All Stories

  1. Characterization of SF3B1 role in prolactin-secreting pituitary tumors
  2. Patients With Pituitary Neuroendocrine Tumours Requiring Neurosurgery –Who Is Referring Them?
  3. Effects of Hypopituitarism Due to Sheehan's Syndrome on Bone Mineral Density: A Multicentric Study in Asian Indians
  4. New directions in MEN1 management: navigating the new clinical practice guidelines
  5. Bone Density, Microarchitecture, and Geometry Assessment in Patients with Pachydermoperiostosis Using Second-Generation High-Resolution Peripheral Quantitative Computed Tomography: A Case–Control Study
  6. A Novel De Novo Nonsense Pathogenic Variant in IGSF1 Resulting in Central Hypothyroidism and Transient GH Deficiency
  7. RET signalling in the pituitary: a double-edged sword for differentiation, apoptosis and therapeutic strategies in acromegaly
  8. Clinical features of acromegaly
  9. Bone mineral density, turnover, and microarchitecture assessed by second-generation high-resolution peripheral quantitative computed tomography in patients with Sheehan’s syndrome
  10. Tall stature and gigantism in adult patients with acromegaly
  11. Consensus guideline for the diagnosis and management of pituitary adenomas in childhood and adolescence: Part 2, specific diseases
  12. Consensus guideline for the diagnosis and management of pituitary adenomas in childhood and adolescence: Part 1, general recommendations
  13. Multiple Endocrine Neoplasia and Familial Isolated Pituitary Adenoma in the Paediatric Population
  14. Genetic Testing in Hereditary Pituitary Tumors
  15. Pharmacological and Genetic Disruption of C-Type Natriuretic Peptide (nppcl) Expression in Zebrafish (Danio rerio) Causes Stunted Growth during Development
  16. Live Fast, Die Young?
  17. Effective Long-term Pediatric Pegvisomant Monotherapy to Final Height in X-linked Acrogigantism
  18. Tumour microenvironment and pituitary tumour behaviour
  19. Insulinomatosis: new aspects
  20. Evaluating home injection compared with healthcare-setting injection of somatostatin analogs: a systematic literature review
  21. Succinate dehydrogenase and MYC-associated factor X mutations in pituitary neuroendocrine tumours
  22. AIP: A double agent? The tissue-specific role of AIP as a tumour suppressor or as an oncogene
  23. Ockham’s Razor for a Retinal Lesion and Acromegaly and Breaking the Vicious Circle
  24. Glucose and lipid metabolism abnormalities in Cushing’s syndrome
  25. Long-term Safety of Growth Hormone in Adults With Growth Hormone Deficiency: Overview of 15 809 GH-Treated Patients
  26. Temozolomide Nonresponsiveness in Aggressive Prolactinomas and Carcinomas: Management and Outcomes
  27. Approach to the Patient With Pseudoacromegaly
  28. Sex-biased islet β cell dysfunction is caused by the MODY MAFA S64F variant by inducing premature aging and senescence in males
  29. Serum Inflammation-based Scores in Endocrine Tumors
  30. Genetics of Acromegaly and Gigantism
  31. Molecular characterization of DICER1-mutated pituitary blastoma
  32. The clinical aspects of pituitary tumour genetics
  33. Patients with rare endocrine conditions have corresponding views on unmet needs in clinical research
  34. Pre-operative serum inflammation-based scores in patients with pituitary adenomas
  35. Update on the Genetics of Pituitary Tumors
  36. The tumour microenvironment of pituitary neuroendocrine tumours
  37. Unusual Combination of MEN-1 and the Contiguous Gene Deletion Syndrome of CAH and Ehlers-Danlos Syndrome (CAH-X)
  38. XAF1 as a modifier of p53 function and cancer susceptibility
  39. Phenotypic and genotypic features of a large kindred with a germline AIP variant
  40. Metformin to reduce metabolic complications and inflammation in patients on systemic glucocorticoid therapy: a randomised, double-blind, placebo-controlled, proof-of-concept, phase 2 trial
  41. Novel Insights into Pituitary Tumorigenesis: Genetic and Epigenetic Mechanisms
  42. Significant Benefits of AIP Testing and Clinical Screening in Familial Isolated and Young-onset Pituitary Tumors
  43. Pachydermoperiostosis mimicking the acral abnormalities of acromegaly
  44. Tumour-infiltrating cytotoxic T lymphocytes in somatotroph pituitary neuroendocrine tumours
  45. Pituitary tumour fibroblast-derived cytokines influence tumour aggressiveness
  46. Chemokines modulate the tumour microenvironment in pituitary neuroendocrine tumours
  47. Redefining the perioperative stress response: a narrative review
  48. Plasma Renin Measurements are Unrelated to Mineralocorticoid Replacement Dose in Patients With Primary Adrenal Insufficiency
  49. Pediatric Parathyroid Carcinoma: A Case Report and Review of the Literature
  50. Surgery, Octreotide, Temozolomide, Bevacizumab, Radiotherapy, and Pegvisomant Treatment of an AIP Mutation‒Positive Child
  51. Acromegaly associated with GIST, non-small cell lung carcinoma, clear cell renal carcinoma, multiple myeloma, medulla oblongata tumour, adrenal adenoma, and follicular thyroid nodules
  52. Aryl Hydrocarbon Receptor Interacting Protein Maintains Germinal Center B Cells through Suppression of BCL6 Degradation
  53. Circulating aryl hydrocarbon receptor-interacting protein (AIP) is independent of GH secretion
  54. Phosphodiesterases and cAMP Pathway in Pituitary Diseases
  55. Tumor microenvironment defines the invasive phenotype of AIP-mutation-positive pituitary tumors
  56. Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective study
  57. Germline and mosaic mutations causing pituitary tumours: genetic and molecular aspects
  58. The current landscape of European registries for rare endocrine conditions
  59. Assessment of Cardiavascular Changes following Trans-sphenoidal Surgery in Acromegalic Patients
  60. Genetics of Pituitary Tumours
  61. Proteomic Analysis of the Human Anterior Pituitary Gland
  62. Pseudoacromegaly
  63. Reduced protein expression of the phosphodiesterases PDE4A4 and PDE4A8 in AIP mutation positive somatotroph adenomas
  64. Pituitary Pathology and Gene Expression in Acromegalic Cats
  65. Coexisting pituitary and non-pituitary gigantism in the same family
  66. International Union of Basic and Clinical Pharmacology. CV. Somatostatin Receptors: Structure, Function, Ligands, and New Nomenclature
  67. Giant Prolactinoma of Young Onset: A Clue to Diagnosis of MEN-1 Syndrome
  68. Clinical and Pathological Aspects of Silent Pituitary Adenomas
  69. Survivin as a potential therapeutic target of acetylsalicylic acid in pituitary adenomas
  70. Macimorelin as a Diagnostic Test for Adult GH Deficiency
  71. A novel DICER1 mutation in familial multinodular goitre
  72. UPDATE ON THE CLINICOPATHOLOGY OF PITUITARY ADENOMAS
  73. Prophylactic thyroidectomy in children with multiple endocrine neoplasia type 2
  74. In vivo bioassay to test the pathogenicity of missense human AIP variants
  75. De novo HNF1 homeobox B mutation as a cause for chronic, treatment-resistant hypomagnesaemia
  76. Tumour compartment transcriptomics demonstrates the activation of inflammatory and odontogenic programmes in human adamantinomatous craniopharyngioma and identifies the MAPK/ERK pathway as a novel therapeutic target
  77. Risk category system to identify pituitary adenoma patients with AIP mutations
  78. MAFA missense mutation causes familial insulinomatosis and diabetes mellitus
  79. Treatment of aggressive pituitary tumours and carcinomas: results of a European Society of Endocrinology (ESE) survey 2016
  80. Cantú syndrome with coexisting familial pituitary adenoma
  81. Multi-chaperone function modulation and association with cytoskeletal proteins are key features of the function of AIP in the pituitary gland
  82. Emergence of Pituitary Adenoma in a Child during Surveillance: Clinical Challenges and the Family Members’ View in anAIPMutation-Positive Family
  83. Metabolic Syndrome in Cushing's Syndrome Patients
  84. Preliminaries
  85. AIP mutations in Brazilian patients with sporadic pituitary adenomas: a single-center evaluation
  86. Somatic USP8 mutations are frequent events in corticotroph tumor progression causing Nelson’s tumor
  87. AIP and the somatostatin system in pituitary tumours
  88. Mechanical, hormonal and metabolic influences on blood vessels, blood flow and bone
  89. Fatal Carney Complex in Siblings Due to De Novo Large Gene Deletion
  90. Pseudoacromegaly: A Differential Diagnostic Problem for Acromegaly With a Genetic Solution
  91. In-frame seven amino-acid duplication in AIP arose over the last 3000 years, disrupts protein interaction and stability and is associated with gigantism
  92. PRKAR1A mutation causing pituitary-dependent Cushing disease in a patient with Carney complex
  93. Cabergoline-related impulse control disorder in an adolescent with a giant prolactinoma
  94. A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics
  95. Pituitary Carcinoma in a Patient with an SDHB Mutation
  96. From pituitary adenoma to pituitary neuroendocrine tumor (PitNET): an International Pituitary Pathology Club proposal
  97. Sporadic pituitary adenomas: the role of germline mutations and recommendations for genetic screening
  98. Genetic Aspects of Pituitary Adenomas
  99. Renin-Angiotensin System Blockade Improves Cardiac Indices in Acromegaly Patients
  100. Social, educational and vocational outcomes in patients with childhood-onset and young-adult-onset growth hormone deficiency
  101. The genetic background of acromegaly
  102. Succinate Dehydrogenase B (SDHB)-Associated Bladder Paragangliomas
  103. Pachydermoperiostosis Masquerading as Acromegaly
  104. Metformin prevents metabolic side effects during systemic glucocorticoid treatment
  105. Diagnostic challenges and management of a patient with acromegaly due to ectopic growth hormone-releasing hormone secretion from a bronchial carcinoid tumour
  106. Echocardiographic improvements following transsphenoidal surgery for acromegaly
  107. Genetics of pituitary adenomas
  108. Systematic Investigation of Expression of G2/M Transition Genes Reveals CDC25 Alteration in Nonfunctioning Pituitary Adenomas
  109. Outcomes of annual surveillance imaging in an adult and paediatric cohort of succinate dehydrogenase B mutation carriers
  110. The clinical, pathological and molecular differences between sparsely and densely granulated somatotroph adenomas
  111. Glioma in an AIP mutation carrier patient
  112. Pseudoacromegaly - a differential diagnostic problem for acromegaly
  113. Olfactory neuroblastoma: a multi centre clinical and pathological review
  114. Metformin alters an anti-proliferative effect of Mitotane in a human adrenocortical cancer (H295R) cell line: preliminary results
  115. The role of the microenvironment in the invasive phenotype of familial pituitary tumours
  116. Polymorphism or mutation? - The role of the R304Q missense AIP mutation in the predisposition to pituitary adenoma
  117. ESR2 mutations in RET mutation-negative familial medullary thyroid carcinoma
  118. Novel Genetic Causes of Pituitary Adenomas
  119. Increased Population Risk ofAIP-Related Acromegaly and Gigantism in Ireland
  120. Gigantism: X-linked acrogigantism and GPR101 mutations
  121. Characterisation of myocardial structure and function in adult-onset growth hormone deficiency using cardiac magnetic resonance
  122. Rapid Proteasomal Degradation of Mutant Proteins Is the Primary Mechanism Leading to Tumorigenesis in Patients With MissenseAIPMutations
  123. Signaling network map of the aryl hydrocarbon receptor
  124. Germline or somatic GPR101 duplication leads to X-linked acrogigantism: a clinico-pathological and genetic study
  125. AIP inactivation leads to pituitary enlargement in the Zebrafish embryo model
  126. The Drosophila AIP orthologue is essential for actin cytoskeleton stabilisation and cell adhesion
  127. cAMP-specific PDE4 phosphodiesterases and AIP in the pathogenesis of pituitary tumors
  128. SomaticGPR101Duplication Causing X-Linked Acrogigantism (XLAG)—Diagnosis and Management
  129. Pheochromocytoma Is Characterized by Catecholamine-Mediated Myocarditis, Focal and Diffuse Myocardial Fibrosis, and Myocardial Dysfunction
  130. AIP mutations in young patients with acromegaly and the Tampico Giant: the Mexican experience
  131. Clinicopathologic features of familial pituitary adenomas
  132. Cancerous leptomeningitis and familial congenital hypopituitarism
  133. AIP and the somatostatin signalling in pituitary tumours
  134. Can immediate postoperative random growth hormone levels predict long-term cure in patients with acromegaly?
  135. Endocrine Tumor Genetics: Challenging Issues
  136. Glucagon-like peptide 1 in the pathophysiology and pharmacotherapy of clinical obesity
  137. Diagnosis of Acromegaly
  138. Clinical Features of Acromegaly☆
  139. Patient-reported outcomes of parenteral somatostatin analogue injections in 195 patients with acromegaly
  140. Additive Anti-Tumor Effects of Lovastatin and Everolimus In Vitro through Simultaneous Inhibition of Signaling Pathways
  141. Factors predicting pasireotide responsiveness in somatotroph pituitary adenomas resistant to first-generation somatostatin analogues: an immunohistochemical study
  142. Childhood somatotroph pituitary adenomas due to aryl hydrocarbon receptor interacting protein (AIP) gene mutations
  143. Pegvisomant treatment for X-linked acrogigantism syndrome
  144. Achieving a consensus on managing idiopathic thickening of the pituitary stalk through a national multidisciplinary forum, meeting virtually
  145. In vitroeffects of Imatinib on somatotrophinoma cell line
  146. Silencing of aryl hydrocarbon receptor protein (AIP) up-regulates the small Rho GTPase, CDC42
  147. Novel targeted treatment combinations for malignant neuroendocrine tumour olfactory neuroblastoma
  148. Potential molecular mechanism of AIP-mediated cellular invasion
  149. The effect of AIP on AHR transcriptional activity: implications forAIPmutations pathogenicity
  150. Investigation of the invasive phenotype of AIP-mutated pituitary adenomas
  151. The epidemiology of pituitary adenomas in Iceland, 1955–2012: a nationwide population-based study
  152. Histopathology and molecular characterisation of intrauterine-diagnosed congenital craniopharyngioma
  153. Landscape of Familial Isolated and Young-Onset Pituitary Adenomas: Prospective Diagnosis inAIPMutation Carriers
  154. The effects of chronic candesartan treatment on cardiac and hepatic adenosine monophosphate-activated protein kinase in rats submitted to surgical stress
  155. Prostatic hyperplasia in acromegaly
  156. Treatment-resistant pediatric giant prolactinoma and multiple endocrine neoplasia type 1
  157. The Gene of the Ubiquitin-Specific Protease 8 Is Frequently Mutated in Adenomas Causing Cushing's Disease
  158. 15 YEARS OF PARAGANGLIOMA: The association of pituitary adenomas and phaeochromocytomas or paragangliomas
  159. Metabolic comorbidities in Cushing's syndrome
  160. Ghrelin
  161. Studying Cat (Felis catus) Diabetes: Beware of the Acromegalic Imposter
  162. The ubiquitin-specific protease 8 gene is frequently mutated in adenomas causing Cushing's disease
  163. Pituitary apoplexy in GH-deficient adults treated with GH - a KIMS database retrospective study
  164. Safety and Efficacy of Oral Octreotide in Acromegaly: Results of a Multicenter Phase III Trial
  165. Excessive Growth Hormone Expression in Male GH Transgenic Mice Adversely Alters Bone Architecture and Mechanical Strength
  166. Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia
  167. Heterogeneous Genetic Background of the Association of Pheochromocytoma/Paraganglioma and Pituitary Adenoma: Results From a Large Patient Cohort
  168. Regulation of Aryl Hydrocarbon Receptor Interacting Protein (AIP) Protein Expression by MiR-34a in Sporadic Somatotropinomas
  169. Evaluation of genotype–phenotype relationships in patients referred for endocrine assessment in suspected Pendred syndrome
  170. Prostatic hyperplasia in acromegaly, a myth or reality: a case–control study
  171. GH deficiency after traumatic brain injury: improvement in quality of life with GH therapy: analysis of the KIMS database
  172. An unusual case of an ACTH-secreting macroadenoma with a germline variant in the aryl hydrocarbon receptor-interacting protein (AIP) gene
  173. Multi-parametric cardiovascular magnetic resonance imaging detects subclinical myocardial involvement in patients diagnosed with phaeochromocytoma
  174. A 25-Year-Old Woman with Headache and Joint Pain
  175. Clinical profile and outcome of patients with acromegaly according to the 2014 consensus guidelines: Impact of a multi-disciplinary team
  176. The role of ghrelin in weight-regulation disorders: Implications in clinical practice
  177. Sequence analysis of the catalytic subunit of PKA in somatotroph adenomas
  178. Low rate of germline AIP mutations in patients with apparently sporadic pituitary adenomas before the age of 40: a single-centre adult cohort
  179. Adrenal cancer in neurofibromatosis type 1: case report and DNA analysis
  180. Paediatric pituitary adenomas: rare, complex, and by no means benign
  181. Common Genetic Variants of the Human Steroid 21-Hydroxylase Gene (CYP21A2) Are Related to Differences in Circulating Hormone Levels
  182. Combination of 13-CisRetinoic Acid and Lovastatin: Marked Antitumor Potential In Vivo in a Pheochromocytoma Allograft Model in Female Athymic Nude Mice
  183. Effects of Long-term Growth Hormone Replacement in Adults With Growth Hormone Deficiency Following Cure of Acromegaly: A KIMS Analysis
  184. 122 Cardiac Abnormalities are Common in Patients Diagnosed with Phaeochromocytoma as Detected by Cardiovascular Magnetic Resonance Imaging
  185. Pituitary blastoma: a pathognomonic feature of germ-line DICER1 mutations
  186. Human AIP gene rescue lethality in a Drosophila melanogaster knockout model of AIP orthologue
  187. The anti-proliferative effect of anti-EGFR tyrosine kinase inhibitor in combination with mitotane on H295R adrenocortical cancer cells
  188. Clinical Experience in the Screening and Management of a Large Kindred With Familial Isolated Pituitary Adenoma Due to an Aryl Hydrocarbon Receptor Interacting Protein (AIP) Mutation
  189. Analysis of the AIP gene promoter
  190. Kallmann syndrome, gender dysphoria, thrombophilia and multiple sclerosis: a complex case report
  191. High incidence of cardiac involvement in patients diagnosed with phaeochromocytoma: a clinical study using cardiovascular magnetic resonance imaging
  192. RET mutation negative familial medullary thyroid carcinoma: four families and literature review
  193. Pre-clinical assessment of the impact of Erlotinib on adrenocortical cancer cells proliferation
  194. Epidemiology and etiopathogenesis of pituitary adenomas
  195. Metformin—mode of action and clinical implications for diabetes and cancer
  196. Preface
  197. Familial pituitary tumors
  198. Characterization of SNARE Proteins in Human Pituitary Adenomas: Targeted Secretion Inhibitors as a New Strategy for the Treatment of Acromegaly?
  199. MicroRNAs: Suggested role in pituitary adenoma pathogenesis
  200. Effects of smoking cessation on  -cell function, insulin sensitivity, body weight, and appetite
  201. The CB1 receptor mediates the peripheral effects of ghrelin on AMPK activity but not on growth hormone release
  202. CB1 receptor mediates the effects of glucocorticoids on AMPK activity in the hypothalamus
  203. A Comprehensive Next Generation Sequencing–Based Genetic Testing Strategy To Improve Diagnosis of Inherited Pheochromocytoma and Paraganglioma
  204. Fasting and postprandial liver glycogen content in patients with type 1 diabetes mellitus after successful pancreas-kidney transplantation with systemic venous insulin delivery
  205. Novel pathway for somatostatin analogs in patients with acromegaly
  206. GH excess in bGH transgenic mice adversely affects bone density, architecture and quality
  207. AIP (aryl hydrocarbon receptor interacting protein)
  208. Gene expression profiling of familial and sporadic pituitary adenomas
  209. Genetic and clinical characteristics of Serbian FIPA families
  210. Drosophila melanogasteras a model organism to study aryl hydrocarbon receptor interacting protein gene function
  211. A Novel Mutation in the Upstream Open Reading Frame of the CDKN1B Gene Causes a MEN4 Phenotype
  212. Familial Pituitary Adenomas
  213. Genes and giants
  214. De Novo HNF1b mutation as a cause for chronic treatment-resistant hypomagnesaemia
  215. Excessive GH expression in bGH transgenic mice adversely alters bone architecture and quality
  216. The role of microRNA miR-34a in the regulation of aryl hydrocarbon receptor interacting protein
  217. Invasion signature' revealed by the analysis of AIP positive and AIP mutation negative human pituitary adenomas
  218. Creation of a locus-specific database for AIP mutations
  219. Genetics of the Ghrelin System
  220. Genetics of Pituitary Adenomas
  221. Ghrelin and cannabinoids require the ghrelin receptor to affect cellular energy metabolism
  222. Structure of the TPR Domain of AIP: Lack of Client Protein Interaction with the C-Terminal α-7 Helix of the TPR Domain of AIP Is Sufficient for Pituitary Adenoma Predisposition
  223. Familial isolated pituitary adenomas: An emerging clinical entity
  224. ACTH-secreting Crooke cell carcinoma of the pituitary
  225. Genetic studies in a coexistence of acromegaly, pheochromocytoma, gastrointestinal stromal tumor (GIST) and thyroid follicular adenoma
  226. 2.7 Expression of a subset of microRNAs in clinically non-functioning pituitary adenomas correlates with tumor size
  227. Familial pituitary adenomas – who should be tested for AIP mutations?
  228. Somatostatin Analogs Modulate AIP in Somatotroph Adenomas: The Role of the ZAC1 Pathway
  229. MicroRNA miR-107 is overexpressed in pituitary adenomas and inhibits the expression of aryl hydrocarbon receptor-interacting protein in vitro
  230. Oncogene-induced senescence in pituitary adenomas and carcinomas
  231. Combined blockade of signalling pathways shows marked anti-tumour potential in phaeochromocytoma cell lines
  232. Mice lacking AMP-activated protein kinase  1 catalytic subunit have increased bone remodelling and modified skeletal responses to hormonal challenges induced by ovariectomy and intermittent PTH treatment
  233. 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
  234. Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis
  235. Genetic analysis in a patient presenting with meningioma and familial isolated pituitary adenoma (FIPA) reveals selective involvement of the R81X mutation of the AIP gene in the pathogenesis of the pituitary tumor
  236. Modifications in basal and stress-induced hypothalamic AMP-activated protein kinase (AMPK) activity in rats chronically treated with an angiotensin II receptor blocker
  237. Ghrelin Regulation of AMPK in the Hypothalamus and Peripheral Tissues
  238. Measurement of AMP-Activated Protein Kinase Activity and Expression in Response to Ghrelin
  239. Cardiovascular changes in patients with adult-onset growth hormone deficiency assessed by CMR
  240. Cardiovascular changes in patients with acromegaly assessed by CMR
  241. Genetic studies on the ghrelin, growth hormone secretagogue receptor (GHSR) and ghrelin O-acyl transferase (GOAT) genes
  242. The Immunophilin-Like Protein XAP2 Is a Negative Regulator of Estrogen Signaling through Interaction with Estrogen Receptor α
  243. Ghrelin in obesity and endocrine diseases
  244. miR-107 Is Overexpressed in Pituitary Adenomas and Inhibits the Expression of Aryl Hydrocarbon Receptor-Interacting Protein (AIP)
  245. Familial isolated pituitary adenoma syndrome
  246. Specific electrocardiographic features associated with Cushing’s disease
  247. AIP and its interacting partners
  248. WITHDRAWN: Ghrelin in obesity and endocrine diseases
  249. The ghrelin/GOAT/GHS-R system and energy metabolism
  250. AIPMutation in Pituitary Adenomas in the 18th Century and Today
  251. 2.3.11 Acromegaly
  252. The expression of ghrelin O-acyltransferase (GOAT) in human tissues
  253. Mechanisms of metformin action on glucose transport and metabolism in human adipocytes
  254. MicroRNA profile indicates downregulation of the TGFβ pathway in sporadic non-functioning pituitary adenomas
  255. Familial isolated pituitary adenomas experience at a single center: clinical importance of AIP mutation screening
  256. Down-Regulation of Wee1 Kinase by a Specific Subset of microRNA in Human Sporadic Pituitary Adenomas
  257. AIP gene and familial isolated pituitary adenomas
  258. Cyclins and their related proteins in pituitary tumourigenesis
  259. Role of the aryl hydrocarbon receptor-interacting protein in familial isolated pituitary adenoma
  260. Down-Regulation of Wee1 Kinase by a Specific Subset of microRNAs in Human Sporadic Pituitary Adenomas
  261. Alterations in Adipose Tissue during Critical Illness
  262. Treatment of acromegaly
  263. AMP-activated protein kinase (AMPK) activation regulates in vitro bone formation and bone mass
  264. Clinical, genetic and molecular characterization of patients with familial isolated pituitary adenomas (FIPA)
  265. AMP-activated protein kinase (AMPK) regulates in vitro bone formation and bone mass in vivo
  266. MicroRNA expression in ACTH-producing pituitary tumors: up-regulation of microRNA-122 and -493 in pituitary carcinomas
  267. Characterization of aryl hydrocarbon receptor interacting protein (AIP) mutations in familial isolated pituitary adenoma families
  268. Ghrelin’s Role as a Major Regulator of Appetite and Its Other Functions in Neuroendocrinology
  269. Molecular Genetics of the Aip Gene in Familial Pituitary Tumorigenesis
  270. PL10 The curious case of ghrelin
  271. Analysis of IMP3 Expression in Normal and Neoplastic Human Pituitary Tissues
  272. Cannabinoids for clinicians: the rise and fall of the cannabinoid antagonists
  273. AMPK as a mediator of hormonal signalling
  274. Activation of RAF/MEK/ERK and PI3K/AKT/mTOR pathways in pituitary adenomas and their effects on downstream effectors
  275. The role of ghrelin and ghrelin-receptor gene variants and promoter activity in type 2 diabetes
  276. Recent Clinical and Pathophysiological Advances in Non-Functioning Pituitary Adenomas
  277. Association Studies onGhrelinandGhrelin ReceptorGene Polymorphisms With Obesity
  278. Shedding light on the intricate puzzle of ghrelin's effects on appetite regulation
  279. AIP, a Protein Mutated in Familial Acromegaly, Plays a Role in the Regulation of Cell Proliferation and Shows Cell-Type Specific Subcellular Localisation
  280. Assessment of p27 (cyclin‐dependent kinase inhibitor 1B) and aryl hydrocarbon receptor‐interacting protein (AIP) genes in multiple endocrine neoplasia (MEN1) syndrome patients without any detectable MEN1 gene mutations
  281. Familial Isolated Pituitary Adenomas
  282. Familial Isolated Pituitary Adenomas
  283. A Genetic Study of the Ghrelin and Growth Hormone Secretagogue Receptor (GHSR) Genes and Stature
  284. STOP AKTING TO TREAT ENDOCRINE TUMOURS
  285. The Yin and Yang of the Ghrelin Gene Products
  286. The potential role of D2 dopamine receptors as a target in the management of neuroendocrine tumors
  287. Changes in Adenosine 5′-Monophosphate-Activated Protein Kinase as a Mechanism of Visceral Obesity in Cushing’s Syndrome
  288. Ghrelin Receptor Gene Polymorphisms and Body Size in Children and Adults
  289. Protein western array analysis in human pituitary tumours: insights and limitations
  290. The Role of the Aryl Hydrocarbon Receptor-Interacting Protein Gene in Familial and Sporadic Pituitary Adenomas
  291. AMP-activated protein kinase mediates glucocorticoid-induced metabolic changes: a novel mechanism in Cushing's syndrome
  292. Somatostatin analogues in the control of neuroendocrine tumours: efficacy and mechanisms
  293. The role of somatostatin analogues in the treatment of neuroendocrine tumours
  294. HLA-DQ3 is a probable risk factor for CMV infection in high-risk kidney transplant patients
  295. The Orexigenic Effect of Ghrelin Is Mediated through Central Activation of the Endogenous Cannabinoid System
  296. The Role of AMP-Activated Protein Kinase in Obesity
  297. Octreotide and the mTOR Inhibitor RAD001 (Everolimus) Block Proliferation and Interact with the Akt-mTOR-p70S6K Pathway in a Neuro-Endocrine Tumour Cell Line
  298. Contents / Foreword / Preface
  299. A new variation in the promoter region, the −604 C>T, and the Leu72Met polymorphism of the ghrelin gene are associated with protection to insulin resistance
  300. Metabolic and hormonal changes during the refeeding period of prolonged fasting
  301. Examining the Candidacy of Ghrelin as a Gene Responsible for Variation in Adult Stature in a United Kingdom Population with Type 2 Diabetes
  302. Ghrelin in neuroendocrine organs and tumours
  303. A mutation and expression analysis of the oncogene BRAF in pituitary adenomas
  304. Ghrelin, the peripheral hunger hormone
  305. Appetite and Metabolic Effects of Ghrelin and Cannabinoids: Involvement of AMP-Activated Protein Kinase
  306. The Farnesoid X Receptor Is Expressed in Breast Cancer and Regulates Apoptosis and Aromatase Expression
  307. PPAR-? expression in pituitary tumours and the functional activity of the glitazones: evidence that any anti-proliferative effect of the glitazones is independent of the PPAR-? receptor
  308. Macro- and micronutrient losses and nutritional status resulting from 44 days of total fasting in a non-obese man
  309. Effect of Gastric Bypass and Gastric Banding on Proneurotensin Levels in Morbidly Obese Patients
  310. Somatostatin analogues stimulate p27 expression and inhibit the MAP kinase pathway in pituitary tumours
  311. Expanding role of AMPK in endocrinology
  312. Ghrelin and cardiovascular health
  313. Refeeding David Blaine — Studies after a 44-Day Fast
  314. Differential gene expression in pituitary adenomas by oligonucleotide array analysis
  315. Enhanced protein kinase B/Akt signalling in pituitary tumours
  316. Fasting and Postprandial Hyperghrelinemia in Prader-Willi Syndrome Is Partially Explained by Hypoinsulinemia, and Is Not Due to Peptide YY3–36Deficiency or Seen in Hypothalamic Obesity Due to Craniopharyngioma
  317. Cannabinoids and Ghrelin Have Both Central and Peripheral Metabolic and Cardiac Effects via AMP-activated Protein Kinase
  318. A HIF1α Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas
  319. Striant™ SR: a novel, effective and convenient testosterone therapy for male hypogonadism
  320. Akting and Cycling: A Tale of the Pituitary
  321. Theobromine inhibits sensory nerve activation and cough
  322. The cannabinoid CB1 receptor antagonist SR141716 blocks the orexigenic effects of intrahypothalamic ghrelin
  323. Ghrelin: update on a novel hormonal system
  324. Ghrelin exerts a proliferative effect on a rat pituitary somatotroph cell line via the mitogen-activated protein kinase pathway
  325. A Comparison of a Novel Testosterone Bioadhesive Buccal System, Striant, with a Testosterone Adhesive Patch in Hypogonadal Males
  326. Ghrelin?a hormone with multiple functions
  327. Elevated Fasting Plasma Ghrelin in Prader-Willi Syndrome Adults Is Not Solely Explained by Their Reduced Visceral Adiposity and Insulin Resistance
  328. Non-Growth Hormone Endocrine Actions of Ghrelin
  329. Identification of Adrenocorticotropin Receptor Messenger Ribonucleic Acid in the Human Pituitary and Its Loss of Expression in Pituitary Adenomas
  330. The Kruppel-like transcription factor 6 gene in sporadic pituitary tumours
  331. Reduced expression of the growth hormone and type 1 insulin‐like growth factor receptors in human somatotroph tumours and an analysis of possible mutations of the growth hormone receptor
  332. Rapid desensitisation of the GH secretagogue (ghrelin) receptor to hexarelin in vitro
  333. Activating point mutations in cyclin-dependent kinase 4 are not seen in sporadic pituitary adenomas, insulinomas or Leydig cell tumours
  334. Ghrelin is Released from Rat Hypothalamic Explants and Stimulates Corticotrophin-releasing Hormone and Arginine-vasopressin
  335. Oral administration of the growth hormone secretagogue NN703 in adult patients with growth hormone deficiency
  336. Macrophage migration inhibitory factor expression is increased in pituitary adenoma cell nuclei
  337. Sequence analysis of the PRKAR1A gene in sporadic somatotroph and other pituitary tumours
  338. A Variation in the Ghrelin Gene Increases Weight and Decreases Insulin Secretion in Tall, Obese Children
  339. A Variation in the Ghrelin Gene Increases Weight and Decreases Insulin Secretion in Tall, Obese Children
  340. Cell Cycle Dysregulation in Human Pituitary Tumours
  341. The Tissue Distribution of the mRNA of Ghrelin and Subtypes of Its Receptor, GHS-R, in Humans
  342. Expression of Phosphorylated p27Kip1Protein and Jun Activation Domain-Binding Protein 1 in Human Pituitary Tumors
  343. Expression of Phosphorylated p27Kip1 Protein and Jun Activation Domain-Binding Protein 1 in Human Pituitary Tumors
  344. The Tissue Distribution of the mRNA of Ghrelin and Subtypes of Its Receptor, GHS-R, in Humans
  345. Optimal Response Criteria for the Human CRH Test in the Differential Diagnosis of ACTH-Dependent Cushing's Syndrome
  346. Response of Serum Macrophage Migration Inhibitory Factor Levels to Stimulation or Suppression of the Hypothalamo-Pituitary-Adrenal Axis in Normal Subjects and Patients with Cushing's Disease
  347. The Effect of Growth Hormone Secretagogues and Neuropeptide Y on Hypothalamic Hormone Release from Acute Rat Hypothalamic Explants
  348. The release of leptin and its effect on hormone release from human pituitary adenomas
  349. Expression of 11β-Hydroxysteroid Dehydrogenase Isoenzymes in the Human Pituitary: Induction of the Type 2 Enzyme in Corticotropinomas and Other Pituitary Tumors
  350. Ghrelin, the endogenous ligand to the growth hormone secretagogue receptor — expression in human hypothalamus and pituitary
  351. Expression of 11 -Hydroxysteroid Dehydrogenase Isoenzymes in the Human Pituitary: Induction of the Type 2 Enzyme in Corticotropinomas and Other Pituitary Tumors
  352. Imprinting of the Gsα gene GNAS1 in the pathogenesis of acromegaly
  353. The Expression of the Growth Hormone Secretagogue Receptor Ligand Ghrelin in Normal and Abnormal Human Pituitary and Other Neuroendocrine Tumors1
  354. Comparison of Somatostatin Analog and Meta-Iodobenzylguanidine Radionuclides in the Diagnosis and Localization of Advanced Neuroendocrine Tumors
  355. The Expression of the Growth Hormone Secretagogue Receptor Ligand Ghrelin in Normal and Abnormal Human Pituitary and Other Neuroendocrine Tumors
  356. Presence of Ghrelin in Normal and Adenomatous Human Pituitary
  357. How common are polycystic ovaries and the polycystic ovarian syndrome in women with Cushing's syndrome?
  358. Expression of the Pituitary Transcription Factor Ptx-1, But Not That of theTrans-Activating Factor Prop-1, Is Reduced in Human Corticotroph Adenomas and Is Associated with Decreasedα -Subunit Secretion1
  359. Expression of the Pituitary Transcription Factor Ptx-1, But Not That of the Trans-Activating Factor Prop-1, Is Reduced in Human Corticotroph Adenomas and Is Associated with Decreased  -Subunit Secretion
  360. Low Expression of the Cell Cycle Inhibitor p27Kip1in Normal Corticotroph Cells, Corticotroph Tumors, and Malignant Pituitary Tumors
  361. Hexarelin as a test of pituitary reserve in patients with pituitary disease
  362. The Growth Hormone Secretagogue Hexarelin Stimulates the Hypothalamo-Pituitary-Adrenal Axis via Arginine Vasopressin
  363. The growth hormone secretagogue receptor
  364. Expression of menin gene mRNA in pituitary tumours
  365. The Effects of GH-Secretagogues on Human Pituitary Cells in Culture and on Rat Hypothalamic Tissue
  366. Leptin and the thyroid — A puzzle with missing pieces
  367. Expression of the Growth Hormone Secretagogue Receptor in Pituitary Adenomas and Other Neuroendocrine Tumors1
  368. Expression of the Growth Hormone Secretagogue Receptor in Pituitary Adenomas and Other Neuroendocrine Tumors
  369. The Pathophysiology of Circulating Corticotropin-Releasing Hormone-Binding Protein Levels in the Human
  370. Leptin levels do not change acutely with food administration in normal or obese subjects, but are negatively correlated with pituitary‐adrenal activity
  371. Differential stimulation of corticol and dehydropiandrosterone levels by food in obese and normal subjects: relation to body fat distribution
  372. Intérêt clinique des neuropeptides GHRH et GHRP
  373. Diagnosis of Growth Hormone Deficiency in Adults
  374. The effect of an opiate antagonist on the hormonal changes induced by hexarelin
  375. Growth hormone-releasing peptide and its analogues
  376. Determination of Direct Effects of Cytokines on Release of Neuropeptides from Rat Hypothalamus by an in Vitro Method