Zespół Scotta (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Zespół Scotta" in Polish language version.

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doi.org

N. Satta, F. Toti, E. Fressinaud, D. Meyer i inni. Scott syndrome: an inherited defect of the procoagulant activity of platelets. „Platelets”. 8 (2–3), s. 117–124, 1997. DOI: 10.1080/09537109709169326. PMID: 20297932.
M. Halliez, M. Fouassier, N. Robillard, C. Ternisien i inni. Detection of phosphatidyl serine on activated platelets’ surface by flow cytometry in whole blood: a simpler test for the diagnosis of Scott syndrome. „Br J Haematol”, 2015. DOI: 10.1111/bjh.13391. PMID: 25823976.

icd9data.com

2014 ICD-9-CM Diagnosis Code 287.1 Qualitative platelet defects. ICD9Data. [dostęp 2015-12-18].

nih.gov

ncbi.nlm.nih.gov

N. Satta, F. Toti, E. Fressinaud, D. Meyer i inni. Scott syndrome: an inherited defect of the procoagulant activity of platelets. „Platelets”. 8 (2–3), s. 117–124, 1997. DOI: 10.1080/09537109709169326. PMID: 20297932.
H.J. Weiss, W.J. Vicic, B.A. Lages, J. Rogers. Isolated deficiency of platelet procoagulant activity. „Am J Med”. 67 (2), s. 206–213, 1979. PMID: 572637.
M. Halliez, M. Fouassier, N. Robillard, C. Ternisien i inni. Detection of phosphatidyl serine on activated platelets’ surface by flow cytometry in whole blood: a simpler test for the diagnosis of Scott syndrome. „Br J Haematol”, 2015. DOI: 10.1111/bjh.13391. PMID: 25823976.

omim.org

Scott Syndrome; SCTS. Johns Hopkins University. [dostęp 2015-12-19]. (ang.).

wiley.com

onlinelibrary.wiley.com

M. Halliez, M. Fouassier, N. Robillard, C. Ternisien i inni. Detection of phosphatidyl serine on activated platelets’ surface by flow cytometry in whole blood: a simpler test for the diagnosis of Scott syndrome. „Br J Haematol”, 2015. DOI: 10.1111/bjh.13391. PMID: 25823976.