All Stories

  1. Evaluation of the analytic performance and macroprolactin sensitivity of a new prolactin immunoassay
  2. Aggressive Pituitary Tumors and Pituitary Carcinomas: definition, management and overview for clinical practice
  3. A promising new direct immunoassay for urinary free cortisol determination
  4. Evidence for somatic mutation screening on aggressive prolactinomas
  5. Acromegaly Disease Control Maintained After Switching From Injected Somatostatin Receptor Ligands to Oral Paltusotine
  6. Impact of exenatide on weight loss and eating behavior in adults with craniopharyngioma-related obesity: the CRANIOEXE randomized placebo-controlled trial
  7. Letter to the Editor From Salle et al.: “A Prospective Multicenter Observational Study of Surgical Versus non-surgical Management for Pituitary Apoplexy”
  8. Carney complex predisposes to breast cancer: prospective study of 50 women
  9. Pasireotide: potential treatment option for McCune–Albright-associated acromegaly
  10. Evidence of Persistent Mild Hypercortisolism in Patients Medically Treated for Cushing Disease: the Haircush Study
  11. The World Health Organization classifications of pituitary neuroendocrine tumours: a clinico-pathological appraisal
  12. Initial pathology in aggressive pituitary tumours and carcinomas: 2b or not 2b?—that is the question
  13. Current Advances in Papillary Craniopharyngioma: State-Of-The-Art Therapies and Overview of the Literature
  14. Outcome and prognostic factors for pituitary carcinomas: lessons from a systematic review
  15. Inhibition of activin signalling reduces the growth of LβT2 gonadotroph pituitary tumours in mouse
  16. IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency
  17. Biological and Therapeutic Implications of the Tumor Microenvironment in Pituitary Adenomas
  18. Aggressive pituitary tumours and carcinomas, characteristics and management of 171 patients
  19. The Challenging Management of Craniopharyngiomas in Adults: Time for a Reappraisal?
  20. Aggressive corticotroph tumors and carcinomas
  21. Prolactin immunoassay: does the high-dose hook effect still exist?
  22. Immunotherapy in aggressive pituitary tumors and carcinomas: a systematic review
  23. Clinical Biology of the Pituitary Adenoma
  24. First case of chronic post-traumatic anterior pituitary dysfunction in a professional rugby player: A case report
  25. Aggressive Pituitary Adenomas
  26. Aggressive pituitary tumours and pituitary carcinomas
  27. Graves’ Disease during Immune Checkpoint Inhibitor Therapy (A Case Series and Literature Review)
  28. Letter to the Editor From Helene Lasolle and Gérald Raverot: “USP8 and TP53 Drivers Are Associated With CNV in a Corticotroph Adenoma Cohort Enriched for Aggressive Tumors”
  29. Anti-PD1 and Anti-PDL1-Induced Hypophysitis: A Cohort Study of 17 Patients with Longitudinal Follow-Up
  30. Immunotherapy in Corticotroph and Lactotroph Aggressive Tumors and Carcinomas: Two Case Reports and a Review of the Literature
  31. Immune Landscape of Pituitary Tumors Reveals Association Between Macrophages and Gonadotroph Tumor Invasion
  32. Treatment Options for Gonadotroph Tumors: Current State and Perspectives
  33. Urinary free cortisol: An automated immunoassay without extraction for diagnosis of Cushing’s syndrome and follow‐up of patients treated by anticortisolic drugs
  34. Gonadotroph Tumors Show Subtype Differences that Might Have Implications for Therapy
  35. How to Classify Pituitary Neuroendocrine Tumors (PitNET)s in 2020
  36. The Microenvironment of Pituitary Tumors—Biological and Therapeutic Implications
  37. Aggressive prolactinomas: how to manage?
  38. Is Gross Total Resection Reasonable in Adults with Craniopharyngiomas with Hypothalamic Involvement?
  39. Emerging and Novel Treatments for Pituitary Tumors
  40. Predicting early post-operative remission in pituitary adenomas: evaluation of the modified knosp classification
  41. Cabergoline in severe ectopic or occult Cushing’s syndrome
  42. Pathological markers of somatotroph pituitary neuroendocrine tumors predicting the response to medical treatment
  43. Pasireotide: A potential therapeutic alternative for resistant prolactinoma
  44. Ectopic acromegaly due to growth hormone-releasing hormone producing bronchial carcinoid causing somatotroph hyperplasia and partial pituitary insufficiency
  45. Clinical, Pathological, and Molecular Factors of Aggressiveness in Lactotroph Tumours
  46. Sex-Related Differences in Lactotroph Tumor Aggressiveness Are Associated With a Specific Gene-Expression Signature and Genome Instability
  47. Correction to: Signs and symptoms of acromegaly at diagnosis: the physician’s and the patient’s perspectives in the ACRO-POLIS study
  48. Signs and symptoms of acromegaly at diagnosis: the physician’s and the patient’s perspectives in the ACRO-POLIS study
  49. Unusual neurologic presentation of aseptic abscesses syndrome
  50. Aggressive pituitary tumours and carcinomas: two sides of the same coin?
  51. Centralization errors in comparative genomic hybridization array analysis of pituitary tumor samples
  52. Dysregulation of cell cycle in animal models and human neuroendocrine pituitary tumors (PitNET)
  53. Hepatic safety of ketoconazole in Cushing’s syndrome: results of a Compassionate Use Programme in France
  54. MANAGEMENT OF ENDOCRINE DISEASE Hyperandrogenic states in women: pitfalls in laboratory diagnosis
  55. Treatment of aggressive pituitary tumours and carcinomas: results of a European Society of Endocrinology (ESE) survey 2016
  56. Prognostic factors of regrowth in nonfunctioning pituitary tumors
  57. Triple-A syndrome: a wide spectrum of adrenal dysfunction
  58. European Society of Endocrinology Clinical Practice Guidelines for the management of aggressive pituitary tumours and carcinomas
  59. Reconsidering olfactory bulb magnetic resonance patterns in Kallmann syndrome
  60. Risks and Benefits of Endoscopic Transsphenoidal Surgery for Nonfunctioning Pituitary Adenomas in Patients of the Ninth Decade
  61. Criteria for the definition of Pituitary Tumor Centers of Excellence (PTCOE): A Pituitary Society Statement
  62. Risk of Recurrence in Pituitary Neuroendocrine Tumors: A Prospective Study Using a Five-Tiered Classification
  63. Transdifferentiation of Neuroendocrine Cells
  64. Temozolomide treatment can improve overall survival in aggressive pituitary tumors and pituitary carcinomas
  65. From pituitary adenoma to pituitary neuroendocrine tumor (PitNET): an International Pituitary Pathology Club proposal
  66. MicroRNAs in pituitary tumors
  67. An old retrocardiac mass fortuitously reclassified as paraganglioma
  68. Silent somatotroph tumour revisited from a study of 80 patients with and without acromegaly and a review of the literature
  69. Dramatic change in skin color after bilateral adrenalectomy in Cushing's disease
  70. Establishment of revised diagnostic cut-offs for adrenal laboratory investigation using the new Roche Diagnostics Elecsys® Cortisol II assay
  71. T2-weighted MRI signal predicts hormone and tumor responses to somatostatin analogs in acromegaly
  72. Therapeutic innovations in endocrine diseases – part 3 : temozolomide and future therapeutics for aggressive pituitary tumors and carcinomas
  73. The silent somatotroph tumours
  74. Pituitary siderosis: the dark side of the pituitary
  75. Differential Effects of PI3K and Dual PI3K/mTOR Inhibition in Rat Prolactin-Secreting Pituitary Tumors
  76. Performance of the 4-mg intravenous dexamethasone suppression test in differentiating Cushing disease from pseudo-Cushing syndrome
  77. Dilated Cardiomyopathy Revealing Cushing Disease
  78. Biological and radiological exploration and management of non-functioning pituitary adenoma
  79. HMGA1-pseudogene expression is induced in human pituitary tumors
  80. Pituitary Involvement in Granulomatosis With Polyangiitis
  81. Expression of estrogen receptor alpha is associated with prolactin pituitary tumor prognosis and supports the sex-related difference in tumor growth
  82. Macroprolactinaemia: a biological diagnostic strategy from the study of 222 patients
  83. A Prognostic Clinicopathologic Classification of Pituitary Endocrine Tumors
  84. Macroprolactinomas in Children and Adolescents: Factors Associated With the Response to Treatment in 77 Patients
  85. Pituitary MRI characteristics in 297 acromegaly patients based on T2-weighted sequences
  86. Pasireotide versus continued treatment with octreotide or lanreotide in patients with inadequately controlled acromegaly (PAOLA): a randomised, phase 3 trial
  87. miR-23b and miR-130b expression is downregulated in pituitary adenomas
  88. Ketoconazole in Cushing's Disease: Is It Worth a Try?
  89. MANAGEMENT OF ENDOCRINE DISEASE: Clinicopathological classification and molecular markers of pituitary tumours for personalized therapeutic strategies
  90. Expression of somatostatin receptors, SSTR2A and SSTR5, in 108 endocrine pituitary tumors using immunohistochemical detection with new specific monoclonal antibodies
  91. Silent GH pituitary tumor: Diagnostic and therapeutic challenges
  92. Non-functioning pituitary macro-incidentalomas benefit from early surgery before becoming symptomatic
  93. Massive prolactinoma in women: a study of 15 cases
  94. BKM120, a pure PI3K inhibitor: a promising treatment for aggressive pituitary tumors or pituitary carcinomas
  95. Expression of somatostatin receptors, SSTR2Aand SSTR5, in 108 pituitary adenomas, using immunohistochemical detection with specific MABs
  96. Aggressive Silent GH Pituitary Tumor Resistant to Multiple Treatments, Including Temozolomide
  97. A new prognostic clinicopathological classification of pituitary adenomas: a multicentric case–control study of 410 patients with 8 years post-operative follow-up
  98. 18F-FDG PET/CT Findings in a Patient With Isolated Intracranial Rosai-Dorfman Disease
  99. Acromegaly induced by ectopic secretion of GHRH: A review 30 years after GHRH discovery
  100. Altered MicroRNA Expression Profile in Human Pituitary GH Adenomas: Down-Regulation of miRNA Targeting HMGA1, HMGA2, and E2F1
  101. Hypothalamo-pituitary sarcoidosis: a multicenter study of 24 patients
  102. Clinical Characteristics and Outcome of Acromegaly Induced by Ectopic Secretion of Growth Hormone-Releasing Hormone (GHRH): A French Nationwide Series of 21 Cases
  103. Pituitary carcinomas and aggressive pituitary tumours: merits and pitfalls of temozolomide treatment
  104. Insuffisances antéhypophysaires post-traumatismes crâniens : quel retentissement ? quel bilan ?
  105. New targeted therapies in pituitary carcinoma resistant to temozolomide
  106. Ectopic ACTH Syndrome in Children and Adolescents
  107. Evidence of improved surgical outcome following endoscopy for nonfunctioning pituitary adenoma removal
  108. Integrated Genomic Profiling Identifies Loss of Chromosome 11p Impacting Transcriptomic Activity in Aggressive Pituitary PRL Tumors
  109. Clinical Characteristics and Therapeutic Responses in Patients with Germ-LineAIPMutations and Pituitary Adenomas: An International Collaborative Study
  110. Temozolomide Treatment in Aggressive Pituitary Tumors and Pituitary Carcinomas: A French Multicenter Experience
  111. Proliferation markers of human pituitary tumors: Contribution of a genome-wide transcriptome approach
  112. Clinical, hormonal and molecular characterization of pituitary ACTH adenomas without (silent corticotroph adenomas) and with Cushing's disease
  113. Prognostic Factors in Prolactin Pituitary Tumors: Clinical, Histological, and Molecular Data from a Series of 94 Patients with a Long Postoperative Follow-Up
  114. Cabergoline therapy of paraneoplastic cushing syndrome in children
  115. Sex hormone-binding globulin gene expression in the liver: Drugs and the metabolic syndrome
  116. Carcinome hypophysaire
  117. Résultats comparés de la chirurgie endoscopique et de la microchirurgie dans une série consécutive de macroadénomes hypophysaires non fonctionnels
  118. Reply
  119. Secondary deterioration of visual field during cabergoline treatment for macroprolactinoma
  120. Predicting Visual Outcome After Treatment of Pituitary Adenomas With Optical Coherence Tomography
  121. Familial pituitary adenomas with a heterogeneous functional pattern: Clinical and genetic features
  122. A diagnostic marker set for invasion, proliferation, and aggressiveness of prolactin pituitary tumors
  123. Aryl Hydrocarbon Receptor-Interacting Protein Gene Mutations in Familial Isolated Pituitary Adenomas: Analysis in 73 Families
  124. P1-038 - Efficacité et tolérance à long terme du traitement médical des macroprolactinomes
  125. Mitotane Has an Estrogenic Effect on Sex Hormone-Binding Globulin and Corticosteroid-Binding Globulin in Humans
  126. Sox3 expression in undifferentiated spermatogonia is required for the progression of spermatogenesis
  127. Nuclear receptors Sf1 and Dax1 function cooperatively to mediate somatic cell differentiation during testis development
  128. X-Linked Sex-Determining Region Y Box 3 (SOX3) Gene Mutations Are Uncommon in Men with Idiopathic Oligoazoospermic Infertility
  129. Influence ofSHBGGene Pentanucleotide TAAAA Repeat and D327N Polymorphism on Serum Sex Hormone-Binding Globulin Concentration in Hirsute Women
  130. Sox3 Is Required for Gonadal Function, but Not Sex Determination, in Males and Females
  131. Syndrome de Klinefelter et microinjections intraovocytaires de spermatozoïdes (revue de la littérature)