Schallmoser K - Search Results

1

Sexually dimorphic estrogen sensing in skeletal stem cells controls skeletal regeneration.

Andrew TW, Koepke LS, Wang Y, Lopez M, Steininger H, Struck D, Boyko T, Ambrosi TH, Tong X, Sun Y, Gulati GS, Murphy MP, Marecic O, Telvin R, Schallmoser K, Strunk D, Seita J, Goodman SB, Yang F, Longaker MT, Yang GP, Chan CKF. Andrew TW, et al. Among authors: schallmoser k. Nat Commun. 2022 Oct 30;13(1):6491. doi: 10.1038/s41467-022-34063-5. Nat Commun. 2022. PMID: 36310174 Free PMC article.

2

Lack of association of the Glu298Asp polymorphism of endothelial nitric oxide synthase with manifest coronary artery disease, carotid atherosclerosis and forearm vascular reactivity in two Austrian populations.

Schmoelzer I, Renner W, Paulweber B, Malaimare L, Iglseder B, Schmid P, Schallmoser K, Wascher TC. Schmoelzer I, et al. Among authors: schallmoser k. Eur J Clin Invest. 2003 Mar;33(3):191-8. doi: 10.1046/j.1365-2362.2003.01108.x. Eur J Clin Invest. 2003. PMID: 12641536

3

Function and activation state of platelets in vitro depend on apheresis modality.

Macher S, Sipurzynski-Budrass S, Rosskopf K, Rohde E, Griesbacher A, Groselj-Strele A, Lanzer G, Schallmoser K. Macher S, et al. Among authors: schallmoser k. Vox Sang. 2010 Nov;99(4):332-40. doi: 10.1111/j.1423-0410.2010.01353.x. Vox Sang. 2010. PMID: 20546206 Clinical Trial.

4

Severe thrombocytopenia due to host-derived anti-HPA-1a after non-myeloablative allogeneic haematopoietic stem cell transplantation for multiple myeloma: a case report.

Macher S, Schallmoser K, Staber PB, Neumeister P, Posch U, Lanzer G, Panzer S. Macher S, et al. Among authors: schallmoser k. Vox Sang. 2005 Nov;89(4):257-60. doi: 10.1111/j.1423-0410.2005.00692.x. Vox Sang. 2005. PMID: 16262760

5

[Evaluation of a newly discovered LDL receptor mutation (exon 10, GAC>AAC, D271N, "FH Graz-1") in familial hypercholesterolemia-- a familystudy].

de Campo A, Toplak H, Wascher TC, Schallmoser K, Friehs A, Schmidt H, Kostner GM. de Campo A, et al. Among authors: schallmoser k. Acta Med Austriaca. 1999;26(1):20-5. Acta Med Austriaca. 1999. PMID: 10230472 German.

6

C242T polymorphism of the p22 phox gene is not associated with peripheral arterial occlusive disease.

Renner W, Schallmoser K, Gallippi P, Krauss C, Toplak H, Wascher TC, Pilger E. Renner W, et al. Among authors: schallmoser k. Atherosclerosis. 2000 Sep;152(1):175-9. doi: 10.1016/s0021-9150(99)00448-7. Atherosclerosis. 2000. PMID: 10996353 Clinical Trial.

7

Thrombin generation before and after multicomponent blood collection.

Cimenti C, Sipurzynski S, Gallistl S, Rosenkranz A, Hiden M, Leschnik B, Schallmoser K, Lanzer G, Muntean WE. Cimenti C, et al. Among authors: schallmoser k. Transfusion. 2008 Aug;48(8):1584-90. doi: 10.1111/j.1537-2995.2008.01757.x. Epub 2008 May 22. Transfusion. 2008. PMID: 18503617 Clinical Trial.

8

Delayed detectability of anti-HPA-3a by the MAIPA assay in a severe neonatal alloimmune thrombocytopenia, but successful transfusion of incompatible donor platelets: a case report.

Schallmoser K, Kutschera J, Macher S, Ulrich S, Eichler P, Panzer S, Lanzer G. Schallmoser K, et al. Vox Sang. 2006 Aug;91(2):181-3. doi: 10.1111/j.1423-0410.2006.00809.x. Vox Sang. 2006. PMID: 16907881 No abstract available.

9

A novel splice-site mutation in intron 7 causes more severe hypercholesterolemia than a combined FH-FDB defect.

deCampo A, Schallmoser K, Schmidt H, Toplak H, Kostner GM. deCampo A, et al. Among authors: schallmoser k. Atherosclerosis. 2001 Aug;157(2):524-5. doi: 10.1016/s0021-9150(01)00535-4. Atherosclerosis. 2001. PMID: 11472756 No abstract available.

10

Reticulocyte hemoglobin content allows early and reliable detection of functional iron deficiency in blood donors.

Semmelrock MJ, Raggam RB, Amrein K, Avian A, Schallmoser K, Lanzer G, Semmelrock HJ, Prueller F, Berghold A, Rohde E. Semmelrock MJ, et al. Among authors: schallmoser k. Clin Chim Acta. 2012 Apr 11;413(7-8):678-82. doi: 10.1016/j.cca.2011.12.006. Epub 2011 Dec 23. Clin Chim Acta. 2012. PMID: 22212625

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