Poor recovery from cystic fibrosis pulmonary exacerbations is associated with poor long-term outcomes.

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Poor recovery from cystic fibrosis pulmonary exacerbations is associated with poor long-term outcomes.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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name

Poor recovery from cystic fibr ...... with poor long-term outcomes.

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Poor recovery from cystic fibr ...... with poor long-term outcomes.

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type

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label

Poor recovery from cystic fibr ...... with poor long-term outcomes.

@en

Poor recovery from cystic fibr ...... with poor long-term outcomes.

@nl

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Poor recovery from cystic fibr ...... with poor long-term outcomes.

@en

Poor recovery from cystic fibr ...... with poor long-term outcomes.

@nl

P1476

Poor recovery from cystic fibr ...... with poor long-term outcomes.

@en

P2093

Philip M Farrell

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Qianqian Zhao

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Zhanhai Li

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P2860

Multi-ethnic reference values for spirometry for the 3-95-yr age range: the global lung function 2012 equations

Predictive 5-year survivorship model of cystic fibrosis.

Association of socioeconomic status with the use of chronic therapies and healthcare utilization in children with cystic fibrosis.

Oral, inhaled, and intravenous antibiotic choice for treating pulmonary exacerbations in cystic fibrosis.

Failure to recover to baseline pulmonary function after cystic fibrosis pulmonary exacerbation

The cost of medical care for patients with cystic fibrosis in a health maintenance organization.

Pulmonary exacerbations in cystic fibrosis: young children with characteristic signs and symptoms

Socioeconomic status and the likelihood of antibiotic treatment for signs and symptoms of pulmonary exacerbation in children with cystic fibrosis

Outcome measures for clinical trials assessing treatment of cystic fibrosis lung disease.

Cystic fibrosis pulmonary exacerbations.

P304

1268-1275

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P31

scholarly article

P356

10.1002/PPUL.23765

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P433

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P478

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P50

Don B Sanders

P577

2017-09-07T00:00:00Z

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P698

28881091

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P921

cystic fibrosis

P932

5639928

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