Gabriela P Finkielstain
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Explore the profile of Gabriela P Finkielstain including associated specialties, affiliations and a list of published articles.
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12
Citations
444
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Recent Articles
1.
Finkielstain G, Rey R
Expert Rev Endocrinol Metab
. 2023 Sep;
18(5):427-439.
PMID: 37694439
Introduction: Disorders of Sex Development (DSD) associated with adrenal dysfunction occur due to different defects in the proteins involved in gonadal and adrenal steroidogenesis. Areas Covered: The deficiencies in 21-hydroxylase...
2.
Finkielstain G, Vieites A, Bergada I, Rey R
Front Endocrinol (Lausanne)
. 2022 Jan;
12:770782.
PMID: 34987475
Disorders of Sex Development (DSD) are anomalies occurring in the process of fetal sexual differentiation that result in a discordance between the chromosomal sex and the sex of the gonads...
3.
Clement F, Grinspon R, Yankelevich D, Martin Benitez S, De La Ossa Salgado M, Ropelato M, et al.
Front Endocrinol (Lausanne)
. 2021 Feb;
11:624684.
PMID: 33613456
Introduction: Practice guidelines cannot recommend establishing a diagnosis of growth hormone deficiency (GHD) without performing growth hormone stimulation tests (GHST) in children with risk factors, due to the lack of...
4.
Finkielstain G, Kim M, Sinaii N, Nishitani M, Van Ryzin C, Hill S, et al.
J Clin Endocrinol Metab
. 2012 Sep;
97(12):4429-38.
PMID: 22990093
Context: Patients with congenital adrenal hyperplasia (CAH) often suffer from long-term complications secondary to chronic glucocorticoid therapy and suboptimal treatment regimens. Objective: The aim of the study was to describe...
5.
Chen W, Xu Z, Sullivan A, Finkielstain G, Van Ryzin C, Merke D, et al.
Clin Chem
. 2011 Dec;
58(2):421-30.
PMID: 22156666
Background: Chimeric CYP21A1P/CYP21A2 genes, caused by homologous recombination between CYP21A2 (cytochrome P450, family 21, subfamily A, polypeptide 2) and its highly homologous pseudogene CYP21A1P (cytochrome P450, family 21, subfamily A,...
6.
Nandagopal R, Sinaii N, Avila N, Van Ryzin C, Chen W, Finkielstain G, et al.
Eur J Endocrinol
. 2011 Mar;
164(6):977-84.
PMID: 21444649
Objective: To comprehensively phenotype parents identified with nonclassic congenital adrenal hyperplasia (NCCAH) by family genetic studies, termed here as cryptic NCCAH and to define the incidence of cryptic NCCAH in...
7.
Forcinito P, Andrade A, Finkielstain G, Baron J, Nilsson O, Lui J
J Endocrinol
. 2010 Oct;
208(1):59-67.
PMID: 20974641
The mammalian growth plate undergoes programmed senescence during juvenile life, causing skeletal growth to slow with age. We previously found that hypothyroidism in rats slowed both growth plate chondrocyte proliferation...
8.
Finkielstain G, Chen W, Mehta S, Fujimura F, Hanna R, Van Ryzin C, et al.
J Clin Endocrinol Metab
. 2010 Oct;
96(1):E161-72.
PMID: 20926536
Background: Genetic analysis is commonly performed in patients with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. Study Objective: The objective of the study was to describe comprehensive CYP21A2 mutation...
9.
Horvath A, Faucz F, Finkielstain G, Nikita M, Rothenbuhler A, Almeida M, et al.
Thyroid
. 2010 Apr;
20(4):363-7.
PMID: 20373981
Background: Human phosphodiesterase (PDE) type 8B (PDE8B) is located at 5q14.1 and is known as the PDE with the highest affinity to cAMP. We recently described a family with bilateral...
10.
Finkielstain G, Forcinito P, Lui J, Barnes K, Marino R, Makaroun S, et al.
Endocrinology
. 2008 Nov;
150(4):1791-800.
PMID: 19036884
Mammalian somatic growth is rapid in early postnatal life but then slows and eventually ceases in multiple tissues. We hypothesized that there exists a postnatal gene expression program that is...