Found: 19
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Rational approach to the primary evaluation of thyroid disease in paediatrics. Full thyroid profile vs. thyroid-stimulating hormone and free thyroxine only.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2018, v. 56, n. 6, p. e144, doi. 10.1515/cclm-2017-0962
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- Publication type:
- Article
The use of a "gray zone" considering measurement uncertainty in pharmacological tests. The serum growth hormone stimulation test as an example.
- Published in:
- 2016
- By:
- Publication type:
- Letter to the Editor
Clinically useful samples and reference change value.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2015, v. 53, n. 2, p. e33, doi. 10.1515/cclm-2014-0657
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- Publication type:
- Article
High prevalence of anti-thyroid antibodies associated with a low vitamin D status in a pediatric cohort.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2014, v. 52, n. 6, p. e119, doi. 10.1515/cclm-2013-0975
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- Publication type:
- Article
Cut-off values of serum growth hormone (GH) in pharmacological stimulation tests (PhT) evaluated in short-statured children using a chemiluminescent immunometric assay (ICMA) calibrated with the International Recombinant Human GH Standard 98/574.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 5, p. e95, doi. 10.1515/cclm-2012-0505
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- Publication type:
- Article
Age-specific thyroid hormone and thyrotropin reference intervals for a pediatric and adolescent population.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2012, v. 50, n. 5, p. 885, doi. 10.1515/cclm-2011-0495
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- Publication type:
- Article
Accelerated Pubertal Tempo in a 46,XY Aromatase-Deficient Patient.
- Published in:
- Hormone Research in Paediatrics, 2018, v. 90, n. 4, p. 275, doi. 10.1159/000492128
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- Publication type:
- Article
Central Adrenal Insufficiency Could Not Be Confirmed by Measurement of Basal Serum DHEAS Levels in Pubertal Children.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 82, n. 5, p. 332, doi. 10.1159/000368318
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- Publication type:
- Article
Preserved Fertility in a Patient with a 46,XY Disorder of Sex Development due to a New Heterozygous Mutation in the NR5A1/SF-1 Gene: Evidence of 46,XY and 46,XX Gonadal Dysgenesis Phenotype Variability in Multiple Members of an Affected Kindred.
- Published in:
- Hormone Research in Paediatrics, 2012, v. 78, n. 2, p. 119, doi. 10.1159/000338346
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- Publication type:
- Article
Three New SF-1 (NR5A1) Gene Mutations in Two Unrelated Families with Multiple Affected Members: Within-Family Variability in 46,XY Subjects and Low Ovarian Reserve in Fertile 46,XX Subjects.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 75, n. 1, p. 70, doi. 10.1159/000320029
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- Publication type:
- Article
Is BaF3 Bioassay Useful to Identify Patients with Bioinactive Growth Hormone?
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2010, v. 23, n. 8, p. 783, doi. 10.1515/jpem.2010.128
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- Publication type:
- Article
Hydrocortisone Treatment in Girls with Congenital Adrenal Hyperplasia Inhibits Serum Dehydroepiandrosterone Sulfate and Affects the GH-IGF-I System.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2009, v. 22, n. 3, p. 255, doi. 10.1515/JPEM.2009.22.3.255
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- Publication type:
- Article
Relationship between the Growth Hormone/Insulin-Like Growth Factor-I Axis, Insulin Sensitivity, and Adrenal Androgens in Normal Prepubertal and Pubertal Girls.
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- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 3, p. 1389, doi. 10.1210/jc.2002-020979
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- Publication type:
- Article
A Novel Missense Mutation in the HSD3B2 Gene, Underlying Nonsalt-Wasting Congenital Adrenal Hyperplasia. New Insight Into the Structure-Function Relationships of 3[beta]-Hydroxysteroid Dehidrogenase Type II.
- Published in:
- 2015
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- Publication type:
- Journal Article
TWO NOVEL HETEROZYGOUS MISSENSE VARIATIONS WITHIN THE GLI2 GENE IN TWO UNRELATED ARGENTINE PATIENTS.
- Published in:
- Medicina (Buenos Aires), 2016, v. 76, n. 4, p. 213
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- Publication type:
- Article
NUEVA MUTACIÓN HETEROCIGOTA EN EL GEN DE LA PROTEÍNA REGULATORIA AGUDA DE LA ESTEROIDEOGÉNESIS (StAR) EN UN PACIENTE 46,XY CON HIPERPLASIA ADRENAL CONGÉNITA LIPOIDEA.
- Published in:
- Medicina (Buenos Aires), 2013, v. 73, n. 4, p. 297
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- Publication type:
- Article
OBESIDAD Y FACTORES DE RIESGO DEL SÍNDROME METABÓLICO EN JÓVENES CON DIABETES TIPO.
- Published in:
- Medicina (Buenos Aires), 2012, v. 72, n. 4, p. 291
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- Publication type:
- Article
Presence of GH1 and absence of GHRHR gene mutations in a large cohort of Argentinian patients with severe short stature and isolated GH deficiency.
- Published in:
- Clinical Endocrinology, 2014, v. 80, n. 4, p. 618, doi. 10.1111/cen.12267
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- Publication type:
- Article
Steroid 21-hydroxylase gene mutational spectrum in 454 Argentinean patients: genotype-phenotype correlation in a large cohort of patients with congenital adrenal hyperplasia.
- Published in:
- Clinical Endocrinology, 2011, v. 75, n. 4, p. 427, doi. 10.1111/j.1365-2265.2011.04123.x
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- Publication type:
- Article