Maria Clemente
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Explore the profile of Maria Clemente including associated specialties, affiliations and a list of published articles.
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63
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597
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Recent Articles
1.
Mercado Santis E, Campos A, Fernandez P, Oriola J, Yeste D, Perez V, et al.
An Pediatr (Engl Ed)
. 2025 Feb;
102(2):503747.
PMID: 39952853
Introduction: 11β-hydroxylase (11β-OH) deficiency is the second most frequent cause of classic congenital adrenal hyperplasia (CAH) (5%-8% of cases). Clinically, it is characterized by virilization and arterial hypertension. The objective...
2.
Perez-Torres Lobato M, Morell M, Solano-Paez P, Ortiz-Palacios M, Menargez A, Panesso M, et al.
Pediatr Blood Cancer
. 2024 Oct;
71(12):e31343.
PMID: 39380174
Purpose: We aim to describe the characteristics of patients with childhood-onset craniopharyngioma and to analyze factors that impair quality of life (QoL) in this population. Methods: Multicenter national study including...
3.
Yeste D, Baz-Redon N, Antolin M, Garcia-Arumi E, Mogas E, Campos-Martorell A, et al.
Int J Mol Sci
. 2024 Sep;
25(18).
PMID: 39337518
Genetic defects in the TSH receptor () can cause poor thyroid differentiation (thyroid dysgenesis) and/or thyroid malfunction (thyroid dyshormonogenesis). The phenotype spectrum is wide: from severe congenital hypothyroidism to mild...
4.
Baz-Redon N, Antolin M, Clemente M, Campos A, Mogas E, Fernandez-Cancio M, et al.
Int J Mol Sci
. 2024 Aug;
25(15).
PMID: 39126042
Thyroid dyshormonogenesis (THD) is a heterogeneous group of genetic diseases caused by the total or partial defect in the synthesis or secretion of thyroid hormones. Genetic variants in can cause...
5.
Fernandez-Cancio M, Antolin M, Clemente M, Campos-Martorell A, Mogas E, Baz-Redon N, et al.
Front Endocrinol (Lausanne)
. 2024 Jul;
15:1367808.
PMID: 39040671
Introduction: Defects in any thyroid hormone synthesis steps cause thyroid dyshormonogenesis (THD). THD due to () gene variants is a cause of congenital hypothyroidism (CH) with a wide clinical spectrum,...
6.
Serafim A, Olive-Cirera G, Ortega-Gonzalez A, Kruer M, Weese-Mayer D, Rand C, et al.
Neurol Neuroimmunol Neuroinflamm
. 2024 Jun;
11(5):e200276.
PMID: 38917381
Objectives: To report the association of zinc finger and SCAN domain containing 1 antibodies (ZSCAN1-abs) with rapid-onset obesity, hypothalamic dysfunction, hypoventilation, and autonomic dysregulation (ROHHAD) syndrome in patients without tumor....
7.
Sarafoglou K, Kim M, Lodish M, Felner E, Martinerie L, Nokoff N, et al.
N Engl J Med
. 2024 Jun;
391(6):493-503.
PMID: 38828945
Background: Children with classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency require treatment with glucocorticoids, usually at supraphysiologic doses, to address cortisol insufficiency and reduce excess adrenal androgens. However,...
8.
Ficial B, Benfari G, Bonafiglia E, Clemente M, Cappelleri A, Flore A, et al.
J Ultrasound Med
. 2023 Dec;
43(4):729-739.
PMID: 38140738
Objectives: To assess the feasibility, accuracy, and reproducibility of tissue-tracking mitral annular displacement (TMAD) compared with other measures of left ventricular systolic function in healthy preterm and term neonates in...
9.
Aguilar-Riera C, Clemente M, Gonzalez-Llorens N, Mogas E, Campos-Martorell A, Fabregas A, et al.
Clin Diabetes Endocrinol
. 2023 Nov;
9(1):5.
PMID: 37908013
Background: Pituitary adenomas (PPAs) are uncommon in childhood and adolescence, accounting for 2-6% of all intracranial neoplasms. Delayed puberty, growth retardation, galactorrhea and weight gain are common features at presentation...
10.
Schroder M, Neacsu M, Adriaansen B, Sweep F, Ahmed S, Ali S, et al.
Eur J Endocrinol
. 2023 Oct;
189(4):460-468.
PMID: 37837609
Importance: Testicular adrenal rest tumors (TARTs), often found in male patients with congenital adrenal hyperplasia (CAH), are benign lesions causing testicular damage and infertility. We hypothesize that chronically elevated adrenocorticotropic...