A. Karow

发表

Clonal evolution and clinical correlates of somatic mutations in myeloproliferative neoplasms.

Christian Beisel, Ronny Nienhold, Jakob Passweg, 2014, Blood.

Loss of Stat1 decreases megakaryopoiesis and favors erythropoiesis in a JAK2-V617F-driven mouse model of MPNs.

R. Skoda, S. Dirnhofer, Takafumi Shimizu, 2014, Blood.

Loss of Stat1 decreases megakaryopoiesis and favors erythropoiesis in a JAK2- V617F driven mouse model of myeloproliferative neoplasms

R. Skoda, S. Dirnhofer, P. Lundberg, 2014 .

Hearing loss and quality of life in survivors of paediatric CNS tumours and other cancers

C. Kuehni, G. Michel, A. Karow, 2018, Quality of Life Research.

Paediatric Cancer Predisposition Documentation Tool – Standardized Reporting Form for Children and Adolescents With Suspected Cancer Predisposition Syndrome

A. Borkhardt, M. Schrappe, M. Kuhlen, 2021 .

The Cytogenetic Landscape of Pediatric Chronic Myeloid Leukemia Diagnosed in Chronic Phase

G. Göhring, M. Metzler, M. Suttorp, 2022, Cancers.

Chromosomal aberrations in congenital bone marrow failure disorders—an early indicator for leukemogenesis?

D. Steinemann, P. Lichter, K. Welte, 2007, Annals of Hematology.

Mutational landscape in children with myelodysplastic syndromes is distinct from adults: specific somatic drivers and novel germline variants

M. Wlodarski, A. Yoshimi, I. Baumann, 2017, Leukemia.

A novel somatic K-Ras mutation in juvenile myelomonocytic leukemia

C. Niemeyer, C. Kratz, H. Hasle, 2006, Leukemia.

Mutational profile of childhood myeloproliferative neoplasms

R. Skoda, A. Karow, R. Nienhold, 2015, Leukemia.

Targeting Telomere Biology in Acute Lymphoblastic Leukemia

T. Dantonello, G. Baerlocher, A. Karow, 2021, International journal of molecular sciences.

JAK2 mutations other than V617F: a novel mutation and mini review.

C. Niemeyer, C. Kratz, C. Waller, 2008, Leukemia research.

Paediatric chronic myeloid leukaemia presenting in de novo or secondary blast phase ‐ a comparison of clinical and genetic characteristics

G. Göhring, M. Metzler, M. Suttorp, 2021, British journal of haematology.

JAK2 V617F-Mutated Myeloproliferative Neoplasia Developing Five Years after Wild-Type JAK2 Acute Myeloid Leukemia: A Case Report

J. Passweg, A. Tichelli, R. Skoda, 2012, Acta Haematologica.

Mutations of the Shwachman-Bodian-Diamond syndrome gene in patients presenting with refractory cytopenia – do we have to screen?

C. Niemeyer, M. Fliegauf, C. Flotho, 2010, Haematologica.

Progressive Thrombosis in a 13-Year-Old Girl with Trisomy 21 Under Therapy with Low Molecular Weight Heparin

I. Hainmann, A. Karow, U. Budde, 2011, Klinische Pädiatrie.

Patient-reported long-term outcome following allogeneic hematopoietic stem cell transplantation in pediatric chronic myeloid leukemia

Friederike Erdmann, M. Metzler, M. Suttorp, 2022, Frontiers in Oncology.

Natural history and early diagnosis of LAD-1/variant syndrome.

O. Sanal, K. Seeger, T. Kuijpers, 2007, Blood.

Hb G-Waimanalo [A1] [α64(E13)Asp→Asn; HBA1: c.193 G > A] with Decreased Oxygen Affinity

A. Karow, M. Schmugge, O. Speer, 2015, Hemoglobin.

Clinical and Molecular Heterogeneity of RTEL1 Deficiency

U. Pannicke, K. Schwarz, S. Ehl, 2017, Front. Immunol..

Morphologic differential diagnosis of juvenile myelomonocytic leukemia--pitfalls apart from viral infection.

I. Baumann, C. Niemeyer, A. Karow, 2009, Journal of pediatric hematology/oncology.

Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30‐year SIOP‐RTSG experience

R. Kuiper, K. Pritchard-Jones, H. van Tinteren, 2020, Cancer.

Myeloid leukemia in children 4 years or older with Down syndrome often lacks GATA1 mutation and cytogenetics and risk of relapse are more akin to sporadic AML

P. Vyas, D. Reinhardt, H. Hasle, 2008, Leukemia.

Clonal Mutational Landscape of Childhood Myelodysplastic Syndromes

M. Wlodarski, J. Maciejewski, P. D. Paepe, 2015 .

Unexpected High Frequency of GATA2 Mutations in Children with Non-Familial MDS and Monosomy 7

M. Wlodarski, I. Baumann, C. Niemeyer, 2012 .

Peripheral blood progenitor cell collection in pediatric patients optimized by high pre-apheresis count of circulating CD34+ cells and high blood flow

T. Pabst, G. Baerlocher, A. Karow, 2018, Bone Marrow Transplantation.

Congenital transfusion-dependent anemia and thrombocytopenia with myelodysplasia due to a recurrent GATA1G208R germline mutation

C. Niemeyer, C. Kratz, A. Schmitt-Gräff, 2008, Leukemia.

Longitudinal Cytokine Profiling Identifies GRO-α and EGF as Potential Biomarkers of Disease Progression in Essential Thrombocythemia

P. Campbell, Mairi S. Shepherd, D. Kent, 2020, HemaSphere.

Reproductive issues for men with cancer: technology and nursing management.

A. Karow, V. Sweet, E. Servy, 1996, Oncology nursing forum.

Management of children and adolescents with chronic myeloid leukemia in blast phase: International pediatric CML expert panel recommendations

C. Zwaan, A. Kiani, B. De Moerloose, 2023, Leukemia.

Temporal evolution and differential patterns of cellular reconstitution after therapy for childhood cancers

A. Karow, M. Krumbholz, Zofia Wotschofsky, 2023, Scientific Reports.

Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working Group

M. Kuhlen, A. Kelsey, F. Lalloo, 2021, Familial Cancer.

Effects of the STAMP-inhibitor asciminib on T cell activation and metabolic fitness compared to tyrosine kinase inhibition by imatinib, dasatinib, and nilotinib

D. Mougiakakos, R. Jitschin, M. Metzler, 2023, Cancer Immunology, Immunotherapy.

Clonal duplication of a germline PTPN11 mutation due to acquired uniparental disomy in acute lymphoblastic leukemia blasts from a patient with Noonan syndrome

D. Steinemann, C. Niemeyer, M. Zenker, 2007, Leukemia.