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Epigenetic Control of Adamantinomatous Craniopharyngiomas.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 10, p. e1867, doi. 10.1210/clinem/dgae006
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- Publication type:
- Article
Nicotinamide Nucleotide Transhydrogenase Is Essential for Adrenal Steroidogenesis: Clinical and In Vitro Lessons.
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- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 6, p. 1464, doi. 10.1210/clinem/dgac705
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- Publication type:
- Article
Integrating Methylome and Transcriptome Signatures Expands the Molecular Classification of the Pituitary Tumors.
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- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 6, p. 1452, doi. 10.1210/clinem/dgac703
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- Publication type:
- Article
Prenatal Dexamethasone Treatment of Congenital Adrenal Hyperplasia: Are We Any Closer to Considering It Safe?
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- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 1, p. e9, doi. 10.1210/clinem/dgac524
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- Publication type:
- Article
Integrating Molecular and Metabolomic Markers in T1D Enables Precocious Interventions: Are We Getting There?
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- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 10, p. e4240, doi. 10.1210/clinem/dgac334
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- Publication type:
- Article
Evaluation of the HPA Axis' Response to Pharmacological Challenges in Experimental and Clinical Early-Life Stress-Associated Depression.
- Published in:
- eNeuro, 2021, v. 8, n. 1, p. 1, doi. 10.1523/ENEURO.0222-20.2020
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- Publication type:
- Article
Quantitative Magnetic Resonance Imaging Evaluation of the Olfactory System in Kallmann Syndrome: Correlation with a Clinical Smell Test.
- Published in:
- Neuroendocrinology, 2011, v. 94, n. 3, p. 209, doi. 10.1159/000328437
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- Publication type:
- Article
Letter to the Editor: Comments on "LGR5 Activates Noncanonical Wnt Signaling and Inhibits Aldosterone Production in the Human Adrenal" by Shaikh L.H., et al.
- Published in:
- 2015
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- Publication type:
- commentary
Sonic hedgehog signaling is active in human adrenal cortex development and deregulated in adrenocortical tumors.
- Published in:
- 2014
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- Publication type:
- Journal Article
Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3.
- Published in:
- 2014
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- Publication type:
- journal article
A Novel ADIPOQ Mutation (p.M40K) Impairs Assembly of High-Molecular-Weight Adiponectin and Is Associated With Early-Onset Obesity and Metabolic Syndrome.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Corrigendum: Transcriptome Analysis Showed a Differential Signature Between Invasive and Non-invasive Corticotrophinomas.
- Published in:
- 2019
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- Publication type:
- Correction Notice
Regulation of Aryl Hydrocarbon Receptor Interacting Protein (AIP) Protein Expression by MiR-34a in Sporadic Somatotropinomas.
- Published in:
- PLoS ONE, 2015, v. 10, n. 2, p. 1, doi. 10.1371/journal.pone.0117107
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- Publication type:
- Article
Components of the Canonical and Non-Canonical Wnt Pathways Are Not Mis-Expressed in Pituitary Tumors.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0062424
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- Publication type:
- Article
TAC3/TACR3 mutations reveal preferential activation of gonadotropin-releasing hormone release by neurokinin B in neonatal life followed by reversal in adulthood.
- Published in:
- 2010
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- Publication type:
- journal article
Novel Mutations in CYP11B1 Gene Leading to 11β-Hydroxylase Deficiency in Brazilian Patients.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 9, p. 3481, doi. 10.1210/jc.2008-2521
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- Publication type:
- Article
Loss-of-Function Mutations in the Genes Encoding Prokineticin-2 or Prokineticin Receptor-2 Cause Autosomal Recessive Kallmann Syndrome.
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- Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 10, p. 4113, doi. 10.1210/jc.2008-0958
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- Publication type:
- Article
Novel Fibroblast Growth Factor Receptor 1 Mutations in Patients with Congenital Hypogonadotropic Hypogonadism with and without Anosmia.
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- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 10, p. 4006, doi. 10.1210/jc.2005-2793
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- Publication type:
- Article
Recurrence of the R947X Mutation in Unrelated Families with Autosomal Dominant Pseudohypoaldosteronism Type 1: Evidence for a Mutational Hot Spot in the Mineralocorticoid Receptor Gene.
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- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 9, p. 3671, doi. 10.1210/jc.2006-0605
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- Publication type:
- Article
Glucocorticoid Sensitivity in Young Healthy Individuals: in Vitro and in Vivo Studies.
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- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 11, p. 5978, doi. 10.1210/jc.2005-0067
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- Publication type:
- Article
Refining Hormonal Diagnosis of Type II 3β- Hydroxysteroid Dehydrogenase Deficiency in Patients with Premature Pubarche and Hirsutism Based on HSD3B2 Genotyping.
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- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 3, p. 1287, doi. 10.1210/jc.2004-1552
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- Publication type:
- Article
Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene.
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- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 4, p. 1805, doi. 10.1210/jcem.87.4.8379
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- Publication type:
- Article
Differential Diagnosis of Major Depressive Disorder and Bipolar Disorder: Genetic and Hormonal Assessment and the Influence of Early-Life Stress.
- Published in:
- Brain Sciences (2076-3425), 2022, v. 12, n. 11, p. 1476, doi. 10.3390/brainsci12111476
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- Publication type:
- Article
gsp Mutation Is Not a Molecular Biomarker of Long-Term Response to First-Generation Somatostatin Receptor Ligands in Acromegaly.
- Published in:
- Cancers, 2021, v. 13, n. 19, p. 4857, doi. 10.3390/cancers13194857
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- Publication type:
- Article
Telomere length and Wnt/β-catenin pathway in adamantinomatous craniopharyngiomas.
- Published in:
- European Journal of Endocrinology, 2022, v. 187, n. 2, p. 219, doi. 10.1530/EJE-21-1269
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- Publication type:
- Article
A sense of time of the glucocorticoid circadian clock: from the ontogeny to the diagnosis of Cushing's syndrome.
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- European Journal of Endocrinology, 2018, v. 179, n. 1, p. R1, doi. 10.1530/EJE-18-0102
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- Publication type:
- Article
Expression profile of apoptosis-related genes in childhood adrenocortical tumors: low level of expression of BCL2 and TNF genes suggests a poor prognosis.
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- European Journal of Endocrinology, 2012, v. 167, n. 2, p. 199, doi. 10.1530/EJE-12-0183
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- Publication type:
- Article
Evaluation of the Tubular and Interstitial Functions of the Testis in 46,XY Patients with Ambiguous Genitalia.
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- Journal of Pediatric Endocrinology & Metabolism, 2000, v. 13, n. 6, p. 605
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- Publication type:
- Article
Restricted Feeding Schedules Modulate in a Different Manner the Expression of Clock Genes in Rat Hypothalamic Nuclei.
- Published in:
- Frontiers in Neuroscience, 2016, p. 1, doi. 10.3389/fnins.2016.00567
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- Publication type:
- Article
A Single Nucleotide Variant in the Promoter Region of 17β-HSD Type 5 Gene Influences External Genitalia Virilization in Females with 21-Hydroxylase Deficiency.
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- Hormone Research in Paediatrics, 2016, v. 85, n. 5, p. 333, doi. 10.1159/000445684
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- Publication type:
- Article
Low expression of HLA-DRA, HLA-DPA1, and HLA-DPB1 is associated with poor prognosis in pediatric adrenocortical tumors (ACT)
- Published in:
- 2014
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- Publication type:
- Journal Article
Low expression of HLA-DRA, HLA-DPA1, and HLA-DPB1 is associated with poor prognosis in pediatric adrenocortical tumors (ACT).
- Published in:
- Pediatric Blood & Cancer, 2014, v. 61, n. 11, p. 1940, doi. 10.1002/pbc.25118
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- Publication type:
- Article
Reduced fibroblast growth factor 21 and β-Klotho secretion in untreated congenital isolated GH deficiency.
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- Endocrine (1355008X), 2021, v. 73, n. 1, p. 160, doi. 10.1007/s12020-021-02700-6
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- Publication type:
- Article
Prostaglandin mediates endotoxaemia-induced hypophagia by activation of pro-opiomelanocortin and corticotrophin-releasing factor neurons in rats.
- Published in:
- Experimental Physiology, 2009, v. 94, n. 3, p. 371, doi. 10.1113/expphysiol.2008.045435
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- Publication type:
- Article
Peripheral Parameters of Thyroid Hormone Action in Resistance to Thyroid Hormone Syndrome: A Focus on Mineral Metabolism.
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- Thyroid, 2009, v. 19, n. 7, p. 785, doi. 10.1089/thy.2008.0211
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- Publication type:
- Article
Hypothalamic-Pituitary Axis and Peripheral Tissue Responses to TRH Stimulation and Liothyronine Suppression Tests in Normal Subjects Evaluated by Current Methods.
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- Thyroid, 2008, v. 18, n. 4, p. 401, doi. 10.1089/thy.2007.0237
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- Publication type:
- Article
Polymorphisms in the RET Proto-Oncogene and the Phenotypic Presentation of Familial Medullary Thyroid Carcinoma.
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- Thyroid, 2004, v. 14, n. 10, p. 848
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- Publication type:
- Article
Spindle assembly checkpoint gene expression in childhood adrenocortical tumors (ACT): Overexpression of Aurora kinases A and B is associated with a poor prognosis.
- Published in:
- Pediatric Blood & Cancer, 2013, v. 60, n. 11, p. 1809, doi. 10.1002/pbc.24653
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- Publication type:
- Article
Enteroendocrine Connections in Congenital Isolated GH Deficiency Due to a GHRH Receptor Gene Mutation.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2019, v. 104, n. 7, p. 2777, doi. 10.1210/jc.2019-00094
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- Publication type:
- Article
Enteroendocrine Connections in Congenital Isolated GH Deficiency Due to a GHRH Receptor Gene Mutation.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Glucocorticoid resistance in dialysis patients may impair the kidney allograft outcome.
- Published in:
- Nephrology Dialysis Transplantation, 2008, v. 23, n. 4, p. 1422
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- Publication type:
- Article
Transcriptome analysis showed a Differential signature between invasive and non-invasive corticotrophinomas.
- Published in:
- Frontiers in Endocrinology, 2017, v. 8, p. 1, doi. 10.3389/fendo.2017.00055
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- Publication type:
- Article
Phenotypic diversity and glucocorticoid sensitivity in patients with familial partial lipodystrophy type 2.
- Published in:
- Clinical Endocrinology, 2019, v. 91, n. 1, p. 94, doi. 10.1111/cen.13984
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- Publication type:
- Article
Postnatal growth and cardiometabolic profile in young adults born large for gestational age.
- Published in:
- Clinical Endocrinology, 2011, v. 75, n. 3, p. 335, doi. 10.1111/j.1365-2265.2011.04054.x
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- Publication type:
- Article
Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1.
- Published in:
- Clinical Endocrinology, 2010, v. 72, n. 3, p. 371, doi. 10.1111/j.1365-2265.2009.03642.x
- By:
- Publication type:
- Article
Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole.
- Published in:
- Clinical Endocrinology, 2008, v. 69, n. 1, p. 93, doi. 10.1111/j.1365-2265.2007.03160.x
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- Publication type:
- Article
Clinical features and genetic analysis of four Brazilian kindreds with resistance to thyroid hormone.
- Published in:
- Clinical Endocrinology, 2007, v. 67, n. 5, p. 748, doi. 10.1111/j.1365-2265.2007.02956.x
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- Publication type:
- Article
Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism.
- Published in:
- Clinical Endocrinology, 2007, v. 66, n. 2, p. 173, doi. 10.1111/j.1365-2265.2006.02702.x
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- Publication type:
- Article
The emergence of the cortisol circadian rhythm in monozygotic and dizygotic twin infants: the twin-pair synchrony.
- Published in:
- Clinical Endocrinology, 2007, v. 66, n. 2, p. 192, doi. 10.1111/j.1365-2265.2006.02706.x
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- Publication type:
- Article
HORMONES - CYTOKINES - SIGNALING Glucocorticoid receptors, in vitro steroid sensitivity, and cytokine secretion in idiopathic nephrotic syndrome.
- Published in:
- Kidney International, 2004, v. 65, n. 2, p. 403, doi. 10.1111/j.1523-1755.2004.00392.x
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- Publication type:
- Article