Published in Thromb Haemost on February 01, 2000
Large-scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,797 individuals. Indian J Hum Genet (2011) 1.16
Factor V leiden and ischemic stroke risk: the Genetics of Early Onset Stroke (GEOS) study. J Stroke Cerebrovasc Dis (2011) 0.97
Haematology and neurology. J Neurol Neurosurg Psychiatry (2007) 0.96
Meta-analysis of factor V Leiden and ischemic stroke in young adults: the importance of case ascertainment. Stroke (2010) 0.87
Prothrombin G20210A mutation is associated with young-onset stroke: the genetics of early-onset stroke study and meta-analysis. Stroke (2014) 0.78
The G79A polymorphism of protein Z gene is an independent risk factor for cerebral venous thrombosis. J Neurol (2008) 0.78
Factor V Leiden does not have a role in cryptogenic ischemic stroke among Iranian young adults. Adv Biomed Res (2014) 0.76
Activated Protein C Resistance Does Not Increase Risk for Recurrent Stroke or Death in Stroke Patients. PLoS One (2016) 0.75
Prevalence and Geographical Variation of Prothrombin G20210A Mutation in Patients with Cerebral Vein Thrombosis: A Systematic Review and Meta-Analysis. PLoS One (2016) 0.75
The Association of Coagulation Factor V (Leiden) and Factor II (Prothrombin) Mutations With Stroke. Iran Red Crescent Med J (2014) 0.75
Factor V Leiden, factor V Cambridge, factor II GA20210, and methylenetetrahydrofolate reductase in cerebral venous and sinus thrombosis: A case-control study. J Res Med Sci (2015) 0.75
Muscle-directed gene transfer and transient immune suppression result in sustained partial correction of canine hemophilia B caused by a null mutation. Mol Ther (2001) 1.93
The role of conventional MR imaging sequences in the evaluation of neurocysticercosis: impact on characterization of the scolex and lesion burden. AJNR Am J Neuroradiol (2007) 1.79
Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost (1998) 1.71
Role of vector in activation of T cell subsets in immune responses against the secreted transgene product factor IX. Mol Ther (2000) 1.55
Risk and prevention of anti-factor IX formation in AAV-mediated gene transfer in the context of a large deletion of F9. Mol Ther (2001) 1.54
Differences in grey and white matter atrophy in amnestic mild cognitive impairment and mild Alzheimer's disease. Eur J Neurol (2009) 1.51
Factor V Leiden is not common in children with portal vein thrombosis. Thromb Haemost (1997) 1.43
Postvaccinal parkinsonism. Mov Disord (1992) 1.41
Hb Rio Claro [beta34(B16)Val-->Met]: a novel electrophoretically silent variant found in association with Hb Hasharon [alpha47(CE5)Asp-->His] and alpha-thalassemia-2(-alpha3.7). Hemoglobin (1999) 1.40
Effect of alpha-thalassemia and beta-globin gene cluster haplotypes on the hematological and clinical features of sickle-cell anemia in Brazil. Am J Hematol (1996) 1.36
Sickle cell disease in a Brazilian population from Sao Paulo: a study of the beta s haplotypes. Hum Hered (1995) 1.20
Factor V Leiden improves in vivo hemostasis in murine hemophilia models. J Thromb Haemost (2005) 1.17
A viable mouse model of factor X deficiency provides evidence for maternal transfer of factor X. J Thromb Haemost (2007) 1.04
The mutation Ala677-->Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis. Thromb Haemost (1997) 1.00
The release of nitric oxide and superoxide anion by neutrophils and mononuclear cells from patients with sickle cell anaemia. Br J Haematol (1996) 0.98
Absence of circulating factor IX antigen in hemophilia B dogs of the UNC-Chapel Hill colony. Thromb Haemost (2000) 0.98
Intravenous administration of an E1/E3-deleted adenoviral vector induces tolerance to factor IX in C57BL/6 mice. Gene Ther (2001) 0.97
Differences in memory performance and other clinical characteristics in patients with mesial temporal lobe epilepsy with and without hippocampal atrophy. Epilepsy Behav (2004) 0.97
The S-100 antigen in cerebrospinal fluid as a possible index of cell injury in the nervous system. J Neurol Sci (1980) 0.95
Frequencies of platelet-specific alloantigen systems 1-5 in three distinct ethnic groups in Brazil. Eur J Immunogenet (1999) 0.95
Prevention of spontaneous bleeding in dogs with haemophilia A and haemophilia B. Haemophilia (2010) 0.94
Association of Hb Santa Ana [alpha 2 beta (2)88(F4)Leu- > Pro] and Hb Porto Alegre [alpha 2 beta (2)9(A6)Ser- > Cys] in a Brazilian female. Hemoglobin (1994) 0.93
Migraine in childhood and adolescence. A critical study of the diagnostic criteria and of the influence of age on clinical findings. Cephalalgia (1998) 0.92
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Wettability control by laser texturing process generating localized gold nanoparticles on polymeric thin films. J Nanosci Nanotechnol (2012) 0.91
Acute multiple mononeuropathy after accidental exposure to oven microwaves. Occup Med (Lond) (1995) 0.91
Osteoarthropathy of hepatolenticular degeneration. Acta Neurol Scand (1978) 0.91
MR imaging texture analysis of the corpus callosum and thalamus in amnestic mild cognitive impairment and mild Alzheimer disease. AJNR Am J Neuroradiol (2010) 0.90
Genetic analysis of beta-thalassemia major and beta-thalassemia intermedia in Brazil. Hemoglobin (1998) 0.90
Minimally invasive radio-guided surgery for primary hyperparathyroidism: From preoperative to intraoperative localization imaging. Ann Endocrinol (Paris) (2010) 0.90
Prevalence of the mutation C677 --> T in the methylene tetrahydrofolate reductase gene among distinct ethnic groups in Brazil. Am J Med Genet (1998) 0.90
Mutation analysis of the HFE gene in Brazilian populations. Blood Cells Mol Dis (2000) 0.89
Wilson's disease: MRI with clinical correlation. Neuroradiology (1994) 0.89
Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease. Thromb Haemost (1997) 0.89
Transcranial Doppler with contrast injection for the detection of patent foramen ovale in stroke patients. Int J Card Imaging (1993) 0.88
Factor V Leiden (FVQ 506) is common in a Brazilian population. Am J Hematol (1995) 0.88
Improved muscle-derived expression of human coagulation factor IX from a skeletal actin/CMV hybrid enhancer/promoter. Blood (2000) 0.87
The Brazilian database on pregnancy in multiple sclerosis. Clin Neurol Neurosurg (2010) 0.87
The nervous system-specific S-100 antigen in cerebrospinal fluid of multiple sclerosis patients. Neurosci Lett (1979) 0.86
Computed tomography in neurocysticercosis: a 10-year long evolution analysis of 100 patients with an appraisal of a new classification. Arq Neuropsiquiatr (1990) 0.86
Heart involvement in hepatolenticular degeneration. Acta Neurol Scand (1978) 0.86
[Brazilian guidelines on platelet antiaggregants and anticoagulants in cardiology]. Arq Bras Cardiol (2013) 0.86
Neurological complications after thrombolytic treatment for acute myocardial infarction: emphasis on unprecedented manifestations. Acta Neurol Scand (1992) 0.85
Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in Brazil. Am J Hematol (1998) 0.85
Normative data for the Brazilian population in the Boston Diagnostic Aphasia Examination: influence of schooling. Braz J Med Biol Res (2004) 0.85
Dual PET/CT with (18)F-DOPA and (18)F-FDG in metastatic medullary thyroid carcinoma and rapidly increasing calcitonin levels: Comparison with conventional imaging. Eur J Surg Oncol (2010) 0.84
The human platelet alloantigen 5 polymorphism as a risk for the development of acute idiopathic thrombocytopenia purpura. Thromb Haemost (2000) 0.84
Abdominal ultrasonography in hepatolenticular degeneration. A study of 33 patients. Arq Neuropsiquiatr (1987) 0.84
Cerebrotendinous xanthomatosis: clinical and laboratory study of 2 cases. Acta Neurol Scand (1983) 0.84
A new regimen of interleukin 2 and lymphokine-activated killer cells. Efficacy without significant toxicity. Arch Intern Med (1988) 0.84
Beta S-gene-cluster haplotypes in sickle cell anemia patients from two regions of Brazil. Am J Hematol (1994) 0.84
An engineered U1 small nuclear RNA rescues splicing-defective coagulation F7 gene expression in mice. J Thromb Haemost (2014) 0.84
Beyond neuropathy in hereditary sensory and autonomic neuropathy type V: cognitive evaluation. Eur J Neurol (2008) 0.84
Diffusion-weighted MR imaging of cystic lesions of neurocysticercosis: a preliminary study. Arq Neuropsiquiatr (2001) 0.84
Mitochondrial dysfunction in myasthenia gravis. Report of a case. Arq Neuropsiquiatr (1989) 0.84
[Benign paroxysmal positioning vertigo]. Arq Neuropsiquiatr (2001) 0.84
The prevalence of multiple sclerosis in the city of São Paulo, Brazil, 1997. Acta Neurol Scand (2001) 0.83
Apoptotic effects of platelet factor VIII on megakaryopoiesis: implications for a modified human FVIII for platelet-based gene therapy. J Thromb Haemost (2014) 0.83
Novel insights into the development of atherosclerosis in hemophilia A mouse models. J Thromb Haemost (2011) 0.83
Strongyloidiasis after unrelated nonmyeloablative allogeneic stem cell transplantation. Bone Marrow Transplant (2006) 0.83
Magnetic resonance imaging in intracranial paracoccidioidomycosis. J Neuroimaging (1993) 0.83
Correlation of magnetization transfer and diffusion magnetic resonance imaging in multiple sclerosis. Mult Scler (2006) 0.82
Management of hydrocephalus in Paget's disease. Case report. Zentralbl Neurochir (1994) 0.82
[Instrument applications of three new Bio-Rad kits for HIV, HCV, HBSAG screening: Combo Genscreen Plus HIV 1/2 AG-AB, Monolisa anti HCV Plus V2, Monolisa HBSAG Plus, with the fully authomatic system Plato 3300]. Minerva Med (2001) 0.82
Acute myocardial infarction in sickle cell anaemia associated with severe hypoxia. Postgrad Med J (1990) 0.81
Bilateral carotid artery dissection with thyrotoxicosis. Neurology (2004) 0.81
Myotonic dystrophy, syringomyelia, and 2/13 translocation in the same family. J Med Genet (1977) 0.81
C282Y mutation in the HLA-H gene is not a risk factor for patients with myocardial infarction. J Cardiovasc Risk (2000) 0.81
Polymorphism of the human platelet antigen-5 system is a risk factor for occlusive vascular complications in patients with sickle cell anemia. Vox Sang (2004) 0.81
Association of TP53 mutation, p53 overexpression, and p53 codon 72 polymorphism with susceptibility to apoptosis in adult patients with diffuse astrocytomas. Int J Biol Markers (2006) 0.81
[Familial hemifacial spasm: report of 2 cases]. Arq Neuropsiquiatr (1998) 0.80
The immunomodulator glatiramer acetate influences spinal motoneuron plasticity during the course of multiple sclerosis in an animal model. Braz J Med Biol Res (2009) 0.80
Detection of somatic mutations of the PIG-A gene in Brazilian patients with paroxysmal nocturnal hemoglobinuria. Braz J Med Biol Res (2001) 0.80
Possible association between cytomegalovirus infection and gastrointestinal bleeding in hemophiliac patients. Acta Haematol (2000) 0.80
Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients. Blood (1995) 0.80
Anisotropic imaging in the dragonfly median ocellus: a matched filter for horizon detection. J Comp Physiol A Neuroethol Sens Neural Behav Physiol (2002) 0.80
Isolated CNS Whipple disease with a variant of oculofacial-skeletal myorhythmia (OFSM). Neurology (2007) 0.80
Prevalence of the prothrombin gene variant 20210 G --> A among patients with myocardial infarction. Cardiovasc Res (1998) 0.80
Determination of the frequency of the 35delG allele in Brazilian neonates. Clin Genet (2000) 0.80
Successful use of hydroxyurea in beta-thalassemia major. N Engl J Med (1997) 0.80
Relationship between environmental factors and gray matter atrophy in refractory MTLE. Neurology (2010) 0.79
Caudate hemorrhage with moyamoya-like vasculopathy from atherosclerotic disease. Stroke (1992) 0.79
Clinical and pathologic prognostic features of leiomyosarcoma of the uterus. Tumori (1983) 0.79
[Paracoccidioidomycosis of the central nervous system: study of 5 cases by magnetic resonance]. Rev Hosp Clin Fac Med Sao Paulo (1993) 0.79
Efficient and wideband horn nanoantenna. Opt Lett (2011) 0.79
Exacerbation of myasthenia gravis by contrast media. AJR Am J Roentgenol (1994) 0.79
Evaluation of the host response to endotoxemia of FVIII and FIX deficient mice. Haemophilia (2011) 0.78
High frequency of vitamin B12 deficiency in a Brazilian population. Public Health Nutr (2010) 0.78
[Neurosyphilis resistant to high doses of penicillin: report of a case]. Arq Neuropsiquiatr (1984) 0.78
[Malignant hyperthermia susceptibility in 3 patients with malignant neuroleptic syndrome]. Arq Neuropsiquiatr (2000) 0.78
HTLV-I associated myelopathy in Brazil: a preliminary report. Arq Neuropsiquiatr (1989) 0.78
Rapid detection of the prothrombin C20209T variant by differential sensitivity to restriction endonuclease digestion. J Thromb Haemost (2003) 0.78
[Precocious Parkinson's disease associated with "eye-of-the-tiger" type pallidal lesions]. Arq Neuropsiquiatr (1995) 0.78