Found: 31
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Targeting dopamine receptors subtype 2 (D2DR) in pheochromocytomas: head-to-head comparison between in vitro and in vivo findings.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Physiopathology of somatolactotroph cells: from transduction mechanisms to cotargeting therapy.
- Published in:
- Annals of the New York Academy of Sciences, 2011, v. 1220, n. 1, p. 60, doi. 10.1111/j.1749-6632.2010.05924.x
- By:
- Publication type:
- Article
Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue.
- Published in:
- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0126648
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- Publication type:
- Article
A Potential Inhibitory Role for the New Truncated Variant of Somatostatin Receptor 5, sst5TMD4, in Pituitary Adenomas Poorly Responsive to Somatostatin Analogs.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 5, p. 2497, doi. 10.1210/jc.2009-2247
- By:
- Publication type:
- Article
Rapid Pituitary Tumor Shrinkage with Dissociation between Antiproliferative and Antisecretory Effects of a Long-Acting Octreotide in an Acromegalic Patient.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 5, p. 1592, doi. 10.1210/jc.2006-2084
- By:
- Publication type:
- Article
Identification and Functional Analysis of the Novel S179R POU1F1 Mutation Associated with Combined Pituitary Hormone Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 12, p. 4981, doi. 10.1210/jc.2005-2289
- By:
- Publication type:
- Article
Genetic Screening of Combined Pituitary Hormone Deficiency: Experience in 195 Patients.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 9, p. 3329, doi. 10.1210/jc.2005-2173
- By:
- Publication type:
- Article
Novel Mutations within the POU1F1 Gene Associated with Variable Combined Pituitary Hormone Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 8, p. 4762, doi. 10.1210/jc.2005-0570
- By:
- Publication type:
- Article
An Uncommon Phenotype with Familial Central Hypogonadism Caused by a Novel PROP1 Gene Mutant Truncated in the Transactivation Domain.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 8, p. 4880, doi. 10.1210/jc.2005-0119
- By:
- Publication type:
- Article
Novel Mutations within the POU1F1 Gene Associated with Variable Combined Pituitary Hormone Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 6, p. 4762, doi. 10.1210/jc.2005-0570
- By:
- Publication type:
- Article
Characterization of the ability of a, second-generation SST-DA chimeric molecule, TBR-065, to suppress GH secretion from human GH-secreting adenoma cells.
- Published in:
- Pituitary, 2021, v. 24, n. 3, p. 351, doi. 10.1007/s11102-020-01113-4
- By:
- Publication type:
- Article
Unilateral agenesis of internal carotid artery associated with congenital combined pituitary hormone deficiency and pituitary stalk interruption without HESX1, LHX4 or OTX2 mutation: a case report.
- Published in:
- 2012
- By:
- Publication type:
- Report
Detection of genetic hypopituitarism in an adult population of idiopathic pituitary insufficiency patients with growth hormone deficiency.
- Published in:
- Pituitary, 2011, v. 14, n. 3, p. 208, doi. 10.1007/s11102-010-0278-8
- By:
- Publication type:
- Article
In vivo and in vitro response to octreotide LAR in a TSH-secreting adenoma: characterization of somatostatin receptor expression and role of subtype 5.
- Published in:
- Pituitary, 2011, v. 14, n. 2, p. 141, doi. 10.1007/s11102-010-0271-2
- By:
- Publication type:
- Article
Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports.
- Published in:
- Journal of Neuroendocrinology, 2023, v. 35, n. 6, p. 1, doi. 10.1111/jne.13287
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- Publication type:
- Article
IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency.
- Published in:
- European Journal of Endocrinology, 2022, v. 187, n. 6, p. 787, doi. 10.1530/EJE-22-0520
- By:
- Publication type:
- Article
Germinal defects of SDHx genes in patients with isolated pituitary adenoma.
- Published in:
- European Journal of Endocrinology, 2020, v. 183, n. 4, p. 369, doi. 10.1530/EJE-20-0054
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- Publication type:
- Article
Pituitary stalk interruption syndrome: etiology and clinical manifestations.
- Published in:
- European Journal of Endocrinology, 2019, v. 181, n. 5, p. R199, doi. 10.1530/EJE-19-0168
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- Publication type:
- Article
An update in the genetic aetiologies of combined pituitary hormone deficiency.
- Published in:
- European Journal of Endocrinology, 2016, v. 174, n. 6, p. R239, doi. 10.1530/EJE-15-1095
- By:
- Publication type:
- Article
The analysis of quantitative expression of somatostatin and dopamine receptors in gastro-entero-pancreatic tumours opens new therapeutic strategies.
- Published in:
- European Journal of Endocrinology, 2006, v. 155, n. 6, p. 849, doi. 10.1530/eje.1.02307
- By:
- Publication type:
- Article
Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and man.
- Published in:
- Human Molecular Genetics, 2023, v. 32, n. 3, p. 367, doi. 10.1093/hmg/ddac192
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- Publication type:
- Article
Congenital Central Hypothyroidism Caused by a Novel IGSF1 Variant Identified in a French Family.
- Published in:
- Hormone Research in Paediatrics, 2022, v. 95, n. 3, p. 296, doi. 10.1159/000524233
- By:
- Publication type:
- Article
Hypopituitarism in Patients with Blepharophimosis and FOXL2 Mutations.
- Published in:
- Hormone Research in Paediatrics, 2020, v. 93, n. 1, p. 30, doi. 10.1159/000507249
- By:
- Publication type:
- Article
Genetic analysis of adult Slovenian patients with combined pituitary hormone deficiency.
- Published in:
- Endocrine (1355008X), 2019, v. 65, n. 2, p. 379, doi. 10.1007/s12020-019-01949-2
- By:
- Publication type:
- Article
Pituitary stalk interruption and olfactory bulbs aplasia/hypoplasia in a man with Kallmann syndrome and reversible gonadotrope and somatotrope deficiencies.
- Published in:
- Endocrine (1355008X), 2015, v. 49, n. 3, p. 865, doi. 10.1007/s12020-014-0475-8
- By:
- Publication type:
- Article
Somatostatin and Dopamine-Somatostatin Multiple Ligands Directed towards Somatostatin and Dopamine Receptors in Pituitary Adenomas.
- Published in:
- Neuroendocrinology, 2006, v. 83, n. 3/4, p. 258, doi. 10.1159/000095536
- By:
- Publication type:
- Article
Proposition of adjustments to the ACMG‐AMP framework for the interpretation of MEN1 missense variants.
- Published in:
- Human Mutation, 2019, v. 40, n. 6, p. 661, doi. 10.1002/humu.23746
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- Publication type:
- Article
Octreotide therapy in meningiomas: in vitro study, clinical correlation, and literature review.
- Published in:
- Journal of Neurosurgery, 2017, v. 127, n. 3, p. 660, doi. 10.3171/2016.8.JNS16995
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- Publication type:
- Article
Case seminar: a young female with acute hyponatremia and a sellar mass.
- Published in:
- Endocrine (1355008X), 2011, v. 40, n. 3, p. 325, doi. 10.1007/s12020-011-9516-8
- By:
- Publication type:
- Article
Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort.
- Published in:
- Clinical Endocrinology, 2021, v. 94, n. 2, p. 277, doi. 10.1111/cen.14355
- By:
- Publication type:
- Article
Balance between somatostatin and D2 receptor expression drives TSH-secreting adenoma response to somatostatin analogues and dopastatins.
- Published in:
- Clinical Endocrinology, 2012, v. 76, n. 3, p. 407, doi. 10.1111/j.1365-2265.2011.04200.x
- By:
- Publication type:
- Article