Found: 14
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Congenital Hyperinsulinism in Brazilian Neonates: A Study of Histology, KATP Channel Genes, and Proliferation of β Cells.
- Published in:
- Pediatric & Developmental Pathology, 2010, v. 13, n. 5, p. 375, doi. 10.2350/08-12-0578.1
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- Publication type:
- Article
CONGENITAL HYPERINSULINISM IN BRAZILIAN NEONATES: A STUDY OF HISTOLOGY, KATP CHANNEL GENES AND PROLIFERATION OF β-CELLS.
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- Pediatric & Developmental Pathology, 2010, v. 13, n. 3, p. 1
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- Publication type:
- Article
Surgery for adrenal tumours with thrombus in the supra-diaphragmatic infra-atrial inferior vena cava, with no cardiopulmonary bypass.
- Published in:
- BJU International, 2004, v. 94, n. 1, p. 70, doi. 10.1111/j.1464-410X.2004.04903.x
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- Publication type:
- Article
Novel Mutations in CYP11B1 Gene Leading to 11β-Hydroxylase Deficiency in Brazilian Patients.
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- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 9, p. 3481, doi. 10.1210/jc.2008-2521
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- Article
Extraadrenal 21-hydroxylation by CYP2C19 and CYP3A4: effect on 21-hydroxylase deficiency.
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- 2009
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- Publication type:
- journal article
The common P450 oxidoreductase variant A503V is not a modifier gene for 21-hydroxylase deficiency.
- Published in:
- 2008
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- Publication type:
- journal article
Absence of Mutations Involving the Lim Homeobox Domain Gene LHX9 in 46,XY Gonadal Agenesis and Dysgenesis.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 6, p. 2465, doi. 10.1210/jcem.86.6.7539
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- Publication type:
- Article
17β-Hydroxysteroid Dehydrogenase-3 Deficiency: Diagnosis, Phenotypic Variability, Population Genetics, and Worldwide Distribution of Ancient and de Novo Mutations.
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- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 12, p. 4713, doi. 10.1210/jc.84.12.4713
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- Publication type:
- Article
The desmopressin stimulation test in the differential diagnosis of Cushing's syndrome.
- Published in:
- Clinical Endocrinology, 1993, v. 38, n. 5, p. 463, doi. 10.1111/j.1365-2265.1993.tb00341.x
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- Publication type:
- Article
A Novel Homozygous Missense FSHR Variant Associated with Hypergonadotropic Hypogonadism in Two Siblings from a Brazilian Family.
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- Sexual Development, 2017, v. 11, n. 3, p. 137, doi. 10.1159/000477193
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- Publication type:
- Article
Heterozygous Nonsense Mutation in the Androgen Receptor Gene Associated with Partial Androgen Insensitivity Syndrome in an Individual with 47,XXY Karyotype.
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- Sexual Development, 2017, v. 11, n. 2, p. 78, doi. 10.1159/000468957
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- Publication type:
- Article
A Bayesian Approach to Diagnose Growth Hormone Deficiency in Children: Insulin-Like Growth Factor Type 1 Is Valuable for Screening and IGF-Binding Protein Type 3 for Confirmation.
- Published in:
- Hormone Research in Paediatrics, 2020, v. 93, n. 3, p. 197, doi. 10.1159/000509840
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- Publication type:
- Article
Severe and Mild Neonatal Hypothyroidism Mediate Opposite Effects on Leydig Cells of Rats.
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- Thyroid, 2002, v. 12, n. 1, p. 13, doi. 10.1089/105072502753451913
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- Publication type:
- Article
A study of patients with Nelson's syndrome.
- Published in:
- Clinical Endocrinology, 1998, v. 49, n. 4, doi. 10.1046/j.1365-2265.1998.00578.x
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- Publication type:
- Article