Gefragt von: Isabelle Monk
Fragesteller Allgemeines

Journal Of Cystic Fibrosis Login

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Zuletzt aktualisiert: 2021-04-09

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Cystic Fibrosis - Physiopedia

Cystic fibrosis (CF) is the most frequent cause of suppurative lung disease in the younger Caucasian population. A depleted volume of the airway surface liquid (ASL) layer in the respiratory system leads to abnormal mucociliary clearance[2]. A chronic cycle of infection and inflammation results in progressive suppurative bronchiectasis and lung damage.
Url: https://www.physio-pedia.com/Cystic_Fibrosis
Cystic Fibrosis - Physiopedia

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Home Page: Journal of Vascular Surgery

21.07.2020 · Journal of Vascular Surgery® is dedicated to the science and art of vascular surgery and aims to be the premier international journal of medical, endovascular and surgical care of vascular diseases. Since the first issue was released in 1984, the goal of the journal has been to improve the management of patients with vascular diseases by publishing relevant papers that report important ...
Url: https://www.jvascsurg.org/
Home Page: Journal of Vascular Surgery

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Supplemental Materials for The association …

Staphylococcus aureus (S. aureus) may be related to more rapid progression of cystic fibrosis (CF) lung disease. Supplemental Materials for The association between Staphylococcus aureus and subsequent bronchiectasis in children with cystic fibrosis - Journal of Cystic Fibrosis
Url: https://www.cysticfibrosisjournal.com/article/S1569-1993(17)30980-3/addons
Supplemental Materials for The association …

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Keep them breathing: Cystic fibrosis …

Cystic fibrosis (CF) affects more than 30,000 people in the United States and 80,000 people worldwide. This life-threatening genetic disorder causes a buildup of thick, viscous mucus secretions in various organ systems, most commonly the gastrointestinal, pulmonary, and genitourinary systems. This article reviews the clinical manifestations, diagnosis, and monitoring of patients with CF as ...
Url: https://journals.lww.com/jaapa/Fulltext/2017/05000/Keep_them_breathing__Cystic_fibrosis.4.aspx
Keep them breathing: Cystic fibrosis …

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Cystic Fibrosis | American Academy of Pediatrics

Cystic fibrosis (CF) is one of the most commonly diagnosed genetic disorders. Clinical characteristics include progressive obstructive lung disease, sinusitis, exocrine pancreatic insufficiency leading to malabsorption and malnutrition, liver and pancreatic dysfunction, and male infertility. Although CF is a life-shortening disease, survival has continued to improve to a median age of 46.2 ...
Url: https://pedsinreview.aappublications.org/content/42/2/55
Cystic Fibrosis | American Academy of Pediatrics

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Clinical Practice Guidelines From the Cystic …

Cystic fibrosis (CF) clinical care guidelines exist for the care of infants up to age 2 years and for individuals ≥6 years of age. An important gap exists for preschool children between the ages of 2 and 5 years. This period marks a time of growth and development that is critical to achieve optimal nutritional status and maintain lung health.
Url: https://pediatrics.aappublications.org/content/137/4/e20151784
Clinical Practice Guidelines From the Cystic …

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Home Page: Respiratory Medicine

Respiratory Medicine is a leading, International journal devoted to the rapid publication of the most up-to-date information in the field of respiratory medicine. It publishes a wide range of original articles and topical reviews dealing with all aspects of respiratory diseases and therapy. Topics include adult and paediatric medicine, epidemiology, immunology and cell biology, physiology ...
Url: https://www.resmedjournal.com/
Home Page: Respiratory Medicine

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Soft "sweat stickers" may streamline diagnosis of …

31.03.2021 · New ''sweat stickers'' may streamline the early diagnosis of cystic fibrosis by enabling scientists to easily gather and analyze sweat from the skin of infants and children.
Url: https://www.eurekalert.org/pub_releases/2021-03/aaft-ss033121.php
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Therapy for most common cause of cystic …

Cystic fibrosis is a progressive genetic disease that damages multiple organs, including the lungs and pancreas. Currently, average life expectancy is 47 years. The disease is caused by mutations ...
Url: https://www.eurekalert.org/pub_releases/2021-03/arh-tfm031821.php
Therapy for most common cause of cystic …

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Cystic Fibrosis: Professor Jane Davies | PaeCH Teaching for Trainees

Cystic Fibrosis: Professor Jane Davies | PaeCH Teaching for Trainees

Added by: Journal of General Physiology

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Identifying the molecular target sites for CFTR potentiators GLPG1837 and VX-770 - Yeh et al.

Identifying the molecular target sites for CFTR potentiators GLPG1837 and VX-770 - Yeh et al.

Added by: JoVE (Journal of Visualized Experiments)

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Testing Antibiotic Efficacy Against Pseudomonas aeruginosa: Cystic Fibrosis Lung l Protocol Preview

Testing Antibiotic Efficacy Against Pseudomonas aeruginosa: Cystic Fibrosis Lung l Protocol Preview

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CF Journal Creating Nutrition Content

CF Journal Creating Nutrition Content

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Nana.scookingcraftcorner-Cystic Fibrosis Journal-Finish Project Jun 6,2020

Nana.scookingcraftcorner-Cystic Fibrosis Journal-Finish Project Jun 6,2020

Added by: Cystic Fibrosis Foundation

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ResearchCon 2021 | Exploring the Unique Cystic Fibrosis Challenges Within the GI Tract

ResearchCon 2021 | Exploring the Unique Cystic Fibrosis Challenges Within the GI Tract

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Genomics in the Virtual Lab, Student Project Presentation: Cystic Fibrosis and CTFR mutations

Genomics in the Virtual Lab, Student Project Presentation: Cystic Fibrosis and CTFR mutations

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Nana.scookingcraftcorner-Cystic Fibrosis Journal=Livechat

Nana.scookingcraftcorner-Cystic Fibrosis Journal=Livechat

Added by: The University of Edinburgh

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UK's first cystic fibrosis gene therapy trial

UK's first cystic fibrosis gene therapy trial

Added by: Duke Health

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Leading an Active Life with Cystic Fibrosis | Duke Health

Leading an Active Life with Cystic Fibrosis | Duke Health
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