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Acute promyelocytic leukemia: evaluation of diagnostic tests from 2000 to 2018 in a public hospital

Abstract: Introduction: Acute promyelocytic leukemia (APL) is caused by t(15;17)(q24;q21) translocation, which product is the fusion oncoprotein PML-RARa (promyelocytic leukemia-retinoic acid receptor alpha). The morphology of leukemic promyelocytes is usually charact

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Prevalence of inversions in introns 1 and 22 of the factor VIII gene and inhibitors in patients from southern Brazil

Abstract: Objectives: The development of antibodies (inhibitors) against exogenous factors is the main complication in the treatment of hemophilia. Both genetic and non-genetic factors are related to inhibitor development. Among the genetic factors, the type of mutati

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Anticancer drug screening: standardization of in vitro wound healing assay

Abstract: Introduction: Gliomas are characterized by rapid proliferation and aggressive invasion into normal surrounding brain tissue. In medical laboratories, the in vitro wound healing assay stands out as a simple, easy, inexpensive and affordable method to evaluate

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Method of histopathological diagnosis of mammary nodules through deep learning algorithm

Abstract: Introduction: Artificial intelligence systems are promising health care technologies, mainly in medical subareas such as pathology, and can be used as support methods for the histological diagnosis of mammary nodules.Objective: This study describes the meth

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Medical Residency Training in Clinical Pathology/ Laboratory Medicine at the Paulista School of Medicine, Federal University of São Paulo
Adagmar Andriolo

Abstract: Teaching and learning in medicine has its own characteristics, requiring from their actors, in addition to intellectual skills, great dedication and personal commitment. The object of study, learning and practice is a person, punctually placed in the position

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Results of laboratory tests not accessed in Brazilian private laboratories

Abstract: Background: Laboratory medicine is an important part of the health care system and directly contributes to preventive actions, diagnostics, treatment, and management of diseases. The level and quality of laboratory resources utilization have been frequently

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Juvenile ossifying fibroma: series of seven cases focusing on clinical and pathological aspects

Abstract: Juvenile ossifying fibroma (JOF) is an uncommon benign fibro-osseous lesion that affects young individuals and deserves attention because it presents an aggressive clinical behavior and high rates of recurrence. This paper aims to report seven cases diagnosed

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Bloodstream infection by Acinetobacter radioresistens: the first case report in Brazil

Abstract: This report is the description of the first case in Brazil of community-acquired bloodstream infection caused byAcinetobacter radioresistens. A 73-year-old male patient with Alzheimer’s and Parkinson’s disease was hospitalized and diagnosed with pneumonia at

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Choroid plexus papilloma: case report
Wilker D. Martins Wander N. Naves

Abstract: Choroid plexus papillomas (CPP) are a rare oncological condition. They affect mostly the pediatric population, and the diagnosis is associated with clinical findings, imaging and anatomopathological methods. We report the case of a 49-year-old woman who under

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Glandular odontogenic cyst: report of an unusual case in the posterior mandible

Abstract: The glandular odontogenic cyst (GOC) is an uncommon developmental cyst that presents glandular differentiation and has potential for recurrence. Clinically, it is asymptomatic and it has slow growing. This report proposes to describe a clinical case of GOC di

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Investigation of Chagas disease within the same family: case study

Abstract: Chagas disease (CD) is a neglected endemic disease. Its classic form of transmission occurs through hematophagous triatomine insects. Its classic form of transmission occurs through hematophagous triatomine insects. There are cases of the disease in non-endem

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Clinical difference between identical twins with sickle cell anemia

Abstract: Sickle cell anemia (SCA) is a genetic disease that causes important clinical manifestations due to chronic hemolysis and vascular occlusion. The aim of this study was to report a rare case of monozygotic twins diagnosed with SCA, presenting a different clinic

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Criterios de Evaluación
Criterios Básicos de Admisión Criterios Básicos de Admisión
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Criterios Altamente Valorados / Criterios Deseables Criterios Cualitativos
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Criterios Altamente Valorados Cuantitativos
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