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Detection of human disease conditions by single-cell morpho-rheological phenotyping of blood.
Elife. 2018 Jan 13;7:e29213. doi: 10.7554/eLife.29213.
Elife. 2018.
PMID: 29331015
Free PMC article.
Congenital macrothrombocytopenia associated with a combination of functional polymorphisms in the TUBB1 gene.
Stächele J, Bakchoul T, Najm J, Felbor U, Knöfler R.
Stächele J, et al.
Hamostaseologie. 2015;35 Suppl 1:S18-21.
Hamostaseologie. 2015.
PMID: 26540125
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Significance of platelet function diagnostics for clarification of suspected battered child syndrome.
Knöfler R, Lohse J, Stächele J, Heilmann A, Schwier F, Schmidt U, Erfurt C.
Knöfler R, et al. Among authors: stachele j.
Hamostaseologie. 2014;34 Suppl 1:S53-6. doi: 10.5482/HAMO-14-02-0011.
Hamostaseologie. 2014.
PMID: 25382772
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Successful thrombolytic treatment of neonatal arterial thromboses.
Stächele J, Dinger J, Brenner S, Hofmann SR, Ifflaender S, Knöfler R.
Stächele J, et al.
Hamostaseologie. 2014;34 Suppl 1:S57-9. doi: 10.5482/HAMO-14-02-0014.
Hamostaseologie. 2014.
PMID: 25382773
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