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Linkage disequilibrium of the common mutations 677C > T and 1298A > C of the human methylenetetrahydrofolate reductase gene as proven by the novel polymorphisms 129C > T, 1068C > T.
- Published in:
- 2000
- By:
- Publication type:
- Letter
Age-Dependent Control of Collagen-Dependent Platelet Responses by Thrombospondin-1—Comparative Analysis of Platelets from Neonates, Children, Adolescents, and Adults.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 9, p. 4883, doi. 10.3390/ijms22094883
- By:
- Publication type:
- Article
Health-Related Quality of Life in Children and Adolescents with Hereditary Bleeding Disorders and in Children and Adolescents with Stroke: Cross-Sectional Comparison to Siblings and Peers.
- Published in:
- BioMed Research International, 2016, v. 2016, p. 1, doi. 10.1155/2016/1579428
- By:
- Publication type:
- Article
Interferences in coagulation tests - evaluation of the 570-nm method on the Dade Behring BCS analyser.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2005, v. 43, n. 2, p. 244, doi. 10.1515/CCLM.2005.041
- By:
- Publication type:
- Article
Intracardiac thrombus associated with resistance to activated protein C.
- Published in:
- 1998
- By:
- Publication type:
- journal article
Impact of high-risk thrombophilia status on recurrence among children with a first non-central-venous-catheter-associated VTE: an observational multicentre cohort study.
- Published in:
- British Journal of Haematology, 2016, v. 175, n. 1, p. 133, doi. 10.1111/bjh.14192
- By:
- Publication type:
- Article
Clinical and laboratory characteristics of children with venous thromboembolism and protein C-deficiency: an observational Israeli-German cohort study.
- Published in:
- British Journal of Haematology, 2014, v. 167, n. 3, p. 385, doi. 10.1111/bjh.13039
- By:
- Publication type:
- Article
Advances in understanding stroke risk in children - a geneticist's view.
- Published in:
- British Journal of Haematology, 2014, v. 164, n. 5, p. 636, doi. 10.1111/bjh.12706
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- Publication type:
- Article
Subcutaneous protein C concentrate in the management of severe protein C deficiency - experience from 12 centres.
- Published in:
- British Journal of Haematology, 2014, v. 164, n. 3, p. 414, doi. 10.1111/bjh.12640
- By:
- Publication type:
- Article
Hämostaseologische Abklärung der klinisch relevanten Blutungsneigung im Kindesalter.
- Published in:
- Journal of Laboratory Medicine / Laboratoriums Medizin, 2003, v. 27, n. 9/10, p. 371
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- Publication type:
- Article
DNA- and Plasma-based Screening for Risk Factors in Infants and Children with Symptomatic Thromboembolism.
- Published in:
- Journal of Laboratory Medicine / Laboratoriums Medizin, 2002, v. 26, n. 5/6, p. 317
- By:
- Publication type:
- Article
Der Methylentetrahydrofolat-Reduktase (MTHFR) C677T-Polymorphismus und andere genetische Ursachen der Hyperhomocysfeinämie bei venösen Gefäßverschlüssen.
- Published in:
- Journal of Laboratory Medicine / Laboratoriums Medizin, 2001, v. 25, n. 7/8, p. 239
- By:
- Publication type:
- Article
The Prothrombin G20210A Mutation - A Common Cause of Thrombophilia?
- Published in:
- Journal of Laboratory Medicine / Laboratoriums Medizin, 1998, v. 22, n. 9, p. 472
- By:
- Publication type:
- Article
Coagulation and fibrinolysis in children, adolescents, and young adults with inflammatory bowel disease.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Detection and characterisation of large SERPINC1 deletions in type I inherited antithrombin deficiency.
- Published in:
- Human Genetics, 2010, v. 127, n. 1, p. 45, doi. 10.1007/s00439-009-0742-6
- By:
- Publication type:
- Article
Clinical Course and Management of Patients with Emergency Surgery Treated with Direct Oral Anticoagulants or Vitamin K Antagonists—Results of the German Prospective RADOA-Registry.
- Published in:
- Journal of Clinical Medicine, 2024, v. 13, n. 1, p. 272, doi. 10.3390/jcm13010272
- By:
- Publication type:
- Article
Genotype–Phenotype Relationship among 785 Unrelated White Women with Inherited Congenital Factor VII Deficiency: A Three-Center Database Study.
- Published in:
- Journal of Clinical Medicine, 2024, v. 13, n. 1, p. 49, doi. 10.3390/jcm13010049
- By:
- Publication type:
- Article
Severe Pulmonary Bleeding after Assist Device Implantation: Incidence, Risk Factors and Prognostic Impact.
- Published in:
- Journal of Clinical Medicine, 2022, v. 11, n. 7, p. 1908, doi. 10.3390/jcm11071908
- By:
- Publication type:
- Article
Quantitative Systems Pharmacology Model-Based Predictions of Clinical Endpoints to Optimize Warfarin and Rivaroxaban Anti-Thrombosis Therapy.
- Published in:
- Frontiers in Pharmacology, 2020, v. 11, p. 1, doi. 10.3389/fphar.2020.01041
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- Publication type:
- Article
Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease.
- Published in:
- Cardiovascular Research, 2001, v. 51, n. 2, p. 251, doi. 10.1016/S0008-6363(01)00286-3
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- Publication type:
- Article
Genetics of Hemostasis: Differential Effects of Heritability and Household Components Influencing Lipid Concentrations and Clotting Factor Levels in 282 Pediatric Stroke Families.
- Published in:
- Environmental Health Perspectives, 2008, v. 116, n. 6, p. 839, doi. 10.1289/ehp.10754
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- Publication type:
- Article
ADAMTS12, a new candidate gene for pediatric stroke.
- Published in:
- PLoS ONE, 2020, v. 14, n. 8, p. 1, doi. 10.1371/journal.pone.0237928
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- Publication type:
- Article
Role of reduced ADAMTS13 in arterial ischemic stroke: A Pediatric Cohort Study.
- Published in:
- Annals of Neurology, 2013, v. 73, n. 1, p. 58, doi. 10.1002/ana.23735
- By:
- Publication type:
- Article
Health-related quality of life in children and adolescents with stroke, self-reports, and parent/proxies reports: Cross-sectional investigation.
- Published in:
- Annals of Neurology, 2011, v. 70, n. 1, p. 70, doi. 10.1002/ana.22381
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- Publication type:
- Article
Role of endogenous testosterone concentration in pediatric stroke.
- Published in:
- Annals of Neurology, 2009, v. 66, n. 6, p. 754, doi. 10.1002/ana.21840
- By:
- Publication type:
- Article
The factor V G1691A mutation is a risk for porencephaly: A case–control study.
- Published in:
- Annals of Neurology, 2004, v. 56, n. 2, p. 287
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- Publication type:
- Article
Prothrombotic Risk Factors and Acute Kidney Transplant Rejection.
- Published in:
- Kidney & Blood Pressure Research, 1998, v. 21, n. 2-4, p. 293, doi. 10.1159/000025883
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- Publication type:
- Article
Zerebrale Venen- und Sinusthrombose.
- Published in:
- Der Nervenarzt, 2019, v. 90, n. 4, p. 379, doi. 10.1007/s00115-018-0654-6
- By:
- Publication type:
- Article
Intracranial bleeding under vitamin K antagonists or direct oral anticoagulants: results of the RADOA registry.
- Published in:
- Neurological Research & Practice, 2022, v. 4, n. 1, p. 1, doi. 10.1186/s42466-022-00183-y
- By:
- Publication type:
- Article
Abdominal venous thrombosis in neonates and infants: role of prothrombotic risk factors – a multicentre case–control study.
- Published in:
- British Journal of Haematology, 2000, v. 111, n. 2, p. 534
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- Publication type:
- Article
Spectrum of molecular defects and mutation detection rate in patients with mild and moderate hemophilia A.
- Published in:
- Human Mutation, 2007, v. 28, n. 1, p. 54, doi. 10.1002/humu.20403
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- Publication type:
- Article
Erratum: Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene.
- Published in:
- Human Mutation, 2006, v. 27, n. 11, p. 1160, doi. 10.1002/humu.9468
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- Publication type:
- Article
Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene.
- Published in:
- Human Mutation, 2006, v. 27, n. 6, p. 600, doi. 10.1002/humu.9425
- By:
- Publication type:
- Article
Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A.
- Published in:
- Human Mutation, 2005, v. 26, n. 3, p. 249, doi. 10.1002/humu.20208
- By:
- Publication type:
- Article
Targeted resequencing of a locus for heparin-induced thrombocytopenia on chromosome 5 identified in a genome-wide association study.
- Published in:
- Journal of Molecular Medicine, 2018, v. 96, n. 8, p. 765, doi. 10.1007/s00109-018-1661-6
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- Publication type:
- Article
Screening for Platelet Dysfunction and Use of Prophylactic Tranexamic Acid in Patients Undergoing Deep Brain Stimulation: A Retrospective Analysis of Incidence and Outcome of Intracranial Hemorrhage.
- Published in:
- Stereotactic & Functional Neurosurgery, 2020, v. 98, n. 3, p. 176, doi. 10.1159/000505714
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- Publication type:
- Article
Eptacog beta efficacy and safety in the treatment and control of bleeding in paediatric subjects (<12 years) with haemophilia A or B with inhibitors.
- Published in:
- Haemophilia, 2022, v. 28, n. 4, p. 548, doi. 10.1111/hae.14563
- By:
- Publication type:
- Article
Two Novel Variants in the Protein S Gene PROS1 Are Associated with Protein S Deficiency and Thrombophilia.
- Published in:
- Acta Haematologica, 2021, v. 144, n. 2, p. 222, doi. 10.1159/000508525
- By:
- Publication type:
- Article
Cross-Sectional and Longitudinal Construct Validity of the Generic KINDL-A(dult)B(rief) Questionnaire in Adults with Thrombophilia or with Hereditary and Acquired Bleeding Disorders.
- Published in:
- Acta Haematologica, 2021, v. 144, n. 2, p. 166, doi. 10.1159/000507602
- By:
- Publication type:
- Article
Psychometric Properties of a Modified KINDL-R Questionnaire for Adolescents and Adults, and Construction of a Brief Version, the KINDL-A(dult)B(rief) Questionnaire, KINDL-AB.
- Published in:
- Acta Haematologica, 2018, v. 140, n. 1, p. 1, doi. 10.1159/000490408
- By:
- Publication type:
- Article
Challenging Aspects of Managing Hemostasis in Adolescents.
- Published in:
- Acta Haematologica, 2014, v. 132, n. 3/4, p. 326, doi. 10.1159/000360237
- By:
- Publication type:
- Article
Bleeding and Thrombosis Issues in Pediatric Patients: Current Approach to Diagnosis and Treatment.
- Published in:
- Acta Haematologica, 2006, v. 115, n. 3/4, p. 137, doi. 10.1159/000090926
- By:
- Publication type:
- Article
Elevated α<sub>1</sub>-Antitrypsin Is a Risk Factor for Arterial Ischemic Stroke in Childhood.
- Published in:
- Acta Haematologica, 2006, v. 115, n. 3/4, p. 186, doi. 10.1159/000090933
- By:
- Publication type:
- Article
ADAMTS genes and the risk of cerebral aneurysm.
- Published in:
- Journal of Neurosurgery, 2016, v. 125, n. 2, p. 269, doi. 10.3171/2015.7.JNS154
- By:
- Publication type:
- Article
Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A.
- Published in:
- Human Mutation, 2002, v. 20, n. 3, p. 236, doi. 10.1002/humu.9062
- By:
- Publication type:
- Article
Risk factors for high-titer inhibitor development in children with hemophilia a: results of a cohort study.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Risk Factors for High-Titer Inhibitor Development in Children with Hemophilia A: Results of a Cohort Study.
- Published in:
- BioMed Research International, 2013, v. 2013, p. 1, doi. 10.1155/2013/901975
- By:
- Publication type:
- Article
Proteomic and other mass spectrometry based 'omics' biomarker discovery and validation in pediatric venous thromboembolism and arterial ischemic stroke: Current state, unmet needs, and future directions.
- Published in:
- Proteomics - Clinical Applications, 2014, v. 8, n. 11/12, p. 828, doi. 10.1002/prca.201400062
- By:
- Publication type:
- Article
Changes in coagulation and fibrinolysis in childhood ALL: a two-step dose reduction of one E. coli asparaginase preparation.
- Published in:
- British Journal of Haematology, 1996, v. 95, n. 1, p. 123, doi. 10.1046/j.1365-2141.1996.d01-1873.x
- By:
- Publication type:
- Article