Publications by authors named "Florian Oyen"

38Publications

Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw-Schulman Syndrome Investigated in Germany.

Thromb Haemost 2018 04 19;118(4):709-722. Epub 2018 Mar 19.

Department of Paediatric Haematology and Oncology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1055/s-0038-1637749DOI Listing
April 2018

Molecular Analysis of Hybrid Neurofibroma/Schwannoma Identifies Common Monosomy 22 and α-T-Catenin/CTNNA3 as a Novel Candidate Tumor Suppressor.

Am J Pathol 2016 12 17;186(12):3285-3296. Epub 2016 Oct 17.

Institute of Neuropathology, University Hospital Münster, Münster, Germany; Institute of Pathology, Health Care Center, Brandenburg Hospital, Brandenburg Medical School Theodor Fontane, Brandenburg an der Havel, Germany. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ajpath.2016.08.019DOI Listing
December 2016

Inherited Thrombotic Thrombocytopenic Purpura (Upshaw Schulman Syndrome) as Differential Diagnosis to Neonatal Septicaemia with Disseminated Intravascular Coagulation - a Case Series.

Z Geburtshilfe Neonatol 2017 Feb 6;221(1):39-42. Epub 2016 Jul 6.

Pediatric Hematology and Oncology, University Medical Center Hamburg Eppendorf, Hamburg, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1055/s-0042-109404DOI Listing
February 2017

Small cell undifferentiated (SCUD) hepatoblastomas: All malignant rhabdoid tumors?

Genes Chromosomes Cancer 2016 12 29;55(12):925-931. Epub 2016 Jul 29.

Department of Pediatric Pathology, Kiel Pediatric Tumor Registry, Christian-Albrechts-University Kiel, Kiel, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/gcc.22390DOI Listing
December 2016

Rapid Diagnosis of an AT/RT by the Detection of a Heterozygous SMARCB1 Germ Line Deletion in an Infant.

Pediatr Blood Cancer 2016 08 19;63(8):1451-3. Epub 2016 Apr 19.

Department of Pediatric Hematology and Oncology, University Children's Hospital Münster, Münster, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pbc.25996DOI Listing
August 2016

Long-term survival of an infant with an atypical teratoid/rhabdoid tumor following subtotal resection and low-cumulative dose chemotherapy: a case report.

Childs Nerv Syst 2016 Jun 8;32(6):1157-61. Epub 2016 Jan 8.

Department of Pediatric Oncology/Hematology/BMT, Charité - Universitätsmedizin Berlin, Augustenburger Platz 1, 13353, Berlin, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00381-015-2999-5DOI Listing
June 2016

The Prevalence of Sickle Cell Disease and Its Implication for Newborn Screening in Germany (Hamburg Metropolitan Area).

Pediatr Blood Cancer 2016 Jan 14;63(1):168-70. Epub 2015 Aug 14.

Bernhard-Nocht-Institute for Tropical Medicine, Hamburg, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pbc.25706DOI Listing
January 2016

Detection of SMARCB1 loss in ascites cells in the diagnosis of an abdominal rhabdoid tumor.

Pediatr Blood Cancer 2015 May 7;62(5):897-900. Epub 2015 Feb 7.

Pediatric Hematology and Oncology, University Childrens Hospital Münster, Münster, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pbc.25412DOI Listing
May 2015

Platelet-free shear flow assay facilitates analysis of shear-dependent functions of VWF and ADAMTS13.

Thromb Res 2014 Dec 28;134(6):1285-91. Epub 2014 Aug 28.

Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.thromres.2014.08.013DOI Listing
December 2014

Identifying molecular markers for the sensitive detection of residual atypical teratoid rhabdoid tumor cells.

Cancer Genet 2014 Sep 21;207(9):390-7. Epub 2014 May 21.

Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Electronic address:

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S22107762140009
Publisher Site
http://dx.doi.org/10.1016/j.cancergen.2014.05.008DOI Listing
September 2014

Clinical and genetic features of rhabdoid tumors of the heart registered with the European Rhabdoid Registry (EU-RHAB).

Cancer Genet 2014 Sep 21;207(9):379-83. Epub 2014 Apr 21.

Children's Hospital Augsburg, Swabian Children's Cancer Center, Augsburg, Germany; Department of Pediatric Hematology and Oncology, University Children's Hospital Münster, Germany. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.cancergen.2014.04.005DOI Listing
September 2014

Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion.

Thromb Haemost 2014 Apr 12;111(4):777-9. Epub 2013 Dec 12.

Florian Langer MD, II. Medizinische Klinik und Poliklinik, Hubertus Wald Tumorzentrum, Universitäres Cancer Center Hamburg (UCCH), Universitätsklinikum Eppendorf, Martinistr. 52, 20246 Hamburg, Germany, Tel.: +49 40 7410 52453, Fax: +49 40 7410 55193, E-mail:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1160/TH13-06-0462DOI Listing
April 2014

Phenotypic and molecular characterisation of type 3 von Willebrand disease in a cohort of Indian patients.

Thromb Haemost 2013 Apr 14;109(4):652-60. Epub 2013 Feb 14.

Department of Hematology, All India Institute of Medical Sciences, New Delhi, 110029, India.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1160/TH12-10-0737DOI Listing
April 2013

Administration of recombinant erythropoietin alone does not improve the phenotype in iron refractory iron deficiency anemia patients.

Ann Hematol 2013 Mar 20;92(3):387-94. Epub 2012 Nov 20.

Department of Pediatric Hematology and Oncology, University Medical Center Eppendorf, Martinistrasse 52, 20246, Hamburg, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00277-012-1618-8DOI Listing
March 2013

Characterisation of mutations and molecular studies of type 2 von Willebrand disease.

Thromb Haemost 2013 Jan 22;109(1):39-46. Epub 2012 Nov 22.

Department of Hematology, All India Institute of Medical Sciences AIIMS, New Delhi 110029, India.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1160/TH12-07-0475DOI Listing
January 2013

Characterisation of two novel large F8 deletions in patients with severe haemophilia A and factor VIII inhibitors.

Thromb Haemost 2011 Feb 23;105(2):279-84. Epub 2010 Nov 23.

Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany.

View Article

Download full-text PDF

Source
http://www.thieme-connect.de/DOI/DOI?10.1160/TH10-09-0570
Publisher Site
http://dx.doi.org/10.1160/TH10-09-0570DOI Listing
February 2011

Difficulties in diagnosing congenital thrombotic thrombocytopenic purpura.

J Pediatr Hematol Oncol 2010 Mar;32(2):103-7

Department of Paediatrics, Haematology and Oncology, Warsaw Medical University, Warsaw, Poland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/MPH.0b013e3181cbd265DOI Listing
March 2010

Clinical and molecular features in patients with atypical teratoid rhabdoid tumor or malignant rhabdoid tumor.

Genes Chromosomes Cancer 2010 Feb;49(2):176-81

Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/gcc.20729
Publisher Site
http://dx.doi.org/10.1002/gcc.20729DOI Listing
February 2010

Analysis of the CC chemokine receptor 5Delta32 polymorphism in pediatric liver transplant recipients.

Pediatr Transplant 2008 Nov 8;12(7):769-72. Epub 2008 Jan 8.

Department of Pediatrics, Pediatrics Hepatology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1399-3046.2007.00900.xDOI Listing
November 2008

Intracranial hemorrhage in a term newborn with severe von Willebrand disease type 3 associated with sinus venous thrombosis.

Haematologica 2006 Dec;91(12 Suppl):ECR60

University Medical Center Hamburg-Eppendorf, Department of Pediatric Hematology and Oncology, Martinistrasse 52, D-20246 Hamburg, Germany.

View Article

Download full-text PDF

Source
December 2006

A common origin of the 4143insA ADAMTS13 mutation.

Thromb Haemost 2006 Jul;96(1):3-6

University Medical Center Hamburg-Eppendorf, Department of Pediatric Hematology and Oncology, Martinistrasse 52, D-20246 Hamburg, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1160/TH05-12-0817DOI Listing
July 2006