Cystic Fibrosis Research Today is a free monthly online journal that collates and summarizes the latest research about Cystic Fibrosis, including details on symptoms, genetics, treatment, information.
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Volume 2 (2005), Issue 3 (March)
- Epidemiology of Pseudomonas aeruginosa in a cystic fibrosis rehabilitation centre.
Eur Respir J, 25(3): 474-81. [Abstract] [Full-text]
- The CFTR 3849+10kbC->T and 2789+5G->A alleles are associated with a mild CF phenotype.
Eur Respir J, 25(3): 468-73. [Abstract] [Full-text]
- Antimicrobial use and Pseudomonas aeruginosa susceptibility profile in a cystic fibrosis centre.
Int J Antimicrob Agents, 25(3): 193-7. [Abstract] [Full-text]
- Optimum peripheral drug deposition in patients with cystic fibrosis.
J Aerosol Med, 18(1): 45-54. [Abstract] [Full-text]
- Structural changes to airway smooth muscle in cystic fibrosis.
Thorax, 60(3): 226-8. [Abstract] [Full-text]
- Safety and tolerability of denufosol tetrasodium inhalation solution, a novel P2Y2 receptor agonist: results of a phase 1/phase 2 multicenter study in mild to moderate cystic fibrosis.
Pediatr Pulmonol, 39(4): 339-48. [Abstract] [Full-text]
- Misdiagnosing cystic fibrosis in the era of gene analysis: case reports.
Pediatr Pulmonol, 39(4): 379-81. [Abstract] [Full-text]
- Thrombophilia in children with cystic fibrosis.
Pediatr Pulmonol, 39(4): 306-10. [Abstract] [Full-text]
- Beyond chloride transport: CFTR in the 21st century-introductory remarks to a new state of the art series.
Pediatr Pulmonol, 39(4): 289-91. [Abstract] [Full-text]
- Insulin-secretion abnormalities and clinical deterioration related to impaired glucose tolerance in cystic fibrosis.
Eur J Endocrinol, 152(2): 241-7. [Abstract] [Full-text]
- Airway colonization by Acrophialophora fusispora in patients with cystic fibrosis.
J Clin Microbiol, 43(3): 1484-7. [Abstract] [Full-text]
- The impact of cystic fibrosis and PSTI/SPINK1 gene mutations on susceptibility to chronic pancreatitis.
Clin Lab Med, 25(1): 79-100. [Abstract] [Full-text]
- Salivary secretion assay for drug efficacy for cystic fibrosis in mice.
Exp Physiol, 90(2): 189-93. [Abstract] [Full-text]
- Rapidly progressive lung disease in a patient with cystic fibrosis on long-term azithromycin: possible role of mycoplasma infection.
J Cyst Fibros, 4(1): 71-3. [Abstract] [Full-text]
- A pilot study of oral L-arginine in cystic fibrosis.
J Cyst Fibros, 4(1): 67-9. [Abstract] [Full-text]
- Associations between clinical variables and quality of life in adults with cystic fibrosis.
J Cyst Fibros, 4(1): 59-66. [Abstract] [Full-text]
- Asians with cystic fibrosis in the UK have worse disease outcomes than clinic matched white homozygous delta F508 controls.
J Cyst Fibros, 4(1): 53-8. [Abstract] [Full-text]
- Risk factors for acquisition of methicillin-resistant Staphylococcus aureus (MRSA) by patients with cystic fibrosis.
J Cyst Fibros, 4(1): 49-52. [Abstract] [Full-text]
- Prospective evaluation of emerging bacteria in cystic fibrosis.
J Cyst Fibros, 4(1): 41-8. [Abstract] [Full-text]
- Long-term azitromycin treatment of cystic fibrosis patients with chronic Pseudomonas aeruginosa infection; an observational cohort study.
J Cyst Fibros, 4(1): 35-40. [Abstract] [Full-text]
- Late diagnosis defines a unique population of long-term survivors of cystic fibrosis.
Am J Respir Crit Care Med, 171(6): 621-6. [Abstract] [Full-text]
- Growth hormone treatment enhances nutrition and growth in children with cystic fibrosis receiving enteral nutrition.
J Pediatr, 146(3): 324-8. [Abstract] [Full-text]
- Guide to bone health and disease in cystic fibrosis.
J Clin Endocrinol Metab, 90(3): 1888-96. [Abstract] [Full-text]
- Uncertainty management following a positive newborn screening for cystic fibrosis.
J Health Commun, 10(1): 57-76. [Abstract] [Full-text]
- Cystic fibrosis airway epithelial Ca2+ i signaling: the mechanism for the larger agonist-mediated Ca2+ i signals in human cystic fibrosis airway epithelia.
J Biol Chem, 280(11): 10202-9. [Abstract] [Full-text]
- Fat absorption in cystic fibrosis mice is impeded by defective lipolysis and post-lipolytic events.
Am J Physiol Gastrointest Liver Physiol, 288(4): G646-53. [Abstract] [Full-text]
- Heat-stable enterotoxin of Escherichia coli stimulates a non-CFTR-mediated duodenal bicarbonate secretory pathway.
Am J Physiol Gastrointest Liver Physiol, 288(4): G654-63. [Abstract] [Full-text]
- Identification of N-acylhomoserine lactones in mucopurulent respiratory secretions from cystic fibrosis patients.
FEMS Microbiol Lett, 244(2): 297-304. [Abstract] [Full-text]
- Erythrocytes of humans with cystic fibrosis fail to stimulate nitric oxide synthesis in isolated rabbit lungs.
Am J Physiol Heart Circ Physiol, 288(4): H1580-5. [Abstract] [Full-text]
- Novel molecular approaches to cystic fibrosis gene therapy.
Biochem J, 387: 1-15. [Abstract] [Full-text]
- Increased prevalence of chronic rhinosinusitis in carriers of a cystic fibrosis mutation.
Arch Otolaryngol Head Neck Surg, 131(3): 237-40. [Abstract] [Full-text]
- Novel mouse model of chronic Pseudomonas aeruginosa lung infection mimicking cystic fibrosis.
Infect Immun, 73(4): 2504-14. [Abstract] [Full-text]
- Lack of association of common cystic fibrosis transmembrane conductance regulator gene mutations with primary sclerosing cholangitis.
Am J Gastroenterol, 100(4): 874-8. [Abstract] [Full-text]
- Cystic fibrosis prenatal screening in genetic counseling practice: recommendations of the National Society of Genetic Counselors.
J Genet Couns, 14(1): 1-15. [Abstract] [Full-text]
- A survey of sexual and reproductive health in men with cystic fibrosis: new challenges for adolescent and adult services.
Thorax, 60(4): 326-30. [Abstract] [Full-text]
- Association of tumour necrosis factor alpha variants with the CF pulmonary phenotype.
Thorax, 60(4): 320-5. [Abstract] [Full-text]
- Airway gene therapy and cystic fibrosis.
J Paediatr Child Health, 41(3): 94-6. [Abstract] [Full-text]
- Optical detection and discrimination of cystic fibrosis-related genetic mutations using oligonucleotide-nanoparticle conjugates.
Anal Bioanal Chem, 381(6): 1122-9. [Abstract] [Full-text]
- Bcl-2 sustains increased mucous and epithelial cell numbers in metaplastic airway epithelium.
Am J Respir Crit Care Med, 171(7): 764-72. [Abstract] [Full-text]
- The effect of varying tonicity on nasal epithelial ion transport in cystic fibrosis.
Am J Respir Crit Care Med, 171(7): 760-3. [Abstract] [Full-text]
- Assessment of nutritional status in adult patients with cystic fibrosis: whole-body bioimpedance vs body mass index, skinfolds, and leg-to-leg bioimpedance.
J Am Diet Assoc, 105(4): 549-55. [Abstract] [Full-text]
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