Halimeh S - Search Results

1

Multiplate whole blood impedance point of care aggregometry: preliminary reference values in healthy infants, children and adolescents.

Halimeh S, Angelis Gd, Sander A, Edelbusch C, Rott H, Thedieck S, Mesters R, Schlegel N, Nowak-Göttl U. Halimeh S, et al. Klin Padiatr. 2010 May;222(3):158-63. doi: 10.1055/s-0030-1249081. Epub 2010 May 31. Klin Padiatr. 2010. PMID: 20514620

2

A Cross-sectional Analysis of Treatment in PUPs in 2021 in Germany - First Data from the GEPHARD Study Group.

GEPHARD Investigators; Contributors:; Contributors to the cross-sectional analysis:; Study commission. GEPHARD Investigators, et al. Hamostaseologie. 2022 Oct;42(S 01):S24-S31. doi: 10.1055/s-0042-1757552. Epub 2022 Oct 26. Hamostaseologie. 2022. PMID: 36288733 Free PMC article.

3

Thrombolysis in newborns and infants.

Nowak-Göttl U, Auberger K, Halimeh S, Junker R, Klinge J, Kreuz WD, Ries M, Schlegel N. Nowak-Göttl U, et al. Among authors: halimeh s. Thromb Haemost. 1999 Sep;82 Suppl 1:112-6. Thromb Haemost. 1999. PMID: 10695499 Review.

4

Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors.

Escuriola Ettingshausen C, Halimeh S, Kurnik K, Schobess R, Wermes C, Junker R, Kreuz W, Pollmann H, Nowak-Göttl U. Escuriola Ettingshausen C, et al. Among authors: halimeh s. Thromb Haemost. 2001 Feb;85(2):218-20. Thromb Haemost. 2001. PMID: 11246535

5

Effects of primary and secondary prophylaxis on the clinical expression of joint damage in children with severe haemophilia A. Results of a multicenter non-concurrent cohort study.

Schobess R, Kurnik K, Friedrichs F, Halimeh S, Krümpel A, Bidlingmaier C, Nowak-Göttl U. Schobess R, et al. Among authors: halimeh s. Thromb Haemost. 2008 Jan;99(1):71-6. doi: 10.1160/TH07-06-0417. Thromb Haemost. 2008. PMID: 18217137

6

[Contraception and thrombophilia].

Rott H, Kruempel A, Kappert G, Nowak-Göttl U, Halimeh S. Rott H, et al. Among authors: halimeh s. Hamostaseologie. 2009 May;29(2):193-6. Hamostaseologie. 2009. PMID: 19404523 German.

7

Long-term secondary prophylaxis in children, adolescents and young adults with von Willebrand disease. Results of a cohort study.

Halimeh S, Krümpel A, Rott H, Bogdanova N, Budde U, Manner D, Faeser B, Mesters R, Nowak-Göttl U. Halimeh S, et al. Thromb Haemost. 2011 Apr;105(4):597-604. doi: 10.1160/TH10-09-0616. Epub 2011 Feb 8. Thromb Haemost. 2011. PMID: 21301780

8

Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 families.

Sandrock K, Halimeh S, Wiegering V, Kappert G, Sauer K, Deeg N, Busse E, Zieger B. Sandrock K, et al. Among authors: halimeh s. Klin Padiatr. 2012 Apr;224(3):174-8. doi: 10.1055/s-0032-1306346. Epub 2012 Apr 18. Klin Padiatr. 2012. PMID: 22513797

9

[Treatment of haemophilia with an integrated therapeutical concept--Duisburg model].

Halimeh S, Rott H, Kappert G. Halimeh S, et al. Hamostaseologie. 2012;32 Suppl 1:S25-8. Hamostaseologie. 2012. PMID: 22961178 German.

10

Risk factors for high-titer inhibitor development in children with hemophilia A: results of a cohort study.

Halimeh S, Bidlingmaier C, Heller C, Gutsche S, Holzhauer S, Kenet G, Kurnik K, Manner D, Iorio A, Nowak-Göttl U. Halimeh S, et al. Biomed Res Int. 2013;2013:901975. doi: 10.1155/2013/901975. Epub 2013 Oct 2. Biomed Res Int. 2013. PMID: 24199202 Free PMC article.

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