All Stories

  1. A rare challenging case of co-existent craniopharyngioma, acromegaly and squamous cell lung cancer
  2. Recent advances in molecular pathology of craniopharyngioma
  3. Outcome of Nonfunctioning Pituitary Adenomas That Regrow After Primary Treatment: A Study From Two Large UK Centers
  4. THERAPY OF ENDOCRINE DISEASE: Surgery in microprolactinomas: effectiveness and risks based on contemporary literature
  5. Childhood Hypothalamic and Pituitary Tumors∗
  6. Patient-reported outcomes of parenteral somatostatin analogue injections in 195 patients with acromegaly
  7. Recent advances in the management of acromegaly
  8. Effectiveness of Metyrapone in Treating Cushing's Syndrome: A Retrospective Multicenter Study in 195 Patients
  9. Mortality of patients with non-functioning pituitary macroadenoma is significantly elevated: systematic analysis of 546 cases in a tertiary referral centre in the UK
  10. The burden of AIP mutations in pituitary adenoma patients from the UK
  11. Treating prolactinomas with dopamine agonists: always worth the gamble?
  12. Landscape of Familial Isolated and Young-Onset Pituitary Adenomas: Prospective Diagnosis inAIPMutation Carriers
  13. SDHC Mutations are Associated with Cardiac Paragangliomas: A Case Report of a Patient With a Dopamine-Secreting Tumor and Review of the Literature
  14. Diabetes Insipidus after Traumatic Brain Injury
  15. Mortality of patients with non-functioning pituitary macroadenoma is significantly elevated: systematic analysis of 546 cases in a tertiary referral centre in the UK
  16. Prevention of adrenal crisis in stress (The PACS Study): serum cortisol during elective surgery, acute trauma and sepsis in comparison to 'stress dose' hydrocortisone administration in adrenal insufficiency
  17. Efficacy and Complications of Pituitary Irradiation
  18. Mortality in patients with non-functioning pituitary adenoma is increased: systematic analysis of 546 cases with long follow-up
  19. Clinical and biochemical manifestations of Cushing’s
  20. Cushing’s Disease – Quality of Life, Recurrence and Long-term Morbidity
  21. Multi-parametric cardiovascular magnetic resonance imaging detects subclinical myocardial involvement in patients diagnosed with phaeochromocytoma
  22. Cushing’s Disease – Quality of Life, Recurrence and Long-term Morbidity
  23. Sequence analysis of the catalytic subunit of PKA in somatotroph adenomas
  24. MANAGEMENT OF ENDOCRINE DISEASE: Pituitary tumour apoplexy
  25. Functioning Gonadotroph Adenomas
  26. Low rate of germline AIP mutations in patients with apparently sporadic pituitary adenomas before the age of 40: a single-centre adult cohort
  27. The Wnt Signalling Cascade and the Adherens Junction Complex in Craniopharyngioma Tumorigenesis
  28. Diagnosis and management of prolactinomas and non-functioning pituitary adenomas
  29. 122 Cardiac Abnormalities are Common in Patients Diagnosed with Phaeochromocytoma as Detected by Cardiovascular Magnetic Resonance Imaging
  30. Refractory hypercalcaemia secondary to parathyroid carcinoma: response to high-dose denosumab
  31. Quality of life in patients with non-functioning pituitary adenomas
  32. BRAF V600E mutations are characteristic for papillary craniopharyngioma and may coexist with CTNNB1-mutated adamantinomatous craniopharyngioma
  33. A Patient with an Apparently Sporadic Pheochromocytoma with a Rearranged During Transfection Codon 635 Variant: A Mild Form of Multiple Endocrine Neoplasia Type 2?
  34. High incidence of cardiac involvement in patients diagnosed with phaeochromocytoma: a clinical study using cardiovascular magnetic resonance imaging
  35. The Prevention of Adrenal Crisis in Stress (PACS) study: serum cortisol during elective surgery and acute trauma in comparison to stress dose hydrocortisone in adrenal insufficiency
  36. Effectiveness of metyrapone in 195 patients with Cushing's syndrome
  37. Management of craniopharyngiomas
  38. Adrenal insufficiency in acute oral opiate therapy
  39. Rathke's cleft cyst
  40. Transsphenoidal pituitary surgery in the elderly is safe and effective
  41. Dandy-Walker Malformation, Papillary Thyroid Carcinoma, and SDHD-Associated Paraganglioma Syndrome
  42. Mortality in Cushing's syndrome: systematic analysis of a large series with prolonged follow-up
  43. The management of head-and-neck paragangliomas
  44. Hypophyseal Wegener's granulomatosis presenting by visual field constriction without hypopituitarism
  45. Does hypopituitarism recover when macroprolactinomas are treated with cabergoline?
  46. Confusing genes: a patient with MEN2A and Cushing's disease
  47. A thyroxine absorption test followed by weekly thyroxine administration: a method to assess non-adherence to treatment
  48. Bilateral third nerve palsy secondary to an apoplexy in a pituitary macroadenoma causing Cushing's disease: a very rare complication of a rare entity
  49. Whole-Exome Sequencing Studies of Nonfunctioning Pituitary Adenomas
  50. Epidemiology and natural history of pituitary tumours
  51. Craniopharyngiomas and Wnt signalling pathways
  52. Densely and sparsely granulated somatotroph adenomas: clinical, genetic and histological differences
  53. Whole-exome sequencing studies of non-functioning pituitary adenomas
  54. Granulation pattern, but not GSP or GHR mutation, is associated with clinical characteristics in somatostatin-naive patients with somatotroph adenomas
  55. Mitotane Therapy in Adrenocortical Cancer Induces CYP3A4 and Inhibits 5α-Reductase, Explaining the Need for Personalized Glucocorticoid and Androgen Replacement
  56. THERAPY IN ENDOCRINE DISEASE: Etomidate in the management of hypercortisolaemia in Cushing's syndrome: a review
  57. Current treatment protocols can offer a normal or near-normal quality of life in the majority of patients with non-functioning pituitary adenomas
  58. Neurofibromatosis Type 1 and pancreatic islet cell tumours: an association which should be recognized
  59. Pasireotide in the Management of Cushing’s Disease: A Review
  60. Somatostatin Analogs Modulate AIP in Somatotroph Adenomas: The Role of the ZAC1 Pathway
  61. Expression of guanylyl cyclase-B (GC-B/NPR2) receptors in normal human fetal pituitaries and human pituitary adenomas implicates a role for C-type natriuretic peptide
  62. Etomidate in the Management of Hypercortisolaemia in Cushing's Syndrome
  63. Pituitary Tumor Surgery in the Elderly: Perioperative Complications and Long-Term Outcome
  64. MECHANISMS IN ENDOCRINOLOGY: Ipilimumab: a novel immunomodulating therapy causing autoimmune hypophysitis: a case report and review
  65. Prevalence and incidence of pituitary adenomas
  66. Mini-review: pheochromocytomas causing the ectopic ACTH syndrome
  67. Disconnection hyperprolactinaemia in nonadenomatous sellar/parasellar lesions practically never exceeds 2000 mU/l
  68. The endocrine glands
  69. Rathke’s cleft cysts
  70. Craniopharyngiomas: An Overview
  71. IGF2-induced hypoglycemia unresponsive to everolimus
  72. Can we ever stop imaging in surgically treated and radiotherapy-naive patients with non-functioning pituitary adenoma?
  73. Pituitary apoplexy in non‐functioning pituitary adenomas: long term follow up is important because of significant numbers of tumour recurrences
  74. 13.3 Disorders of the posterior pituitary gland
  75. Outcome in surgically treated Rathke's cleft cysts: long-term monitoring needed
  76. The postoperative monitoring of nonfunctioning pituitary adenomas
  77. 2.3.15 Pituitary incidentalomas
  78. 2.4.2 Craniopharyngiomas
  79. Somatostatin Analogue Treatment Increases AIP Protein Expression in Somatotroph Tumours from Patients with Acromegaly and in GH3 Cells in vitro
  80. Opioid induced hypogonadism
  81. Nelson's syndrome
  82. Disorders of the anterior pituitary gland
  83. Disorders of the anterior pituitary gland
  84. Disorders of the posterior pituitary gland
  85. Prevalence of pituitary adenomas: a community-based, cross-sectional study in Banbury (Oxfordshire, UK)
  86. Post-operative Replacement and Assessment of HPA Axis Recovery in Cushing’s Syndrome
  87. The value of the oral glucose tolerance test, random serum growth hormone and mean growth hormone levels in assessing the postoperative outcome of patients with acromegaly
  88. Non-adenomatous pituitary tumours
  89. Nonfunctioning pituitary adenomas: the Oxford experience
  90. An e-mail GP advisory service: a more efficient way of dealing with clinical enquiries
  91. Radiation-induced hypopituitarism
  92. GH replacement in patients with non-functioning pituitary adenoma (NFA) treated solely by surgery is not associated with increased risk of tumour recurrence
  93. Valvular heart disease and the use of cabergoline for the treatment of prolactinoma
  94. Craniopharyngiomas. Historical aspects of their management
  95. Surgical debulking of pituitary macroadenomas causing acromegaly improves control by lanreotide
  96. Radiotherapy of other sellar lesions
  97. Craniopharyngiomas
  98. What is the natural history of nonoperated nonfunctioning pituitary adenomas?
  99. Acromegaly and anaplastic astrocytoma: coincidence or pathophysiological relation?
  100. Silent corticotroph adenomas
  101. Collision lesions of the sella: co-existence of craniopharyngioma with gonadotroph adenoma and of Rathke’s cleft cyst with corticotroph adenoma
  102. What are the markers of aggressiveness in prolactinomas? Changes in cell biology, extracellular matrix components, angiogenesis and genetics
  103. Hypopituitarism Oddities: Craniopharyngiomas
  104. Do the limits of serum prolactin in disconnection hyperprolactinaemia need re-definition? A study of 226 patients with histologically verified non-functioning pituitary macroadenoma
  105. Craniopharyngiomas
  106. GH replacement does not increase the risk of recurrence in patients with craniopharyngioma
  107. A case of post-traumatic isolated ACTH deficiency with spontaneous recovery 9 months after the event
  108. The impact of chronic in vivo glucocorticoid excess on the functional characteristics of human skin fibroblasts obtained from patients with endogenous Cushing's syndrome
  109. Evaluation of GH reserve in patients with adrenal incidentalomas and biochemical evidence of subclinical autonomous glucocorticoid hypersecretion
  110. Craniopharyngiomas in children and adults: systematic analysis of 121 cases with long-term follow-up
  111. The value of an acute octreotide suppression test in predicting long-term responses to depot somatostatin analogues in patients with active acromegaly
  112. Treatment of Pituitary Tumors: History
  113. Evaluation of bone mineral density of the peripheral skeleton in pre- and postmenopausal women with newly diagnosed endogenous Cushing's syndrome
  114. Pegvisomant: a new treatment modality for acromegaly
  115. Assessment of GH reserve before and after successful treatment of adult patients with Cushing's syndrome
  116. Craniopharyngioma
  117. Benign Cysts: Rathke's Cleft Cysts, Mucoceles, Arachnoid Cysts, and Dermoid and Epidermoid Cysts