Search Results - "Perglerovà, K"

Number of RUNX1 mutations, wild-type allele loss and additional mutations impact on prognosis in adult RUNX1-mutated AML by Stengel, A, Kern, W, Meggendorfer, M, Nadarajah, N, Perglerovà, K, Haferlach, T, Haferlach, C

“…RUNX1 -mutated acute myeloid leukemia (AML) show a distinct pattern of genetic abnormalities and an adverse prognosis. We analyzed the impact of multiple RUNX1…”
Get full text

Subtype-specific patterns of molecular mutations in acute myeloid leukemia by Rose, D, Haferlach, T, Schnittger, S, Perglerová, K, Kern, W, Haferlach, C

“…Acute myeloid leukemia (AML) can be grouped into morphologically or genetically defined subtypes. Today, the AML phenotype–genotype associations, that is,…”
Get full text

The new provisional WHO entity ‘RUNX1 mutated AML’ shows specific genetics but no prognostic influence of dysplasia by Haferlach, T, Stengel, A, Eckstein, S, Perglerová, K, Alpermann, T, Kern, W, Haferlach, C, Meggendorfer, M

Get full text

Next-generation deep-sequencing detects multiple clones of CALR mutations in patients with BCR-ABL1 negative MPN by Jeromin, S, Kohlmann, A, Meggendorfer, M, Schindela, S, Perglerová, K, Nadarajah, N, Kern, W, Haferlach, C, Haferlach, T, Schnittger, S

Get full text

Karyotype evolution and acquisition of FLT3 or RAS pathway alterations drive progression of myelodysplastic syndrome to acute myeloid leukemia by Meggendorfer, Manja, de Albuquerque, Andreia, Nadarajah, Niroshan, Alpermann, Tamara, Kern, Wolfgang, Steuer, Kimberly, Perglerová, Karolína, Haferlach, Claudia, Schnittger, Susanne, Haferlach, Torsten

Get full text

The new provisional WHO entity 'RUNX1 mutated AML%apos; shows specific genetics but no prognostic influence of dysplasia by Haferlach, T, Stengel, A, Eckstein, S, Perglerová, K, Alpermann, T, Kern, W, Haferlach, C, Meggendorfer, M

Get full text