Agnes Linglart
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Explore the profile of Agnes Linglart including associated specialties, affiliations and a list of published articles.
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215
Citations
3915
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Recent Articles
1.
Lambert A, Marie-Agathe T, Fouatih K, Lecoeuvre A, Thomas-Teinturier C, Rothenbuhler A, et al.
Endocr Connect
. 2025 Mar;
PMID: 40042209
Introduction: We previously observed that continuous subcutaneous gonadotropin infusion (CSGI) in infants with congenital hypogonadotropic hypogonadism (CHH) can mimic minipuberty. Objective: to describe the early adolescence outcome of boys treated...
2.
De Luca A, Bocquet A, Brancato-Bouet S, Chalumeau M, Dupont C, Darmaun D, et al.
Nutr Res Rev
. 2025 Feb;
:1-48.
PMID: 40008435
In Europe, organic food must comply with specific regulations which do not include nutritional criteria. The ability of organic food to meet the nutritional needs of children is not assessed....
3.
Kishnani P, Seefried L, Dahir K, Martos-Moreno G, Hogler W, Greenberg C, et al.
J Med Genet
. 2025 Feb;
PMID: 39965917
Background: Hypophosphatasia (HPP) is a rare metabolic disease caused by autosomal dominant or recessive inheritance of variants resulting in low alkaline phosphatase activity. The objective of this analysis was to...
4.
Del Sal A, Haumont E, Pigeolet M, Gaume M, Riouallon G, Bahi Buisson N, et al.
J Clin Med
. 2025 Feb;
14(3).
PMID: 39941520
: This is a retrospective study. The aim of this study is to report the results of bipolar minimally invasive fusionless surgery for scoliosis in Rett syndrome with a minimum...
5.
Haffner D, Emma F, Seefried L, Hogler W, Javaid K, Bockenhauer D, et al.
Nat Rev Nephrol
. 2025 Feb;
PMID: 39905262
No abstract available.
6.
Seefried L, Aliberti F, Heier C, Arango-Sancho P, Biosse Duplan M, Sakka S, et al.
Orphanet J Rare Dis
. 2025 Feb;
19(Suppl 2):497.
PMID: 39901153
No abstract available.
7.
Lemaitre M, Picart C, Gueorguieva I, Charbit J, Edouard T, Linglart A, et al.
Ann Endocrinol (Paris)
. 2025 Jan;
86(1):101696.
PMID: 39818293
Primary hyperparathyroidism is rare in children. A germline mutation is identified in half of all children with primary hyperparathyroidism (70% of newborns and infants, and 40% of children and adolescents)....
8.
Haffner D, Emma F, Seefried L, Hogler W, Javaid K, Bockenhauer D, et al.
Nat Rev Nephrol
. 2025 Jan;
PMID: 39814982
X-linked hypophosphataemia (XLH) is a rare metabolic bone disorder caused by pathogenic variants in the PHEX gene, which is predominantly expressed in osteoblasts, osteocytes and odontoblasts. XLH is characterized by...
9.
Munteanu M, Resch E, Bildheim V, Hoffjan S, Erdlenbruch B, Linglart A, et al.
Horm Res Paediatr
. 2025 Jan;
:1-8.
PMID: 39799940
Introduction: Pseudohypoparathyroidism 1A (PHP1A) is the best-known representative of inactivating parathyroid hormone (PTH)/PTHrP-signaling disorders (iPPSD). The associated phenotype develops over time and often includes hormonal resistances, short stature, and osteoma...
10.
Pechabrier M, Bacchetta J, Tounian P, Eddiry S, Linglart A, Edouard T
Arch Pediatr
. 2024 Nov;
32(1):4-11.
PMID: 39567315
Background And Objective: In 2022, recommendations for vitamin D supplementation in children were updated in France. The objective of this study was to assess real-life practices of vitamin D supplementation...