False-positive rapid tests for malaria in patients with rheumatoid factor von Grobusch, MP, Alpermann, U, Schwenke, S, Jelinek, T, Warhurst, DC

Volltext

Anti-CD4-Therapie in der Behandlung der rheumatoiden Arthritis - sind die Würfel schon gefallen? von Keyßer, G., Alpermann, U., Burmester, G.-R.

Volltext

Anti-CD4 therapy in treatment of rheumatoid arthritis--have the die been cast? von Keysser, G, Alpermann, U, Burmester, G R

Volltext

Anti-CD4 therapy in treatment of rheumatoid arthritis--have the die been cast? von Keysser, G, Alpermann, U, Burmester, G R

Volltext

Landscape of genetic lesions in 944 patients with myelodysplastic syndromes von Haferlach, T, Nagata, Y, Grossmann, V, Okuno, Y, Bacher, U, Nagae, G, Schnittger, S, Sanada, M, Kon, A, Alpermann, T, Yoshida, K, Roller, A, Nadarajah, N, Shiraishi, Y, Shiozawa, Y, Chiba, K, Tanaka, H, Koeffler, H P, Klein, H-U, Dugas, M, Aburatani, H, Kohlmann, A, Miyano, S, Haferlach, C, Kern, W, Ogawa, S

Volltext

SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations von Meggendorfer, M, Bacher, U, Alpermann, T, Haferlach, C, Kern, W, Gambacorti-Passerini, C, Haferlach, T, Schnittger, S

Volltext

Prognostic impact of FLT3-ITD load in NPM1 mutated acute myeloid leukemia von Schnittger, S, Bacher, U, Kern, W, Alpermann, T, Haferlach, C, Haferlach, T

Volltext

Clinical impact of FLT3 mutation load in acute promyelocytic leukemia with t(15;17)/PML-RARA von SCHNITTGER, Susanne, BACHER, Ulrike, HAFERIACH, Claudia, KERN, Wolfgang, ALPERMANN, Tamara, HAFERLACH, Torsten

Volltext

WT1 mutations are secondary events in AML, show varying frequencies and impact on prognosis between genetic subgroups von Krauth, M-T, Alpermann, T, Bacher, U, Eder, C, Dicker, F, Ulke, M, Kuznia, S, Nadarajah, N, Kern, W, Haferlach, C, Haferlach, T, Schnittger, S

Volltext

Age, JAK2(V617F) and SF3B1 mutations are the main predicting factors for survival in refractory anaemia with ring sideroblasts and marked thrombocytosis von Broséus, J, Alpermann, T, Wulfert, M, Florensa Brichs, L, Jeromin, S, Lippert, E, Rozman, M, Lifermann, F, Grossmann, V, Haferlach, T, Germing, U, Luño, E, Girodon, F, Schnittger, S

Volltext

Allelochemical interactions and short-term effects of the dinoflagellate Alexandrium on selected photoautotrophic and heterotrophic protists von Tillmann, Urban, Alpermann, Tilman, John, Uwe, Cembella, Allan

Volltext

High number of additional genetic lesions in acute myeloid leukemia with t(8;21)/RUNX1-RUNX1T1: frequency and impact on clinical outcome von Krauth, M-T, Eder, C, Alpermann, T, Bacher, U, Nadarajah, N, Kern, W, Haferlach, C, Haferlach, T, Schnittger, S

Volltext

Comparison of genetic and clinical aspects in patients with acute myeloid leukemia and myelodysplastic syndromes all with more than 50% of bone marrow erythropoietic cells von BACHER, Ulrike, HAFERLACH, Claudia, ALPERMANN, Tamara, KERN, Wolfgang, SCHNITTGER, Susanne, HAFERLACH, Torsten

Volltext

Use of CBL exon 8 and 9 mutations in diagnosis of myeloproliferative neoplasms and myelodysplastic/myeloproliferative disorders: an analysis of 636 cases von SCHNITTGER, Susanne, BACHER, Ulrike, KERN, Wolfgang, HAFERLACH, Claudia, HAFERLACH, Torsten, ALPERMANN, Tamara, REITER, Andreas, ULKE, Madlen, DICKER, Frank, EDER, Christiane, KOHLMANN, Alexander, GROSSMANN, Vera, KOWARSCH, Andreas

Volltext

The inv(3)(q21q26)/t(3;3)(q21;q26) is frequently accompanied by alterations of the RUNX1, KRAS and NRAS and NF1 genes and mediates adverse prognosis both in MDS and in AML: a study... von Haferlach, C, Bacher, U, Haferlach, T, Dicker, F, Alpermann, T, Kern, W, Schnittger, S

Volltext

Molecular analyses of 15,542 patients with suspected BCR-ABL1-negative myeloproliferative disorders allow to develop a stepwise diagnostic workflow von SCHNITTGER, Susanne, BACHER, Ulrike, EDER, Christiane, DICKER, Frank, ALPERMANN, Tamara, GROSSMANN, Vera, KOHLMANN, Alexander, KERN, Wolfgang, HAFERLACH, Claudia, HAFERLACH, Torsten

Volltext

Intra-population clonal variability in allelochemical potency of the toxigenic dinoflagellate Alexandrium tamarense von Tillmann, Urban, Alpermann, Tilman L., da Purificação, Rodrigo C., Krock, Bernd, Cembella, Allan

Volltext

Characterization of NPM1-mutated AML with a history of myelodysplastic syndromes or myeloproliferative neoplasms von Schnittger, S, Bacher, U, Haferlach, C, Alpermann, T, Dicker, F, Sundermann, J, Kern, W, Haferlach, T

Volltext

CDKN1B, encoding the cyclin-dependent kinase inhibitor 1B (p27), is located in the minimally deleted region of 12p abnormalities in myeloid malignancies and its low expression is a... von HAFERLACH, Claudia, BACHER, Ulrike, KOHLMANN, Alexander, SCHINDELA, Sonja, ALPERMANN, Tamara, KERN, Wolfgang, SCHNITTGER, Susanne, HAFERIACH, Torsten

Volltext

Molecular mutations are prognostically relevant in AML with intermediate risk cytogenetics and aberrant karyotype von Bacher, U, Haferlach, T, Alpermann, T, Kern, W, Schnittger, S, Haferlach, C

Volltext