Pituitary

Papers
(The median citation count of Pituitary is 3. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-09-01 to 2024-09-01.)
ArticleCitations
A Pituitary Society update to acromegaly management guidelines184
COVID-19 and the pituitary76
Postoperative diabetes insipidus: how to define and grade this complication?54
Pituitary apoplexy associated with acute COVID-19 infection and pregnancy50
Isolated ACTH deficiency induced by cancer immunotherapy: a systematic review46
Descriptive epidemiology of craniopharyngiomas in the United States39
Skull base repair following endonasal pituitary and skull base tumour resection: a systematic review32
Clinical, biological, radiological, and pathological comparison of sparsely and densely granulated somatotroph adenomas: a single center experience from a cohort of 131 patients with acromegaly31
Pituitary society expert Delphi consensus: operative workflow in endoscopic transsphenoidal pituitary adenoma resection29
Managing pasireotide-associated hyperglycemia: a randomized, open-label, Phase IV study28
Glucocorticoid use in patients with adrenal insufficiency following administration of the COVID-19 vaccine: a pituitary society statement27
Mice with gene alterations in the GH and IGF family26
Consensus on criteria for acromegaly diagnosis and remission25
Glucocorticoid Withdrawal Syndrome following treatment of endogenous Cushing Syndrome24
Prevalence of comorbidities and concomitant medication use in acromegaly: analysis of real-world data from the United States24
Pre-operative serum inflammation-based scores in patients with pituitary adenomas22
Diabetes insipidus after endoscopic transsphenoidal surgery: multicenter experience and development of the SALT score21
Selective resection of cushing microadenoma guided by preoperative hybrid 18-fluoroethyl-L-tyrosine and 11-C-methionine PET/MRI20
Impact of intraoperative magnetic resonance imaging on gross total resection, extent of resection, and residual tumor volume in pituitary surgery: systematic review and meta-analysis19
Levoketoconazole improves clinical signs and symptoms and patient-reported outcomes in patients with Cushing’s syndrome18
Diagnostic value of Knosp grade and modified Knosp grade for cavernous sinus invasion in pituitary adenomas: a systematic review and meta‐analysis18
Machine learning in predicting early remission in patients after surgical treatment of acromegaly: a multicenter study18
Cephalocaudal tumor diameter is a predictor of diabetes insipidus after endoscopic transsphenoidal surgery for non-functioning pituitary adenoma18
Safety of growth hormone (GH) treatment in GH deficient children and adults treated for cancer and non-malignant intracranial tumors—a review of research and clinical practice17
Differences between immunotherapy-induced and primary hypophysitis—a multicenter retrospective study17
Cardiovascular health and mortality in Cushing’s disease17
Opioids and pituitary function: expert opinion17
Corticotroph tumor progression during long-term therapy with osilodrostat in a patient with persistent Cushing’s disease16
Impact of the diagnostic delay of acromegaly on bone health: data from a real life and long term follow-up experience16
Immune profiling of pituitary tumors reveals variations in immune infiltration and checkpoint molecule expression16
Virtual magnetic resonance elastography has the feasibility to evaluate preoperative pituitary adenoma consistency16
Incidence, mortality, and cardiovascular diseases in pituitary adenoma in Korea: a nationwide population-based study16
Real-world experience with pasireotide-LAR in resistant acromegaly: a single center 1-year observation16
Neural network modeling for prediction of recurrence, progression, and hormonal non-remission in patients following resection of functional pituitary adenomas16
Cushing’s disease: adrenal steroidogenesis inhibitors16
The direct and indirect impact of the COVID-19 pandemic on the care of patients with pituitary disease: a cross sectional study15
Levoketoconazole in the treatment of patients with endogenous Cushing’s syndrome: a double-blind, placebo-controlled, randomized withdrawal study (LOGICS)15
The microenvironment of pituitary adenomas: biological, clinical and therapeutical implications15
The NETting of pituitary adenoma: a gland illusion15
Complication avoidance protocols in endoscopic pituitary adenoma surgery: a retrospective cohort study in 514 patients15
Epidemiology of common and uncommon adult pituitary tumors in the U.S. according to the 2017 World Health Organization classification15
Clinical profiles of silent corticotroph adenomas compared with silent gonadotroph adenomas after adopting the 2017 WHO pituitary classification system15
Pilot study to define criteria for Pituitary Tumors Centers of Excellence (PTCOE): results of an audit of leading international centers15
Effects of adult growth hormone deficiency and replacement therapy on the cardiometabolic risk profile14
Determinants of skeletal fragility in acromegaly: a systematic review and meta-analysis14
Pituitary adenomas in older adults (≥ 65 years): 90-day outcomes and readmissions: a 10-year endoscopic endonasal surgical experience14
Paltusotine, a novel oral once-daily nonpeptide SST2 receptor agonist, suppresses GH and IGF-1 in healthy volunteers14
HOMA-IR in acromegaly: a systematic review and meta-analysis14
Prognostic value of nadir GH levels for long-term biochemical remission or recurrence in surgically treated acromegaly14
Extending lifespan by modulating the growth hormone/insulin-like growth factor-1 axis: coming of age14
Surgery is a safe, effective first-line treatment modality for noninvasive prolactinomas14
Treatment of Cushing’s syndrome with osilodrostat: practical applications of recent studies with case examples14
Modern imaging in Cushing’s disease14
Long-term efficacy and safety of osilodrostat in Cushing’s disease: final results from a Phase II study with an optional extension phase (LINC 2)13
Oral octreotide capsules for the treatment of acromegaly: comparison of 2 phase 3 trial results13
Endocrine disorders after primary gamma knife radiosurgery for pituitary adenomas: A systematic review and meta-analysis13
Normative data for pituitary size and volume in the general population between 50 and 66 years13
Gut microbiota in patients with newly diagnosed acromegaly: a pilot cross-sectional study13
Prolactin immunoassay: does the high-dose hook effect still exist?13
Quality of life impairment after a diagnosis of Cushing’s syndrome12
Glucocorticoid receptor blockers12
Novel approaches to bone comorbidity in Cushing’s disease: an update12
Implementation of functional imaging using 11C-methionine PET-CT co-registered with MRI for advanced surgical planning and decision making in prolactinoma surgery12
AIP variant causing familial prolactinoma12
Targeted therapies in the medical management of craniopharyngioma12
Predictive factors of postoperative diabetes insipidus in 333 patients undergoing transsphenoidal surgery for non-functioning pituitary adenoma12
The sellar barrier on preoperative imaging predicts intraoperative cerebrospinal fluid leak: a prospective multicenter cohort study12
Frailty does not preclude surgical success after endoscopic transsphenoidal surgery for pituitary adenomas11
11C-methionine PET aids localization of microprolactinomas in patients with intolerance or resistance to dopamine agonist therapy11
Genetics of Cushing’s disease: from the lab to clinical practice11
Effect of long-term growth hormone replacement on glucose metabolism in adults with growth hormone deficiency: a systematic review and meta-analysis11
Prevalence of Nelson’s syndrome after bilateral adrenalectomy in patients with cushing’s disease: a systematic review and meta-analysis10
Comparison between extended transsphenoidal and transcranial surgery for craniopharyngioma: focus on hypothalamic function and obesity10
Surgical outcomes of medically failed prolactinomas: a systematic review and meta-analysis10
Pituitary stalk interruption syndrome: phenotype, predictors, and pathophysiology of perinatal events10
HLA analysis of immune checkpoint inhibitor-induced and idiopathic isolated ACTH deficiency9
Late Night Salivary Cortisol in the diagnosis of neoplastic hypercortisolism (including cyclic Cushing’s syndrome)9
Genetic spectrum and predictors of mutations in four known genes in Asian Indian patients with growth hormone deficiency and orthotopic posterior pituitary: an emphasis on regional genetic diversity9
How to rule out non-neoplastic hypercortisolemia (previously known as pseudo-cushing)9
Rathke’s cleft cyst infections and pituitary abscesses: case series and review of the literature9
Typing of inflammatory lesions of the pituitary9
Professor Rathke’s gift to neurosurgery: the cyst, its diagnosis, surgical management, and outcomes9
Cystic appearance on magnetic resonance imaging in bihormonal growth hormone and prolactin tumors in acromegaly9
The epidemiology and management patterns of pediatric pituitary tumors in the United States9
Prevalence of clinical signs, symptoms and comorbidities at diagnosis of acromegaly: a systematic review in accordance with PRISMA guidelines9
Anastrozole as add-on therapy for cabergoline-resistant prolactin-secreting pituitary adenomas: real-life experience in male patients9
Pituitary Society Delphi Survey: An international perspective on endocrine management of patients undergoing transsphenoidal surgery for pituitary adenomas9
Refractory nonfunctioning pituitary adenomas8
Serum copeptin levels at day two after pituitary surgery and ratio to baseline predict postoperative central diabetes insipidus8
Increased risk of preneoplastic colonic lesions and colorectal carcinoma in acromegaly: multicenter case–control study8
Machine learning as a clinical decision support tool for patients with acromegaly8
Proportion and predictors of Hypogonadism Recovery in Men with Macroprolactinomas treated with dopamine agonists8
A study on clinical outcomes of Rathke’s cleft cyst in patients managed conservatively8
Pregnancy outcomes in women receiving growth hormone replacement therapy enrolled in the NordiNet® International Outcome Study (IOS) and the American Norditropin® Studies: Web-Enabled Research (ANSWER8
Management of prolactinomas in children and adolescents; which factors define the response to treatment?8
Diagnosis and treatment outcomes of Cushing’s disease during pregnancy8
Radiological evolution of autograft fat used for skull base reconstruction after transsphenoidal surgery for pituitary adenomas8
Effects of oral macimorelin on copeptin and anterior pituitary hormones in healthy volunteers8
Efficacy of temozolomide combined with capecitabine (CAPTEM) on refractory prolactinomas as assessed using an ex vivo 3D spheroid assay8
Clinical and radiographic assessment of peripheral joints in controlled acromegaly8
Outcomes of pituitary apoplexy: a comparison of microadenomas and macroadenomas8
Treatment and prognostic factors of pituicytoma: a single-center experience and comprehensive literature review8
How to manage intolerance to dopamine agonist in patients with prolactinoma7
Integrated multi-omics profiling of nonfunctioning pituitary adenomas7
Biliary adverse events in acromegaly during somatostatin receptor ligands: predictors of onset and response to ursodeoxycholic acid treatment7
Biochemical testing to differentiate Cushing’s disease from ectopic ACTH syndrome7
The role of endoscopic endonasal surgery in the management of prolactinomas based on their invasiveness into the cavernous sinus7
Patient-reported outcomes in patients with acromegaly treated with pegvisomant in the ACROSTUDY extension: A real-world experience7
Prevalence of coronary calcium deposits in Sheehan’s syndrome patients on long term replacement treatment7
Reported outcomes in transsphenoidal surgery for pituitary adenomas: a systematic review7
Long-term hepatic and cardiac health in patients diagnosed with Sheehan’s syndrome7
Growth hormone alters gross anatomy and morphology of the small and large intestines in age- and sex-dependent manners7
Surgical strategies in the treatment of MR-negative Cushing’s Disease: a systematic review and treatment algorithm7
Evaluation of acromegaly treatment direct costs with respect to biochemical control and follow-up length7
Refractory lactotroph adenomas7
Cushing’s disease: risk of recurrence following trans-sphenoidal surgery, timing and methods for evaluation7
A systematic literature review to evaluate extended dosing intervals in the pharmacological management of acromegaly7
Pituitary acting drugs: cabergoline and pasireotide7
Usefulness of a clinicopathological classification in predicting treatment-related outcomes and multimodal therapeutic approaches in pituitary adenoma patients: retrospective analysis on a Portuguese 6
Effectiveness of the intraoperative magnetic resonance imaging during endoscopic endonasal approach for acromegaly6
Responsiveness to DDAVP in Cushing’s disease is associated with USP8 mutations through enhancing AVPR1B promoter activity6
Identification of mutant K-RAS in pituitary macroadenoma6
Pituitary metastases from neuroendocrine neoplasms: case report and narrative review6
Characteristics and overall survival in pediatric versus adult pituitary adenoma: a National Cancer Database analysis6
Functioning gonadotroph adenomas in premenopausal women: clinical and molecular characterization and review of the literature6
Hypopituitarism and pregnancy: clinical characteristics, management and pregnancy outcome6
Genetics, clinical features and outcomes of non-syndromic pituitary gigantism: experience of a single center from Sao Paulo, Brazil6
Differences in clinical, hormonal, and radiological presentation and in surgical outcomes in patients presenting with and without pituitary apoplexy. A multicenter study of 245 cases6
Psychosocial effects and clinic reflections of the COVID-19 outbreak in patients with acromegaly and Cushing’s disease6
Chiasmal herniation following treatment of pituitary macroadenoma6
Treatment of recurrent and persistent Cushing’s disease after first transsphenoidal surgery: lessons learned from an international meta-analysis6
A prospective study on the efficacy of oral estrogen in female patients with acromegaly6
A comparison of macular ganglion cell and retinal nerve fibre layer optical coherence tomographic parameters as predictors of visual outcomes of surgery for pituitary tumours6
The effect of glucose dynamics on plasma copeptin levels upon glucagon, arginine, and macimorelin stimulation in healthy adults6
Preoperative differentiation of hypophysitis and pituitary adenomas using a novel clinicoradiologic scoring system6
Treatment of non-functioning pituitary adenoma with cabergoline: a systematic review and meta-analysis6
Vasculometabolic effects in patients with congenital growth hormone deficiency with and without GH replacement therapy during adulthood6
Pituitary tumor centers of excellence for Cushing’s disease6
Predicting hypogonadotropic hypogonadism persistence in male macroprolactinoma6
Vascular anomalies in patients with growth hormone-secreting pituitary adenomas: illustrative case report and systematic review of the literature6
Acromegaly and pregnancy: a systematic review and meta-analysis6
Hypercoagulability in Cushing’s syndrome: incidence, pathogenesis and need for thromboprophylaxis protocols6
Role of biological effective dose for prediction of endocrine remission in acromegaly patients treated with stereotactic radiosurgery6
Management of sellar and parasellar tumors becoming symptomatic during pregnancy: a practical algorithm based on multi-center experience and systematic literature review5
Long-term cardiometabolic outcome in patients with pituitary adenoma diagnosed in chilhood and adolescence5
Risk factors for tumor recurrence and progression of spindle cell oncocytoma of the pituitary gland: a systematic review and pooled analysis5
Long-term safety of gamma knife radiosurgery (SRS) for acromegaly5
Transcriptome profiling of insulin sensitive tissues from GH deficient mice following GH treatment5
POU1F1 mutations in combined pituitary hormone deficiency: differing spectrum of mutations in a Western-Indian cohort and systematic analysis of world literature5
Exploring the role of the tumor microenvironment in refractory pituitary tumor pathogenesis5
Characterization of the ability of a, second-generation SST-DA chimeric molecule, TBR-065, to suppress GH secretion from human GH-secreting adenoma cells5
Giant prolactinoma in children and adolescents: a single-center experience and systematic review5
Pituitary surgery in Cushing’s disease: first line treatment and role of reoperation5
Pituitary apoplexy and panhypopituitarism following acute leptospirosis5
Development of a cost-effective diagnostic algorithm incorporating transcription factor immunohistochemistry in the evaluation of pituitary tumours5
Quality of life after long-term biochemical control of acromegaly5
Healthcare utilization and costs among prolactinoma patients: a cross-sectional study and analysis of determinants5
Acromegaly is associated with a distinct oral and gut microbiota5
Increased oxytocin release precedes hyponatremia after pituitary surgery5
Prior testosterone replacement therapy may impact spermatogenic response to combined gonadotropin therapy in severe congenital hypogonadotropic hypogonadism5
Weekly somapacitan had no adverse effects on glucose metabolism in adults with growth hormone deficiency5
Impact of patient-reported nasal symptoms on quality of life after endoscopic pituitary surgery: a prospective cohort study4
Pituitary metastases: a case series and scoping review4
The treatment of aggressive prolactinomas with everolimus4
Machine learning models predict delayed hyponatremia post-transsphenoidal surgery using clinically available features4
Changing presentation of acromegaly in half a century: a single-center experience4
Surgical outcomes and quality of life in Rathke’s cleft cysts undergoing endoscopic transsphenoidal resection: a multicentre study and systematic review of the literature4
Familial neurohypophyseal diabetes insipidus: clinical, genetic and functional studies of novel mutations in the arginine vasopressin gene4
Refractory somatotroph adenomas4
Predicting tumor consistency and extent of resection in non-functioning pituitary tumors4
Double adenomas of the pituitary reveal distinct lineage markers, copy number alterations, and epigenetic profiles4
Thyrotropin-secreting pituitary adenomas induce left atrial enlargement with subclinical atrial fibrillation: an echocardiographic study4
The role of stereotactic radiosurgery in the multidisciplinary management of pituitary metastases4
Psychological well-being and illness perceptions in patients with hypopituitarism4
Standards of care for medical management of acromegaly in pituitary tumor centers of excellence (PTCOE)4
Deficiency of WFS1 leads to the impairment of AVP secretion under dehydration in male mice4
Surgically treated acromegaly patients have a similar quality of life whether controlled by surgery or requiring additional medical therapy (QuaLAT Study)4
Venous thromboembolism chemical prophylaxis after endoscopic trans-sphenoidal pituitary surgery4
Discrimination between non-functioning pituitary adenomas and hypophysitis using machine learning methods based on magnetic resonance imaging‑derived texture features4
Growth hormone secreting pituitary adenomas show distinct extrasellar extension patterns compared to nonfunctional pituitary adenomas4
Safety of endoscopic endonasal biopsy for the pituitary stalk-hypothalamic lesions4
Role of Radiation in the treatment of Cushing Disease4
Predictive value of macular ganglion cell-inner plexiform layer thickness in visual field defect of pituitary adenoma patients: a case-control study4
Fully endoscopic endonasal approach for the treatment of intrasellar arachnoid cysts3
The diagnosis and prevalence of hypoprolactinemia in patients with panhypopituitarism and the effects on depression and sexual functions3
Evaluating the burden of endogenous Cushing’s syndrome using a web-based questionnaire and validated patient-reported outcome measures3
An Infundibular Unidentified Object (IUO): a new pituitary stalk marker?3
GnRH agonist-associated pituitary apoplexy: a case series and review of the literature3
Cushing’s disease: role of bilateral adrenalectomy3
Internal carotid artery stenosis and risk of cerebrovascular ischemia following stereotactic radiosurgery for recurrent or residual pituitary adenomas3
Contemporary radiotherapy and radiosurgery techniques for refractory pituitary adenomas3
Chiasmapexy for secondary empty sella syndrome: diagnostic and therapeutic considerations3
Co-expression of intermediate filaments glial fibrillary acidic protein and cytokeratin in pituitary adenoma3
Glucose metabolism, gut-brain hormones, and acromegaly treatment: an explorative single centre descriptive analysis3
Overnight 1 mg dexamethasone suppression test and 24 h urine free cortisol—accuracy and pitfalls when screening for Cushing’s syndrome3
Pituitary apoplexy score, toward standardized decision-making: a descriptive study3
The impact of facility type and volume on treatment and overall survival in craniopharyngioma3
Mental health disorders in newly diagnosed non-functional pitutary adenoma under initial observation: an observational cohort study using the nationwide MarketScan database3
Clinico-radiological correlation of pituitary stalk interruption syndrome in children with growth hormone deficiency3
Regional genotypic variations in normosmic congenital hypogonadotropic hypogonadism: our experience and systematic review3
Antiplatelet and anticoagulation therapy and the risk of pituitary apoplexy in pituitary adenoma patients3
The role of the dentist and orthodontist in recognizing oro-facial manifestations of acromegaly: a questionnaire-based study3
Endoscopic endonasal marsupialization of rathke cleft cysts: clinical outcomes and risk factors analysis of visual impairment, pituitary dysfunction, and CSF leak3
Patient-reported outcomes in refractory hormone-producing pituitary adenomas: an unmet need3
Historical and future trends in emergency pituitary referrals: a machine learning analysis3
Impact of histopathological classification of non-functioning adenomas on long term outcomes: comparison of the 2004 and 2017 WHO classifications3
Post-operative surveillance for somatotroph, lactotroph and non-functional pituitary adenomas after curative resection: a systematic review3
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