Results 21 to 30 of about 6,359 (170)
Renal symptoms in the Joubert syndrome [PDF]
, 2009 OBJECTIVE:To describe the case of a patient with Joubert syndrome associated with renal impairments. CASE DESCRIPTION: A 2 month-old patient was admitted with hypotonia and hyperpneia.
Andrade, Maria Cristina de +2 more
core +4 more sources
Mediators of Inflammation, Volume 2017, Issue 1, 2017., 2017 Cystic fibrosis (CF) is the most common autosomal genetic recessive disease caused by mutations of gene encoding for the cystic fibrosis transmembrane conductance regulator. Patients with CF display a wide spectrum of symptoms, the most severe being chronic lung infection and inflammation, which lead to onset of cystic fibrosis lung disease.
Domitilla Schiumarini +14 more
wiley +1 more source
Mediators of Inflammation, Volume 2017, Issue 1, 2017., 2017 The angelicin analogue 4,6,4′‐trimethylangelicin (TMA) was recently reported as a strong inhibitor of nuclear factor‐κB (NF‐κB) activity and of the expression of the interleukin‐8 (IL‐8) gene in bronchial epithelial cells in which the inflammatory response has been challenged with P.
Ilaria Lampronti +14 more
wiley +1 more source
Immunology &Cell Biology, Volume 92, Issue 8, Page 659-670, September 2014., 2014 Unlike induced Foxp3+ regulatory T cells (Foxp3+ iTreg) that have been shown to play an essential role in the development of protective immunity to the ubiquitous mold Aspergillus fumigatus, type‐(1)‐regulatory T cells (Tr1) cells have, thus far, not been implicated in this process.
Tanja Bedke +9 more
wiley +1 more source
Prevalence of sickle cell trait and sickle cell anemia among newborns in the Federal District, Brazil, 2004 to 2006 [PDF]
, 2009 Para determinar a prevalência da anemia e traço falciforme em recém-nascidos no Distrito Federal, Brasil, no período de 2004 a 2006, foi realizado um estudo seccional de prevalência.
Barbosa, Lívia +4 more
core +1 more source
Brazilian Journal of Otorhinolaryngology, 2010 Embora o perfil das citocinas na polipose nasossinusal seja bem documentado, pouco se sabe sobre estas proteínas quando associadas à Fibrose Cística. OBJETIVOS: Avaliar a expressão das citocinas IL¬4, IL¬5, IL¬6, IL¬8, GM¬C-SF e IFN--y analisada pela RT¬-
Flávio Barbosa Nunes +6 more
doaj +1 more source
Effects of Pilates mat exercises on muscle strength and on pulmonary function in patients with cystic fibrosis [PDF]
, 2014 Objective: To analyze the effects of Pilates mat exercises in patients with cystic fibrosis (CF). Methods: This was a clinical trial involving 19 CF patients recruited from either the CF Outpatient Clinic of the State University at Campinas Hospital de ...
Almeida, Marina Buarque +5 more
core +4 more sources
Clinical, nutritional and spirometric evaluation of patients with cystic fibrosis after the implementation of multidisciplinary treatment [PDF]
, 2010 OBJETIVO: A fibrose cística (FC) é uma doença hereditária, multissistêmica e crônica, para a qual é importante uma abordagem multidisciplinar. O objetivo deste estudo foi mostrar a evolução de um grupo de pacientes com FC após a implantação desse tipo de
Almeida, Giseli Barbiero de +5 more
core +1 more source
Prática fisioterapêutica no tratamento da fibrose cística
ABCS Health Sciences, 2014 A fibrose cística (FC), denominada também de mucoviscidose, é uma doença genética do tipo autossômica recessiva que acomete principalmente crianças e indivíduos de raça branca.
Carolina Lazzarim de Conto +6 more
doaj +1 more source
Relevância clínica em não fi brose cística bronquiectasia seguida em uma prática real [PDF]
, 2013 INTRODUCTION: Bronchiectasis is a chronic disorder characterized by permanent dilation of the bronchi and bronchioles accompanied by inflammatory changes in the walls of these structures and adjacent lung parenchyma.
Bigatão, Amilcar Marcelo +5 more
core +3 more sources