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M

Michelle Shaw

The Hospital for Sick Children

H指数:12

被引数:511

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Reducing multiple-breath washout test burden in cystic fibrosis: agreement between the first acceptable trial and mean lung clearance index

减少囊性纤维化中多呼吸洗出试验的负担：首次可接受试验与平均肺清除指数的一致性

Journal of Cystic Fibrosis

IF6

2026-09-120

PRE

Persistence of large P. aeruginosa aggregates despite reduced airway burden in people with cystic fibrosis on CFTR modulator therapy

尽管囊性纤维化患者在使用CFTR调节剂治疗后气道负荷降低，但仍存在大型铜绿假单胞菌聚集物

Journal of Cystic Fibrosis

IF6

2026-06-280

PRE

The Impact of Nutritional Status on Lung Function Trajectories in Pediatric Patients With Primary Ciliary Dyskinesia

营养状况对原发性纤毛运动障碍儿科患者肺功能轨迹的影响

Pediatric Pulmonology

IF2.3

2026-04-190

PRE

Sputum Biomarkers of Inflammation to Track Acute Respiratory Events in School-Age Children with Cystic Fibrosis

International Journal of Molecular Sciences

IF4.9

2026-02-070

OAAI

Long-Term Outcomes of Transarterial Embolization for Pulmonary Arteriovenous Malformations in Pediatric Hereditary Hemorrhagic Telangiectasia

经动脉栓塞术治疗儿童遗传性出血性毛细血管扩张症相关肺动静脉畸形的长期疗效

CardioVascular and Interventional Radiology

IF2.9

2025-12-280

PRE

Biomarkers associated with clinical response to cystic fibrosis pulmonary exacerbation treatment and adjuvant prednisone therapy

与囊性纤维化肺部恶化治疗临床反应及辅助泼尼松疗法相关的生物标志物

Journal of Cystic Fibrosis

IF6

2025-09-010

OAAI

Variability of lung function tests in primary ciliary dyskinesia

EUROPEAN RESPIRATORY JOURNAL

IF21

2024-10-300

PRE

Ventilation distribution efficiency or lung clearance index: Does it matter?

EUROPEAN RESPIRATORY JOURNAL

IF21

2024-10-300

PRE

A randomised trial of oral prednisone for cystic fibrosis pulmonary exacerbation treatment

EUROPEAN RESPIRATORY JOURNAL

IF21

2024-05-021

PRE

Cardiopulmonary Exercise Testing Provides Prognostic Information in Advanced Cystic Fibrosis Lung Disease

ANNALS OF THE AMERICAN THORACIC SOCIETY

IF5.4

2024-03-014

OAAI

Radtke, Thomas; Urquhart, Don S.; Braun, Julia; Barry, Peter J.; Waller, Ian; Petch, Nicole; Mei-Zahav, Meir; Kramer, Mordechai R.; Hua-Huy, Thong; Dinh-Xuan, Anh Tuan; Innes, J. Alastair; McArthur, Sara; Sovtic, Aleksandar; Gojsina, Bojana; Verges, Samuel; De Maat, Tanguy; Morrison, Lisa; Wood, Jamie; Crute, Samantha; Williams, Craig A.; Tomlinson, Owen W.; Bar-Yoseph, Ronen; Hebestreit, Alexandra; Quon, Bradley S.; Kwong, Eugenie; Saynor, Zoe L.; Causer, Adam J.; Stephenson, Anne L.; Schneiderman, Jane E.; Shaw, Michelle; Dwyer, Tiffany; Stevens, Daniel; Remus, Natascha; Douvry, Benoit; Foster, Karla; Benden, Christian; Ratjen, Felix; Hebestreit, Helge

SPLUNC1 as a biomarker of pulmonary exacerbations in children with cystic fibrosis

JOURNAL OF CYSTIC FIBROSIS

IF6

2024-03-012

PRE

Longitudinal Assessment of Curacao Criteria in Children with Hereditary Hemorrhagic Telangiectasia

JOURNAL OF PEDIATRICS

IF3.5

2023-12-017

PRE

Does timing of diagnosis effect outcome in primary ciliary dyskinesia?

EUROPEAN RESPIRATORY JOURNAL

IF21

2023-10-270

PRE

Disease manifestations in siblings with primary ciliary dyskinesia

EUROPEAN RESPIRATORY JOURNAL

IF21

2023-10-270

PRE

Factors associated with lung function response with oral antibiotic treatment of pulmonary exacerbations in cystic fibrosis

口服抗生素治疗囊性纤维化肺恶化与肺功能反应相关的因素

JOURNAL OF CYSTIC FIBROSIS

IF6

2023-09-012

PRE

Efficacy of Antibiotic Eradication Therapy of Early Pseudomonas aeruginosa Infection in Children with Primary Ciliary Dyskinesia

ANNALS OF THE AMERICAN THORACIC SOCIETY

IF5.4

2023-06-016

PRE

Comparative analysis of respiratory symptom scores to detect acute respiratory events in children with cystic fibrosis

JOURNAL OF CYSTIC FIBROSIS

IF6

2023-03-015

PRE

Impact of antibiotic eradication therapy of Pseudomonas aeruginosa on long term lung function in cystic fibrosis

JOURNAL OF CYSTIC FIBROSIS

IF6

2023-01-0112

PRE

The effect of antibiotic changes during treatment of cystic fibrosis pulmonary exacerbations

JOURNAL OF CYSTIC FIBROSIS

IF6

2022-09-016

PRE

Interleukin-1 beta is a potential mediator of airway nitric oxide deficiency in cystic fibrosis

JOURNAL OF CYSTIC FIBROSIS

IF6

2022-07-013

PRE