• A case of suspected IgG4-related hypophysitis presented with panhypopituitarism and central diabetes insipidus
• A Comprehensive Review of the Role of Biomarkers in the Early Detection of Endocrine Disorders in Critical Illnesses
• A Diagnosis of Sheehan's Syndrome: Better Late Than Never
• A prognostic model for use before elective surgery to estimate the risk of postoperative pulmonary complications (GSU-Pulmonary Score): a development and validation study in three international cohorts
• Accuracy of Glucagon Testing Across Transition in Young Adults with Childhood-Onset Growth Hormone Deficiency
• Acquired thyroid-stimulating hormone, luteinizing hormone, and follicle-stimulating hormone deficiencies with circulating anti-glycoprotein hormones alpha chain-positive cell antibodies
• Acromegaly and COVID-19, lessons, and new opportunities
• Acute neuroendocrine changes after traumatic brain injury
• Acute parkinsonism in a patient with myxedema crisis: A case report
• Advancement in perioperative management of pituitary adenomas-Current concepts and best practices
• An invasive nasopharyngeal carcinoma with extension to the pituitary gland mimicking an invasive pituitary macroadenoma: A case report
• Anterior and Posterior Pituitary Function in Patients with Sheehan Syndrome - Combining the use of Insulin Tolerance Test and Copeptin Assay
• Anterior pituitary dysfunction after traumatic brain injury: A prospective study
• Bilateral Sixth Nerve Palsy: A Rare Presentation of Primary Hypophysitis
• Cardiovascular Risk Factors in Sheehan's Syndrome: A Case-Control Study
• Clinical presentation and surgical outcomes of very large and giant pituitary adenomas: 80 cases in a cohort study of 306 patients with pituitary adenomas
• Clinical Presentation, Diagnosis, and Management of Hyperinsulinemic Hypoglycemia in Adults: A Single-center Experience
• Combined Pituitary Hormone Deficiency in <em>lhx4</em>-Knockout Zebrafish
• Comparison of Surgical Modalities for Giant Pituitary Adenoma: A Systematic Review and Meta-Analysis of 1413 Patients
• Congenital Combined Pituitary Hormone Deficiency Attributable to a Novel PROP1 Mutation (467insT)
• Congenital Hypopituitarism: Current Agnostic Genetics Faces Its Limits
• Could low prolactin levels after radiotherapy predict the onset of hypopituitarism?
• Cutis verticis gyrata in a patient with acromegaly: an unusual case and review of literature
• Development and validation of a novel treatment adherence, satisfaction and knowledge questionnaire (TASK-Q) for adult patients with hypothalamic-pituitary disorders
• Diabetes Insipidus Complicating Diabetes Mellitus Type 1: A Pituitary Abscess Diagnosis
• Diagnosis and management of children and adult craniopharyngiomas: a French Endocrine Society/French Society for Paediatric Endocrinology &amp; Diabetes Consensus Statement
• Diagnosis of hypoprolactinemia
• Diagnostic, therapeutic, and prognostic characteristics of patients with acromegaly according to tumor size at diagnosis
• Ectopic Sphenoid Sinus Prolactinoma Associated With Empty Sella and Recurrent Meningitis Treated Successfully With Cabergoline
• Effects of glucocorticoid replacement therapy in patients with pituitary disease: A new perspective for personalized replacement therapy
• Efficacy and safety of Aviandr in the treatment of anxiety in patients with adjustment disorders after COVID-19
• Efficacy and safety of radiosurgery in acromegaly
• Endocrine Petrified Ear: Associated Endocrine Conditions in Auricular Calcification/Ossification (A Sample-Focused Analysis)
• Endoscopic endonasal resection of Rathke cleft cysts: a single-institution analysis of 148 consecutive patients
• Endoscopic endonasal resection of symptomatic Rathke's cleft cysts: outcomes of the strategy to maintain the fenestration open
• Endoscopic endonasal transsphenoidal approach improves endocrine function and surgical outcome in primary craniopharyngioma resection: a systematic review and meta-analysis
• Endoscopic transsphenoidal resection of parasellar abducens nerve schwannoma: A video demonstration
• Epidemiology of Endocrine Dysfunctions in Pediatric Patients with Previous Central Nervous System Infection: A Scoping Review of the Literature
• Evolving growth hormone deficiency: proof of concept
• Exome Sequencing has a high diagnostic rate in sporadic congenital hypopituitarism and reveals novel candidate genes
• Exploring risk factors of severe pituitary apoplexy: Insights from a multicenter study of 71 cases
• Gonadotropic status in adult women with pituitary stalk interruption syndrome
• Graves' Disease in Hypopituitarism Due to Pituitary Apoplexy
• High fever in a 39 year-old woman
• High prevalence of morphometric vertebral fractures opportunistically detected on thoracic radiograms in patients with non-functioning pituitary adenoma
• Histologic Assessment of Lumbosacral Transitional Vertebrae Pseudoarticulation as a Source of Pain in Bertolotti Syndrome
• Histological assessment of lumbosacral transitional vertebrae pseudoarticulation as a source of pain in Bertolotti's Syndrome
• Hyponatremia due to preserved non-osmotic arginine vasopressin secretion in adipsic diabetes insipidus: a case report with review of literature
• Hypopituitarism
• Hypopituitarism after gamma knife radiosurgery for pituitary adenomas: long-term results from a single-center experience
• Hypopituitarism with secondary adrenocortical insufficiency and arginine vasopressin deficiency due to hypophysitis after COVID-19 vaccination: a case report
• Immunoglobulin G4-related Autoimmune Pancreatitis and Hypopituitarism Following Immune Checkpoint Inhibitor Therapy: A Case Report
• Insights into Central Congenital Hypothyroidism: A Multicenter Retrospective Analysis
• Knockout mice with pituitary malformations help identify human cases of hypopituitarism
• Langerhans cell histiocytosis of the suprasellar region: diagnosis based on thyroid cytology
• Langerhans Cell Histiocytosis of the Suprasellar Region: Diagnosis on Thyroid Cytology
• Long-term outcomes of neuroendoscopic cyst partial resection combined with stereotactic radiotherapy for craniopharyngioma
• Lymphocytic hypophysitis - various course of the disease and individualized therapeutic approach. An algorithm of the follow-up
• Metastatic malignant struma ovarii to the pituitary presenting as a sellar mass and responding to total thyroidectomy with adjuvant radioactive iodine therapy
• Morbidities and mortality among hospitalized patients with hypopituitarism: Prevalence, causes and management
• Neuroendocrine challenges and clinical outcomes in men with chronic traumatic brain injury: a cross-sectional study
• Neuropathy target esterase activity defines phenotypes among PNPLA6 disorders
• Neurosarcoidosis With Panhypopituitarism: Two Cases and Literature Review
• Old woman with Sheehan's syndrome suffered severe hyponatremia following percutaneous coronary intervention: a case report and review of literature
• Outcomes of Ovulation Induction Aimed to Pregnancy in Eight Hypopituitarism Patients
• Panhypopituitarism in a Patient with Burkitt Lymphoma: A Diagnostic and Therapeutic Challenge
• Partial hypopituitarism with ACTH deficiency as the main manifestation as a complication of hemorrhagic fever with renal syndrome
• Pegvisomant and pasireotide in PRL and GH co-secreting vs GH-secreting Pit-NETs
• Pegvisomant or pasirotide in PRL and GH co-secreting vs GH-secreting Pit-NETs
• Pituitary Apoplexy and the Current Understanding of Its Management: A Meta-Analysis of 908 Patients
• Pituitary Apoplexy: An Updated Review
• Pituitary Apoplexy: Pitfalls in Diagnosis
• Pituitary Complications of Checkpoint Inhibitor Use
• Pituitary deficiencies related to optic nerve hypoplasia and visual acuity
• Pituitary Hyperplasia Due to Longstanding Primary Hypothyroidism: A Case Report and Comprehensive Review of the Literature
• Pituitary Involvement in Langerhans Cell Histiocytosis: A Challenging Case
• Plasma oxytocin levels in response to glucagon in patients with arginine vasopressin deficiency (central diabetes insipidus) and healthy controls
• Post-traumatic pituitary stalk transection syndrome (PSTS) expeditiously manifested after a fall from a height combined with acute traumatic spinal cord injury: a rare case report with review of literature
• Pregnancy in Autoimmune Hypophysitis: Management of a Rare Condition
• Progress, challenges and perspectives in the management of hypopituitarism
• Proteomic and metabolomic analysis of GH deficiency-induced NAFLD in hypopituitarism: insights into oxidative stress
• Rare coexistence of hypopituitarism with osteogenesis imperfecta - A double-trouble for bone
• Recurrent p.H119Y variant in MAP2K1 expands the phenotypic spectrum of MAP2K1-related RASopathy
• Response to Letter to the Editor From Josef Finsterer: "Explaining Long COVID: A Pioneer Cross-Sectional Study Supporting the Endocrine Hypothesis"
• Response to Recombinant Human Growth Hormone (rhGH) Therapy in Children with Growth Hormone Deficiency
• Rethinking the role of surgical resection in the management of primary pituitary lymphoma
• Robust growth hormone responses to GH-releasing peptide 2 in adolescents
• Segmental Agenesis of the Corpus Callosum With Pituitary Hypoplasia
• Serum phosphate levels at diagnosis predict long-term risk for hypopituitarism in patients with acromegaly
• Severe hypoglycemia in a diabetic patient with pituitary apoplexy: a case report
• Sheehan's Syndrome in a Patient With Factor XI Deficiency
• Sheehan's syndrome presenting with panhypopituitarism and central diabetes insipidus: a case report
• Somapacitan-induced reversible lipoatrophy in an adult woman with hypopituitarism
• Staged surgical treatment of the giant Pituitary Neuroendocrine Tumors
• The comprehensive evaluation of oral and fecal microbiota in patients with acromegaly
• Treatment of an Aggressive Gonadotroph Pituitary Neuroendocrine Tumor With ¹⁷⁷Lutetium DOTATATE Radionuclide Therapy
• Trio-based whole exome sequencing in patients with ectopic posterior pituitary
• Understanding oxytocin in human physiology and pathophysiology: A path towards therapeutics
• Worster-Drought Syndrome (Congenital Bilateral Perisylvian Syndrome) with Posterior Pituitary Ectopia, Pituitary Hypoplasia, Empty Sella and Panhypopituitarism: A Patient Report
• Wrong Tissue at the Wrong Place: A Rare Case of Hypopituitarism Secondary to Metastatic Renal Cell Carcinoma