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Mark Chilvers

seattle children's hospital
H指数:33
被引数:4,743

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European Respiratory Society and American Thoracic Society guidelines for the diagnosis of primary ciliary dyskinesia

欧洲呼吸学会和美国胸科学会关于原发性纤毛运动障碍诊断指南。Eur. Respir. J. 26, 2500745

2025-12-016
PRE
A Review of Newborn Screening Programs for Cystic Fibrosis: Are Current Protocols Appropriate for Canada's Diverse Population?

对囊性纤维化新生儿筛查计划的综述:现行的方案是否适用于加拿大多元化人口?

2025-11-180
OAAI
A Germline Heterozygous Dominant Negative IKZF2 Variant Causing Syndromic Primary Immune Regulatory Disorder and ICHAD

一个导致综合征性原发性免疫调节紊乱和ICHAD的生殖系杂合显性负性IKZF2变异体

2025-04-280
OA
Standards for the care of people with cystic fibrosis; establishing and maintaining health
2024-01-0130
OAAI
High-quality read-based phasing of cystic fibrosis cohort informs genetic understanding of disease modification
2023-01-013
OAAI
A Phase 3, open-label, 96-week trial to study the safety, tolerability, and efficacy of tezacaftor/ivacaftor in children ≥ 6 years of age homozygous for F508del or heterozygous for F508del and a residual function CFTR variant
2022-07-018
OAAI
Outcomes of Cystic Fibrosis Screening-Positive Infants With Inconclusive Diagnosis at School Age
2021-12-0128
PRE
Cystic fibrosis-related diabetes onset can be predicted using biomarkers measured at birth (vol 23, pg 927, 2021)
2021-11-010
OAAI
Cystic fibrosis-related diabetes onset can be predicted using biomarkers measured at birth
2021-05-0116
OAAI
Epidemiology of Clonal Pseudomonas aeruginosa Infection in a Canadian Cystic Fibrosis Population
2018-07-0114
PREAI
Diagnosis of Primary Ciliary Dyskinesia An Official American Thoracic Society Clinical Practice Guideline
2018-06-15307
OAAI