False normal Lung Clearance Index in infants with cystic fibrosis due to software algorithms. - Wikidata - awgldk - TriplyDB

False normal Lung Clearance Index in infants with cystic fibrosis due to software algorithms.

False normal Lung Clearance Index in infants with cystic fibrosis due to software algorithms.

http://www.wikidata.org/entity/Q50865804

about

Key paediatric messages from Amsterdam Feasibility of multiple breath washout measurements in infants with bronchiolitis: A pilot study.Pediatric Pulmonology year in review 2015: Part 1.The use of multiple breath washout for assessing cystic fibrosis in infants.Lack of transparency in software used to analyze multiple breath washout data.End-inspiratory molar mass step correction for analysis of infant multiple breath washout tests.In vitro and in vivo functional residual capacity comparisons between multiple-breath nitrogen washout devices.The effect of inert gas choice on multiple breath washout in healthy infants: differences in lung function outcomes and breathing pattern.Unexpected results in infant multiple breath washout: Is the truth hidden in the washin?Multiple breath washout: From Renaissance to Enlightenment?Novel methodology to perform sulfur hexafluoride (SF6)-based multiple-breath wash-in and washout in infants using current commercially available equipment.Lung clearance index and moment ratios at different cut-off values in infant multiple-breath washout measurements.How to Monitor Early Cystic Fibrosis Lung Disease. By Multiple-Breath Washout, Chest Computed Tomography, or Both?Last Word on Viewpoint: Using the same cut-off for sulfur hexafluoride and nitrogen multiple-breath washout may not be appropriate.Accurate lung volume measurements in vitro using a novel inert gas washout method suitable for infants.

P2860

Q28596669-A243211F-0051-4B0C-8E82-26539DCDA8AC Q38754980-E54099E6-19EA-42CC-9920-389913F127E4 Q38819881-425AB153-64A5-40FC-A917-64E766C16DB9 Q39031790-763AFCE7-F583-4930-806C-C7E0C3C09A57 Q44484012-30898BF4-BCEF-4C56-9724-9648E4F1683A Q44705966-898B84AD-5925-44E9-B6B7-26AAB2CFB9BC Q47123658-C264565E-0E14-4EAE-B2AE-86F8D3009FC6 Q47690732-16D20AB7-5CD2-4792-81E2-1D106052D1D9 Q47901076-6E09DA9E-2FB2-4AAD-B685-0856B45E7928 Q50802755-4122A9AC-D9F4-4CC5-98D7-B80DF7A3AF52 Q51427842-1CC8EC40-3C42-483F-AA35-76B3EE15D841 Q51519754-229CE53B-FEB8-4A6C-A215-7D5BA4701FA1 Q51560369-1DB07CAE-2349-467E-928F-3B7D31BACF88 Q51564965-C530733D-2C73-4867-B078-34AFB601D5A2 Q51569128-43B039D8-B96F-4F07-B8E4-241AB0A7F7C6

P2860

False normal Lung Clearance Index in infants with cystic fibrosis due to software algorithms.

http://www.wikidata.org/entity/Q50865804

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh-hant

name

False normal Lung Clearance In ...... is due to software algorithms.

@en

False normal Lung Clearance In ...... is due to software algorithms.

@nl

type

label

False normal Lung Clearance In ...... is due to software algorithms.

@en

False normal Lung Clearance In ...... is due to software algorithms.

@nl

prefLabel

False normal Lung Clearance In ...... is due to software algorithms.

@en

False normal Lung Clearance In ...... is due to software algorithms.

@nl

P1433

Q50865804-366D98B8-D87C-4C6C-A0C2-37826C4018DD

P1476

Q50865804-20AF69D8-DE1D-4511-83DC-43AA5CEA5AA9

P2093

Q50865804-11F1CAA3-1636-4C20-82E6-8964612AD622

Q50865804-191439EA-7A8A-4E13-93FD-A004D61CF450

Q50865804-417D1AAF-AF60-430A-BAE2-D23D6C1BFB52

Q50865804-4C7307D6-49AD-43C7-8CB9-D2D631B51C4F

Q50865804-572C4661-42DD-47C8-B53C-68BBF51F9C13

Q50865804-664A807A-5F5A-4A75-82EA-8A25AE429E42

Q50865804-A249A2BC-B9BF-4861-BA2A-D3F1AEFB787F

Q50865804-C454B5B3-D1DE-4D4B-BEB8-CEE32A9A98B5

P2860

Q50865804-020408E8-2C7C-4C2F-B0DE-402355598F3F

Q50865804-0EEE462A-DF22-4AEC-AF40-EF40B0D9B9B1

Q50865804-127FA97E-BC14-486B-89DD-7777DDCE25B8

Q50865804-13C75177-81D3-43F7-9B05-B52A1D0F16B2

Q50865804-14BE2503-6A96-4976-B44B-ED2726570813

Q50865804-15682E93-A492-49E5-8CCC-BD136407742B

Q50865804-19D38DE2-CC17-4A9C-BB8C-CA108260F57C

Q50865804-1A7013EA-95EF-4D17-8AD0-E49E16FBF85A

Q50865804-1A7AA081-5E21-408C-8CAA-D5B8F974144A

Q50865804-2D7B80E9-B256-4CC4-ACDB-B89B426C0C7C

P304

Q50865804-7C931FE8-A223-43F9-A736-3406F27FAB9A

P31

Q50865804-69B9A83F-9492-4299-AEC5-B6854DC72341

P356

Q50865804-00FEFF20-592D-4D72-AA54-681934C82A78

P433

Q50865804-D194A707-1C1B-465D-9104-83662E06B75D

P478

Q50865804-C22C26F4-C5F5-4B7E-8135-5AFDB23B0296

P50

Q50865804-1EE82463-8212-4B3B-80F3-B67F0E3638A7

Q50865804-A2602FE7-24D8-4333-BDEB-EA49833ED509

Q50865804-CB31FCD9-E55A-4D2C-8C3F-2099DF15858A

P577

Q50865804-9580F717-50F8-402B-8904-662526682E9B

P698

Q50865804-756F32FE-70E6-4B1F-94A1-A311FF046AC5

P921

Q50865804-597D8764-B0B4-4250-9A35-61B4125D642A

P356

P1433

Pediatric Pulmonology

P1476

False normal Lung Clearance In ...... sis due to software algorithms

@en

P2093

Anne Schmidt

http://www.w3.org/2001/XMLSchema#string

Carmen Casaulta

http://www.w3.org/2001/XMLSchema#string

Daniel Trachsel

http://www.w3.org/2001/XMLSchema#string

Elisabeth Kieninger

http://www.w3.org/2001/XMLSchema#string

Gaudenz Hafen

http://www.w3.org/2001/XMLSchema#string

Ines Mack

http://www.w3.org/2001/XMLSchema#string

Insa Korten

http://www.w3.org/2001/XMLSchema#string

Sophie Yammine

http://www.w3.org/2001/XMLSchema#string

P2860

Lung clearance index: evidence for use in clinical trials in cystic fibrosis

Lung volume, breathing pattern and ventilation inhomogeneity in preterm and term infants.

Normative data for lung function and exhaled nitric oxide in unsedated healthy infants.

Air trapping on chest CT is associated with worse ventilation distribution in infants with cystic fibrosis diagnosed following newborn screening.

Retrospective analysis of stored dried blood spots from children with cystic fibrosis and matched controls to assess the performance of a proposed newborn screening protocol in Switzerland.

Lung function in African infants: a pilot study

Lung clearance index as an outcome measure for clinical trials in young children with cystic fibrosis. A pilot study using inhaled hypertonic saline

Interpretation of lung function in infants and young children with cystic fibrosis.

Consensus statement for inert gas washout measurement using multiple- and single- breath tests.

Practicability of nitrogen multiple-breath washout measurements in a pediatric cystic fibrosis outpatient setting.

P304

970-977

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/PPUL.23256

http://www.w3.org/2001/XMLSchema#string

P433

10

http://www.w3.org/2001/XMLSchema#string

P478

50

http://www.w3.org/2001/XMLSchema#string

P50

Alexander Moeller

Pinelopi Anagnostopoulou

P577

2015-08-18T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

26285162

http://www.w3.org/2001/XMLSchema#string

P921

cystic fibrosis