Keyword Connections

cystic fibrosis

Journals

33

1 Scientific reports

2 PloS one

3 eLife

4 Medicine

5 ACS omega

6 Physical Therapy

7 Free radical biology & medicine

8 molecular microbiology

9 scientific data

10 oncotarget

11 canadian medical education journal

12 new biotechnology

13 bmj open respiratory research

14 jbi database of systematic reviews and implementation reports

15 pediatric pulmonology

16 african health sciences

17 Journal of pain and symptom management

18 Clinical nutrition (Edinburgh, Scotland)

19 health (london, england : 1997)

20 surgery

21 journal of biological methods

22 Journal of the Royal Society, Interface

23 BMC pulmonary medicine

24 clinical nutrition espen

25 clinical medicine & research

26 seminars in cardiothoracic and vascular anesthesia

27 Thorax

28 The Turkish journal of pediatrics

29 virology journal

30 journal of cystic fibrosis : official journal of the european cystic fibrosis society

31 science (new york, ny)

32 cell stem cell

33 epidemiology (sunnyvale, calif)

Research Groups

0

No Research Group Connected

Bibliographies

43

1 Pathways, practices and architectures: Containing antimicrobial resistance in the cystic fibrosis clinic.

2 A Novel Tool to Evaluate the Accuracy of Predicting Survival and Guiding Lung Transplantation in Cystic Fibrosis.

3 High-Efficiency, Selection-free Gene Repair in Airway Stem Cells from Cystic Fibrosis Patients Rescues CFTR Function in Differentiated Epithelia.

4 Cystic fibrosis in Tunisian children: a review of 32 children.

5 Venous thromboembolic events during warm autoimmune hemolytic anemia.

6 Current infection control practices used in Australian and New Zealand cystic fibrosis centers.

7 Interspecies interactions induce exploratory motility in .

8 Respect the poster.

9 New insights into the mycobacterial PE and PPE proteins provide a framework for future research.

10 Utility and validity of dynamic chest radiography in cystic fibrosis (dynamic CF): an observational, non-controlled, non-randomised, single-centre, prospective study.

11 Intention to control low central venous pressure reduced blood loss during laparoscopic hepatectomy: A double-blind randomized clinical trial.

12 Development and Validation of the AdT-Physio Scale: A Tool to Assess Adherence and Perception of Physical Therapist Intervention in Patients With Cystic Fibrosis.

13 Activated L-Arginine/Nitric Oxide Pathway in Pediatric Cystic Fibrosis and Its Association with Pancreatic Insufficiency, Liver Involvement and Nourishment: An Overview and New Results

14 cftr mutation analysis of a caucasian father with congenital bilateral absence of vas deferens, a taiwanese mother, and twins resulting from icsi procedure

15 liver cirrhosis and portal hypertension in cystic fibrosis

16 bronchial epithelial cells from cystic fibrosis patients express a specific long non-coding rna signature upon pseudomonas aeruginosa infection

17 draft genome sequence of acinetobacter pittii st643 shared by cystic fibrosis patients

18 animals devoid of pulmonary system as infection models in the study of lung bacterial pathogens

19 methicillin-resistant staphylococcus aureus in cystic fibrosis patients: do we need to care? a cohort study

20 lying in wait: modeling the control of bacterial infections via antibiotic-induced proviruses

21 perfil nutricional, clínico e socioeconômico de pacientes com fibrose cística atendidos em um centro de referência no nordeste do brasil nutritional, clinical and socioeconomic profile of patients with cystic fibrosis treated at a referral center in northeastern brazil

22 ivs8 polyt and m470v polymorphisms in healthy individuals and cystic fibrosis patients in mazandaran province, iran

23 hyponatremic hypochloremic dehydration in children with cystic fibrosis in slovenia; the incidence and recommendations for prevention and treatment

24 o que é ser mãe de uma criança com fibrose cística qué significa ser madre de un niño con fibrosis quística what is being a mother of a child with cystic fibrosis

25 non-antimicrobial airway management of non-cystic fibrosis bronchiectasis

26 β-sitosterol reduces the expression of chemotactic cytokine genes in cystic fibrosis bronchial epithelial cells

27 densidade mineral óssea, função pulmonar, idade cronológica e idade de diagnóstico em crianças e adolescentes com fibrose cística bone mineral density, pulmonary function, chronological age, and age at diagnosis in children and adolescents with cystic fibrosis

28 chronic cough with normal sweat chloride: phenotypic descriptions of two rare cystic fibrosis genotypes

29 deve-se extrapolar o tratamento de bronquiectasias em pacientes com fibrose cística para aqueles com bronquiectasias de outras etiologias? should the bronchiectasis treatment given to cystic fibrosis patients be extrapolated to those with bronchiectasis from other causes?

30 respiratory muscle strength and exercise performance in cystic fibrosis–a cross sectional study

31 stenotrophomonas maltophilia phenotypic and genotypic diversity during a 10-year colonization in the lungs of a cystic fibrosis patient

32 peritonitis meconial y fibrosis quística meconium peritonitis and cystic fibrosis

33 evolution of stenotrophomonas maltophilia in cystic fibrosis lung over chronic infection: a genomic and phenotypic population study

34 interactions between neutrophils and pseudomonas aeruginosa in cystic fibrosis

35 acute appendicitis mimicking intestinal obstruction in a patient with cystic fibrosis

36 patient’s perception of the meaning of life in cystic fibrosis – its evaluation with respect to the stage of the disease and treatment

37 tobramycin and amikacin delay adhesion and microcolony formation in pseudomonas aeruginosa cystic fibrosis isolates

38 nets and cf lung disease: current status and future prospects

39 sweat conductivity and coulometric quantitative test in neonatal cystic fibrosis screening

40 a vsv-g pseudotyped last generation lentiviral vector mediates high level and persistent gene transfer in models of airway epithelium in vitro and in vivo

41 Evaluation of clinically relevant changes in the lung clearance index in children with cystic fibrosis and healthy controls.

42 Cystic fibrosis related bone disease in children: Can it be predicted?

43 The predictive role of lung clearance index on FEV decline in cystic fibrosis.