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Frequency distribution of RHD alleles among Greek donors with weak D phenotypes demonstrates a distinct pattern in central European countries

Transfusion medicine (Oxford, England), 2019-12, Vol.29 (6), p.468-470

2019

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Coexisting dysfibrinogenemia (γArg275His) and FV Leiden associated with thrombosis (Fibrinogen Crete)

Thrombosis research, 2010-08, Vol.126 (2), p.e162-e164

2010

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Effect of angiotensin converting enzyme gene I/D polymorphism and its expression on clinical outcome in acute respiratory distress syndrome

Minerva anestesiologica, 2013-08, Vol.79 (8), p.861

2013

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Coagulation disorders and the role of tissue factor and tissue factor pathway inhibitor in critically ill patients

Intensive care medicine experimental, 2015-10, Vol.3 (Suppl 1), p.1, Article A297

2015

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No evidence of frequent association of the JAK2 V617F mutation with acute myocardial infarction in young patients

Leukemia, 2009-05, Vol.23 (5), p.1008-1009

2009

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Predicting response to chronic antihypertensive treatment with fosinopril : The role of angiotensin-converting enzyme gene polymorphism

Cardiovascular drugs and therapy, 2000-08, Vol.14 (4), p.427-432

2000

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P43 Successful pregnancy outcome in a woman with dysfibrinogenemia and FVLeiden associated with thrombosis

Thrombosis research, 2009, Vol.123, p.S152-S152

2009

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HEMOSTASIS DISORDERS IN CORONARY ARTERY DISEASE: A PROSPECTIVE COMPARATIVE STUDY OF 130 PATIENTS

Georgian medical news, 2022-11 (332), p.12-21

2022

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P1735Factor V Leiden and prothrombin G20210A mutations in patients with premature myocardial infarction

European heart journal, 2017-08, Vol.38 (suppl_1)

2017

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The prevalence of hepatitis B and C in HIV-positive Greek patients: relationship to survival of deceased AIDS patients

The Journal of infection, 2000-03, Vol.40 (2), p.127-131

2000

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Resistance to activated protein C and FV Leiden mutation in patients with a history of acute myocardial infarction or primary hypertension

American journal of hypertension, 2000, Vol.13 (1), p.61-65

2000

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HAEMOSTASIS BALANCE DISORDERS IN PATIENTS WITH ESSENTIAL HYPERTENSION

Thrombosis research, 1997-10, Vol.88 (2), p.99-107

1997

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Prevalence of the FVQ506 mutation in the Hellenic population

Thrombosis and haemostasis, 1996-07, Vol.76 (1), p.127-127

1996

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Epidemiology of haemophilia in Greece: an overview

Thrombosis and haemostasis, 1994-12, Vol.72 (6), p.808-813

1994

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ACE/DD genotype is associated with hemostasis balance disturbances reflecting hypercoagulability and endothelial dysfunction in patients with untreated hypertension

The American heart journal, 2000-11, Vol.140 (5), p.760-765

2000

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Prevalence of prothrombotic polymorphisms in Greece

Genetic testing, 2008-12, Vol.12 (4), p.541-547

2008

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Family studies in an extremely large mild haemophilia A pedigree which includes 10% of Greek haemophiliacs

British journal of haematology, 1995-01, Vol.89 (1), p.203-206

1995

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Antibody Responses to Hepatitis C Virus by Second-Generation Immunoassays in a Cohort of Patients with Bleeding Disorders

Vox sanguinis, 1992-01, Vol.63 (3), p.204-209

1992

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Combination treatment with interferon (IFN) and ribavirin (RBV) inHCV(+)HIV(−) haemophilia PTS, non responders (NR) to IFNmonotherapy

Journal of hepatology, 2000, Vol.32, p.189-189

2000

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Determinants of progression of HIV infection in a Greek hemophilia cohort followed for up to 16 years after seroconversion

Journal of acquired immune deficiency syndromes and human retrovirology, 1998-09, Vol.19 (1), p.89-97

1998

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HIV Seropositivity in Greek Blood Donors (1985-1990)

Vox sanguinis, 1991-01, Vol.61 (3), p.215-216

1991

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The Pervalence of Hepatitis B and C in HIV-positive Greek Patients: Relationship to Survival of Deceased AIDS Patients

The Journal of infection, 2000-03, Vol.40 (2), p.127-131

2000

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1.P.383 Inherited factor V (MF) mis-sense mutation in patients with essential hypertension

Atherosclerosis, 1997-10, Vol.134 (1-2), p.98-98

1997

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Allele frequency of the CCR5 mutant chemokine receptor in Greek Caucasians

Journal of acquired immune deficiency syndromes and human retrovirology, 1998-02, Vol.17 (2), p.181-182

1998

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Abstract: P884 LACK OF ASSOCIATION OF ANGIOTENSIN CONVERTING ENZYME GENE INSERTION/DELETION POLYMORPHISM AND MYOCARDIAL INFARCTION AT VERY YOUNG AGES

Atherosclerosis. Supplements, 2009-06, Vol.10 (2), p.e1029-e1029

2009

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Frequency distribution of RHD alleles among Greek donors with weak D phenotypes demonstrates a distinct pattern in central European countries

Coexisting dysfibrinogenemia (γArg275His) and FV Leiden associated with thrombosis (Fibrinogen Crete)

Effect of angiotensin converting enzyme gene I/D polymorphism and its expression on clinical outcome in acute respiratory distress syndrome

Coagulation disorders and the role of tissue factor and tissue factor pathway inhibitor in critically ill patients

No evidence of frequent association of the JAK2 V617F mutation with acute myocardial infarction in young patients

Predicting response to chronic antihypertensive treatment with fosinopril : The role of angiotensin-converting enzyme gene polymorphism

P43 Successful pregnancy outcome in a woman with dysfibrinogenemia and FVLeiden associated with thrombosis

HEMOSTASIS DISORDERS IN CORONARY ARTERY DISEASE: A PROSPECTIVE COMPARATIVE STUDY OF 130 PATIENTS

P1735Factor V Leiden and prothrombin G20210A mutations in patients with premature myocardial infarction

The prevalence of hepatitis B and C in HIV-positive Greek patients: relationship to survival of deceased AIDS patients

Resistance to activated protein C and FV Leiden mutation in patients with a history of acute myocardial infarction or primary hypertension

HAEMOSTASIS BALANCE DISORDERS IN PATIENTS WITH ESSENTIAL HYPERTENSION

Prevalence of the FVQ506 mutation in the Hellenic population

Epidemiology of haemophilia in Greece: an overview

ACE/DD genotype is associated with hemostasis balance disturbances reflecting hypercoagulability and endothelial dysfunction in patients with untreated hypertension

Prevalence of prothrombotic polymorphisms in Greece

Family studies in an extremely large mild haemophilia A pedigree which includes 10% of Greek haemophiliacs

Antibody Responses to Hepatitis C Virus by Second-Generation Immunoassays in a Cohort of Patients with Bleeding Disorders

Combination treatment with interferon (IFN) and ribavirin (RBV) inHCV(+)HIV(−) haemophilia PTS, non responders (NR) to IFNmonotherapy

Determinants of progression of HIV infection in a Greek hemophilia cohort followed for up to 16 years after seroconversion

HIV Seropositivity in Greek Blood Donors (1985-1990)

The Pervalence of Hepatitis B and C in HIV-positive Greek Patients: Relationship to Survival of Deceased AIDS Patients

1.P.383 Inherited factor V (MF) mis-sense mutation in patients with essential hypertension

Allele frequency of the CCR5 mutant chemokine receptor in Greek Caucasians

Abstract: P884 LACK OF ASSOCIATION OF ANGIOTENSIN CONVERTING ENZYME GENE INSERTION/DELETION POLYMORPHISM AND MYOCARDIAL INFARCTION AT VERY YOUNG AGES

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