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Bone Marrow Transplantation|January 11, 2007
Substitution of cyclophosphamide and busulfan by fludarabine, treosulfan and melphalan in a preparative regimen for children and adolescents with Shwachman-Diamond syndromeM Sauer, C Zeidler, B Meissner, et al.
Transplantation|May 16, 1998
Early loss of renal transplants in patients with thrombophiliaM Fischereder, P Göhring, H Schneeberger, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|September 30, 2010
Concurrent TNFRSF1A R92Q and pyrin E230K mutations in a child with multiple sclerosisA Blaschek, P Lohse, K Huss, et al.
Casopis Lekaru Ceskych|April 4, 2000
[Lysosomal acid lipase deficiency. Overview of Czech patients]M Elleder, H Poupĕtová, J Ledvinová, et al.
The Journal of Clinical Investigation|October 1, 1989
A nonsense mutation in the apolipoprotein C-IIPadova gene in a patient with apolipoprotein C-II deficiencyS S Fojo, P Lohse, C Parrott, et al.
Alimentary Pharmacology & Therapeutics|December 5, 2008
The role of fatty acid hydrolase gene variants in inflammatory bowel diseaseM Storr, D Emmerdinger, J Diegelmann, et al.
Klinische Padiatrie|November 9, 2010
Analysis of cryopyrin-associated periodic syndromes (CAPS) in German children: epidemiological, clinical and genetic characteristicsE Lainka, U Neudorf, P Lohse, et al.
The Journal of Clinical Investigation|August 1, 1995
Dominant expression of type III hyperlipoproteinemia. Pathophysiological insights derived from the structural and kinetic characteristics of ApoE-1 (Lys146-->Glu)W A Mann, P Lohse, R E Gregg, et al.
The Journal of Clinical Investigation|August 1, 1993
Rapid in vivo transport and catabolism of human apolipoprotein A-IV-1 and slower catabolism of the apoA-IV-2 isoproteinD J Rader, J Schäfer, P Lohse, et al.
Leukemia & Lymphoma|June 30, 2004
Genetic analyses permit the differentiation between reactive malfunctions ('promyelocyte arrest') and arising promyelocyte leukemia in a pregnant patient with a history of a medulloblastomaBrigitte Poleck-Dehlin, T Duell, R Bartl, et al.
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