All Stories

  1. Octreotide therapy in meningiomas: in vitro study, clinical correlation, and literature review
  2. LHX4 et déficit hypophysaire congénital : nouveaux variants, nouveau phénotype, nouvelle surveillance
  3. Hypopituitarisme congénital : description phénotypique et analyse génétique de 990 patients. Expérience du réseau Genhypopit
  4. Combined pituitary hormone deficiency: current and future status
  5. Pasireotide and octreotide antiproliferative effects and sst2 trafficking in human pancreatic neuroendocrine tumor cultures
  6. Neuroendocrine tumors: insights into innovative therapeutic options and rational development of targeted therapies
  7. Targeting Dopamine Receptors Subtype 2 (D2DR) in Pheochromocytomas: Head-to-Head Comparison Between In Vitro and In Vivo Findings
  8. 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
  9. PROKR2 Variants in Multiple Hypopituitarism with Pituitary Stalk Interruption
  10. Somatostatin receptor sst2 gene transfer in human prolactinomas in vitro: Impact on sensitivity to dopamine, somatostatin and dopastatin, in the control of prolactin secretion
  11. Genetic causes of combined pituitary hormone deficiencies in humans
  12. Phenotypic Homogeneity and Genotypic Variability in a Large Series of Congenital Isolated ACTH-Deficiency Patients withTPITGene Mutations
  13. Balance between somatostatin and D2 receptor expression drives TSH‐secreting adenoma response to somatostatin analogues and dopastatins
  14. Case seminar: a young female with acute hyponatremia and a sellar mass
  15. Quelles causes génétiques rechercher en présence d’un déficit en hormone de croissance ?
  16. Physiopathology of somatolactotroph cells: from transduction mechanisms to cotargeting therapy
  17. Expression of somatostatin receptors, dopamine D2 receptors, noradrenaline transporters, and vesicular monoamine transporters in 52 pheochromocytomas and paragangliomas
  18. Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms
  19. Detection of genetic hypopituitarism in an adult population of idiopathic pituitary insufficiency patients with growth hormone deficiency
  20. Effet de l’octréotide et du SOM 230 sur la viabilité cellulaire de méningiomes in vitro
  21. In vivo and in vitro response to octreotide LAR in a TSH-secreting adenoma: characterization of somatostatin receptor expression and role of subtype 5
  22. A Potential Inhibitory Role for the New Truncated Variant of Somatostatin Receptor 5, sst5TMD4, in Pituitary Adenomas Poorly Responsive to Somatostatin Analogs
  23. Ciblage des récepteurs de la somatostatine dans les tumeurs neuroendocrines gastroentéropancréatiques (TNE-GEP) : quels radiotraceurs pour quelles tumeurs ?
  24. Donnees genetiques actuelles
  25. Lanreotide for the treatment of acromegaly
  26. Mécanismes de tumorigenèse hypophysaire
  27. Somatostatin Receptor sst2 Decreases Cell Viability and Hormonal Hypersecretion and Reverses Octreotide Resistance of Human Pituitary Adenomas
  28. Congenital pituitary hormone deficiencies: role ofLHX3/LHX4genes
  29. OR2,6 Interrelationship between somatostatin/dopamine pathways and growth factors in non-small lung cancer cells
  30. Somatostatin–dopamine ligands in the treatment of pituitary adenomas
  31. A Novel Dysfunctional LHX4 Mutation with High Phenotypical Variability in Patients with Hypopituitarism
  32. Efficacy of a dopamine-somatostatin chimeric molecule, BIM-23A760, in the control of cell growth from primary cultures of human non-functioning pituitary adenomas: a multi-center study
  33. Relevance of coexpression of somatostatin and dopamine D2 receptors in pituitary adenomas
  34. Somatostatinergic ligands in dopamine-sensitive and -resistant prolactinomas
  35. Déficit hypophysaire combiné multiple : aspects cliniques et génétiques
  36. Rapid Pituitary Tumor Shrinkage with Dissociation between Antiproliferative and Antisecretory Effects of a Long-Acting Octreotide in an Acromegalic Patient
  37. Novel chimeric somatostatin analogs: facts and perspectives
  38. saveanu
  39. Identification and Functional Analysis of the Novel S179RPOU1F1Mutation Associated with Combined Pituitary Hormone Deficiency
  40. The analysis of quantitative expression of somatostatin and dopamine receptors in gastro-entero-pancreatic tumours opens new therapeutic strategies
  41. Genetic Screening of Combined Pituitary Hormone Deficiency: Experience in 195 Patients
  42. Somatostatin and Dopamine-Somatostatin Multiple Ligands Directed towards Somatostatin and Dopamine Receptors in Pituitary Adenomas
  43. An Uncommon Phenotype with Familial Central Hypogonadism Caused by a NovelPROP1Gene Mutant Truncated in the Transactivation Domain
  44. Novel Mutations within thePOU1F1Gene Associated with Variable Combined Pituitary Hormone Deficiency
  45. Efficacy of chimeric molecules directed towards multiple somatostatin and dopamine receptors on inhibition of GH and prolactin secretion from GH-secreting pituitary adenomas classified as partially responsive to somatostatin analog therapy
  46. Génétique des hypopituitarismes antérieurs
  47. Novel modalities of somatostatin actions
  48. Pituitary hormone deficiencies due to transcription factor gene alterations
  49. P222 - Expression quantitative des arnm de récepteurs de la somatostatine (sst2 et sst5) et dopamine d2 (d2dr) dans les tumeurs endocrines digestives
  50. Hypopituitarisme congénital
  51. Demonstration of Enhanced Potency of a Chimeric Somatostatin-Dopamine Molecule, BIM-23A387, in Suppressing Growth Hormone and Prolactin Secretion from Human Pituitary Somatotroph Adenoma Cells
  52. A luteinizing hormone-, alpha-subunit- and prolactin-secreting pituitary adenoma responsive to somatostatin analogs: in vivo and in vitro studies
  53. BIM-23244, a Somatostatin Receptor Subtype 2- and 5-Selective Analog with Enhanced Efficacy in Suppressing Growth Hormone (GH) from Octreotide-Resistant Human GH-Secreting Adenomas
  54. BIM-23244, a Somatostatin Receptor Subtype 2- and 5-Selective Analog with Enhanced Efficacy in Suppressing Growth Hormone (GH) from Octreotide-Resistant Human GH-Secreting Adenomas1
  55. Human Somatostatin Receptor Subtypes in Acromegaly: Distinct Patterns of Messenger Ribonucleic Acid Expression and Hormone Suppression Identify Different Tumoral Phenotypes1
  56. Quantitative and Functional Expression of Somatostatin Receptor Subtypes in Human Prolactinomas1