Carine Villanueva
Overview
Explore the profile of Carine Villanueva including associated specialties, affiliations and a list of published articles.
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21
Citations
104
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Recent Articles
1.
Cuny T, Reynaud R, Raverot G, Coutant R, Chanson P, Kariyawasam D, et al.
Ann Endocrinol (Paris)
. 2024 Jul;
86(1):101631.
PMID: 39002896
No abstract available.
2.
Bazus L, Perge K, Cabet S, Mottolese C, Villanueva C
Childs Nerv Syst
. 2024 May;
40(9):2677-2683.
PMID: 38761265
Introduction: Disturbances in plasma sodium levels are a major complication following recent resections of craniopharyngiomas in children. They must be properly managed to avoid neurological sequelae. We aimed to describe...
3.
Castets S, Thomas-Teinturier C, Villanueva C, Amsellem J, Barat P, Brun G, et al.
Arch Pediatr
. 2024 Mar;
31(3):165-171.
PMID: 38538470
Hypopituitarism (or pituitary deficiency) is a rare disease with an estimated prevalence of between 1/16,000 and 1/26,000 individuals, defined by insufficient production of one or several anterior pituitary hormones (growth...
4.
Janot C, Perrin P, Raverot V, Bretones P, Ecochard R, Malburet-Testori S, et al.
Hum Reprod
. 2024 Mar;
39(5):1003-1012.
PMID: 38514451
Study Question: Is the 24-h urinary gonadotropin assay an effective diagnostic tool in central precocious puberty (CPP) in girls? Summary Answer: This study is the first to provide 24-h urinary...
5.
Perge K, Capel E, Villanueva C, Gautheron J, Diallo S, Auclair M, et al.
Eur J Endocrinol
. 2024 Jan;
190(2):151-164.
PMID: 38245004
Objective: SOFT syndrome (MIM#614813), denoting Short stature, Onychodysplasia, Facial dysmorphism, and hypoTrichosis, is a rare primordial dwarfism syndrome caused by biallelic variants in POC1A, encoding a centriolar protein. SOFT syndrome,...
6.
Zhang M, Thieux M, Arvis L, Lin J, Guyon A, Plancoulaine S, et al.
Sleep
. 2023 Mar;
46(7).
PMID: 36971181
Study Objectives: To determine the prevalence of metabolic syndrome (MS) in children with narcolepsy and to evaluate their clinical and sleep characteristics according to the different components of MS. Methods:...
7.
Levaillant L, Bouhours-Nouet N, Illouz F, Amsellem Jager J, Bachelot A, Barat P, et al.
J Clin Endocrinol Metab
. 2023 Mar;
108(9):e779-e788.
PMID: 36884306
Introduction: Congenital hypothyroidism with gland-in-situ (CH-GIS) is usually attributed to mutations in the genes involved in thyroid hormone production. The diagnostic yield of targeted next-generation sequencing (NGS) varied widely between...
8.
Puvilland C, Villanueva C, Hemmendinger A, Kornreich L, Gueorguieva I, Karnoub M, et al.
Cancers (Basel)
. 2023 Jan;
15(1).
PMID: 36612052
Purpose: to compare the recurrence rate in children with midline LGG, depending on whether or not they have received GHRT, in order to assess its impact on the risk of...
9.
Arvis L, Doye E, Perge K, Zhang M, Thieux M, Guyon A, et al.
Sleep
. 2022 Nov;
46(5).
PMID: 36433727
Study Objectives: Narcolepsy with cataplexy is associated with obesity in children. We proposed to assess whether metabolic complications were linked to narcolepsy regardless of obesity. The second aim of the...
10.
Zhang M, Thieux M, Inocente C, Vieux N, Arvis L, Villanueva C, et al.
CNS Neurosci Ther
. 2022 Feb;
28(6):829-841.
PMID: 35212159
Objectives: To characterize the rapid weight gain (RWG) phenotype associated with the onset of childhood narcolepsy and to determine whether it could constitute a marker of severity of the disease....