Arlene Stecenko
Overview
Explore the profile of Arlene Stecenko including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
18
Citations
555
Followers
0
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Recent Articles
1.
Zaveri S, Stecenko A, Hunt W, Goss A, Sharma P, Hartman T, et al.
BMJ Open
. 2024 Dec;
14(12):e092503.
PMID: 39725418
Introduction: People with cystic fibrosis (PwCF) are at high risk for developing cystic fibrosis (CF)-related diabetes (CFRD), which worsens morbidity and mortality. Although the pathological events leading to the development...
2.
Song J, McNeany J, Wang Y, Daley T, Stecenko A, Kamaleswaran R
Comput Biol Med
. 2024 Oct;
183:109255.
PMID: 39405732
Background: Continuous Glucose Monitoring (CGM) provides a detailed representation of glucose fluctuations in individuals, offering a rich dataset for understanding glycemic control in diabetes management. This study explores the potential...
3.
Gonzalez-Rosales N, Kasi A, McCracken C, Silva G, Starks M, Stecenko A, et al.
Pediatr Pulmonol
. 2022 Dec;
58(3):871-877.
PMID: 36479634
Background: Viral respiratory infections trigger pulmonary exacerbations (PEs) in children with cystic fibrosis (CF), but their clinical impact is not well understood. Methods: A retrospective review of pediatric patients with...
4.
Dilernia D, Amin P, Flores J, Stecenko A, Sorscher E
Hum Mutat
. 2022 Feb;
43(5):595-603.
PMID: 35170824
Current approaches to characterize the mutational profile of the cystic fibrosis transmembrane conductance regulator (CFTR) gene are based on targeted mutation analysis or whole gene studies derived from short-read next...
5.
Patel M, McCracken C, Daley T, Stecenko A, Linnemann R
Pediatr Pulmonol
. 2021 Aug;
56(5):901-909.
PMID: 34402224
Introduction: Annual oral glucose tolerance testing (OGTT) is the recommended screening modality for cystic fibrosis-related diabetes (CFRD) in patients with cystic fibrosis (CF). This study aimed to determine if there...
6.
Middour-Oxler B, Bergman S, Blair S, Pendley S, Stecenko A, Hunt W
J Pediatr Nurs
. 2021 Jun;
62:177-183.
PMID: 34172371
Background: The aim of this study was to survey young adults who participated in either a formal or semi-formal transition program at one cystic fibrosis (CF) care center to compare...
7.
Bedi B, Lin K, Maurice N, Yuan Z, Bijli K, Koval M, et al.
Clin Sci (Lond)
. 2020 Jun;
134(14):1911-1934.
PMID: 32537652
Cystic fibrosis (CF) is a progressive multiorgan autosomal recessive disease with devastating impact on the lungs caused by derangements of the CF transmembrane conductance regulator (CFTR) gene. Morbidity and mortality...
8.
Zang X, Monge M, Gaul D, McCarty N, Stecenko A, Fernandez F
J Proteome Res
. 2019 Oct;
19(1):144-152.
PMID: 31621328
The most common cause of death in cystic fibrosis (CF) patients is progressive lung function decline, which is punctuated by acute pulmonary exacerbations (APEs). A major challenge is to discover...
9.
Yadav R, Yoo D, Kahlenberg J, Bridges Jr S, Oni O, Huang H, et al.
J Cyst Fibros
. 2019 Jan;
18(5):636-645.
PMID: 30638826
Cystic fibrosis (CF) airway disease is characterized by the long-term presence of neutrophil granulocytes. Formation of neutrophil extracellular traps (NETs) and/or autoantibodies directed against extracellular components of NETs are possible...
10.
DeMuth K, Stecenko A, Sullivan K, Fitzpatrick A
Allergy Asthma Proc
. 2013 May;
34(3):227-32.
PMID: 23676571
Food allergy affects 8% of preschool children, but factors responsible for food allergy in children are poorly understood. Use of antacid medication may be a contributing factor. The purpose of...