Metastatic disease and major adverse cardiovascular events preceding diagnosis are the main determinants of disease-specific survival of pheochromocytoma/paraganglioma: long-term follow-up of 303 patients
Raber, Wolfgang, Schendl, Raphael, Arikan, Melisa, Scheuba, Andreas, Mazal, Peter, Stadlmann, Valerie, Lehner, Reinhard, Zeitlhofer, Petra, Baumgartner-Parzer, Sabina, Gabler, Cornelia, Esterbauer, Harald
Published in Frontiers in endocrinology (Lausanne) (21.08.2024)
Published in Frontiers in endocrinology (Lausanne) (21.08.2024)
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Journal Article
Case Report: Refractory Cytopenia With a Switch From a Transient Monosomy 7 to a Disease-Ameliorating del(20q) in a NHEJ1-Deficient Long-term Survivor
Poyer, Fiona, Jimenez Heredia, Raúl, Novak, Wolfgang, Zeitlhofer, Petra, Nebral, Karin, Dworzak, Michael N., Haas, Oskar A., Boztug, Kaan, Kager, Leo
Published in Frontiers in immunology (24.06.2022)
Published in Frontiers in immunology (24.06.2022)
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Journal Article
Copy Number Changes and Allele Distribution Patterns of Chromosome 21 in B Cell Precursor Acute Lymphoblastic Leukemia
Abbasi, M. Reza, Nebral, Karin, Haslinger, Sabrina, Inthal, Andrea, Zeitlhofer, Petra, König, Margit, Schinnerl, Dagmar, Köhrer, Stefan, Strehl, Sabine, Panzer-Grümayer, Renate, Mann, Georg, Attarbaschi, Andishe, Haas, Oskar A.
Published in Cancers (13.09.2021)
Published in Cancers (13.09.2021)
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Journal Article
A single‐center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease‐causing genotypes
Kager, Leo, Jimenez‐Heredia, Raúl, Zeitlhofer, Petra, Novak, Wolfgang, Eder, Sebastian K., Segarra‐Roca, Anna, Frohne, Alexandra, Nebral, Karin, Haimel, Matthias, Geyeregger, René, Roetzer‐Londgin, Katharina, Haas, Oskar A., Boztug, Kaan
Published in HemaSphere (01.01.2024)
Published in HemaSphere (01.01.2024)
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Journal Article
Novel Compound Heterozygous Mutations in Two Families With Bernard-Soulier Syndrome
Minkov, Milen, Zeitlhofer, Petra, Zoubek, Andreas, Kager, Leo, Panzer, Simon, Haas, Oskar A
Published in Frontiers in pediatrics (22.01.2021)
Published in Frontiers in pediatrics (22.01.2021)
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Journal Article
Band 3 nullVIENNA, a novel homozygous SLC4A1 p.Ser477X variant causing severe hemolytic anemia, dyserythropoiesis and complete distal renal tubular acidosis
Kager, Leo, Bruce, Lesley J., Zeitlhofer, Petra, Flatt, Joanna F., Maia, Tabita M., Ribeiro, M. Leticia, Fahrner, Bernhard, Fritsch, Gerhard, Boztug, Kaan, Haas, Oskar A.
Published in Pediatric blood & cancer (01.03.2017)
Published in Pediatric blood & cancer (01.03.2017)
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Journal Article
Dominant inherited β‐thalassemia intermedia in a Polish family due to a novel frameshift mutation in HBB
Novak, Wolfgang, Sunder‐Plassmann, Raute, Berner, Jakob, Köhrer, Stefan, Zeitlhofer, Petra, Haas, Oskar A., Riedl, Julia, Kager, Leo, Sillaber, Christian
Published in Pediatric blood & cancer (01.10.2023)
Published in Pediatric blood & cancer (01.10.2023)
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Journal Article
Targeted mutation screening of 292 candidate genes in 38 children with inborn haematological cytopenias efficiently identifies novel disease‐causing mutations
Kager, Leo, Jimenez Heredia, Raúl, Hirschmugl, Tatjana, Dmytrus, Jasmin, Krolo, Ana, Müller, Heiko, Bock, Christoph, Zeitlhofer, Petra, Dworzak, Michael, Mann, Georg, Holter, Wolfgang, Haas, Oskar, Boztug, Kaan
Published in British journal of haematology (01.07.2018)
Published in British journal of haematology (01.07.2018)
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Journal Article
Absence of Band 3 in Severe Dyserythropoietic/Hemolytic Anemia with Complete Distal Renal Acidosis and a Novel Homozygous Exon 12 C.1430C>a (p.Ser477X) SLC4A1 Gene Mutation
Kager, Leo, Bruce, Lesley J, Flatt, Joanna F, Zeitlhofer, Petra, Fritsch, Gerhard, Fahrner, Bernhard, Haas, Oskar A.
Published in Blood (03.12.2015)
Published in Blood (03.12.2015)
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Journal Article
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: Novel Variants in PKLR and Severe Chronic Hemolysis
Kager, Leo, Minkov, Milen, Zeitlhofer, Petra, Fahrner, Bernhard, Ratzinger, Franz, Boztug, Kaan, Dossenbach-Glaninger, Astrid, Haas, Oskar A.
Published in Pediatric blood & cancer (01.05.2016)
Published in Pediatric blood & cancer (01.05.2016)
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Journal Article
Band 3 null super(VIENNA), a novel homozygous SLC4A1 p.Ser477X variant causing severe hemolytic anemia, dyserythropoiesis and complete distal renal tubular acidosis
Kager, Leo, Bruce, Lesley J, Zeitlhofer, Petra, Flatt, Joanna F, Maia, Tabita M, Ribeiro, MLeticia, Fahrner, Bernhard, Fritsch, Gerhard, Boztug, Kaan, Haas, Oskar A
Published in Pediatric blood & cancer (01.03.2017)
Published in Pediatric blood & cancer (01.03.2017)
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Journal Article
Thiamine-responsive megaloblastic anemia (TRMA) in an Austrian boy with compound heterozygous SLC19A2 mutations
Pichler, Herbert, Zeitlhofer, Petra, Dworzak, Michael N., Diakos, Christopher, Haas, Oskar A., Kager, Leo
Published in European journal of pediatrics (01.11.2012)
Published in European journal of pediatrics (01.11.2012)
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Journal Article
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
Kager, Leo, Minkov, Milen, Zeitlhofer, Petra, Fahrner, Bernhard, Ratzinger, Franz, Boztug, Kaan, Dossenbach-Glaninger, Astrid, Haas, Oskar A.
Published in Pediatric blood & cancer (01.05.2016)
Published in Pediatric blood & cancer (01.05.2016)
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Journal Article
High-resolution analysis of alterations in medullary thyroid carcinoma genomes
Flicker, Karin, Ulz, Peter, Höger, Harald, Zeitlhofer, Petra, Haas, Oskar A., Behmel, Annemarie, Buchinger, Wolfgang, Scheuba, Christian, Niederle, Bruno, Pfragner, Roswitha, Speicher, Michael R.
Published in International journal of cancer (15.07.2012)
Published in International journal of cancer (15.07.2012)
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Journal Article
Band 3 null VIENNA , a novel homozygous SLC4A1 p.Ser477X variant causing severe hemolytic anemia, dyserythropoiesis and complete distal renal tubular acidosis
Kager, Leo, Bruce, Lesley J, Zeitlhofer, Petra, Flatt, Joanna F, Maia, Tabita M, Ribeiro, M Leticia, Fahrner, Bernhard, Fritsch, Gerhard, Boztug, Kaan, Haas, Oskar A
Published in Pediatric blood & cancer (01.03.2017)
Published in Pediatric blood & cancer (01.03.2017)
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Journal Article
A Novel DNA/RNA FISH X Inactivation Assay Reveals a Nonrandom, Ploidy-Dependent Acquisition of the Active and Inactive X Chromosomes in Childhood Hyperdiploid Acute Lymphoblastic Leukemia (ALL) and Non-Hodgkin Lymphoma (NHL)
Haas, Oskar A., Zeitlhofer, Petra, Strehl, Sabine, Pfeilstoecker, Michael, Koenig, Margit, Weinhaeusel, Andreas
Published in Blood (16.11.2004)
Published in Blood (16.11.2004)
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Journal Article
Evidence of a polyclonal nature of myositis ossificans
LEITHNER, Andreas, WEINHAEUSEL, Andreas, ZEITLHOFER, Petra, KOCH, Horst, RADL, Roman, WINDHAGER, Reinhard, BEHAM, Alfred, HAAS, Oskar A
Published in Virchows Archiv : an international journal of pathology (01.04.2005)
Published in Virchows Archiv : an international journal of pathology (01.04.2005)
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Journal Article
Case Report: Refractory Cytopenia With a Switch From a Transient Monosomy 7 to a Disease-Ameliorating del(20q) in a NHEJ1-Deficient Long-term Survivor
Poyer, Fiona, Jimenez Heredia, Raúl, Novak, Wolfgang, Zeitlhofer, Petra, Nebral, Karin, Dworzak, Michael N, Haas, Oskar A, Boztug, Kaan, Kager, Leo
Published in Frontiers in immunology (01.01.2022)
Published in Frontiers in immunology (01.01.2022)
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