نتایج جستجو برای: condition factor cf

تعداد نتایج: 1162104  

Journal: :Pediatric pulmonology. Supplement 1991
L A Mieles D M Orenstein R M Toussaint R Selby R D Gordon T E Starzl

Im~rovements in l'ulmonary care and other refinements in management allow more patients WIth cystic fibroSIS (CF) to survive long enough for liver disease to become a limiting factor in their life expectancy (1, 2, 3). Since liver transplantation is considered the treatment of choice for patients with end-stage liver disease, it is predictable that more patients with CF and liver failure will b...

Journal: :The Journal of pharmacology and experimental therapeutics 1999
D W Johnson H J Saunders F J Johnson S O Huq M J Field C A Pollock

To assess the direct fibrogenic effects of cyclosporin A (CyA) on the human tubulointerstitium, primary cultures of human renal proximal tubule cells (PTC) and renal cortical fibroblasts (CF) were incubated for 24 h with various concentrations of CyA. Cytotoxicity was confirmed in both cell populations by dose-dependent inhibition of thymidine incorporation, viability, and PTC apical sodium-hyd...

2013
Robin H. Ballard Amy Holtzworth-Munroe Amy G. Applegate Brian M. D’Onofrio John E. Bates

With over 1 million children in the United States affected by parental divorce or separation each year, there is interest in interventions to mitigate the potential negative consequences of divorce on children. Family mediation has been widely heralded as a better solution than litigation; however, mediation does not work for all families. One proposed improvement involves bringing the child’s ...

Journal: :Arquivos brasileiros de endocrinologia e metabologia 2011
Renata Maria de Noronha Luís Eduardo Procópio Calliari Neiva Damaceno Lucia Harumi Muramatu Osmar Monte

Cystic fibrosis (CF) is the most common recessive autosomal disease among Caucasian. Children with CF have benefitted from advances in medical and nutritional treatments, and this can be gleaned from the improvement in the survival of these patients. The increase in the survival rate brought with it the appearance of co-morbidities related to CF. Nowadays cystic fibrosis-related diabetes (CFRD)...

2016
R Andres Floto Kenneth N Olivier Lisa Saiman Charles L Daley Jean-Louis Herrmann Jerry A Nick Peadar G Noone Diana Bilton Paul Corris Ronald L Gibson Sarah E Hempstead Karsten Koetz Kathryn A Sabadosa Isabelle Sermet-Gaudelus Alan R Smyth Jakko van Ingen Richard J Wallace Kevin L Winthrop Bruce C Marshall Charles S Haworth

Non-tuberculous mycobacteria (NTM) are ubiquitous environmental organisms that can cause chronic pulmonary infection, particularly in individuals with pre-existing inflammatory lung disease, such as cystic fibrosis (CF). Pulmonary disease (PD) caused by NTM has emerged as a major threat to the health of individuals with CF, but remains difficult to diagnose and problematic to treat. In response...

2015
Mohammad A Wazzan

Cystic fibrosis (CF) is a multisystemic, autosomal recessive disorder that predominantly affects infants, children, and young adults. Manifestations of CF involve the lung and gastrointestinal tract, including the pancreas. Pancreatic cystosis is a rare condition typically seen in CF during the second decade of life. It has characteristic magnetic resonance imaging (MRI) and ultrasound (US) fea...

2009
Dimitrios Manolopoulos Ingo Runkel

Starting from an abelian rigid braided monoidal category C we define an abelian rigid monoidal category CF which captures some aspects of perturbed conformal defects in two-dimensional conformal field theory. Namely, for V a rational vertex operator algebra we consider the charge-conjugation CFT constructed form V (the Cardy case). Then C = Rep(V ) and an object in CF corresponds to a conformal...

Journal: :Thorax 2008
A Smyth S Lewis C Bertenshaw I Choonara J McGaw A Watson

BACKGROUND There has been a recent increase in the number of reported cases of acute renal failure (ARF) in cystic fibrosis (CF). A case-control study was conducted to determine the factors which are associated with an increased risk of ARF. METHODS 24 cases of confirmed ARF were identified in patients with CF from 20 UK CF centres presenting between 1997 and 2004. Using the UK CF database, s...

Journal: :The European respiratory journal 2013
Catriona Kelly Mark T Williams Kathryn Mitchell J Stuart Elborn Madeleine Ennis Bettina C Schock

A20 is a lipopolysaccharide (LPS)-inducible, cytoplasmic zinc finger protein, which inhibits Toll-like receptor-activated nuclear factor (NF)-κB signalling by deubiquitinating tumour necrosis factor receptor-associated factor (TRAF)-6. The action of A20 is facilitated by complex formation with ring finger protein (RNF)-11, Itch and TAX-1 binding protein-1 (TAX1BP1). This study investigated whet...

Journal: :The European respiratory journal 1999
I Eichler M Nilsson R Rath I Enander P Venge D Y Koller

Cystic fibrosis (CF) is characterized by the production of abnormally thick secretions in the airways, chronic bacterial endobronchial infections and a chronic, predominantly neutrophilic inflammatory response. Therefore, myeloperoxidase (MPO) and lactoferrin are frequently used as inflammatory markers. Recently, a new protein in the neutrophil granules, human neutrophil lipocalin (HNL) has bee...

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