Zobrazeno 1 - 10
of 296
pro vyhledávání: '"I. Tatarsky"'
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis. 1:260-264
Previous preliminary data and case reports have suggested an association of von Willebrand's disease (vWD) with factor XI deficiency and platelet abnormalities. We have analyzed the prevalence of factor XI deficiency and thrombocytopathy in a cohort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6014e4e773a566f6b8e53a335e324ed6
https://doi.org/10.1177/107602969500100402
https://doi.org/10.1177/107602969500100402
Publikováno v:
European Journal of Cardiovascular Prevention & Rehabilitation. 2:57-62
Increasing evidence suggests that oxidized low-density lipoprotein (LDL) is associated with the development of atherosclerosis in vivo. Because endothelial injury contributes to the development of the atherogenic , we investigated the efficacy of oxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14eceda03ce49bb3df6aa70533c5b878
https://doi.org/10.1177/174182679500200109
https://doi.org/10.1177/174182679500200109
Autor:
Rivka Sharon, I. Tatarsky
Publikováno v:
American Journal of Hematology. 46:87-90
Forty-six mothers with immune thrombocytopenic purpura (ITP) gave birth to 72 babies. Sixty-two babies were delivered vaginally and 10 babies by cesarean section. There was no mortality among mothers or babies. Eighteen infants were born thrombocytop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d827ab77874738eaa044669ef1f42b5d
https://doi.org/10.1002/ajh.2830460206
https://doi.org/10.1002/ajh.2830460206
Publikováno v:
Fibrinolysis. 6:183-186
Thrombotic events are common in patients with myeloproliferative disorders. Since abnormalities in the fibrinolytic system have been reported in patients with thrombotic phenomena, we have evaluated fibrinolytic parameters in 48 polycythaemia vera (P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e5cd3f520da45a33366c80f37e5a772
https://doi.org/10.1016/0268-9499(92)90058-p
https://doi.org/10.1016/0268-9499(92)90058-p
Publikováno v:
Vox Sanguinis. 65:328-330
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d13de1c4095aa06aca12b52f5aa0f3cb
https://doi.org/10.1159/000462451
https://doi.org/10.1159/000462451
Publikováno v:
The Israel Medical Association journal : IMAJ. 2(1)
The etiology of bone marrow failure, a prominent feature of paroxysmal nocturnal hemoglobulinuria, is presently unknown.To evaluate the possible influence of cellular immune mechanisms in the bone marrow failure of PNH.We studied marrow erythroid col
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7a385ce69cca2c56b19c35f095561c09
https://pubmed.ncbi.nlm.nih.gov/10892366
https://pubmed.ncbi.nlm.nih.gov/10892366
Publikováno v:
Thrombosis and Haemostasis. 63:036-038
SummaryTo account for the lack of correlation between the level of factor XI (FXI) in deficient patients and haemorrhagic manifestations, we correlated the prevalence of combined FXI and von Willebrand’s factor (vWF) deficiency in 212 FXI-deficient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a02b589efe56f25f8f782c6b4718cabc
https://doi.org/10.1055/s-0038-1645682
https://doi.org/10.1055/s-0038-1645682
Autor:
I, Tatarsky, R, Sharon
Publikováno v:
Seminars in hematology. 34(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::508a1a393b5ad1e03717d3ddaba2da11
https://pubmed.ncbi.nlm.nih.gov/9025159
https://pubmed.ncbi.nlm.nih.gov/9025159
Publikováno v:
Israel journal of medical sciences. 30(12)
The prevalence, clinical manifestations and serological markers of hepatitis C virus (HCV), hepatitis B virus (HBV) and human immunodeficiency virus (HIV) infections were studied in 112 multiply transfused patients (49 hemophiliacs receiving either n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9a0b180dcaba1f54354c187c347b0b41
https://pubmed.ncbi.nlm.nih.gov/8002269
https://pubmed.ncbi.nlm.nih.gov/8002269
Publikováno v:
American journal of hematology. 46(4)
We describe the results of clinical, cytogenetic, and molecular biological studies of a patient who, after two courses of treatment with Busulphan, has remained free of symptoms of Philadelphia chromosome-positive chronic myeloid leukemia for 27 year
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef62ba7747df299d411b5195ee36dfaa
https://pubmed.ncbi.nlm.nih.gov/8037191
https://pubmed.ncbi.nlm.nih.gov/8037191