Last Posted: Jul 31, 2019
- Advances In Gene Therapy For Cystic Fibrosis Lung Disease.
Yan Ziying et al. Human molecular genetics 2019 Jul - Making precision medicine personal for cystic fibrosis.
Manfredi Candela et al. Science (New York, N.Y.) 2019 365(6450) 220-221 - Positive Newborn Screening for Cystic Fibrosis, What to Do Next?
Kumar Prawin et al. Indian journal of pediatrics 2019 Jul - Next generation microbiology and cystic fibrosis diagnostics: are we there yet?
Moser Claus et al. Current opinion in pulmonary medicine 2018 11 (6) 599-605 - Interventions for treating neuropathic pain in people with sickle cell disease.
Asnani Monika R et al. The Cochrane database of systematic reviews 2019 Jul 7CD012943 - [Selection of lung transplant candidates in France in 2019].
Falque L et al. Revue des maladies respiratoires 2019 Apr 36(4) 508-518 - Unraveling the CFTR Function-Phenotype Connection for Precision Treatment in Cystic Fibrosis.
Zemanick Edith T et al. American journal of respiratory and critical care medicine 2019 May 199(9) 1053-1054 - Epidemiology of rare diseases detected by newborn screening in the Czech Republic.
David Jan et al. Central European journal of public health 2019 Jun 27(2) 153-159 - Identification of 99% of CFTR gene mutations in Bulgarian-, Bulgarian Turk-, and Roma cystic fibrosis patients.
Petrova Guergana et al. Molecular genetics & genomic medicine 2019 Jun e696 - Late diagnosis and poor nutrition in cystic fibrosis diagnosed before implementation of newborn screening.
Pedersen Maya Graham et al. Acta paediatrica (Oslo, Norway : 1992) 2019 Jun
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