Louise S Conwell
Overview
Explore the profile of Louise S Conwell including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
35
Citations
436
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
De Leon D, Arnoux J, Banerjee I, Bergada I, Bhatti T, Conwell L, et al.
Horm Res Paediatr
. 2023 Jul;
97(3):279-298.
PMID: 37454648
Background: Hyperinsulinism (HI) due to dysregulation of pancreatic beta-cell insulin secretion is the most common and most severe cause of persistent hypoglycemia in infants and children. In the 65 years...
2.
Jeffery T, Chang A, Conwell L
Cochrane Database Syst Rev
. 2023 Jan;
1:CD002010.
PMID: 36625789
Background: Osteoporosis is a disorder of bone mineralisation occurring in about one third of adults with cystic fibrosis. Bisphosphonates can increase bone mineral density and decrease the risk of new...
3.
Vanderniet J, Neville K, Conwell L, Wegner E, Craig M, Adams S, et al.
J Paediatr Child Health
. 2022 Dec;
59(2):398-400.
PMID: 36511518
No abstract available.
4.
Musthaffa Y, Conwell L
J Paediatr Child Health
. 2020 Nov;
57(9):1519-1523.
PMID: 33233026
No abstract available.
5.
Musthaffa Y, Papadimos E, Fairchild J, Titmuss A, Corpus S, Huynh T, et al.
J Paediatr Child Health
. 2020 Aug;
57(5):727-731.
PMID: 32808382
No abstract available.
6.
Papadimos E, Perry E, Goodwin B, Conwell L
J Paediatr Child Health
. 2019 Dec;
56(7):1140-1143.
PMID: 31868246
No abstract available.
7.
Johnson S, Carter H, Leo P, Hollingworth S, Davis E, Jones T, et al.
Diabetes Care
. 2019 Apr;
42(5):e79-e80.
PMID: 31010948
No abstract available.
8.
Maharaj A, Buonocore F, Meimaridou E, Ruiz-Babot G, Guasti L, Peng H, et al.
J Endocr Soc
. 2019 Jan;
3(1):201-221.
PMID: 30620006
Primary adrenal insufficiency (PAI) is a potentially life-threatening condition that can present with nonspecific features and can be difficult to diagnose. We undertook next generation sequencing in a cohort of...
9.
Johnson S, Carter H, Leo P, Hollingworth S, Davis E, Jones T, et al.
Diabetes Care
. 2018 Dec;
42(1):69-76.
PMID: 30523035
Objective: Maturity-onset diabetes of the young (MODY) is an autosomal dominant form of diabetes, with multiple causative genes. Some MODY subtypes can be treated with sulfonylureas instead of insulin, improving...
10.
Johnson S, Ellis J, Leo P, Anderson L, Ganti U, Harris J, et al.
Pediatr Diabetes
. 2018 Sep;
20(1):57-64.
PMID: 30191644
Background: Maturity-onset diabetes of the young (MODY) is caused by autosomal dominant mutations in one of 13 confirmed genes. Estimates of MODY prevalence vary widely, as genetic screening is usually...