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Showing 37 to 44 of 44 entries
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[Pulmonary form of mucoviscidosis in 2 related infants. Report of 2 cases].

Polski tygodnik lekarski (Warsaw, Poland : 1960)

USZYCKA-KARCZ M, ZYCHOWICZ C.
PMID: 13779406
Pol Tyg Lek. 1960 Aug 08;15:1239-41.

No abstract available.

[Diabetes mellitus in cystic fibrosis].

Pneumologie (Stuttgart, Germany)

Ratjen F, Konietzko N.
PMID: 14732892
Pneumologie. 2004 Jan;58(1):5-6. doi: 10.1055/s-2003-812439.

No abstract available.

Cystic fibrosis since 1938.

American journal of respiratory and critical care medicine

Davis PB.
PMID: 16126935
Am J Respir Crit Care Med. 2006 Mar 01;173(5):475-82. doi: 10.1164/rccm.200505-840OE. Epub 2005 Aug 26.

Cystic fibrosis (CF) was distinguished from celiac disease in 1938. Then, it was a pathologic diagnosis, life expectancy was approximately 6 months, and the autosomal recessive disease was believed to arise from abnormal mucus plugging exocrine ducts. Death often...

Changing patterns of gastrointestinal manifestations of cystic fibrosis. Survey of recent progress in diagnosis and treatment.

Clinical pediatrics

Grand RJ.
PMID: 4952803
Clin Pediatr (Phila). 1970 Oct;9(10):588-93. doi: 10.1177/000992287000901008.

No abstract available.

Rebuttal from Mr Shepherd et al.

Chest

Shepherd SL, Goodrich EJ, Desch J, Quinton PM.
PMID: 24136087
Chest. 2014 Apr;145(4):684-685. doi: 10.1378/chest.13-2407.

No abstract available.

Cystic Fibrosis-Related Diabetes in Children: An Update.

Pediatric annals

Kim RJ.
PMID: 27622916
Pediatr Ann. 2016 Sep 01;45(9):e321-6. doi: 10.3928/19382359-20160815-01.

Cystic fibrosis-related diabetes mellitus (CFRD) is the most common endocrine complication of cystic fibrosis (CF), affecting more than 50% of patients by the 4th decade of life. CFRD is often preceded by worsening pulmonary status and nutritional decline. Treatment...

Gaps in the evidence for treatment decisions in cystic fibrosis: a systematic review.

Thorax

Rowbotham NJ, Smith S, Prayle AP, Robinson KA, Smyth AR.
PMID: 30301819
Thorax. 2019 Mar;74(3):229-236. doi: 10.1136/thoraxjnl-2017-210858. Epub 2018 Oct 09.

INTRODUCTION: Cystic fibrosis (CF) is a multisystem disorder. Treatment is complex and evidence for treatment decisions may be absent. Characterising gaps in the research evidence will highlight treatment uncertainties and help prioritise research questions. We systematically identified the evidence...

Female reproductive health in cystic fibrosis.

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Hughan KS, Daley T, Rayas MS, Kelly A, Roe A.
PMID: 31679735
J Cyst Fibros. 2019 Oct;18:S95-S104. doi: 10.1016/j.jcf.2019.08.024.

Women with cystic fibrosis (CF) are living longer and healthier lives, and opportunities for childbearing are increasingly promising. However, this population can also face sexual and reproductive health concerns, including menstrual irregularities, unplanned pregnancies, infertility and pregnancy complications. Additionally,...

Showing 37 to 44 of 44 entries