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Methylome profiling of healthy and central precocious puberty girls.
- Published in:
- Clinical Epigenetics, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13148-018-0581-1
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- Publication type:
- Article
Evidence for a Founder Effect of SDHB Exon 1 Deletion in Brazilian Patients With Paraganglioma.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 8, p. 2105, doi. 10.1210/clinem/dgad028
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- Publication type:
- Article
Novel MKRN3 Missense Mutations Associated With Central Precocious Puberty Reveal Distinct Effects on Ubiquitination.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 7, p. 1646, doi. 10.1210/clinem/dgad151
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- Publication type:
- Article
Clinical and Genetic Characterization of Familial Central Precocious Puberty.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 7, p. 1758, doi. 10.1210/clinem/dgac763
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- Publication type:
- Article
Primary Adrenal Insufficiency Due to Bilateral Adrenal Infarction in COVID-19.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 1, p. e394, doi. 10.1210/clinem/dgab557
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- Publication type:
- Article
Brain MRI in Girls With Central Precocious Puberty: A Time for New Approaches.
- Published in:
- 2021
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- Publication type:
- Editorial
Novel Genetic and Biochemical Findings of DLK1 in Children with Central Precocious Puberty: A Brazilian-Spanish Study.
- Published in:
- 2020
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- Publication type:
- journal article
Receptors for Melanocortin Peptides in the Hypothalamic-Pituitary-Adrenal Axis and Skin.
- Published in:
- Annals of the New York Academy of Sciences, 1995, v. 771, n. 1, p. 352, doi. 10.1111/j.1749-6632.1995.tb44694.x
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- Publication type:
- Article
SIN3A Defects Associated with Syndromic Congenital Hypogonadotropic Hypogonadism: An Overlap with Witteveen-Kolk Syndrome.
- Published in:
- Neuroendocrinology, 2023, v. 113, n. 8, p. 834, doi. 10.1159/000529615
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- Publication type:
- Article
Clinical and Genetic Characterization of a Constitutional Delay of Growth and Puberty Cohort.
- Published in:
- Neuroendocrinology, 2020, v. 110, n. 11/12, p. 959, doi. 10.1159/000504783
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- Publication type:
- Article
Outcomes of Patients with Central Precocious Puberty Due to Loss-of-Function Mutations in the MKRN3 Gene after Treatment with Gonadotropin-Releasing Hormone Analog.
- Published in:
- Neuroendocrinology, 2020, v. 110, n. 7/8, p. 705, doi. 10.1159/000504446
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- Publication type:
- Article
Central Precocious Puberty Caused by a Heterozygous Deletion in the <bold>MKRN3</bold> Promoter Region.
- Published in:
- Neuroendocrinology, 2018, v. 107, n. 2, p. 127, doi. 10.1159/000490059
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- Publication type:
- Article
High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic.
- Published in:
- Neuroendocrinology, 2017, v. 105, n. 1, p. 17, doi. 10.1159/000446963
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- Publication type:
- Article
New Causes of Central Precocious Puberty: The Role of Genetic Factors.
- Published in:
- Neuroendocrinology, 2014, v. 100, n. 1, p. 1, doi. 10.1159/000366282
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- Publication type:
- Article
The Role of Prokineticins in the Pathogenesis of Hypogonadotropic Hypogonadism.
- Published in:
- Neuroendocrinology, 2010, v. 91, n. 4, p. 283, doi. 10.1159/000308880
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- Publication type:
- Article
The neurokinin B pathway in human reproduction.
- Published in:
- Nature Genetics, 2009, v. 41, n. 3, p. 269, doi. 10.1038/ng0309-269
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- Publication type:
- Article
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2017, p. 1557, doi. 10.1210/jc.2016-3677
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- Publication type:
- Article
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty.
- Published in:
- 2017
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- Publication type:
- journal article
Expanding the Spectrum of Founder Mutations Causing Isolated Gonadotropin-Releasing Hormone Deficiency.
- Published in:
- 2015
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- Publication type:
- journal article
Approach to the patient with hypogonadotropic hypogonadism.
- Published in:
- 2013
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- Publication type:
- Journal Article
Nonsense mutations in FGF8 gene causing different degrees of human gonadotropin-releasing deficiency.
- Published in:
- 2010
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- Publication type:
- journal article
Steroidogenic Factor 1 Overexpression and Gene Amplification Are More Frequent in Adrenocortical Tumors from Children than from Adults.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 3, p. 1458, doi. 10.1210/jc.2009-2040
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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.
- Published in:
- 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
Expression of Insulin-Like Growth Factor-II and Its Receptor in Pediatric and Adult Adrenocortical Tumors.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 9, p. 3524, doi. 10.1210/jc.2008-0065
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- Publication type:
- Article
Factors Determining Normal Adult Height in Girls with Gonadotropin-Dependent Precocious Puberty Treated with Depot Gonadotropin-Releasing Hormone Analogs.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 7, p. 2662, doi. 10.1210/jc.2007-2183
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- Publication type:
- Article
Evaluating the Roles of Follicle-Stimulating Hormone Receptor Polymorphisms in Gonadal Hyperstimulation Associated with Severe Juvenile Primary Hypothyroidism.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 6, p. 2312, doi. 10.1210/jc.2006-2086
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- Publication type:
- Article
Novel Fibroblast Growth Factor Receptor 1 Mutations in Patients with Congenital Hypogonadotropic Hypogonadism with and without Anosmia.
- Published in:
- 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.
- Published in:
- 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
Allelic Variants of the γ-Aminobutyric Acid-A Receptor α1-Subunit Gene (GABRA1) Are Not Associated with Idiopathic Gonadotropin-Dependent Precocious Puberty in Girls with and without Electroencephalographic Abnormalities.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 6, p. 2432, doi. 10.1210/jc.2005-2657
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- Publication type:
- Article
Letter re: FSH Receptor Polymorphisms and Iatrogenic Ovarian Hyperstimulation.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 8, p. 4978, doi. 10.1210/jc.2005-0650
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- Publication type:
- Article
Deletion Mapping of Chromosome 17 in Benign and Malignant Adrenocortical Tumors Associated with the Arg337His Mutation of the p53 Tumor Suppressor Protein.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 5, p. 2976, doi. 10.1210/jc.2004-0963
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- Publication type:
- Article
Familial Hyperestrogenism in Both Sexes: Clinical, Hormonal, and Molecular Studies of Two Siblings.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 7, p. 3027, doi. 10.1210/jc.2002-021780
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- Publication type:
- Article
Familial Hyperestrogenism in Both Sexes: Clinical, Hormonal, and Molecular Studies of Two Siblings.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 7, p. 3027, doi. 10.1210/jc.2002-021780
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- Publication type:
- Article
Cushing’s Syndrome Secondary to Adrenocorticotropin-Independent Macronodular Adrenocortical Hyperplasia due to Activating Mutations of GNAS1 Gene.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 5, p. 2147, doi. 10.1210/jc.2002-021362
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- Publication type:
- Article
Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene.
- Published in:
- 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
An Inherited Mutation Outside the Highly Conserved DNA-Binding Domain of the p53 Tumor Suppressor Protein in Children and Adults with Sporadic Adrenocortical Tumors.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 10, p. 4970, doi. 10.1210/jcem.86.10.7957
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- Publication type:
- Article
Adrenocorticotropin-Dependent Precocious Puberty of Testicular Origin in a Boy with X-Linked Adrenal Hypoplasia Congenita Due to a Novel Mutation in the DAX1 Gene.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 9, p. 4068, doi. 10.1210/jcem.86.9.7816
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- Publication type:
- Article
The Importance of Autosomal Genes in Kallmann Syndrome: Genotype-Phenotype Correlations and Neuroendocrine Characteristics.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 4, p. 1532, doi. 10.1210/jcem.86.4.7420
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- Publication type:
- Article
Gonadotropin-Independent Precocious Puberty Due to Luteinizing Hormone Receptor Mutations in Brazilian Boys: A Novel Constitutively Activating Mutation in the First Transmembrane Helix.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 12, p. 4799, doi. 10.1210/jcem.85.12.7071
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- Publication type:
- Article
Origin of an Ovarian Steroid Cell Tumor Causing Isosexual Pseudoprecocious Puberty Demonstrated by the Expression of Adrenal Steroidogenic Enzymes and Adrenocorticotropin Receptor.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 3, p. 1211, doi. 10.1210/jcem.85.3.6454
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- Publication type:
- Article
Longitudinal Hormonal and Pituitary Imaging Changes in Two Females with Combined Pituitary Hormone Deficiency due to Deletion of A301,G302 in the PROP1 Gene.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 3, p. 942, doi. 10.1210/jcem.84.3.5537
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- Publication type:
- Article
Activating Mutation of the Stimulatory G Protein (gsp) as a Putative Cause of Ovarian and Testicular Human Stromal Leydig Cell Tumors
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 6, p. 2074, doi. 10.1210/jcem.83.6.4847
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- Publication type:
- Article
Clinical and Pathological Predictors of Death for Adrenocortical Carcinoma.
- Published in:
- Journal of the Endocrine Society, 2024, v. 8, n. 4, p. 1, doi. 10.1210/jendso/bvad170
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- Publication type:
- Article
Efficacy of Oral Furosemide Test for Primary Aldosteronism Diagnosis.
- Published in:
- Journal of the Endocrine Society, 2024, v. 8, n. 1, p. 1, doi. 10.1210/jendso/bvad147
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- Publication type:
- Article
High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort.
- Published in:
- Journal of the Endocrine Society, 2022, v. 6, n. 9, p. 1, doi. 10.1210/jendso/bvac106
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- Publication type:
- Article
New Insights Into Pheochromocytoma Surveillance of Young Patients With VHL Missense Mutations.
- Published in:
- Journal of the Endocrine Society, 2019, v. 3, n. 9, p. 1682, doi. 10.1210/js.2019-00225
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- Publication type:
- Article
MKRN3 Mutations in Central Precocious Puberty: A Systematic Review and Meta-Analysis.
- Published in:
- Journal of the Endocrine Society, 2019, v. 3, n. 5, p. 979, doi. 10.1210/js.2019-00041
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- Publication type:
- Article
Retrospective Analysis of Prognostic Factors in Pediatric Patients with Adrenocortical Tumor from Unique Tertiary Center with Long-Term Follow-Up.
- Published in:
- Journal of Clinical Medicine, 2022, v. 11, n. 22, p. 6641, doi. 10.3390/jcm11226641
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- Publication type:
- Article
Myocardial Inactivation of Thyroid Hormones in Patients with Aortic Stenosis.
- Published in:
- Thyroid, 2017, v. 27, n. 5, p. 738, doi. 10.1089/thy.2016.0514
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- Publication type:
- Article
Intraoperative radiofrequency ablation for unresectable abdominal paraganglioma: a case report.
- Published in:
- Frontiers in Endocrinology, 2024, p. 1, doi. 10.3389/fendo.2024.1346052
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- Publication type:
- Article