Nabarrete, Juliana Moura;
Pereira, Andrea Z;
Garófolo, Adriana;
Seber, Adriana;
Venancio, Angela Mandelli;
Grecco, Carlos Eduardo Setanni;
Bonfim, Carmem Maria Sales;
Nakamura, Claudia Harumi;
Fernandes, Daieni;
Campos, Denise Johnsson;
Oliveira, Fernanda Luisa Ceragioli;
Cousseiro, Flávia Krüger;
Rossi, Flávia Feijó Panico;
Gurmini, Jocemara;
Viani, Karina Helena Canton;
Guterres, Luciana Fernandes;
Mantovani, Luiz Fernando Alves Lima;
Darrigo Junior, Luiz Guilherme;
Albuquerque, Maria Isabel Brandão Pires e;
Brumatti, Melina;
Neves, Mirella Aparecida;
Duran, Natália;
Villela, Neysimelia Costa;
Zecchin, Victor Gottardello;
Fernandes, Juliana Folloni.
ABSTRACT The Brazilian Nutritional Consensus in Hematopoietic Stem Cell Transplantation: Children and Adolescents was developed by dietitians, physicians, and pediatric hematologists from 10 Brazilian reference centers in hematopoietic stem cell transplantation. The aim was to emphasize the importance of...
Soares, Rodolfo Daniel de Almeida;
Fonseca, Patricia Belintani Blum;
Fertrin, Kleber Yotsumoto;
Marinato, André;
Melo, Andresa Lima;
Nascimento, Ana Clara Kneese;
Moreno, Adrienne Bunn;
Vecina, Antonianna;
Dias, Bruno Vieira;
Lima, Carlos Bernardo Loureiro;
Souza, Fernando Vieira Pericole de;
Cantadori, Lucas Oliveira;
Reis, Marcos Laercio Ponte;
Ganacini, Paulo Roberto;
Helman, Ricardo.
Objective: To report the outcomes of a systematic literature review of guidelines and consensus on the management of paroxysmal nocturnal hemoglobinuria (PNH) and describe the main therapeutic options available worldwide. Methods: A systematic literature review was conducted in April 2018 with no time li...
Trucco, José I;
Berro, Mariano;
Basquiera, Ana Lisa;
García, Pablo;
Yantorno, Sebastián;
Palmer, Silvina;
Requejo, Alejandro;
Vitriú, Adriana;
Bentolila, Gonzalo;
Rivas, María Marta;
Ferini, Gonzalo;
García, Juan José;
Milone, Jorge;
Stemmelin, German;
Jaimovich, Gregorio;
Foncuberta, Cecilia;
Martinez Rolón, Juliana;
Kusminsky, Gustavo D.
Abstract We retrospectively analyzed 570 adult patients who received allogeneic stem cell transplantation for malignant diseases. The outcomes were compared according to donor type. Most of the patients (60%) were transplanted for acute leukemia. Median follow-up was 1.6 years. Haploidentical allogeneic ...
Introdução: O Transplante de Células-Tronco Hematopoiéticas é um procedimento com alto risco de complicações, as quais impactam nos cuidados da equipe de enfermagem. Na realização desse cuidado, valer-se de práticas padronizadas, sustentadas em evidências científicas e na experiência de enfe...
ABSTRACT Introduction: Acute graft-versus-host disease (GVHD) is one of the major causes of morbidity and mortality in patients undergoing allogeneic hematopoietic stem cell transplantation (AHSCT) and has become the subject of several studies to understand and treat it. Objective: This study does a de...
Getz, Joselito;
Goldenstein, Monica;
Bonfim, Carmem;
Funke, Vaneuza Moreira;
Colturato, Vergílio;
Hamerschlak, Nelson;
Torres, Margareth;
Sayer, David;
Boldt, Angelica;
Pasquini, Ricardo;
Pereira, Noemi Farah.
ABSTRACT Background: Immunological life-threatening complications frequently occur in post-hematopoietic stem cell transplantation (HSCT), despite matching recipient and donor (R/D) pairs for classical human leukocyte antigens (HLA). Studies have shown that R/D non-HLA disparities within the major histo...
A deficiência de mevalonato quinase (MVK; MIM #142680; ORPHA #343) é uma doença genética, espectral, rara, associadas a mutações ao longo do gene MVK causando distúrbios na síntese do colesterol, que culminam em: inflamação sistêmica com febre, adenopatia, sintomas abdominais e outros achados ...
PubMed,
Deficiencia de Mevalonato Quinasa,
Conductas Terapéuticas Homeopáticas,
Enfermedades Genéticas Congénitas,
Inmunoglobulina D,
Terapia Genética,
Fiebre,
Linfadenopatía,
Meningitis Aséptica,
Vasculitis,
Interleucina-1,
Sistema Hematopoyético,
Inflamación,
Signos y Síntomas,
Amiloidosis,
Terapéutica,
Trasplante de Células Madre Hematopoyéticas,
Sistema Nervioso Central
Introducción: La aplasia medular adquirida grave es una enfermedad hematológica infrecuente caracterizada por una disminución o ausencia de precursores hematopoyéticos en la médula ósea, lo cual se expresa con distintos grados de citopenias. Varios factores, infecciosos o no, pueden incidir en su ...
