B. Fahrner

CREBBP HAT domain mutations prevail in relapse cases of high hyperdiploid childhood acute lymphoblastic leukemia

E. Froňková, M. Morak, M. Zeginigg, 2012, Leukemia.

Central nervous system disease in Langerhans cell histiocytosis.

R. Arceci, D. Prayer, H. Lassmann, 2010, The Journal of pediatrics.

L Central Nervous System Disease in Langerhans Cell Histiocytosis

R. Arceci, D. Prayer, H. Lassmann, 2010 .

Management of chronic immune thrombocytopenia in children and adolescents: lessons from an Austrian national cross-sectional study of 81 patients.

R. Crazzolara, W. Holter, L. Kager, 2016, Seminars in hematology.

Long‐term outcome of hypothalamic pituitary tumors in Langerhans cell histiocytosis

D. Prayer, H. Prosch, H. Gadner, 2012, Pediatric blood & cancer.

Band 3 nullVIENNA, a novel homozygous SLC4A1 p.Ser477X variant causing severe hemolytic anemia, dyserythropoiesis and complete distal renal tubular acidosis

O. Haas, L. Bruce, G. Fritsch, 2017, Pediatric blood & cancer.

Two Novel Missense Mutations and a 5bp Deletion in the Erythroid‐Specific Promoter of the PKLR Gene in Two Unrelated Patients With Pyruvate Kinase Deficient Transfusion‐Dependent Chronic Nonspherocytic Hemolytic Anemia

O. Haas, L. Kager, F. Ratzinger, 2016, Pediatric blood & cancer.