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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1896 1
1945 2
1946 3
1947 9
1948 14
1949 12
1950 17
1951 19
1952 25
1953 22
1954 17
1955 28
1956 17
1957 12
1958 7
1959 8
1960 10
1961 7
1962 17
1963 27
1964 53
1965 32
1966 24
1967 34
1968 31
1969 28
1970 44
1971 47
1972 50
1973 35
1974 30
1975 33
1976 24
1977 26
1978 26
1979 34
1980 31
1981 36
1982 35
1983 41
1984 56
1985 52
1986 60
1987 51
1988 55
1989 61
1990 61
1991 73
1992 47
1993 70
1994 77
1995 92
1996 83
1997 110
1998 133
1999 159
2000 166
2001 175
2002 201
2003 196
2004 221
2005 261
2006 254
2007 265
2008 264
2009 267
2010 292
2011 301
2012 332
2013 369
2014 347
2015 356
2016 340
2017 335
2018 308
2019 296
2020 317
2021 293
2022 212
2023 208
2024 102

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8,095 results

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Page 1
Inherited factor II deficiency with paradoxical hypercoagulability: a case report.
Watson H, Perez A, Ayesu K, Musa F, Sarriera J, Madruga M, Carlan SJ. Watson H, et al. Blood Coagul Fibrinolysis. 2018 Mar;29(2):223-226. doi: 10.1097/MBC.0000000000000710. Blood Coagul Fibrinolysis. 2018. PMID: 29389674
: Congenital deficiency of factor II is a very rare autosomal recessive disorder that can result in a bleeding diathesis. ...Paradoxical thrombosis in patients born from a nonconsanguineous marriage with factor II deficiency has not been …
: Congenital deficiency of factor II is a very rare autosomal recessive disorder that can result in a bleeding diathesi …
Congenital factor II deficiency: moroccan cases.
Imane S, Laalej Z, Faez S, Oukkache B. Imane S, et al. Int J Lab Hematol. 2013 Aug;35(4):416-20. doi: 10.1111/ijlh.12033. Epub 2012 Nov 28. Int J Lab Hematol. 2013. PMID: 23190616
This study highlights the rarity of inherited factor II deficiency and the importance of coagulation testing in the diagnosis of this condition. ...Three patients were female, and one was male. Symptoms of factor II deficiency were report …
This study highlights the rarity of inherited factor II deficiency and the importance of coagulation testing in the dia …
Antibiotic-associated hypoprothrombinaemia.
Lipsky JJ. Lipsky JJ. J Antimicrob Chemother. 1988 Mar;21(3):281-300. doi: 10.1093/jac/21.3.281. J Antimicrob Chemother. 1988. PMID: 3283095 Review.
This effect has commonly been attributed to the potential of these drugs to kill intestinal bacteria, a possible source of vitamin K, which is a necessary co-factor in the synthesis of four of the clotting factors. This review examines the evidence for and against this hyp …
This effect has commonly been attributed to the potential of these drugs to kill intestinal bacteria, a possible source of vitamin K, which …
Congenital deficiencies and abnormalities of prothrombin.
Girolami A, Scarano L, Saggiorato G, Girolami B, Bertomoro A, Marchiori A. Girolami A, et al. Blood Coagul Fibrinolysis. 1998 Oct;9(7):557-69. doi: 10.1097/00001721-199810000-00001. Blood Coagul Fibrinolysis. 1998. PMID: 9863703 Review.
Prothrombin (factor II) deficiency was first described in 1947 by Quick et al., although the first prothrombin abnormality was reported in 1969 by Shapiro et al. ...Usually, activity levels less than 10% of normal are found in homozygotes, and between 40 and …
Prothrombin (factor II) deficiency was first described in 1947 by Quick et al., although the first prothrombin abnormal …
A severe neonatal presentation of factor II deficiency.
Pasmant E, Dumont B, Lacapere JJ, Dautzenberg MD, Bezeaud A. Pasmant E, et al. Eur J Haematol. 2011 Nov;87(5):464-6. doi: 10.1111/j.1600-0609.2011.01670.x. Epub 2011 Aug 11. Eur J Haematol. 2011. PMID: 21692854
Prothrombin deficiency is an autosomal recessive disorder associated with moderate or severe bleeding tendency. ...
Prothrombin deficiency is an autosomal recessive disorder associated with moderate or severe bleeding tendency. ...
Vitamin K.
[No authors listed] [No authors listed] Br Med J. 1969 Apr 5;2(5648):40. Br Med J. 1969. PMID: 5776219 Free PMC article. No abstract available.
Prevalence of coagulation factor II G20210A and factor V G1691A Leiden polymorphisms in Chechans, a genetically isolated population in Jordan.
Dajani R, Fatahallah R, Dajani A, Al-Shboul M, Khader Y. Dajani R, et al. Mol Biol Rep. 2012 Sep;39(9):9133-8. doi: 10.1007/s11033-012-1785-7. Epub 2012 Jun 29. Mol Biol Rep. 2012. PMID: 22744422
BACKGROUND: Coagulation factor II G20210A and coagulation factor V (Leiden) G1691A single nucleotide polymorphisms (SNPs) are major inherited risk factors of venous thromboembolism. ...No homozygous factor II allele was found. Factor V Le …
BACKGROUND: Coagulation factor II G20210A and coagulation factor V (Leiden) G1691A single nucleotide polymorphisms (SNP …
Congenital bleeding disorders of the vitamin K-dependent clotting factors.
Girolami A, Scandellari R, Scapin M, Vettore S. Girolami A, et al. Vitam Horm. 2008;78:281-374. doi: 10.1016/S0083-6729(07)00014-3. Vitam Horm. 2008. PMID: 18374200 Review.
The different bleeding condition will be dealt with separately, namely, prothrombin or Factor II, Factor VII, Factor IX (hemophilia B), and Factor X deficiencies. An additional heading deals with the combined defect of the prothrombin complex, n …
The different bleeding condition will be dealt with separately, namely, prothrombin or Factor II, Factor VII, Factor …
8,095 results