Inflammation in Cystic Fibrosis

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Lobectomy in Patients with Cystic Fibrosis by Shahid I Sheikh, Karen McCoy, Nancy A Ryan-Wenger, Alpa Patel, Stephen Kirkby

“…BACKGROUND: Some patients with cystic fibrosis (CF) develop severe but localized lung disease or recurrent hemoptysis/pneumothorax refractory to conventional medical therapies.…”
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Pseudomonas cepacia in cystic fibrosis by Ronald Gold

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Imaging the Abdominal Manifestations of Cystic Fibrosis by C. D. Gillespie, M. K. O’Reilly, G. N. Allen, S. McDermott, V. O. Chan, C. A. Ridge

“…Cystic fibrosis (CF) is a multisystem disease with a range of abdominal manifestations including those involving the liver, pancreas, and kidneys. …”
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MicroRNA Dysregulation in Cystic Fibrosis by Paul J. McKiernan, Catherine M. Greene

“…The cystic fibrosis lung is a complex milieu comprising multiple factors that coordinate its physiology. …”
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Cystic Fibrosis: Bench to Bedside 2003 by Bruce K Rubin

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Cough in non-cystic fibrosis bronchiectasis by Ahmad Kantar, Woo-Jung Song, Andrew Bush, Grigorios Chatziparasidis

“…Non-cystic fibrosis bronchiectasis (NCFBE) belongs to the spectrum of chronic suppurative lung diseases and is characterised by persistent wet/sputum-productive cough and airway dilatation. …”
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Liver Transplantation for Cirrhosis in Cystic Fibrosis by T Lamireau, S Martin, M Lallier, JE Marcotte, F Alvarez

“…BACKGROUND: Liver disease is the third most common cause of death in children with cystic fibrosis (CF). Liver transplantation is an effective treatment in children with hepatic failure.…”
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Epidemiology of Pseudomonas cepacia in Cystic Fibrosis by Statement from the Medical/Scientific Advisory Committee Canadian Cystic Fibrosis Foundation

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A Roadmap to the Brittle Bones of Cystic Fibrosis by Ashwini P. Gore, Soon Ho Kwon, Antine E. Stenbit

“…Cystic fibrosis (CF) is an autosomal recessive disorder which despite advances in medical care continues to be a life-limiting and often fatal disease. …”
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Characterization of Patients with Cystic Fibrosis in Multidisciplinary Consultation by Caridad Llull Tombo, Mercedes Fonseca Hernández, Ileana García Rodríguez, Juan Carlos Yanes Macías, Daymí Tió González, Yoandra León Rayas

“…<strong><br />Objective:</strong> to characterize patients with cystic fibrosis in the province of Cienfuegos.<strong><br /> Methods:</strong> an observational, descriptive and cross-sectional study was carried out at the Paquito González Cueto de Cienfuegos University Pediatric Hospital in the cystic fibrosis consultation, from January 1 to December 31, 2018. …”
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Paradoxical Embolization in an Adult Cystic Fibrosis Patient by Nabil M Al Lawati, Pearce Wilcox

“…Cystic fibrosis patients with an implantable venous access device (IVAD) and a patent foramen ovale (PFO) are at an increased risk of developing paradoxical embolism. …”
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New Developments in Cystic Fibrosis Airway Inflammation by Nades Palaniyar, Marcus A. Mall, Christian Taube, Stefan Worgall, Hartmut Grasemann

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Progression and mortality of patients with cystic fibrosis in China by Wangji Zhou, Yaqi Wang, Yanli Yang, Yanyan Sun, Chongsheng Cheng, Jinrong Dai, Shuzhen Meng, Keqi Chen, Yang Zhao, Xueqi Liu, Dingding Zhang, Song Liu, Weiguo Zhu, Yaping Liu, Kai-Feng Xu, Xinlun Tian

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Progressive Scoliosis in a Child with Cystic Fibrosis by Lauren M. Castner, Samya Z. Nasr, Manuel Arteta

“…We discuss an adolescent female with cystic fibrosis, asthma, and scoliosis who had a rapid decline in her pulmonary function despite typical treatment for a cystic fibrosis exacerbation. …”
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Pancreatic Cystosis in Two Adolescents with Cystic Fibrosis by Elpis Hatziagorou, Asterios Kampouras, Maria Sidiropoulou, Andreas Markou, Athanasia Anastasiou, John Tsanakas

“…We present pancreatic cystosis in two adolescents with cystic fibrosis, a 13-year-old girl and an 18-year-old boy. …”
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Pulmonary Nocardiosis in an Immunocompetent Patient with Cystic Fibrosis by Lucy Schoen, Jonathan D. Santoro, Carlos Milla, Sumit Bhargava

“…Nocardia spp. are bacteria of low virulence that cause infection classically in immunocompromised hosts with the lungs as the primary site of infection in the majority of cases. Patients with cystic fibrosis have pulmonary disease characterized by frequent and progressive bacterial infections. …”
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Microbial Contamination of Nebulizers in Patients With Cystic Fibrosis by Cansu Yilmaz Yegit, Pinar Ergenekon, Nurcan Duman, Hakan Mursaloglu, Muruvvet Cenk, Burcu Suzer Uzunoglu, Gamze Tastan, Yasemin Gokdemir, Ela Erdem Eralp, Aysegul Karahasan Yagci, Fazilet Karakoc, Bulent Karadag

“…The aim was to investigate the contamination profile of the nebulizers in cystic fibrosis patients and evaluate the relationship between hygiene practices and microbial contamination. …”
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Psychometric validation of the Cystic Fibrosis Impact Questionnaire (CF-IQ): A patient-reported outcome assessing impacts of cystic fibrosis. by Daniel Serrano, Alyssa Uzumcu, Maya Gerstein, Nicolai D Ayasse, Ella Engstrom, Frederick B Barnes, Charles Iaconangelo, Teja Thorat, Lisa J McGarry, Isabelle Sermet-Gaudelus

“…The Cystic Fibrosis (CF) Impact Questionnaire (CF-IQ) was qualitatively developed to assess the impact of CF in the context of treatment advancements and increased longevity. …”
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Normalization of Cystic Fibrosis Immune System Reverses Intestinal Neutrophilic Inflammation and Significantly Improves the Survival of Cystic Fibrosis MiceSummary by Callie E. Scull, Yawen Hu, Scott Jennings, Guoshun Wang

Subjects: “…Cystic Fibrosis…”
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