Found: 18
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Prevalence and Causes of Anemia in Hospitalized Patients: Impact on Diseases Outcome.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 4, p. 950, doi. 10.3390/jcm9040950
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- Publication type:
- Article
Genetic analysis of erythrocytosis reveals possible causative and modifier gene mutations.
- Published in:
- British Journal of Haematology, 2019, v. 186, n. 4, p. e100, doi. 10.1111/bjh.15931
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- Publication type:
- Article
<italic>HFE</italic> mutations in idiopathic erythrocytosis.
- Published in:
- British Journal of Haematology, 2018, v. 181, n. 2, p. 270, doi. 10.1111/bjh.14555
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- Publication type:
- Article
Idiopathic erythrocytosis: a study of a large cohort with a long follow-up.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years).
- Published in:
- European Journal of Haematology, 2016, v. 97, n. 6, p. 547, doi. 10.1111/ejh.12767
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- Publication type:
- Article
Thrombotic risk correlates with mutational status in true essential thrombocythemia.
- Published in:
- European Journal of Clinical Investigation, 2016, v. 46, n. 8, p. 683, doi. 10.1111/eci.12647
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- Publication type:
- Article
Thrombotic and hemorrhagic complications in idiopathic erythrocytosis.
- Published in:
- American Journal of Hematology, 2017, v. 92, n. 11, p. E639, doi. 10.1002/ajh.24873
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- Publication type:
- Article
A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Thrombotic events in severe FXII deficiency in comparison with unaffected family members during a long observation period.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2019, v. 47, n. 3, p. 481, doi. 10.1007/s11239-019-01819-8
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- Publication type:
- Article
Impact of HFE mutations on thrombotic risk in patients with idiopathic erythrocytosis: A single‐centre study.
- Published in:
- EJHaem, 2024, v. 5, n. 5, p. 1086, doi. 10.1002/jha2.1019
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- Publication type:
- Article
Increased Prevalence of Reported Cases of Congenital Prekallikrein Deficiency Among African Americans as Compared With the General Population of the United States.
- Published in:
- 2020
- By:
- Publication type:
- Editorial
The Dysprothrombinemias due to Arg596 Mutations: A Conundrum With No Bleeding Tendency and Venous Thrombosis due to Antithrombin Resistance.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2019, v. 25, p. 1, doi. 10.1177/1076029619841701
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- Publication type:
- Article
Vitamin K-Dependent Coagulation Factors That May be Responsible for Both Bleeding and Thrombosis (FII, FVII, and FIX).
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2018, v. 24, n. 9S, p. 42S, doi. 10.1177/1076029618811109
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- Publication type:
- Article
Prothrombin: Another Clotting Factor After FV That Is Involved Both in Bleeding and Thrombosis.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2018, v. 24, n. 6, p. 845, doi. 10.1177/1076029618770741
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- Publication type:
- Article
Thrombotic and Hemorrhagic Conditions Due to a Gain of Function of Coagulation Proteins: A Special Type of Clotting Disorders.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2018, v. 24, n. 4, p. 560, doi. 10.1177/1076029617721012
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- Publication type:
- Article
Factor X Friuli Coagulation Disorder: Almost 50 Years Later.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2018, v. 24, n. 1, p. 33, doi. 10.1177/1076029616686423
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- Publication type:
- Article
Acquired Isolated FVII Deficiency.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2016, v. 22, n. 8, p. 705, doi. 10.1177/1076029615599440
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- Publication type:
- Article
Myocardial Infarctions and Other Acute Coronary Syndromes in Rare Congenital Bleeding Disorders: A Critical Analysis of All Reported Cases.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2015, v. 21, n. 4, p. 359, doi. 10.1177/1076029614548056
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- Publication type:
- Article