27 Einträge gefunden

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

   1. Lehmberg, K
   2. Hassenpflug, W A
   3. Klaassen, I
   4. Hillebrand, G
   5. Oyen, F
   6. Budde, U
   7. Singer, D

   2017 - Forschungsinformationssystem des UKE
2. Identification and characterization of the elusive mutation causing the historical von Willebrand Disease type IIC Miami

   1. Obser, T
   2. Ledford-Kraemer, M
   3. Oyen, F
   4. Brehm, M A
   5. Denis, C V
   6. Marschalek, R
   7. Montgomery, R R

   2016 - Forschungsinformationssystem des UKE
3. Germline de novo mutations and linkage markers vs. DNA sequencing for carrier detection in von Willebrand disease

   1. Ahmad, F
   2. Oyen, F
   3. Jan, R
   4. Budde, U
   5. Schneppenheim, R
   6. Saxena, R

   2014 - Forschungsinformationssystem des UKE
4. Interactions of von Willebrand factor and ADAMTS13 in von Willebrand disease and thrombotic thrombocytopenic purpura

   1. Budde, U
   2. Schneppenheim, R

   2014 - Forschungsinformationssystem des UKE
5. von Willebrand disease type 2A phenotypes IIC, IID and IIE: A day in the life of shear-stressed mutant von Willebrand factor

   1. Brehm, M A
   2. Huck, Volker
   3. Aponte-Santamaría, C
   4. Obser, T
   5. Grässle, S
   6. Oyen, F
   7. Budde, U

   2014 - Forschungsinformationssystem des UKE
6. Identification of a homozygous Cys410Ser mutation in the von Willebrand factor D2 domain causing type 2A(IIC) von Willebrand disease phenotype in an Iranian patient

   1. Enayat, M S
   2. Ravanbod, S
   3. Rassoulzadegan, M
   4. Jazebi, M
   5. Ala, F
   6. Budde, U
   7. Schneppenheim, S

   2013 - Forschungsinformationssystem des UKE
7. Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formation.

   1. Castaman, G
   2. Giacomelli, S H
   3. Jacobi, P M
   4. Obser, Tobias
   5. Budde, U
   6. Rodeghiero, F
   7. Schneppenheim, Reinhard

   2012 - Forschungsinformationssystem des UKE
8. A comparison between two semi-quantitative bleeding scales for the diagnosis and assessment of bleeding severity in type 1 von Willebrand disease.

   1. Tosetto, A
   2. Rodeghiero, F
   3. Castaman, G
   4. Goodeve, A
   5. Federici, A B
   6. Batlle, J
   7. Meyer, D

   2011 - Forschungsinformationssystem des UKE
9. [Von Willebrand factor and ADAMTS13 balancing primary haemostasis].

   1. Schneppenheim, Reinhard
   2. Budde, U

   2011 - Forschungsinformationssystem des UKE
10. von Willebrand factor: the complex molecular genetics of a multidomain and multifunctional protein.

    1. Schneppenheim, Reinhard
    2. Budde, U

    2011 - Forschungsinformationssystem des UKE
11. Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype.

    1. Castaman, G
    2. Giacomelli, S H
    3. Jacobi, P
    4. Obser, Tobias
    5. Budde, U
    6. Rodeghiero, F
    7. Haberichter, S L

    2010 - Forschungsinformationssystem des UKE
12. von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levels

    1. Hickson, N
    2. Hampshire, D
    3. Winship, P
    4. Goudemand, J
    5. Schneppenheim, R
    6. Budde, U
    7. Castaman, G

    2010 - Forschungsinformationssystem des UKE
13. Validation of a rapid test (VWF-LIA) for the quantitative determination of von Willebrand factor antigen in type 1 von Willebrand disease diagnosis within the European multicenter study MCMDM-1VWD.

    1. Castaman, G
    2. Tosetto, A
    3. Cappelletti, A
    4. Goodeve, A
    5. Federici, A B
    6. Batlle, J
    7. Meyer, D

    2010 - Forschungsinformationssystem des UKE
14. Severe bleeding diathesis associated with moderate thrombocytopenia - diagnostic workup of seven family members with type 2B von Willebrand's disease.

    1. Zdziarska, J
    2. Iwaniec, T
    3. Skotnicki, A B
    4. Musia, J
    5. Schneppenheim, Reinhard
    6. Budde, U
    7. Kentouche, K

    2010 - Forschungsinformationssystem des UKE
15. Acquired von Willebrand syndrome as side effect of valproic acid therapy in children is rare.

    1. Eberl, Wolfgang
    2. Budde, U
    3. Bentele, Karl H. P.
    4. Christen, H-J
    5. Knapp, R
    6. Mey, A
    7. Schneppenheim, Reinhard

    2009 - Forschungsinformationssystem des UKE
16. Response to DDAVP in children with von Willebrand disease type 2.

    1. Schneppenheim, Reinhard
    2. Budde, U
    3. Beutel, Karin
    4. Hassenpflug, W-A
    5. Hauch, H
    6. Obser, Tobias
    7. Oyen, Florian

    2009 - Forschungsinformationssystem des UKE
17. Shear-induced unfolding activates von Willebrand factor A2 domain for proteolysis.

    1. Schneppenheim, Reinhard
    2. Baldauf, C
    3. Stacklies, W
    4. Obser, T
    5. Pieconka, A
    6. Schneppenheim, S
    7. Budde, U

    2009 - Forschungsinformationssystem des UKE
18. [Inborn and acquired von Willebrand disease]

    1. Schneppenheim, Reinhard
    2. Budde, U

    2008 - Forschungsinformationssystem des UKE
19. Genetic defects in von Willebrand disease type 3 in Indian and Greek patients.

    1. Gupta, P K
    2. Saxena, R
    3. Adamtziki, E
    4. Budde, U
    5. Oyen, Florian
    6. Obser, Tobias
    7. Schneppenheim, Reinhard

    2008 - Forschungsinformationssystem des UKE
20. Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD).

    1. Budde, U
    2. Schneppenheim, Reinhard
    3. Eikenboom, J
    4. Goodeve, A
    5. Will, K
    6. Drewke, E
    7. Castaman, G

    2008 - Forschungsinformationssystem des UKE