Sonya Heltshe
Overview
Explore the profile of Sonya Heltshe including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
256
Followers
0
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Recent Articles
1.
Somayaji R, Wessels M, Milinic T, Ramos K, Mayer-Hamblett N, Ramsey B, et al.
J Cyst Fibros
. 2023 Jun;
22(4):669-673.
PMID: 37286384
Introduction: Although work to date in cystic fibrosis (CF) has elucidated frequencies and characteristics of adverse events, the accuracy of attribution of relatedness to study drug by investigators has not...
2.
Roesch E, Bonfield T, Lazarus H, Reese J, Hilliard K, Hilliard J, et al.
J Cyst Fibros
. 2022 Dec;
22(3):407-413.
PMID: 36549988
Background: Mesenchymal stem cells are of particular interest in cystic fibrosis (CF) as a potential therapeutic. Data from pre-clinical studies suggest that allogeneic bone marrow-derived human mesenchymal stem cells (hMSCs)...
3.
Magaret A, Warden M, Simon N, Heltshe S, Retsch-Bogart G, Ramsey B, et al.
J Cyst Fibros
. 2021 Dec;
21(2):293-299.
PMID: 34879997
Background: Given future challenges in conducting large randomized, placebo controlled trials for future CF therapeutics development, we evaluated the potential for using external historical controls to either enrich or replace...
4.
Sathe M, Huang R, Heltshe S, Eng A, Borenstein E, Miller S, et al.
J Pediatr Gastroenterol Nutr
. 2021 May;
73(3):395-402.
PMID: 34016873
Objectives: To identify factors that increase the risk of gastrointestinal-related (GI-related) hospitalization of infants with cystic fibrosis (CF) during the first year of life. Methods: The Baby Observational and Nutrition...
5.
Pittman J, Khan U, Laguna T, Heltshe S, Goss C, Sanders D
J Cyst Fibros
. 2021 Mar;
20(6):972-977.
PMID: 33745860
Background: Cystic fibrosis (CF) is an autosomal recessive disease characterized by chronic sinopulmonary symptoms and chronic gastrointestinal symptoms that begins in infancy. Children with CF are increasingly being included in...
6.
Holtrop M, Heltshe S, Shabanova V, Keller A, Schumacher L, Fernandez L, et al.
Ann Am Thorac Soc
. 2021 Feb;
18(7):1158-1166.
PMID: 33544657
Epidemiologic studies demonstrate worse outcomes in women with cystic fibrosis (CF) than men. Women are colonized earlier with respiratory pathogens and have increased rates of pulmonary exacerbations after puberty and...
7.
Magaret A, Warden M, Simon N, Heltshe S, Mayer-Hamblett N
J Cyst Fibros
. 2020 Apr;
19(3):e11-e12.
PMID: 32291159
No abstract available.
8.
Gelfond D, Heltshe S, Ma C, Rowe S, Frederick C, Uluer A, et al.
Clin Transl Gastroenterol
. 2017 Mar;
8(3):e81.
PMID: 28300821
Objectives: A defect in bicarbonate secretion contributes to the pathophysiology of gastrointestinal complications in patients with cystic fibrosis (CF). We measured gastrointestinal pH, clinical outcomes, and intestinal transit profiles in...
9.
Koutros S, Silverman D, Alavanja M, Andreotti G, Lerro C, Heltshe S, et al.
Int J Epidemiol
. 2015 Sep;
45(3):792-805.
PMID: 26411407
Background: In the developed world, occupational exposures are a leading cause of bladder cancer. A few studies have suggested a link between pesticide exposures among agricultural populations and bladder cancer....
10.
Subbarao P, Milla C, Aurora P, Davies J, Davis S, Hall G, et al.
Ann Am Thorac Soc
. 2015 Jun;
12(6):932-9.
PMID: 26075554
The lung clearance index (LCI) is a lung function parameter derived from the multiple-breath washout (MBW) test. Although first developed 60 years ago, the technique was not widely used for...