Cristiane Kopacek
Overview
Explore the profile of Cristiane Kopacek including associated specialties, affiliations and a list of published articles.
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Articles
15
Citations
107
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0
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Recent Articles
1.
Cheuiche A, da Silveira L, Lucena I, Punales M, Costenaro F, Kopacek C, et al.
Neuroendocrinology
. 2025 Mar;
:1-19.
PMID: 40031895
Introduction: Pelvic ultrasound has been studied for the follow-up of girls with precocious puberty during gonadotropin-releasing hormone agonists (GnRHa) therapy. The addition of Doppler evaluation of uterine arteries needs to...
2.
Bertoncello F, Beust M, Tagliari C, Herter L, Kopacek C
Rev Bras Ginecol Obstet
. 2024 May;
46.
PMID: 38765514
Objectives: This study aims to correlate pelvic ultrasound with female puberty and evaluate the usual ultrasound parameters as diagnostic tests for the onset of puberty and, in particular, a less...
3.
Castro S, Wiest P, Spritzer P, Kopacek C
Endocr Connect
. 2023 Oct;
12(12).
PMID: 37902057
Congenital adrenal hyperplasia (CAH) occurs due to enzyme defects in adrenal steroidogenesis. The 21-hydroxylase deficiency accounts for 90-95% of cases, triggering accumulation of 17-hydroxyprogesterone (17-OHP). Early diagnosis through neonatal screening...
4.
Boff M, Kopacek C, de Souza V, Ribeiro S, Kreisner E, Vargas P, et al.
Arch Endocrinol Metab
. 2023 May;
67(4):e000606.
PMID: 37252695
Objective: To determine the incidence of congenital hypothyroidism (CH) over a 10-year period at the Reference Service in Neonatal Screening of the state of Rio Grande do Sul (RSNS-RS). Subjects...
5.
Prado M, Singh S, Ligabue-Braun R, Meneghetti B, Rispoli T, Kopacek C, et al.
Int J Mol Sci
. 2022 Jan;
23(1).
PMID: 35008721
Deficiency of 21-hydroxylase enzyme (CYP21A2) represents 90% of cases in congenital adrenal hyperplasia (CAH), an autosomal recessive disease caused by defects in cortisol biosynthesis. Computational prediction and functional studies are...
6.
Cheuiche A, da Silveira L, Escott G, Lucena I, Punales M, Costenaro F, et al.
Endocrine
. 2021 Nov;
76(1):172-178.
PMID: 34846680
Purpose: To evaluate the accuracy of the uterine artery pulsatility index (PI) for the diagnosis of pubertal onset in girls. Methods: Cross-sectional study of girls with normal pubertal development. Puberty...
7.
Dos Santos T, Rodrigues T, Punales M, Arrais R, Kopacek C
Curr Pediatr Rep
. 2021 Aug;
9(4):142-153.
PMID: 34430071
Purpose Of Review: This review aims to address the actual state of the most advanced diabetes devices, as follows: continuous subcutaneous insulin infusions (CSII), continuous glucose monitoring systems (CGM), hybrid-closed...
8.
Eisenstein E, Kopacek C, Cavalcante S, Neves A, Fraga G, Messina L
Curr Pediatr Rep
. 2020 Aug;
8(3):93-98.
PMID: 32837801
Purpose Of The Review: The purpose of the review is to describe the Brazilian Telemedicine University Network RUTE concerning the Special Interest Group of Children and Adolescents, the new SIG-COVID19-BR...
9.
Deconte D, Kreusch T, Salvaro B, Perin W, Ferreira M, Kopacek C, et al.
J Pediatr Genet
. 2020 Aug;
9(4):263-269.
PMID: 32765931
Kenny-Caffey syndrome (KCS) is a rare genetic condition characterized by growth retardation, bone abnormalities, and hypoparathyroidism. Herein, we report an unusual case of a 10-year-old girl with Kenny-Caffey syndrome type...
10.
Beltrao L, Correia E, Rosa E, Correia J, Kopacek C, Faria A, et al.
Pediatr Int
. 2019 Feb;
61(1):113-114.
PMID: 30734433
No abstract available.