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Lung Diseases

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Last Posted: May 04, 2018

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• Cystic Fibrosis Disease Modifiers: Complex Genetics Defines the Phenotypic Diversity in a Monogenic Disease.  
  O'Neal Wanda K et al. Annual review of genomics and human genetics 2018 Apr
• Disease-modifying genetic factors in cystic fibrosis.  
  Marson Fernando A L et al. Current opinion in pulmonary medicine 2018 May (3) 296-308
• [Precision medicine: A major step forward in specific situations, a myth in refractory cancers?]  
  Albin Nicolas et al. Bulletin du cancer 2018 Apr 105(4) 375-396
• Delays in adding new newborn screening tests harm babies, families  
  R Moy et al, STatNews, Apr 30, 2018
• Diagnostic and prognostic values of endothelial-cell-specific molecule-1 with malignant pleural effusions in patients with non-small cell lung cancer.  
  Lu Guo-Jun et al. Oncotarget 2017 Jul 8(30) 49217-49223
• Early diagnosis from newborn screening maximises survival in severe cystic fibrosis. 
  Tridello Gloria et al. ERJ open research 2018 Apr 4(2)
• Exploiting molecular genomics in precision radiation oncology: a marriage of biological and physical precision.  
  Tan Janice S H et al. Chinese clinical oncology 2017 Sep 6(Suppl 2) S19
• Living With COPD 
• NIH statement on World Asthma Day 2018  
  NIH video: patients and scientists work together to advance asthma research.
• The CF Canada-Sick Kids Program in individual CF therapy: A resource for the advancement of personalized medicine in CF.  
  Eckford Paul D W et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2018 Apr
• The detection and significance of EGFR and BRAF in cell-free DNA of peripheral blood in NSCLC.  
  Yang Yang et al. Oncotarget 2017 Jul 8(30) 49773-49782
• A Qualitative Analysis of the Information Needs of Parents of Children with Cystic Fibrosis prior to First Admission.  
  Fixter Vera et al. Journal of pediatric nursing 34e29-e33
• At-Home Genetic Testing Is Blurring Lines Between Patient and Consumer  
  E Glowatz, Newsweek, Apr 24, 2018
• Clinical experience with multigene carrier panels in the reproductive setting.  
  Terhaar Catherine et al. Prenatal diagnosis 2018 Apr
• Detection of oncogenic mutations in resected bronchial margins by next-generation sequencing indicates early relapse in stage IA lung adenocarcinoma patients.  
  Lv Tangfeng et al. Oncotarget 2017 Jun 8(25) 40643-40653