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Sequential acquisition of IgH and TCR rearrangements during the preleukemic phase of acute lymphoblastic leukemia in an adolescent patient. Linden T, Furlan I, Schwarz S, Stoehr R, Niemeyer CM, Rossig C (2011) In: Pediatric Blood and Cancer, 56(2), 301-303. doi:10.1002/pbc.22734 Research article (journal) \| Published
Molecular diagnosis of Shwachman-Diamond syndrome in a child with incomplete clinical disease phenotype. Linden T, Ehlert K, Niemeyer CM, Fleischhack G, Jürgens H, Rossig C (2010) In: Pediatric Blood and Cancer, 55(1), 177-179. doi:10.1002/pbc.22424 Research article (journal) \| Published
Childhood B-cell precursor acute lymphoblastic leukaemia in a patient with familial thrombocytopenia and RUNX1 mutation. Linden T, Schnittger S, Groll AH, Juergens H, Rossig C (2010) In: British Journal of Haematology, 151(5), 528-530. doi:10.1111/j.1365-2141.2010.08370.x Research article (journal) \| Published
Hereditary thrombocytopenia and acute myeloid leukemia: a common link due to a germline mutation in the AML1 gene. Appelmann I, Linden T, Rudat A, Mueller-Tidow C, Berdel WE, Mesters RM (2009) In: Annals of Hematology, 88(10), 1037-1038. Research article (journal) \| Published
UICC-2002 TNM classification is not suitable for differentiated thyroid cancer in children and adolescents. Oommen PT, Romahn A, Linden T, Frühwald MC, Bucsky P (2008) In: Pediatric Blood and Cancer, 50(6), 1159-1162. doi:10.1002/pbc.21385 Research article (journal) \| Published

Duration: since 01/07/2010

Type of project: Own resources project

Sequential acquisition of IgH and TCR rearrangements during the preleukemic phase of acute lymphoblastic leukemia in an adolescent patient. Linden T, Furlan I, Schwarz S, Stoehr R, Niemeyer CM, Rossig C (2011) In: Pediatric Blood and Cancer, 56(2), 301-303. doi:10.1002/pbc.22734 Research article (journal) \| Published
Molecular diagnosis of Shwachman-Diamond syndrome in a child with incomplete clinical disease phenotype. Linden T, Ehlert K, Niemeyer CM, Fleischhack G, Jürgens H, Rossig C (2010) In: Pediatric Blood and Cancer, 55(1), 177-179. doi:10.1002/pbc.22424 Research article (journal) \| Published
Childhood B-cell precursor acute lymphoblastic leukaemia in a patient with familial thrombocytopenia and RUNX1 mutation. Linden T, Schnittger S, Groll AH, Juergens H, Rossig C (2010) In: British Journal of Haematology, 151(5), 528-530. doi:10.1111/j.1365-2141.2010.08370.x Research article (journal) \| Published
Hereditary thrombocytopenia and acute myeloid leukemia: a common link due to a germline mutation in the AML1 gene. Appelmann I, Linden T, Rudat A, Mueller-Tidow C, Berdel WE, Mesters RM (2009) In: Annals of Hematology, 88(10), 1037-1038. Research article (journal) \| Published
UICC-2002 TNM classification is not suitable for differentiated thyroid cancer in children and adolescents. Oommen PT, Romahn A, Linden T, Frühwald MC, Bucsky P (2008) In: Pediatric Blood and Cancer, 50(6), 1159-1162. doi:10.1002/pbc.21385 Research article (journal) \| Published