Mercedes Maceiras
B, Argentina
Last Updated: 09/26/2026
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Found 15 publications
Predictive outcome measures of adult short stature in patients with severe acquired autoimmune hypothyroidism.
Journal: Archivos argentinos de pediatria
Published: August 21, 2018
Accelerated Pubertal Tempo in a 46,XY Aromatase-Deficient Patient.
Journal: Hormone research in paediatrics
Published: January 08, 2018
Rational approach to the primary evaluation of thyroid disease in paediatrics. Full thyroid profile vs. thyroid-stimulating hormone and free thyroxine only.
Journal: Clinical chemistry and laboratory medicine
Published: October 19, 2017
The use of a "gray zone" considering measurement uncertainty in pharmacological tests. The serum growth hormone stimulation test as an example.
Journal: Clinical chemistry and laboratory medicine
Published: September 30, 2015
A novel missense mutation in the HSD3B2 gene, underlying nonsalt-wasting congenital adrenal hyperplasia. new insight into the structure-function relationships of 3β-hydroxysteroid dehidrogenase type II.
Journal: The Journal of clinical endocrinology and metabolism
Published: October 17, 2014
Clinically useful samples and reference change value.
Journal: Clinical chemistry and laboratory medicine
Published: June 23, 2014
Central adrenal insufficiency could not be confirmed by measurement of basal serum DHEAS levels in pubertal children.
Journal: Hormone research in paediatrics
Published: April 09, 2014
High prevalence of anti-thyroid antibodies associated with a low vitamin D status in a pediatric cohort.
Journal: Clinical chemistry and laboratory medicine
Published: November 12, 2013
Novel heterozygous mutation in the steroidogenic acute regulatory protein gene in a 46,XY patient with congenital lipoid adrenal hyperplasia
Journal: Medicina
Published: August 09, 2013
Presence of GH1 and absence of GHRHR gene mutations in a large cohort of Argentinian patients with severe short stature and isolated GH deficiency.
Journal: Clinical endocrinology
Published: June 25, 2013
Unique dominant negative mutation in the N-terminal mitochondrial targeting sequence of StAR, causing a variant form of congenital lipoid adrenal hyperplasia.
Journal: The Journal of clinical endocrinology and metabolism
Published: November 24, 2012
Last Updated: 09/26/2026