Results 51 to 60 of about 4,191 (194)
Impact of Family History of Haemophilia on Diagnosis, Management and Outcomes in Severe Haemophilia
ABSTRACT Introduction Patients with severe haemophilia A (HA) with no family history of haemophilia will be diagnosed upon their first bleeding event. Methods Herein, we studied the effects of lack of family history in HA and the subsequent delay of diagnosis on bleeding pattern and early treatment, as well as on the risk of inhibitor development.
Ana Mendoza +9 more
wiley +1 more source
HEMOSTASIA: DESAFIOS NA EDUCAÇÃO DE HEMATOLOGIA
Objetivos: Relatar na forma de relato de experiência a participação de alunos monitores na disciplina de Hematologia da UNIRIO no ensino da Hemostasia. Material e métodos: Relato de experência de monitores e o aproveitamento de discentes da aula prática de Hemostasia para os alunos do sétimo período da UNIRIO, como parte de um projeto acadêmico ...
RC Bokehi +9 more
openaire +2 more sources
JUSTIFICATIVA E OBJETIVOS: A hemodiluição normovolêmica produz resultados conflitantes na hemostasia, pois os trabalhos diferem quanto a tipo de líquido utilizado, profundidade da hemodiluição, método utilizado para avaliar a hemostasia e forma de se ...
Marco Aurélio Beloto de Souza +2 more
doaj +1 more source
Mieloma Múltiplo e distúrbios da hemostasia [PDF]
O mieloma múltiplo (MM) é o tumor de células plasmocitárias que corresponde a aproximadamente 10% das neoplasias hematológicas. Durante o seu curso clínico, relata-se que 15-30% dos pacientes podem apresentar manifestações hemorrágicas, decorrentes de vários mecanismos fisiopatológicos.
D'Amico, Elbio A., Villaça, Paula R.
openaire +3 more sources
How to explain the beneficial effects of leukocyte‐ and platelet‐rich fibrin
Abstract The survival of an organism relies on its ability to repair the damage caused by trauma, toxic agents, and inflammation. This process involving cell proliferation and differentiation is driven by several growth factors and is critically dependent on the organization of the extracellular matrix. Since autologous platelet concentrates (APCs) are
Juan Blanco +3 more
wiley +1 more source
Abstract Introduction Haemophilia A is an X‐linked bleeding disorder resulting from a deficiency of factor VIII (FVIII). To date, multiple gene therapies have entered clinical trials with the goal of providing durable haemostatic protection from a single dose. TAK 754 (BAX 888) is an investigational AAV8‐based gene therapy containing a FVIII transgene.
John Chapin +13 more
wiley +1 more source
Alterações da hemostasia em crianças submetidas a cirurgia cardíaca com circulação extracorpórea [PDF]
OBJETIVO: Avaliar as alterações de hemostasia encontradas em crianças submetidas a cirurgia cardíaca com circulação extracorpórea (CEC). MÉTODOS: Estudamos 17 crianças no pré e pós-operatório (PO) imediato, no 1° PO e entre o 4º e 7º PO, analisando o ...
Fernanda Maria Rebouças da Costa Silveira +5 more
doaj +1 more source
Fukumori and colleagues compared the short‐term results of robotic liver surgery with those of conventional open liver surgery in elderly patients aged 70 years and over and used propensity score‐matched analysis to assess safety and efficacy. Robotic liver surgery can be safely performed in patients aged 70 years and older.
Daisuke Fukumori +6 more
wiley +1 more source
Background: Hyperhomocysteinemia, a thrombotic risk factor, may have several causes. Among the genetic causes of hyperhomocysteinemia, there are polymorphisms in the enzymes methylenetetrahydrofolate reductase (C677T) and cystathionine β-synthase (C699T,
Anahi Guadalupe Figueroa-Torres +10 more
doaj +1 more source
Abstract The study aimed to examine matrix metalloproteinase‐2 (MMP‐2) expression in a rat ligamentum flavum (LF) hypertrophy model in vivo, and the effect of elastin‐derived peptides (EDPs) on MMP‐2 and tissue inhibitors of metalloproteinases (TIMPs) in rat LF cells in vitro.
Wen‐Hai Zhuo +6 more
wiley +1 more source

