event in the pathogenesis of therapy-related acute myeloid leukemias with C-RAF germline mutationsA Zebisch, M Haller, K Hiden, et al.
Pediatric Research|July 1, 1989
Genetic and phenotypic heterogeneity in disorders of peroxisome biogenesis--a complementation study involving cell lines from 19 patientsA A Roscher, S Hoefler, G Hoefler, et al.
Pageof 6