Trasplante pulmonar en pacientes con fibrosis pulmonar idiopática [PDF]
Pulmonary transplantation represents a therapeutic option in patients with advanced pulmonary fibrosis who have a progressive course despite medical treatment, improving their survival and quality of life. It is vital that the pulmonologist knows when to refer a patient and be familiar with the requirements and contraindications. Timely referral grants
BRICEÑO V, CATALINA +2 more
openaire +2 more sources
Cell therapy in pulmonary diseases: are there perspectives? [PDF]
A terapia celular poderia ser conceituada de forma ampla e genérica como o emprego de células para tratamento de doenças. Apesar de um número não tão expressivo de relatos tendo o pulmão como objeto de estudo na terapia celular em pacientes humanos, há ...
ALVES-DE-MORAES, Luis B. C. +6 more
core +1 more source
Histological features and survival in idiopathic pulmonary fibrosis [PDF]
BACKGROUND: Idiopathic pulmonary fibrosis was recently redefined as usual interstitial pneumonia of unknown etiology. Consequently, the prognostic value of histological findings needs to be reassessed.
Coletta, Ester Nei Aparecida Martins +6 more
core +2 more sources
Fibroelastosis pleuroparenquimatosa e hipertension pulmonar: un fenotipo diferente?
La fibroelastosis pleuroparenquimatosa es una enfermedad pulmonar inusual con características clínicas, radiológicas y patológicas únicas, que se ha incluido recientemente en el consenso actualizado sobre neumonías intersticiales idiopáticas.
Lourdes González +3 more
doaj +1 more source
Hipertensión pulmonar en pacientes con fibrosis pulmonar y sobrevida post-trasplante pulmonar [PDF]
Introduccion: La presencia de hipertension pulmonar (HTP) en pacientes con fibrosis pulmonar es un predictor de gravedad y pobre sobrevida en pacientes en espera de trasplante pulmonar. Poco se sabe del impacto de la HTP en la sobrevida de los pacientes en el periodo post trasplante.
BRICEÑO V, CATALINA +4 more
openaire +2 more sources
Evaluation of the histological parameters in usual interstitial pneumonia (idiopathic pulmonary fibrosis) [PDF]
Idiopathic pulmonary fibrosis (cryptogenic fibrosing alveolitis) is a progressive interstitial pulmonary disease of unknown etiology. Since Hamman's and Rich's (1944) reports, many studies have tried to find a histological marker for the correlation ...
Coletta, Ester Nei Aparecida Martins +2 more
core +3 more sources
Results of nutritional intervention in children and adolescents with cystic fibrosis [PDF]
Objective: few studies have verified longitudinally the evolution of the nutritional status of patients with cystic fibrosis. The objective of this study is to follow the evolution of the nutritional status, body composition and energy consumption ...
Ancona-Lopez, Fabio +5 more
core +3 more sources
Abstract Book for the 27th Congress of the European Hematology Association
HemaSphere, Volume 6, Issue S3, Page 1-4130, June 2022.
wiley +1 more source
Introducción: la fibrosis pulmonar idiopática (FPI) es una enfermedad progresiva y crónica con muy mal pronóstico. Actualmente, existen dos fármacos para esta patología.
Raquel López Vime +3 more
doaj +1 more source
Treatment with DNases rescues hidden neutrophil elastase from aggregated NETs
DNase 1 releases hidden neutrophil elastase activity from aggNETs. Abstract The release of neutrophil extracellular traps (NETs) is one of the weapons neutrophils have in their armory. NETs consist of extracellular chromatin fibers decorated with a plethora of cytoplasmic and granular proteins, such as the antimicrobial serine protease neutrophil ...
Malgorzata J. Podolska +11 more
wiley +1 more source

