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1.
J Phys Condens Matter ; 33(45)2021 Aug 31.
Artigo em Inglês | MEDLINE | ID: mdl-34388733

RESUMO

The knowledge of the magnon dispersion relations in antiferromagnetic materials with nontrivial spin textures has considerable interest to the understanding of magnonic and spintronic phenomena involving these materials. One particularly interesting nontrivial spin texture existing in several antiferromagnets has spins at an angle of 120° with the in-plane neighbors and arranged in kagome lattices. Here we present a spin-wave calculation for antiferromagnets with kagome spin lattices considering exchange and single-ion anisotropy interactions between the spins. The theory yields exact analytical expressions for the frequencies of magnons at high-symmetry points of the Brillouin zone, that can be readily use to obtain the interaction parameters from experimental data with one-and two-magnon inelastic light scattering. The analytical expressions are used to obtain the field parameters for the kagome lattice antiferromagnet L12-IrMn3from four experimentally measured frequencies. Both exchange field parameters are in reasonable agreement with the values obtained withab initiocalculations, while the anisotropy field is in very good agreement with the one calculated with atomistic spin models and Monte Carlo simulations.

2.
J Phys Condens Matter ; 33(43)2021 Aug 13.
Artigo em Inglês | MEDLINE | ID: mdl-34293724

RESUMO

We report the investigation of spin-to-charge current interconversion process in hybrid structures of yttrium iron garnet (YIG)/metallic bilayers by means of two different experimental techniques: spin pumping effect (SPE) and spin Hall magnetoresistance (SMR). We demonstrate the evidence of a correlation between spin-to-charge conversion and SMR in bilayers of YIG/Pd, YIG/Pt, and YIG/IrMn. The correlation was verified directly in the spin Hall angles and the amplitudes of the voltage signals measured by the SPE and SMR techniques. The detection of SMR was carried out using the modulated magnetoresistance technique and lock-in amplifier detection. For these measurements, we present a simple model for the interpretation of the results. The results allow us to conclude that indeed the interface in the YIG/metallic bilayers has a dominant role in the spin-to-charge current conversion and SMR.

3.
Contraception ; 102(4): 254-258, 2020 10.
Artigo em Inglês | MEDLINE | ID: mdl-32470465

RESUMO

OBJECTIVE: To evaluate the efficacy of a levonorgestrel 52-mg intrauterine system (LNG 52-mg IUS) in controlling abnormal uterine bleeding and improving quality of life in women with inherited bleeding disorders. STUDY DESIGN: We assessed 20 participants laboratory diagnosed with inherited bleeding disorders, who presented with abnormal uterine bleeding and were registered in a Central Blood Center. The primary outcomes were menstrual bleeding volume and quality of life before and after LNG 52-mg IUS placement. We used the Pictorial Blood Loss Assessment Chart (PBAC) score for measuring menstrual bleeding and the Short Form-36 Health Survey to assess quality of life before and after LNG 52-mg IUS placement. We also conducted blood tests to evaluate the hematimetric level. Follow-up visits were conducted at 1, 3, 6, and 12 months after LNG 52-mg IUS placement. Statistical analyses were performed using the Friedman non-parametric test. RESULTS: The use of LNG 52-mg IUS reduced uterine bleeding in women with inherited bleeding disorders. The median PBAC score was higher before LNG 52-mg IUS placement than at 3, 6, and 12 months after placement (p < 0.001). The amenorrhea rate was 70% after 12 months. There was an improvement in all eight parameters of quality of life (p < 0.001). The mean hemoglobin, ferritin, and serum iron levels were also higher at 12 months than before LNG 52-mg IUS placement. CONCLUSION: LNG 52-mg IUS placement can effectively control abnormal uterine bleeding in women with inherited bleeding disorders and consequently improve their quality of life. IMPLICATIONS: The results from our study suggest that women with inherited bleeding disorders who present with heavy menstrual bleeding can benefit from the use of a levonorgestrel-releasing intrauterine system similar to women without bleeding disorders.


Assuntos
Anticoncepcionais Femininos/uso terapêutico , Dispositivos Intrauterinos Medicados , Levanogestrel/uso terapêutico , Menorragia/tratamento farmacológico , Hemorragia Uterina/tratamento farmacológico , Adulto , Transtornos Herdados da Coagulação Sanguínea/tratamento farmacológico , Anticoncepcionais Femininos/administração & dosagem , Feminino , Humanos , Levanogestrel/administração & dosagem , Qualidade de Vida
5.
J Thromb Haemost ; 14(1): 3-27, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26439670

RESUMO

UNLABELLED: Essentials The priority of ISTH was to establish a global core curriculum in thrombosis and hemostasis. International survey to determine competencies required for clinical specialists was carried out in the field. Competency framework provides a reference point for mapping and developing regional curricula. Core curriculum informs and links to a variety of ISTH educational materials. SUMMARY: Background The International Society on Thrombosis and Haemostasis (ISTH) identified the need for an international core curriculum on thrombosis and hemostasis for its society members and the larger thrombosis and hemostasis community. Aims The current research sought consensus on the core competencies required by medical doctors who are ready to practise as independent clinical specialists in thrombosis and hemostasis with the aim of developing a core clinical curriculum for specialists in the field. Method A draft list of competencies was developed by the Working Group and formed the basis of an online survey. ISTH members and the larger thrombosis and hemostasis community were asked to rate the importance of each competency, on a Likert scale, for clinical specialists in thrombosis and hemostasis. Results There were a total of 644 responses to the online survey with broad geographical representation. There was general agreement on what level of competency would be required for clinical specialists in thrombosis and hemostasis at the specified level of training. Conclusions Using the survey to gain consensus on the level of competency required by clinical specialists in the field of thrombosis and hemostasis enabled the development of a core clinical curriculum that has been endorsed by the ISTH Council. The curriculum will offer a framework and international reference that will be used by the society, by national and regional organizations, and for further research.


Assuntos
Cardiologia/educação , Competência Clínica , Currículo , Hematologia/educação , Hemostasia , Trombose/terapia , Cardiologia/métodos , Geografia , Hematologia/métodos , Humanos , Cooperação Internacional , Sociedades Médicas , Inquéritos e Questionários
6.
Phys Rev Lett ; 115(22): 226601, 2015 Nov 27.
Artigo em Inglês | MEDLINE | ID: mdl-26650313

RESUMO

The use of graphene in spintronic devices depends, among other things, on its ability to convert a spin excitation into an electric charge signal, a phenomenon that requires a spin-orbit coupling (SOC). Here we report the observation of two effects that show the existence of SOC in large-area CVD grown single-layer graphene deposited on a single crystal film of the ferrimagnetic insulator yttrium iron garnet (YIG). The first is a magnetoresistance of graphene induced by the magnetic proximity effect with YIG. The second is the detection of a dc voltage along the graphene layer resulting from the conversion of the spin current generated by spin pumping from microwave driven ferromagnetic resonance into a charge current, which is attributed to the inverse Rashba-Edelstein effect.

7.
J Chem Phys ; 143(12): 124706, 2015 Sep 28.
Artigo em Inglês | MEDLINE | ID: mdl-26429031

RESUMO

We report experiments with polyaniline-Fe3O4 (PANI-Fe3O4) nanocomposites synthesized under several different conditions. With a reaction carried out at room temperature and assisted by intense ultra-violet (UV) irradiation, we observe sustained oscillations in the magnetization with a period of about 25 min. The oscillations are interpreted as the result of an oscillatory chemical reaction in which part of the Fe(+2) ions of magnetite, Fe3O4, are oxidized by the UV irradiation to form Fe(+3) so that a fraction of the magnetite content transforms into maghemite, γ-Fe2O3. Then, Fe(+3) ions at the nanoparticle surfaces are reduced and transformed back into Fe(+2), when acting as an oxidizing agent for polyaniline in the polymerization process. Since maghemite has smaller magnetization than magnetite, the oscillating chemical reaction results in the oscillatory magnetization. The observations are interpreted with the Lotka-Volterra nonlinear coupled equations with parameters that can be adjusted to fit very well the experimental data.

8.
Haemophilia ; 21(5): 670-80, 2015 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-25828579

RESUMO

Inherited factor VII (FVII) deficiency is the most common among the rare bleeding disorders. It is transmitted as an autosomal recessive inheritance, due to mutations in the FVII gene (F7). Molecular studies of FVII deficiency are rare in non-Caucasian populations. The aim of the study was to evaluate the molecular basis behind low levels of FVII activity (FVII:C) levels in a cohort of Brazilian patients. A total of 34 patients with low FVII levels were clinically evaluated and submitted to laboratory tests, among these, prothrombin time and FVII:C, with different thromboplastins. All exons and intron/exon boundaries of F7 were amplified and sequenced. A total of 14 genetic alterations were identified, of which six were described previously, c.1091G>A, c.1151C>T, c.-323_-313insCCTATATCCT, c.285G>A, c.525C>T, c.1238G>A and eight (54.0%) and eight were new, c.128G>A, c.252C>T, c.348G>A, c.417G>A, c.426G>A, c.745_747delGTG, c.843G>A and c.805+52C>T. In addition to the mutation c.1091G>A, known as FVII Padua, the mutation c.1151C>T also presented discrepant FVII:C levels when tested with human and rabbit brain thromboplastin. There was no association between phenotype and genotype. Most of the identified genetic alterations found were polymorphisms. Low levels of FVII:C in this population were mostly related to polymorphisms in F7 and associated with a mild clinical phenotype. Mutation c.1151C>T was associated with discrepant levels of FVII:C using different thromboplastins, such as reported with FVII Padua.


Assuntos
Fator VII/genética , Adolescente , Adulto , Idoso , Brasil , Criança , Estudos de Coortes , Feminino , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Fenótipo , Adulto Jovem
10.
Braz. j. med. biol. res ; 45(1): 1-7, Jan. 2012. tab
Artigo em Inglês | LILACS | ID: lil-610551

RESUMO

Venous thrombosis, including deep vein thrombosis and pulmonary embolism, is a common disease that frequently recurs. Recurrence can be prevented by anticoagulants, but this comes at the risk of bleeding. Therefore, assessment of the risk of recurrence is important to balance the risks and benefits of anticoagulant treatment. This review briefly outlines what is currently known about the epidemiology of recurrent venous thrombosis, and focuses in more detail on potential new risk factors for venous recurrence. The general implications of these findings in patient management are discussed.


Assuntos
Feminino , Humanos , Anticoagulantes/uso terapêutico , Trombose Venosa/epidemiologia , Medição de Risco , Fatores de Risco , Recidiva/prevenção & controle , Trombose Venosa/prevenção & controle
11.
Braz J Med Biol Res ; 45(1): 1-7, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22183247

RESUMO

Venous thrombosis, including deep vein thrombosis and pulmonary embolism, is a common disease that frequently recurs. Recurrence can be prevented by anticoagulants, but this comes at the risk of bleeding. Therefore, assessment of the risk of recurrence is important to balance the risks and benefits of anticoagulant treatment. This review briefly outlines what is currently known about the epidemiology of recurrent venous thrombosis, and focuses in more detail on potential new risk factors for venous recurrence. The general implications of these findings in patient management are discussed.


Assuntos
Anticoagulantes/uso terapêutico , Trombose Venosa/epidemiologia , Feminino , Humanos , Masculino , Medição de Risco , Fatores de Risco , Prevenção Secundária , Trombose Venosa/prevenção & controle
12.
Phys Rev Lett ; 107(19): 197203, 2011 Nov 04.
Artigo em Inglês | MEDLINE | ID: mdl-22181640

RESUMO

We observe amplification of spin-wave packets propagating along a film of single-crystal yttrium iron garnet subject to a transverse temperature gradient. The spin waves are excited and detected with standard techniques used in magnetostatic microwave delay lines in the 1-2 GHz frequency range. The amplification is attributed to the action of a thermal spin-transfer torque acting on the magnetization that opposes the relaxation and which is created by spin currents generated through the spin-Seebeck effect. The experimental data are interpreted with a spin-wave model that gives an amplification gain in very good agreement with the data.

14.
J Ethnopharmacol ; 135(2): 393-8, 2011 May 17.
Artigo em Inglês | MEDLINE | ID: mdl-21420480

RESUMO

ETHNOPHARMACOLOGICAL RELEVANCE: Lychnophora passerina (Asteraceae), popularly known as "arnica," is used to treat inflammation, pain, rheumatism, contusions, bruises and insect bites in Brazilian traditional medicine. MATERIALS AND METHODS: The anti-inflammatory activity of crude ethanolic extract of aerial parts of L. passerina and its ethyl acetate and methanolic fractions had their abilities to modulate the production of NO, TNF-α and IL-10 inflammatory mediators in LPS/IFN-γ-stimulated J774.A1 macrophages evaluated. Moreover, the crude ethanolic extract and derived fractions were also in vivo assayed by carrageenan-induced paw oedema in mice. RESULTS: In vitro assays showed remarkable anti-inflammatory activity of L. passerina crude ethanolic extract (EE) and its ethyl acetate (A) and methanolic (M) fractions, through the inhibition of production of NO and TNF-α inflammatory mediators and induction of production of IL-10 anti-inflammatory cytokine. In vivo assays showed anti-inflammatory activity for EE 10% ointment, similar to the standard drug diclofenac gel. The A and M fraction ointments 20% presented anti-inflammatory activity. CONCLUSION: The results obtained showed that possible anti-inflammatory effects of EE and its A and M fractions may be attributed to inhibition pro-inflammatory cytokines production, TNF-α and NO and to increased IL-10 production. EE, A and M ointments showed topical in vivo anti-inflammatory activity. The in vivo anti-inflammatory activity of EE of L. passerina may be related to synergistic effects of different substances in the crude extract. Therefore, traditional use of aerial parts of L. passerina in the inflammatory conditions could be beneficial to treat topical inflammatory conditions, as evidenced by the present study.


Assuntos
Anti-Inflamatórios/farmacologia , Asteraceae/química , Extratos Vegetais/farmacologia , Animais , Anti-Inflamatórios/uso terapêutico , Linhagem Celular , Edema/induzido quimicamente , Edema/tratamento farmacológico , Etanol/química , Interleucina-10/biossíntese , Macrófagos/efeitos dos fármacos , Macrófagos/metabolismo , Masculino , Camundongos , Extratos Vegetais/uso terapêutico , Inibidores do Fator de Necrose Tumoral
16.
Int J Lab Hematol ; 33(2): 117-24, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21118380

RESUMO

INTRODUCTION: Thrombotic complications are a main concern in patients with myeloproliferative neoplasms. Recently, a gain-of-function mutation of the gene encoding the JAK2 tyrosine kinase that results in a valine-to-phenylalanine substitution at position 617 (V617F) has been described. Since the description of the JAK2-V617F mutation and its finding in patients with splanchnic vein thrombosis without an overt myeloproliferative neoplasm, many groups have studied the prevalence of this mutation in patients with unexplained venous and arterial thrombosis. METHODS: A literature search was made using the key words thrombosis, JAK2V617F mutation, myeloproliferative neoplasms, cerebral vein thrombosis and splanchnic vein thrombosis. RESULTS: JAK2V617F is frequent in patients with splanchnic vein thrombosis, but is rare in patients with venous thrombosis at other locations or with arterial thrombosis. CONCLUSION: Routine testing for JAK2V617F is not currently recommended for patients with unexplained thromboses, except for those with splanchnic vein thrombosis. In patients with cerebral vein thrombosis, the value of testing for JAK2V617F mutation is yet to be established.


Assuntos
Testes Genéticos , Janus Quinase 2/genética , Mutação , Trombose/genética , Veias Cerebrais/patologia , Predisposição Genética para Doença , Testes Genéticos/normas , Humanos , Veias Mesentéricas/patologia , Transtornos Mieloproliferativos/complicações , Transtornos Mieloproliferativos/genética , Trombose/etiologia
17.
Parasite Immunol ; 31(1): 41-9, 2009 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-19121082

RESUMO

Protein-energy malnutrition and visceral leishmaniasis are important problems of public health affecting millions of people worldwide. Vaccine efficacy depends on the ability of individuals to mount an appropriate immune response and may be inadequate in malnourished persons. In this study, we used a mouse model to verify the effect of combined protein, iron and zinc deficiency in the response to Leishmania chagasi antigen vaccine. BALB/c mice were fed with a low-protein (3% casein), iron- and zinc-deficient diet or control diet (14% casein and sufficient in zinc and iron). After malnutrition establishment, mice were vaccinated subcutaneously with L. chagasi Ag plus saponin. After vaccination, mice were nutritionally repleted and then all mice were challenged with L. chagasi promastigotes. Four weeks later, liver and spleen parasite load was evaluated. Our data show that vaccine caused a significant reduction in parasite load in spleen and liver from mice fed with control diet. However, splenic parasitism was increased in mice fed with deficient diet and this diet caused a reduction in splenocyte IFN-gamma production in response to the vaccine in repleted mice. These data suggest that malnutrition may alter immune response to L. chagasi vaccine in BALB/c model of infection, even after nutritional repletion.


Assuntos
Leishmania infantum/imunologia , Vacinas contra Leishmaniose/imunologia , Desnutrição Proteico-Calórica/imunologia , Adjuvantes Imunológicos/administração & dosagem , Animais , Antígenos de Protozoários/imunologia , Peso Corporal , Dieta , Feminino , Humanos , Injeções Subcutâneas , Interferon gama/biossíntese , Deficiências de Ferro , Fígado/parasitologia , Linfócitos/imunologia , Camundongos , Camundongos Endogâmicos BALB C , Saponinas/administração & dosagem , Baço/parasitologia , Análise de Sobrevida , Zinco/deficiência
18.
Haemophilia ; 15(1): 142-9, 2009 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-18976255

RESUMO

Inherited coagulopathies are bleeding disorders, which require treatment for life. Keeping an updated registry on these diseases is crucial for planning care, documenting prevalence of diseases and evaluating effectiveness of resources. We have analysed data from 26 treatment centres on coagulopathies in Brazil. Information included socio-demographic data, diagnosis of coagulopathies, severity of haemophilias A and B, presence and quantification of inhibitors in haemophilia, type of von Willebrand disease (VWD) and infection status for viral diseases. On 1 July 2007, there were 10 982 patients with inherited coagulopathies in Brazil, of which 6881 (62.7%) corresponded to haemophilia A, 1291 (11.7%) to haemophilia B, 2333 (21.2%) to VWD, 258 (2.4%) to other coagulopathies and 219 (2.0%) to undiagnosed bleeding disorders. Haemophilia A and B inhibitors were present in 9.9% and 1.9% of the patients, respectively. Human immunodeficiency virus infection was present is 6.5%, 4.8% and 1% of patients with haemophilia A, B and VWD, respectively. Hepatitis C virus infection was present in 34.9%, 29.7% and 12% of patients with haemophilia A, B and VWD, respectively. Infection by hepatitis B and human T-cell leukemia-lymphoma virus was also reported. This is the first report on the registry of patients with inherited coagulopathies in Brazil, supposed to be the third largest population of patients with haemophilia.


Assuntos
Transtornos Herdados da Coagulação Sanguínea/epidemiologia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Transtornos Herdados da Coagulação Sanguínea/complicações , Brasil/epidemiologia , Criança , Pré-Escolar , Feminino , Infecções por HIV/complicações , Infecções por HIV/epidemiologia , Infecções por HTLV-I/complicações , Infecções por HTLV-I/epidemiologia , Hemofilia A/epidemiologia , Hemofilia B/epidemiologia , Vacinas contra Hepatite B/provisão & distribuição , Hepatite B Crônica/complicações , Hepatite B Crônica/epidemiologia , Hepatite C Crônica/complicações , Hepatite C Crônica/epidemiologia , Humanos , Lactente , Recém-Nascido , Masculino , Pessoa de Meia-Idade , Prevalência , Sistema de Registros , Adulto Jovem , Doenças de von Willebrand/epidemiologia
19.
Int J Lab Hematol ; 29(3): 153-62, 2007 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-17474891

RESUMO

Venous thromboembolism, represented by deep venous thrombosis and pulmonary embolism, is a common disease with high mortality and morbidity. Within the last 25 years, risk factors for venous thromboembolism have been linked to mutations in the genes of the coagulation/anticoagulation system. Factor V Leiden and the prothrombin G20210A mutations are the most prevalent inherited risk factors predisposing to venous thromboembolism in the Western world. Tests to detect these mutations are carried out when investigating a personal or family history of venous thromboembolism. At the present, there are several different methods available for the detection of these mutations in the laboratory. The choice of the method will depend on many variables. This article is aimed at reviewing the available methods for the detection of factor V Leiden and prothrombin G20210A mutations, their principle, applicability, advantages and disadvantages of use.


Assuntos
Fator V/análise , Protrombina/análise , Protrombina/genética , Resistência à Proteína C Ativada/genética , Ensaio de Imunoadsorção Enzimática , Transferência Ressonante de Energia de Fluorescência , Humanos , Análise de Sequência com Séries de Oligonucleotídeos , Mutação Puntual , Reação em Cadeia da Polimerase/métodos , Polimorfismo Conformacional de Fita Simples , Controle de Qualidade , Análise de Sequência de DNA , Tromboembolia/diagnóstico , Trombose Venosa/diagnóstico
20.
Phys Rev Lett ; 98(8): 087202, 2007 Feb 23.
Artigo em Inglês | MEDLINE | ID: mdl-17359123

RESUMO

A spin-wave theory is presented which explains the frequency pulling and mode locking observed when two closely spaced spin-transfer nanometer-scale oscillators with slightly different frequencies are separately driven in the same magnetic thin film by spin-polarized carriers at high direct-current densities. The theory confirms recent experimental evidence that the origin of the phenomena lies in the nonlinear interaction between two overlapping spin waves excited in the magnetic nanostructure.

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