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Prevention and treatment of bleeding complications in patients receiving vitamin K antagonists, Part 1: Prevention.
- Published in:
- American Journal of Hematology, 2009, v. 84, n. 9, p. 579, doi. 10.1002/ajh.21470
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- Publication type:
- Article
The C677T methylenetetrahydrofolate reductase gene mutation does not influence cardiovascular risk in the dialysis population: results of a multicentre prospective study.
- Published in:
- Nephrology Dialysis Transplantation, 2005, v. 20, n. 2, p. 382
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- Publication type:
- Article
The role of PC‐1 and ACE genes in diabetic nephropathy in type 1 diabetic patients: evidence for a polygenic control of kidney disease progression.
- Published in:
- Nephrology Dialysis Transplantation, 2002, v. 17, n. 8, p. 1402, doi. 10.1093/ndt/17.8.1402
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- Publication type:
- Article
TET2 Mutations in Ph-Negative Myeloproliferative Neoplasms: Identification of Three Novel Mutations and Relationship with Clinical and Laboratory Findings.
- Published in:
- BioMed Research International, 2013, v. 2013, p. 1, doi. 10.1155/2013/929840
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- Publication type:
- Article
Effects of Ethylene Oxide and Steam Sterilization on Dialysis-Induced Cytokine Release by Cuprophan Membrane.
- Published in:
- Artificial Organs, 2002, v. 26, n. 6, p. 543, doi. 10.1046/j.1525-1594.2002.06886_1.x
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- Publication type:
- Article
ASSOCIATIONS BETWEEN PERSONALITY TRAITS, PERCEIVED STRESS AND DEPRESSIVE SYMPTOMS IN GYNECOLOGICAL CANCER PATIENTS CHARACTERIZED BY THE SHORT AND LONG ALLELE VARIANT OF THE 5-HTTLPR GENOTYPE: PRELIMINARY RESULTS.
- Published in:
- Clinical Neuropsychiatry, 2022, v. 19, n. 3, p. 156, doi. 10.36131/cnfioritieditore20220304
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- Publication type:
- Article
MALADAPTIVE COPING STRATEGIES AND NEUROTICISM MEDIATE THE RELATIONSHIP BETWEEN 5HTT-LPR POLYMORPHISMS AND SYMPTOMS OF ANXIETY IN ELITE ATHLETES.
- Published in:
- Clinical Neuropsychiatry, 2019, v. 16, n. 1, p. 62
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- Publication type:
- Article
Mortality and clinical outcome of Italian patients undergoing orthopaedic surgery: effect of peri-operative blood transfusion.
- Published in:
- Blood Transfusion (17232007), 2021, v. 19, n. 4, p. 284, doi. 10.2450/2020.0059-20
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- Publication type:
- Article
Anticoagulation in Italian patients with venous thromboembolism and thrombophilic alterations: findings from START2 register study.
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- Blood Transfusion (17232007), 2020, v. 18, n. 6, p. 486, doi. 10.2450/2020.0091-20
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- Publication type:
- Article
Pattern of use and clinical outcomes with rIX‐FP in pediatric/adolescent patients with haemophilia B in Italy: Results from IDEAL real‐world study.
- Published in:
- European Journal of Haematology, 2024, v. 112, n. 5, p. 765, doi. 10.1111/ejh.14168
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- Publication type:
- Article
A comprehensive on-line digestion-liquid chromatography/mass spectrometry/collision-induced dissociation mass spectrometry approach for the characterization of human fibrinogen.
- Published in:
- Rapid Communications in Mass Spectrometry: RCM, 2001, v. 15, n. 16, p. 1383, doi. 10.1002/rcm.355
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- Publication type:
- Article
A myoferlin gain‐of‐function variant associates with a new type of hereditary angioedema.
- Published in:
- Allergy, 2020, v. 75, n. 11, p. 2989, doi. 10.1111/all.14454
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- Publication type:
- Article
A PC-1 amino acid variant (K121Q) is associated with faster progression of renal disease in patients with type 1 diabetes and albuminuria.
- Published in:
- 2000
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- Publication type:
- journal article
The curious incident of a cavum velum interpositum cyst in twins of a mother carrying May-Hegglin anomaly: a case report and short literature review.
- Published in:
- 2020
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- Publication type:
- journal article
Fetal Sex Identification in Maternal Plasma by Means of Short Tandem Repeats on Chromosome X.
- Published in:
- Annals of the New York Academy of Sciences, 2008, v. 1137, p. 148, doi. 10.1196/annals.1448.038
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- Publication type:
- Article
Modulation of factors involved in placental haemostasis and angiogenesis by low-molecular-weight-heparins.
- Published in:
- Archives of Gynecology & Obstetrics, 2016, v. 294, n. 6, p. 1323, doi. 10.1007/s00404-016-4185-8
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- Publication type:
- Article
Modulation of factors involved in placental haemostasis and angiogenesis by low-molecular-weight-heparins.
- Published in:
- 2016
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- Publication type:
- journal article
Findings from a multicentre, observational study on reproductive outcomes in women with unexplained recurrent pregnancy loss: the OTTILIA registry.
- Published in:
- 2021
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- Publication type:
- journal article
Real‐world experience of rIX‐FP prophylaxis at dosing intervals of 14 days or more in adult patients with haemophilia B in Italy – Results from IDEAL Part B.
- Published in:
- Haemophilia, 2024, v. 30, n. 4, p. 1067, doi. 10.1111/hae.15074
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- Publication type:
- Article
IDEAL study: A real‐world assessment of pattern of use and clinical outcomes with recombinant coagulation factor IX albumin fusion protein (rIX‐FP) in patients with haemophilia B in Italy.
- Published in:
- Haemophilia, 2023, v. 29, n. 1, p. 135, doi. 10.1111/hae.14689
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- Publication type:
- Article
Predictors of inhibitor eradication by primary immune tolerance induction in severe haemophilia A with high responding inhibitors.
- Published in:
- Haemophilia, 2022, v. 28, n. 1, p. 55, doi. 10.1111/hae.14431
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- Publication type:
- Article
Psychosomatic syndromes are associated with IL-6 pro-inflammatory cytokine in heart failure patients.
- Published in:
- PLoS ONE, 2022, v. 17, n. 3, p. 1, doi. 10.1371/journal.pone.0265282
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- Publication type:
- Article
Severe systemic thrombosis in a young COVID-19 patient with a rare homozygous prothrombin G20210A mutation.
- Published in:
- Infezioni in Medicina, 2021, v. 29, n. 2, p. 259
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- Publication type:
- Article
How to handle low-molecular-weight heparins in patients with decreased renal function: an open issue.
- Published in:
- 2008
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- Publication type:
- Editorial
Genome‐Wide Association Study Identifies First Locus Associated with Susceptibility to Cerebral Venous Thrombosis.
- Published in:
- Annals of Neurology, 2021, v. 90, n. 5, p. 777, doi. 10.1002/ana.26205
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- Publication type:
- Article
De Novo p.Asp3368Gly Variant of Dystrophin Gene Associated with X-Linked Dilated Cardiomyopathy and Skeletal Myopathy: Clinical Features and In Silico Analysis.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 5, p. 2787, doi. 10.3390/ijms25052787
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- Publication type:
- Article
The Role of Genetics in the Management of Heart Failure Patients.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 20, p. 15221, doi. 10.3390/ijms242015221
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- Publication type:
- Article
Diet-Related Alterations of Gut Bile Salt Hydrolases Determined Using a Metagenomic Analysis of the Human Microbiome.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 7, p. 3652, doi. 10.3390/ijms22073652
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- Publication type:
- Article
Summary of the Available Molecular Methods for Detection of SARS-CoV-2 during the Ongoing Pandemic.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 3, p. 1298, doi. 10.3390/ijms22031298
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- Publication type:
- Article
Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders.
- Published in:
- International Journal of Molecular Sciences, 2018, v. 19, n. 6, p. 1597, doi. 10.3390/ijms19061597
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- Publication type:
- Article
THE MOLECULAR ORGANIZATION OF ENDOTHELIAL JUNCTIONS IN VASCULAR PERMEABILITY.
- Published in:
- Euromediterranean Biomedical Journal, 2021, v. 16, p. 108, doi. 10.3269/1970-5492.2021.16.26
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- Publication type:
- Article
Investigation of a Large Kindred Reveals Cardiac Calsequestrin (CASQ2) as a Cause of Brugada Syndrome.
- Published in:
- Genes, 2024, v. 15, n. 7, p. 822, doi. 10.3390/genes15070822
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- Publication type:
- Article
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis.
- Published in:
- Genes, 2023, v. 14, n. 7, p. 1380, doi. 10.3390/genes14071380
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- Publication type:
- Article
A Novel DLG1 Variant in a Family with Brugada Syndrome: Clinical Characteristics and In Silico Analysis.
- Published in:
- Genes, 2023, v. 14, n. 2, p. 427, doi. 10.3390/genes14020427
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- Publication type:
- Article
Pathogenic DNM1L Variant (1085G>A) Linked to Infantile Progressive Neurological Disorder: Evidence of Maternal Transmission by Germline Mosaicism and Influence of a Contemporary in cis Variant (1535T>C).
- Published in:
- Genes, 2021, v. 12, n. 9, p. 1295, doi. 10.3390/genes12091295
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- Publication type:
- Article
Genetic Polymorphisms in an Aged Population.
- Published in:
- High Blood Pressure & Cardiovascular Prevention, 2007, v. 14, n. 2, p. 99, doi. 10.2165/00151642-200714020-00007
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- Publication type:
- Article
Genetic Polymorphisms in an Aged Population.
- Published in:
- High Blood Pressure & Cardiovascular Prevention, 2007, v. 14, n. 2, p. 99, doi. 10.2165/00151642-200714020-00007
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- Publication type:
- Article
Prospective evaluation of pregnancy outcome in an Italian woman with late-onset combined homocystinuria and methylmalonic aciduria.
- Published in:
- 2019
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- Publication type:
- journal article
Italian experience with rVIII-single chain: a survey of patients with haemophilia A and their physicians.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2022, v. 53, n. 4, p. 934, doi. 10.1007/s11239-021-02599-w
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- Publication type:
- Article
Correction to: Use of low-molecular weight heparin, transfusion and mortality in COVID-19 patients not requiring ventilation.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Use of low-molecular weight heparin, transfusion and mortality in COVID-19 patients not requiring ventilation.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2021, v. 52, n. 3, p. 772, doi. 10.1007/s11239-021-02429-z
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- Publication type:
- Article
Anemone study: prevalence of risk factors for superficial vein thrombosis in a large Italian population of blood donors.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2020, v. 50, n. 3, p. 689, doi. 10.1007/s11239-020-02140-5
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- Publication type:
- Article
Novel AKAP9 mutation and long QT syndrome in a patient with torsades des pointes.
- Published in:
- 2019
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- Publication type:
- journal article
Hereditary angioedema: Looking for bradykinin production and triggers of vascular permeability.
- Published in:
- Clinical & Experimental Allergy, 2019, v. 49, n. 11, p. 1395, doi. 10.1111/cea.13506
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- Publication type:
- Article
Angiopoietin‐1 haploinsufficiency affects the endothelial barrier and causes hereditary angioedema.
- Published in:
- Clinical & Experimental Allergy, 2019, v. 49, n. 5, p. 626, doi. 10.1111/cea.13349
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- Publication type:
- Article
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant.
- Published in:
- 1998
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- Publication type:
- journal article
Mutational Spectrum of the C1 Inhibitor Gene in a Cohort of Italian Patients with Hereditary Angioedema: Description of Nine Novel Mutations.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 2, p. 73, doi. 10.1111/ahg.12052
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- Publication type:
- Article
The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both.
- Published in:
- British Journal of Haematology, 2000, v. 111, n. 4, p. 1223, doi. 10.1046/j.1365-2141.2000.02502.x
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- Publication type:
- Article
Prognostic Factors in Noncirrhotic Patients With Splanchnic Vein Thromboses.
- Published in:
- American Journal of Gastroenterology (Springer Nature), 2007, v. 102, n. 11, p. 2464, doi. 10.1111/j.1572-0241.2007.01477.x
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- Publication type:
- Article
High Prevalence of Thrombophilic Genotypes in Patients With Acute Mesenteric Vein Thrombosis.
- Published in:
- American Journal of Gastroenterology (Springer Nature), 2001, v. 96, n. 1, p. 146, doi. 10.1111/j.1572-0241.2001.03465.x
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- Publication type:
- Article