Millie Garg
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Explore the profile of Millie Garg including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
208
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Recent Articles
1.
Perron J, Uther P, Coffey M, Lovell-Simons A, Bartlett A, McKay A, et al.
Med Teach
. 2024 Mar;
47(1):126-133.
PMID: 38460191
Purpose: Serious games (SGs) have great potential for pediatric medical education. This study evaluated the efficacy of a SG in improving learner satisfaction, knowledge, and behavior. Materials And Methods: This...
2.
Coffey M, Garg M, Homaira N, Jaffe A, Ooi C
Paediatr Respir Rev
. 2020 Sep;
39:61-64.
PMID: 32917517
No abstract available.
3.
Coffey M, Low I, Stelzer-Braid S, Wemheuer B, Garg M, Thomas T, et al.
PLoS One
. 2020 May;
15(5):e0233557.
PMID: 32442222
Intestinal bacterial dysbiosis is evident in children with cystic fibrosis (CF) and intestinal viruses may be contributory, given their influence on bacterial species diversity and biochemical cycles. We performed a...
4.
Coffey M, Garg M, Homaira N, Jaffe A, Ooi C
Cochrane Database Syst Rev
. 2020 Jan;
1:CD012949.
PMID: 31962375
Background: Cystic fibrosis (CF) is a multisystem disease and the importance of growth and nutrition has been well established, given its implications for lung function and overall survival. It has...
5.
Coffey M, Nielsen S, Wemheuer B, Kaakoush N, Garg M, Needham B, et al.
Sci Rep
. 2019 Dec;
9(1):18593.
PMID: 31819107
Intestinal dysbiosis has been observed in children with cystic fibrosis (CF), yet the functional consequences are poorly understood. We investigated the functional capacity of intestinal microbiota and inflammation in children...
6.
Tham A, Katz T, Sutherland R, Garg M, Liu V, Tong C, et al.
J Cyst Fibros
. 2019 Sep;
19(1):146-152.
PMID: 31530443
Background: Children with CF have been reported to consume significantly more energy-dense, nutrient-poor foods than controls where there are now concerns of inadequate micronutrient intake. There are no current or...
7.
Ooi C, Syed S, Rossi L, Garg M, Needham B, Avolio J, et al.
Sci Rep
. 2018 Dec;
8(1):17834.
PMID: 30546102
Cystic fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Next to progressive airway disease, CF is also associated with intestinal inflammation and dysbiosis....
8.
Garg M, Swab M, Gibney D, Cohen J, Gupta N, Ooi C
JPEN J Parenter Enteral Nutr
. 2017 Dec;
42(3):607-612.
PMID: 29187050
Background: The purpose of this study is to determine whether direct involvement by dietitians in parenteral nutrition (PN) ordering resulted in a reduction in PN prescriptions errors. Methods: A prospective...
9.
Garg M, Leach S, Day A, Ooi C
J Cyst Fibros
. 2017 Nov;
17(1):e10-e11.
PMID: 29128316
No abstract available.
10.
Garg M, Leach S, Pang T, Needham B, Coffey M, Katz T, et al.
J Cyst Fibros
. 2017 Jul;
17(1):109-113.
PMID: 28754328
Background: The pathogenesis of gut inflammation, bacterial dysbiosis and increased rates of malignancy in CF is unclear. Fecal M2-pyruvate kinase (M2-PK) is a biomarker indicative of cellular proliferation that may...