Trombocitička trombocitopenična purpura (Serbo-Croatian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Trombocitička trombocitopenična purpura" in Serbo-Croatian language version.

refsWebsite

Global rank Serbo-Croatian rank

9nih.gov

4^th place

3^rd place

8doi.org

2^nd place

1hematologylibrary.org

low place

1,541^st place

doi.org

dx.doi.org

Moake JL (2002). „Thrombotic microangiopathies”. N. Engl. J. Med. 347 (8): 589–600. DOI:10.1056/NEJMra020528. PMID 12192020.
Moake JL (1998). „Moschcowitz, multimers, and metalloprotease”. N. Engl. J. Med. 339 (22): 1629–31. DOI:10.1056/NEJM199811263392210. PMID 9828253.
Furlan M, Robles R, Galbusera M, et al. (1998). „von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome”. N. Engl. J. Med. 339 (22): 1578–84. DOI:10.1056/NEJM199811263392202. PMID 9828245.
Tsai HM, Lian EC (1998). „Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura”. N. Engl. J. Med. 339 (22): 1585–94. DOI:10.1056/NEJM199811263392203. PMID 9828246.
Upshaw JD (June 1978). „Congenital deficiency of a factor in normal plasma that reverses microangiopathic hemolysis and thrombocytopenia”. N. Engl. J. Med. 298 (24): 1350–2. DOI:10.1056/NEJM197806152982407. PMID 651994.
Levy GG, Nichols WC, Lian EC, et al. (October 2001). „Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura”. Nature 413 (6855): 488–94. DOI:10.1038/35097008. PMID 11586351.
Moake JL (2004). „von Willebrand factor, ADAMTS-13, and thrombotic thrombocytopenic purpura”. Semin. Hematol. 41 (1): 4–14. DOI:10.1053/j.seminhematol.2003.10.003. PMID 14727254.
Zheng XL, Kaufman RM, Goodnough LT, Sadler JE (2004). „Effect of plasma exchange on plasma ADAMTS13 metalloprotease activity, inhibitor level, and clinical outcome in patients with idiopathic and nonidiopathic thrombotic thrombocytopenic purpura”. Blood 103 (11): 4043–9. DOI:10.1182/blood-2003-11-4035. PMID 14982878.

hematologylibrary.org

bloodjournal.hematologylibrary.org

Schulman I, Pierce M, Lukens A, Currimbhoy Z (July 1960). „Studies on thrombopoiesis. I. A factor in normal human plasma required for platelet production; chronic thrombocytopenia due to its deficiency” (PDF). Blood 16: 943–57. PMID 14443744.

nih.gov

ncbi.nlm.nih.gov

Moake JL (2002). „Thrombotic microangiopathies”. N. Engl. J. Med. 347 (8): 589–600. DOI:10.1056/NEJMra020528. PMID 12192020.
Moake JL (1998). „Moschcowitz, multimers, and metalloprotease”. N. Engl. J. Med. 339 (22): 1629–31. DOI:10.1056/NEJM199811263392210. PMID 9828253.
Furlan M, Robles R, Galbusera M, et al. (1998). „von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome”. N. Engl. J. Med. 339 (22): 1578–84. DOI:10.1056/NEJM199811263392202. PMID 9828245.
Tsai HM, Lian EC (1998). „Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura”. N. Engl. J. Med. 339 (22): 1585–94. DOI:10.1056/NEJM199811263392203. PMID 9828246.
Schulman I, Pierce M, Lukens A, Currimbhoy Z (July 1960). „Studies on thrombopoiesis. I. A factor in normal human plasma required for platelet production; chronic thrombocytopenia due to its deficiency” (PDF). Blood 16: 943–57. PMID 14443744.
Upshaw JD (June 1978). „Congenital deficiency of a factor in normal plasma that reverses microangiopathic hemolysis and thrombocytopenia”. N. Engl. J. Med. 298 (24): 1350–2. DOI:10.1056/NEJM197806152982407. PMID 651994.
Levy GG, Nichols WC, Lian EC, et al. (October 2001). „Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura”. Nature 413 (6855): 488–94. DOI:10.1038/35097008. PMID 11586351.
Moake JL (2004). „von Willebrand factor, ADAMTS-13, and thrombotic thrombocytopenic purpura”. Semin. Hematol. 41 (1): 4–14. DOI:10.1053/j.seminhematol.2003.10.003. PMID 14727254.
Zheng XL, Kaufman RM, Goodnough LT, Sadler JE (2004). „Effect of plasma exchange on plasma ADAMTS13 metalloprotease activity, inhibitor level, and clinical outcome in patients with idiopathic and nonidiopathic thrombotic thrombocytopenic purpura”. Blood 103 (11): 4043–9. DOI:10.1182/blood-2003-11-4035. PMID 14982878.