APLASIA SEVERA DE MEDULA ÓSSEA SECUNDÁRIA À APLASIA PURA DE SÉRIE VERMELHA: RELATO DE CASO
Introdução: anemia aplástica é uma doença rara e heterogênea. A maioria (70–80%) é categorizada como idiopática porque sua etiologia primária é desconhecida. É um distúrbio de células-tronco hematopoiéticas com risco de vida que é tratado com transplante
ASA Silva +9 more
doaj +1 more source
Anatomy of a Dispute:Leonardo, Pacioli, and Scientific Entertainment in Renaissance Milan. [PDF]
none1noHistorians have recently paid increasing attention to the role of the disputation in Italian universities and humanist circles. By contrast, the role of disputations as forms of entertainment at fifteenth-century Italian courts has been somewhat ...
Azzolini, Monica
core +1 more source
Targeted modulation of IGFL2‐AS1 reveals its translational potential in cervical adenocarcinoma
Cervical adenocarcinoma patients face worse outcomes than squamous cell carcinoma counterparts despite similar treatment. The identification of IGFL2‐AS1's differential expression provides a molecular basis for distinguishing these histotypes, paving the way for personalized therapies and improved survival in vulnerable populations globally.
Ricardo Cesar Cintra +6 more
wiley +1 more source
LINFOMA DE HODGKIN CLÁSSICO EM PACIENTE VIVENDO COM HIV: RELATO DE CASO
Introdução: O Linfoma de Hodgkin clássico (LHc) é uma doença rara, com predileção por adolescentes e adultos jovens (15 a 39 anos). Até 90% dos recém-diagnosticados com LH podem ser curados com quimioterapia combinada e/ou radioterapia.
ASA Silva +9 more
doaj +1 more source
Importancia en el sistema de salud de la infección por Treponema pallidum, la enfermedad de Chagas y el virus de la inmunodeficiencia humana 1 en amerindios de Argentina: un estudio observacional [PDF]
El objetivo de este trabajo fue estimar la prevalencia de Treponema pallidum, Trypanosoma cruzi y virus de la inmunodeficiencia humana (HIV-1) en 5 comunidades originarias de Argentina.
Berini, Carolina Andrea +10 more
core +2 more sources
Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce +72 more
wiley +1 more source
Anesthesiologists’ knowledge about packed red blood cells transfusion in surgical patients
Introduction: Blood is an important resource in several lifesaving interventions, such as anemia correction and improvement of oxygen transport capacity. Despite advances, packed red blood cell (PRBC) transfusion still involves risks.
Joyce Mendes Soares +6 more
doaj +1 more source
A Systematic Comparison of Alpha‐Synuclein Seed Amplification Assays for Increasing Reproducibility
ABSTRACT Seed amplification assays (SAAs) enable ultrasensitive detection of misfolded α‐synuclein across biofluids and tissues. Yet, heterogeneity in protocols limits cross‐study comparability and clinical translation. Here, we review α‐synuclein SAA methods and their performance across various biological matrices.
Manuela Amaral‐do‐Nascimento +3 more
wiley +1 more source
Introdução: Linfomas Primários de Sistema Nervoso Central (LPSNC) são neoplasias raras, com origem em linfócitos B CD20 positivos. Representam cerca de 7-14% das neoplasias pós transplante de órgãos sólidos, estando o vírus Epstein Barr (EBV) e o estado ...
MP César +6 more
doaj +1 more source
Plan de negocios para un centro de bienestar integral para mujeres [PDF]
Walliq será un centro de bienestar integral de medicina alternativa contemporánea dirigido a mujeres de 31 a 55 años de edad de Lima Metropolitana de los niveles socioeconómicos (NSE) A y B, las cuales mantienen un estilo de vida moderno.
Cáceres Tafur, Sandra Patricia +2 more
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