Found: 137
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IGSF10 mutations dysregulate gonadotropin-releasing hormone neuronal migration resulting in delayed puberty.
- Published in:
- EMBO Molecular Medicine, 2016, v. 8, n. 6, p. 626, doi. 10.15252/emmm.201606250
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- Publication type:
- Article
Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life.
- Published in:
- Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0287-9
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- Publication type:
- Article
Absence of activating mutations in the GnRH receptor gene in human pituitary gonadotroph adenomas.
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- European Journal of Endocrinology, 1998, v. 139, n. 2, p. 157, doi. 10.1530/eje.0.1390157
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- Publication type:
- Article
Personalized Noninvasive Diagnostic Algorithms Based on Urinary Free Cortisol in ACTH-dependant Cushing's Syndrome.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 11, p. 2882, doi. 10.1210/clinem/dgae258
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- Publication type:
- Article
Exome Sequencing as a Tool for Detecting Point Mutations and Deletions in Patients With Hypogonadotropic Hypogonadism.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 10, p. e4254, doi. 10.1210/clinem/dgac377
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- Publication type:
- Article
Reproductive Phenotypes in Men With Acquired or Congenital Hypogonadotropic Hypogonadism: A Comparative Study.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 7, p. e2812, doi. 10.1210/clinem/dgac194
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- Publication type:
- Article
Response to Letter to the Editor from Soghomonian: "Epicardial and Pericardial Adiposity Without Myocardial Steatosis in Cushing Syndrome".
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 1, p. e443, doi. 10.1210/clinem/dgab678
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- Publication type:
- Article
Epicardial and Pericardial Adiposity Without Myocardial Steatosis in Cushing Syndrome.
- Published in:
- 2021
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- Publication type:
- journal article
Compromised Volumetric Bone Density and Microarchitecture in Men With Congenital Hypogonadotropic Hypogonadism.
- Published in:
- 2021
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- Publication type:
- journal article
Does Genetic Susceptibility of the Gonadotropic Axis Explain the Variable Impact of Stressors Causing Functional Hypothalamic Amenorrhea?
- Published in:
- 2021
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- Publication type:
- journal article
Non-invasive Diagnostic Strategy in ACTH-dependent Cushing's Syndrome.
- Published in:
- 2020
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- Publication type:
- journal article
BMPR1A and BMPR1B Missense Mutations Cause Primary Ovarian Insufficiency.
- Published in:
- 2019
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- Publication type:
- journal article
Illicit Upregulation of Serotonin Signaling Pathway in Adrenals of Patients With High Plasma or Intra-Adrenal ACTH Levels.
- Published in:
- 2019
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- Publication type:
- journal article
Letter to the Editor: "Long-Term Outcome of Primary Bilateral Macronodular Adrenocortical Hyperplasia After Unilateral Adrenalectomy".
- Published in:
- 2019
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- Publication type:
- Letter
Hyperprolactinemia-induced ovarian acyclicity is reversed by kisspeptin administration.
- Published in:
- Journal of Clinical Investigation, 2012, v. 122, n. 10, p. 3791, doi. 10.1172/JCI63937
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- Publication type:
- Article
Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome.
- Published in:
- Neuroendocrinology, 2021, v. 111, n. 1/2, p. 99, doi. 10.1159/000506640
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- Publication type:
- Article
Germline Prolactin Receptor Mutation Is Not a Major Cause of Sporadic Prolactinoma in Humans.
- Published in:
- Neuroendocrinology, 2016, v. 103, n. 6, p. 738, doi. 10.1159/000442981
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- Publication type:
- Article
Kisspeptin Restores Pulsatile LH Secretion in Patients with Neurokinin B Signaling Deficiencies: Physiological, Pathophysiological and Therapeutic Implications.
- Published in:
- Neuroendocrinology, 2013, v. 97, n. 2, p. 193, doi. 10.1159/000336376
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- Publication type:
- Article
Hyperprolactinémie et infertilité Approche physiopathologique.
- Published in:
- Médecine Sciences, 2013, v. 29, n. 3, p. 242, doi. 10.1051/medsci/2013293004
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- Publication type:
- Article
Classification of Patients With GH Disorders May Vary According to the IGF-I Assay.
- Published in:
- 2017
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- Publication type:
- journal article
Anti-Müllerian Hormone and Ovarian Morphology in Women With Isolated Hypogonadotropic Hypogonadism/Kallmann Syndrome: Effects of Recombinant Human FSH.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2017, v. 102, n. 4, p. 1102, doi. 10.1210/jc.2016-3799
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- Publication type:
- Article
Anti-Müllerian Hormone and Ovarian Morphology in Women With Isolated Hypogonadotropic Hypogonadism/Kallmann Syndrome: Effects of Recombinant Human FSH.
- Published in:
- 2017
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- Publication type:
- journal article
Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2016, p. 4541, doi. 10.1210/jc.2016-2152
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- Publication type:
- Article
Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency.
- Published in:
- 2016
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- Publication type:
- journal article
Reference Values for IGF-I Serum Concentrations: Comparison of Six Immunoassays.
- Published in:
- 2016
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- Publication type:
- journal article
Unilateral Adrenalectomy as a First-Line Treatment of Cushing's Syndrome in Patients With Primary Bilateral Macronodular Adrenal Hyperplasia.
- Published in:
- 2015
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- Publication type:
- journal article
Macroprolactinomas in children and adolescents: factors associated with the response to treatment in 77 patients.
- Published in:
- 2015
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- Publication type:
- Journal Article
New NOBOX Mutations Identified in a Large Cohort of Women With Primary Ovarian Insufficiency Decrease KIT-L Expression.
- Published in:
- 2015
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- Publication type:
- Journal Article
Sex Steroids, Precursors, and Metabolite Deficiencies in Men With Isolated Hypogonadotropic Hypogonadism and Panhypopituitarism: A GCMS-Based Comparative Study.
- Published in:
- 2015
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- Publication type:
- Journal Article
131I-noriodocholesterol uptake by testicular adrenal rest tumors in a patient with classical 21-hydroxylase deficiency.
- Published in:
- 2014
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- Publication type:
- journal article
Cardiac structure and function in Cushing's syndrome: a cardiac magnetic resonance imaging study.
- Published in:
- 2014
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- Publication type:
- journal article
Insulin-like Peptide 3 (INSL3) in Men With Congenital Hypogonadotropic Hypogonadism/Kallmann Syndrome and Effects of Different Modalities of Hormonal Treatment: A Single-Center Study of 281 Patients.
- Published in:
- 2014
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- Publication type:
- Journal Article
Molecular screening for a personalized treatment approach in advanced adrenocortical cancer.
- Published in:
- 2013
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- Publication type:
- Journal Article
One-year progression-free survival of therapy-naive patients with malignant pheochromocytoma and paraganglioma.
- Published in:
- 2013
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- Publication type:
- Journal Article
Computed tomography of the anterior skull base in Kallmann syndrome reveals specific ethmoid bone abnormalities associated with olfactory bulb defects.
- Published in:
- 2013
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- Publication type:
- journal article
No evidence of a detrimental effect of cabergoline therapy on cardiac valves in patients with acromegaly.
- Published in:
- 2012
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- Publication type:
- journal article
Mitotane, Metyrapone, and Ketoconazole Combination Therapy as an Alternative to Rescue Adrenalectomy for Severe ACTH-Dependent Cushing’s Syndrome.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 9, p. 2796, doi. 10.1210/jc.2011-0536
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- Publication type:
- Article
Endocrine effects of the tyrosine kinase inhibitor vandetanib in patients treated for thyroid cancer.
- Published in:
- 2011
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- Publication type:
- journal article
Ectopic ACTH Syndrome in Children and Adolescents.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 5, p. 1213, doi. 10.1210/jc.2010-2276
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- Publication type:
- Article
Diabetes Mellitus, Extreme Insulin Resistance, and Hypothalamic-Pituitary Langerhans Cells Histiocytosis.
- Published in:
- Case Reports in Endocrinology, 2019, p. 1, doi. 10.1155/2019/2719364
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- Publication type:
- Article
Prenatal testosterone treatment potentiates the aggression-inhibiting effect of the neurosteroid dehydroepiandrosterone in female mice.
- Published in:
- Aggressive Behavior, 2001, v. 27, n. 2, p. 130, doi. 10.1002/ab.5
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- Publication type:
- Article
R31C <i>GNRH1</i> Mutation and Congenital Hypogonadotropic Hypogonadism.
- Published in:
- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0069616
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- Publication type:
- Article
Two Families with Normosmic Congenital Hypogonadotropic Hypogonadism and Biallelic Mutations in KISS1R (KISS1 Receptor): Clinical Evaluation and Molecular Characterization of a Novel Mutation.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0053896
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- Publication type:
- Article
Congenital Hypogonadotropic Hypogonadism Due to GNRH Receptor Mutations in Three Brothers Reveal Sites Affecting Conformation and Coupling.
- Published in:
- PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0038456
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- Publication type:
- Article
Normosmic Congenital Hypogonadotropic Hypogonadism Due to TAC3/TACR3 Mutations: Characterization of Neuroendocrine Phenotypes and Novel Mutations.
- Published in:
- PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0025614
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- Publication type:
- Article
Familial Glucocorticoid Receptor Haploinsufficiency by Non-Sense Mediated mRNA Decay, Adrenal Hyperplasia and Apparent Mineralocorticoid Excess.
- Published in:
- PLoS ONE, 2010, v. 5, n. 10, p. 1, doi. 10.1371/journal.pone.0013563
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- Publication type:
- Article
Female Gonadal Function before and after Treatment of Acromegaly.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 10, p. 4518, doi. 10.1210/jc.2009-2815
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- Publication type:
- Article
TAC3 and TACR3 Defects Cause Hypothalamic Congenital Hypogonadotropic Hypogonadism in Humans.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 5, p. 2287, doi. 10.1210/jc.2009-2600
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- Publication type:
- Article
The paradoxical increase in cortisol secretion induced by dexamethasone in primary pigmented nodular adrenocortical disease involves a glucocorticoid receptor-mediated effect of dexamethasone on protein kinase A catalytic subunits.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Lack of androgen receptor expression in Sertoli cells accounts for the absence of anti-Mullerian hormone repression during early human testis development.
- Published in:
- 2009
- By:
- Publication type:
- journal article