Philippe A Lysy
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Explore the profile of Philippe A Lysy including associated specialties, affiliations and a list of published articles.
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Articles
45
Citations
768
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Recent Articles
1.
Polle O, Pyr Dit Ruys S, Lemmer J, Hubinon C, Martin M, Herinckx G, et al.
Sci Rep
. 2024 Sep;
14(1):20798.
PMID: 39242727
Partial remission (PR) occurs in only half of people with new-onset type 1 diabetes (T1D) and corresponds to a transient period characterized by low daily insulin needs, low glycemic fluctuations...
2.
Beckers M, Polle O, Gallo P, Bernard N, Bugli C, Lysy P
J Diabetes Res
. 2024 Jun;
2023:5568663.
PMID: 38846373
Aims: New-onset type 1 diabetes mellitus (T1D) in pediatric patients represents a clinical challenge for initial total daily insulin dosing (TIDD) due to substantial heterogeneity in practice and lack of...
3.
Welsch S, Harvengt A, Gallo P, Martin M, Beckers D, Mouraux T, et al.
Diabetes Metab J
. 2024 Mar;
48(5):949-959.
PMID: 38523249
Backgruound: Recent diabetes subclassifications have improved the differentiation between patients with type 1 diabetes mellitus (T1DM) and type 2 diabetes mellitus despite several overlapping features, yet without considering genetic forms...
4.
De Schepper J, Thomas M, Huysentruyt K, Becker M, Boros E, Casteels K, et al.
Horm Res Paediatr
. 2024 Mar;
PMID: 38432193
Introduction A variable near adult height (NAH) outcome after growth hormone (GH) therapy in Noonan syndrome (NS) patients with short stature has been reported. The main objective of this study...
5.
Harvengt A, Polle O, Martin M, van Maanen A, Gatto L, Lysy P
PLoS One
. 2023 Nov;
18(11):e0294982.
PMID: 38033011
Aims: To evaluate whether parameters of post-hypoglycemic hyperglycemia (PHH) correlated with glucose homeostasis during the first year after type 1 diabetes onset and helped to distinguish pediatric patients undergoing partial...
6.
Landen L, De Leener A, Le Roux M, Brichard B, Aydin S, Maiter D, et al.
Front Endocrinol (Lausanne)
. 2023 Aug;
14:1204793.
PMID: 37564981
Introduction: Von Hippel Lindau (VHL) syndrome is caused by an autosomal dominant hereditary or sporadic germline mutation of the gene with more than five hundred pathogenic mutations identified. Pheochromocytomas and...
7.
Souabni S, Harvengt A, Legat C, Lysy P
Clin Case Rep
. 2023 May;
11(6):e7336.
PMID: 37257167
Kabuki syndrome is a congenital condition characterized by a set of facial dysmorphic features that often help the clinician to suspect the diagnosis. However, more insidious symptoms can rarely occur,...
8.
Welsch S, Mailleux V, le Hardy de Beaulieu P, Ranguelov N, Godefroid N, Robert A, et al.
Front Pediatr
. 2023 Feb;
11:1080905.
PMID: 36824650
Background: Hyperglycemia (HG) and prediabetes are rarely sought in pediatric liver (LT) and renal (RT) transplantation, yet their presence indicates a high risk of diabetes and cardiovascular disease. The objectives...
9.
Boutsen L, Costenoble E, Polle O, Erdem K, Bugli C, Lysy P
Ther Adv Endocrinol Metab
. 2023 Jan;
14:20420188221145550.
PMID: 36699944
Objective: To evaluate the residual effect of partial remission (PR) on immediate post-PR glycemic control according to its occurrence and duration in a cohort of children with type 1 diabetes...
10.
De Ridder F, Charleer S, Jacobs S, Bolsens N, Ledeganck K, Van Aken S, et al.
Front Pediatr
. 2022 Oct;
10:991633.
PMID: 36275049
Objective: Real-time continuous glucose monitoring (RT-CGM) can improve metabolic control and quality of life (QoL), but long-term real-world data in children with type 1 diabetes (T1D) are scarce. Over a...