Pituitary

Papers
(The median citation count of Pituitary is 2. 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 2021-08-01 to 2025-08-01.)
ArticleCitations
Idiopathic central diabetes insipidus in a large cohort of patients: the hypopituitarism ENEA rare observational (HEROS) study93
Predictors of biochemical remission after transsphenoidal surgery in a large cohort of acromegaly patients44
Substance P and Neurokinin-1 receptor are overexpressed in adamantinomatous craniopharyngioma than in the pituitary gland37
Neuromedin B receptor as a potential therapeutic target for corticotroph adenomas34
The impact of facility type and volume on treatment and overall survival in craniopharyngioma30
Weekly somapacitan had no adverse effects on glucose metabolism in adults with growth hormone deficiency29
Prevalence and risk factors of colon polyps and other colonic lesions in acromegaly: Insights from colonoscopy screening27
A comparison of macular ganglion cell and retinal nerve fibre layer optical coherence tomographic parameters as predictors of visual outcomes of surgery for pituitary tumours26
Correction to: Osilodrostat improves blood pressure and glycemic control in patients with Cushing’s disease: a pooled analysis of LINC 3 and LINC 4 studies26
Development of a cost-effective diagnostic algorithm incorporating transcription factor immunohistochemistry in the evaluation of pituitary tumours26
Pituitary: hic manebimus optime24
The assessment of thiol-disulfide homeostasis and ıschemia-modified albumin levels in patients with acromegaly24
Genetic models of Cushing’s disease23
Discrimination between non-functioning pituitary adenomas and hypophysitis using machine learning methods based on magnetic resonance imaging‑derived texture features21
Acromegaly increases depressive symptoms and reduces quality of life of cohabitants21
Radiological evolution of autograft fat used for skull base reconstruction after transsphenoidal surgery for pituitary adenomas20
Sleep disruption in patients with active and treated endogenous Cushing’s syndrome20
Gigantism: microsurgical treatment by transsphenoidal approach and prognostic factors20
Complications and mortality of Cushing’s disease: report on data collected over a 20-year period at a referral centre19
ACRODAT and SAGIT for the assessment of disease activity in acromegaly: a multicenter study of the Veneto region in Italy19
Machine learning as a clinical decision support tool for patients with acromegaly19
Hospital frailty risk score predicts postoperative outcomes after endoscopic endonasal resection of non-functioning pituitary adenomas19
Functioning gonadotroph adenomas in premenopausal women: clinical and molecular characterization and review of the literature19
Pituitary metastases: a case series and scoping review18
Bone health and skeletal fragility in second- and third-line medical therapies for acromegaly: preliminary results from a pilot single center experience18
Implementation of functional imaging using 11C-methionine PET-CT co-registered with MRI for advanced surgical planning and decision making in prolactinoma surgery18
Predicting tumor consistency and extent of resection in non-functioning pituitary tumors17
Basal cortisol in relation to metyrapone confirmation in predicting adrenal insufficiency after pituitary surgery17
Diagnosis of growth hormone deficiency: searching for Consensus along life16
Medical management pathways for Cushing’s disease in pituitary tumors centers of excellence (PTCOEs)16
Psychiatric morbidity in acromegaly: a cohort study and meta-analysis of the literature15
A post-hoc internal validation of arginine-stimulated copeptin cut-offs for diagnosing AVP deficiency (central diabetes insipidus)15
Correction: Development and validation of a novel treatment adherence, satisfaction and knowledge questionnaire (TASK-Q) for adult patients with hypothalamic-pituitary disorders15
How to rule out non-neoplastic hypercortisolemia (previously known as pseudo-cushing)15
Commentary: The updated European society of endocrinology clinical practice guideline for the management of aggressive pituitary tumors and pituitary carcinomas15
The diagnosis and prevalence of hypoprolactinemia in patients with panhypopituitarism and the effects on depression and sexual functions15
TSH-secreting pituitary adenomas and bone15
IGF-1 is positively associated with BMI in patients with acromegaly14
Cushing’s disease and bone14
Hypopituitarism and bone disease: pathophysiology, diagnosis and treatment outcomes13
Generating novel pituitary datasets from open-source imaging data and deep volumetric segmentation13
Shared decision-making and detection of comorbidities in an online acromegaly consultation with and without the Acromegaly Disease Activity Tool ACRODAT® using the simulated person approach13
Pituitary metastases from neuroendocrine neoplasms: case report and narrative review13
Pituitary surgery in Cushing’s disease: first line treatment and role of reoperation13
Response to letter to the editor “Hypopituitarism and COVID-19, what else?”13
Clinical, surgical, and endocrine outcome following treatment of posterior pituitary tumors: a retrospective cohort study12
Reappraising prediction of surgical complexity of non-functioning pituitary adenomas after transsphenoidal surgery: the modified TRANSSPHER grade12
Glucocorticoid Withdrawal Syndrome following treatment of endogenous Cushing Syndrome12
Muscle dysfunction is associated with poor quality of life in long-term controlled patients with acromegaly12
Acromegaly is associated with a distinct oral and gut microbiota12
Outcomes in surgical management of microprolactinomas: an international multi-institutional series12
Is diabetes with acromegaly for life?11
[68 Ga]-DOTATATE PET/MR-based evaluation of physiologic somatostatin receptor 2 expression in the adult pituitary gland as a function of age and sex in a prospective cohort11
Cabergoline treatment for surgery-naïve non-functioning pituitary macroadenomas11
Copeptin after pituitary surgery: is it worth measuring?11
Pituitary surgery and COVID11
Long COVID and pituitary dysfunctions: a bidirectional relationship?11
Measuring pituitary tumor volume: a comparison of the simplified and non-simplified ellipsoid equation with the 3D planimetric volume assessment10
Effect of antineoplastic drug therapies on carcinoma and aggressive pituitary tumors: a systematic review and meta-analysis10
Clinical and prognostic implications of pituitary macroadenomas (PitNets) grading: a monocentric experience10
Refractory nonfunctioning pituitary adenomas10
Usefulness of a clinicopathological classification in predicting treatment-related outcomes and multimodal therapeutic approaches in pituitary adenoma patients: retrospective analysis on a Portuguese 10
Low prevalence of neuropathic-like pain symptoms in long-term controlled acromegaly10
Prevalence of comorbidities and concomitant medication use in acromegaly: analysis of real-world data from the United States10
Characterization of a paradoxical post-operative increase in serum cortisol in Cushing disease10
Clinical and prognostic significance of granulation patterns in somatotroph adenomas/tumors of the pituitary: a meta-analysis10
Determinants of skeletal fragility in acromegaly: a systematic review and meta-analysis10
Demonstration of the inferior intercavernous sinus is closely linked to the extent of pneumatization of the sphenoid sinus: useful information for the pituitary surgeon10
Surgical treatment of cystic pituitary adenomas: literature-based definitions and postoperative outcomes10
Hypopituitarism and pregnancy: clinical characteristics, management and pregnancy outcome10
Headache in patients with non-functioning pituitary adenoma before and after transsphenoidal surgery – a prospective study10
The effect of glucose dynamics on plasma copeptin levels upon glucagon, arginine, and macimorelin stimulation in healthy adults10
Serum biomarkers of colonic polyps in patients with acromegaly: a meta-analysis and systematic review10
Semaglutide as a promising treatment for hypothalamic obesity: a six-month case series on four females with craniopharyngioma9
Cushing’s disease: role of preoperative and primary medical therapy9
High prevalence of morphometric vertebral fractures opportunistically detected on thoracic radiograms in patients with non-functioning pituitary adenoma9
Posterior hypothalamic involvement on pre-operative MRI predicts hypothalamic obesity in craniopharyngiomas9
Growth hormone insensitivity and adipose tissue: tissue morphology and transcriptome analyses in pigs and humans9
Importance of 24 h ambulatory blood pressure monitoring in patients with acromegaly and correlation with cardiac magnetic resonance findings9
Diffusion-weighted imaging does not seem to be a predictor of consistency in pituitary adenomas9
TGFBR3L is associated with gonadotropin production in non-functioning gonadotroph pituitary neuroendocrine tumours9
An update on, and genetics of refractory adenomas of childhood9
Proportion and predictors of Hypogonadism Recovery in Men with Macroprolactinomas treated with dopamine agonists9
Skeletal fragility in pituitary disease: how can we predict fracture risk?9
Changes in pituitary adenoma patient presentation and outcomes during the COVID pandemic at a Pituitary Center of Excellence9
The somatotroph pituitary gland function in high-aged multimorbid hospitalized patients with IGF-I deficiency9
The diagnosis of GH deficiency in adult β-thalassemic patients: are two different stimulation tests necessary to improve specificity?8
Glucose metabolism, gut-brain hormones, and acromegaly treatment: an explorative single centre descriptive analysis8
The comprehensive evaluation of oral and fecal microbiota in patients with acromegaly8
How to manage intolerance to dopamine agonist in patients with prolactinoma8
Giant prolactinomas, a detailed analysis of 196 adult cases8
Correction: consensus on criteria for acromegaly diagnosis and remission8
HLA analysis of immune checkpoint inhibitor-induced and idiopathic isolated ACTH deficiency8
Idiopathic isolated adrenocorticotropic hormone deficiency: a systematic review of a heterogeneous and underreported disease8
Can we predict the risk of venous thromboembolism in patients with Cushing’s syndrome: a nationwide cohort analysis8
Alert: misinformation that may hurt patients with both adrenal insufficiency and AVP deficiency8
Cushing’s syndrome: Guidance on thromboprophylaxis at last8
Clinical use of [18F]fluoro-ethyl-L-tyrosine PET co-registered with MRI for localizing prolactinoma remnants8
Impulse control disorders in patients with pituitary adenoma managed with or without dopamine agonists: a cross-sectional study from a UK centre7
Syndrome of inappropriate antidiuresis/hyponatremia in COVID-197
Pituitary Tumor Centers of Excellence (PTCOE) should now include neuro-oncologic input7
Non-penetrant Xq26.3 duplication involving the invariant TAD border: clinical evidence for the VGLL1 region as the GPR101 pituitary enhancer of X-linked acrogigantism7
Long-term metabolic effectiveness and safety of growth hormone replacement therapy in patients with adult growth hormone deficiency: a single-institution study in Japan7
Selective resection of the medial wall of the cavernous sinus in pituitary surgery: results of a prospective single center analysis7
Sellar and perisellar meningiomas: effects on pituitary function in a Spanish cohort observational study7
Reported baseline variables in transsphenoidal surgery for pituitary adenoma over a 30 year period: a systematic review7
Correction: Impulse control disorders in patients with dopamine agonist-treated pituitary adenomas: a cross-sectional multicenter study7
Pituitary acting drugs: cabergoline and pasireotide7
Pituitary enlargement in patients with cerebrospinal fluid drainage due to ventricular shunt insertion: know the condition and do not mistake for adenoma6
Pituitary apoplexy: a comprehensive analysis of 93 cases across functioning and non-functioning pituitary adenomas from a single-center6
Prolactin-secreting tumors, dopamine agonists and pregnancy: a longitudinal experience of a tertiary neuroendocrine center6
Responsiveness to DDAVP in Cushing’s disease is associated with USP8 mutations through enhancing AVPR1B promoter activity6
Vitamin D in pituitary driven osteopathies6
Posterior pituitary tumors: an entity unto itself6
Clinico-radiological correlation of pituitary stalk interruption syndrome in children with growth hormone deficiency6
Cushing’s syndrome and COVID-196
Estimation of the biological variation of IGF-I in multimorbid geriatric patients and its clinical implications6
Growth hormone alters gross anatomy and morphology of the small and large intestines in age- and sex-dependent manners6
Exploring the role of the tumor microenvironment in refractory pituitary tumor pathogenesis6
Letter to the editor regarding “Vascular anomalies in patients with growth hormone-secreting pituitary adenomas: illustrative case report and systematic review of the literature”6
Elevated risk of recurrence and retreatment for silent pituitary adenomas6
Metastases to the pituitary gland: insights from the German pituitary tumor registry6
Serum copeptin levels at day two after pituitary surgery and ratio to baseline predict postoperative central diabetes insipidus6
The role of endoscopic endonasal surgery in the management of prolactinomas based on their invasiveness into the cavernous sinus6
Cushing’s disease in children: unique features and update on genetics6
The role of stereotactic radiosurgery in the multidisciplinary management of pituitary metastases6
Surgical outcomes of medically failed prolactinomas: a systematic review and meta-analysis5
Changing the name of diabetes insipidus5
Endoscopic endonasal transcavernous surgery for a contemporary series of 59 prolactinomas5
Role of Radiation in the treatment of Cushing Disease5
Efficacy of temozolomide combined with capecitabine (CAPTEM) on refractory prolactinomas as assessed using an ex vivo 3D spheroid assay5
Treatment of non-functioning pituitary adenoma with cabergoline: a systematic review and meta-analysis5
Preoperative differentiation of hypophysitis and pituitary adenomas using a novel clinicoradiologic scoring system5
GHR disruption in mature adult mice alters xenobiotic metabolism gene expression in the liver5
Novel imaging techniques in refractory pituitary adenomas5
Refractory Pit1 plurihormonal tumours and thyrotroph adenomas5
Sheehan syndrome: a current approach to a dormant disease4
Impact of etiology, sex, diabetes mellitus and remission status on erythrocytic profile in patients with cushing’s syndrome: a large population database study4
Reported outcomes in transsphenoidal surgery for pituitary adenomas: a systematic review4
The efficacy of a visiting surgical service versus that of a hospital-based surgical service in providing endoscopic endonasal surgery to remove nonfunctioning pituitary adenomas in rural communities4
Impact of the diagnostic delay of acromegaly on bone health: data from a real life and long term follow-up experience4
A prospective study on the efficacy of oral estrogen in female patients with acromegaly4
Precocious puberty, pandemic and beyond4
Opioids and pituitary function: expert opinion4
Treatment of recurrent and persistent Cushing’s disease after first transsphenoidal surgery: lessons learned from an international meta-analysis4
The role of the dentist and orthodontist in recognizing oro-facial manifestations of acromegaly: a questionnaire-based study4
Correction: Giant prolactinomas, a detailed analysis of 196 adult cases4
Response to letter to the editor “proposed consideration for targeted immunotherapy in pituitary carcinomas and aggressive pituitary tumors”4
11C-methionine PET aids localization of microprolactinomas in patients with intolerance or resistance to dopamine agonist therapy4
Morphometric study of the pituitary gland and stalk with emphasis on lifestyle factors4
Somapacitan-induced reversible lipoatrophy in an adult woman with hypopituitarism4
Dabrafenib as a diagnostic and therapeutic strategy for the non-surgical management of papillary craniopharyngioma4
Letter to the editor: Pituitary hyperplasia causing visual symptoms in a young woman planning pregnancy4
Impact of patient-reported nasal symptoms on quality of life after endoscopic pituitary surgery: a prospective cohort study4
Exploring sex-specific hematological changes and their impact on quality of life in patients with prolactinoma4
A patient-reported outcome measure for patients with pituitary adenoma undergoing transsphenoidal surgery4
Cushing’s disease: adrenal steroidogenesis inhibitors4
Recovery from hypogonadism in men with prolactinoma treated with dopamine agonists4
High prevalence of overweight/obesity and dyslipidemia in patients with intracranial germ cell tumors4
Hypopituitarism and COVID-194
Differences between immunotherapy-induced and primary hypophysitis—a multicenter retrospective study4
Care trajectories of surgically treated patients with a prolactinoma: why did they opt for surgery?4
Clinical and imaging findings for the evaluation of large Rathke’s cleft cysts and cystic craniopharyngiomas4
Kidney function in acromegaly: evidence from a long-term observational study4
Giant prolactinoma in children and adolescents: a single-center experience and systematic review3
Glucose intolerance in acromegaly is driven by low insulin secretion; results from an intravenous glucose tolerance test3
Standards of care for medical management of acromegaly in pituitary tumor centers of excellence (PTCOE)3
Current status of artificial intelligence technologies in pituitary adenoma surgery: a scoping review3
Sleep quality in patients with non-functioning pituitary adenoma: impact of replacement therapies with an emphasis on the time of hydrocortisone3
Development and validation of a novel treatment adherence, satisfaction and knowledge questionnaire (TASK-Q) for adult patients with hypothalamic-pituitary disorders3
Clinicopathological analysis of non-functioning pituitary adenomas (PAs) according to the 2022 WHO classification3
Post-operative surveillance for somatotroph, lactotroph and non-functional pituitary adenomas after curative resection: a systematic review3
“Intrasellar tumor-to-tumor metastasis: A single center experience with a systematic review”3
Levoketoconazole in the treatment of patients with endogenous Cushing’s syndrome: a double-blind, placebo-controlled, randomized withdrawal study (LOGICS)3
Surgical strategies in the treatment of MR-negative Cushing’s Disease: a systematic review and treatment algorithm3
Epigenetic implications in the pathogenesis of corticotroph tumors3
Differential diagnosis between Cushing’s syndrome and non-neoplastic hypercortisolism: are we getting there?3
Enhancing diagnostic tools for vasopressin deficiency: insights from a single-center cohort study3
FGFR1 variation in the divergent settings of congenital hypopituitarism and pituitary tumours3
A procedure in mice to obtain intact pituitary-infundibulum-hypothalamus preparations: a method to evaluate the reconstruction of hypothalamohypophyseal system3
Predictive factors for post-therapeutic biochemical discordance in acromegaly: a monocentric analysis of 156 cases3
Consensus and controversies about diagnosing GH deficiency: a Delphi survey by the GH research society3
Efficacy and safety of pasireotide treatment in acromegaly: A systematic review and single arm meta-analysis3
Impact of insurance on outcomes of patients undergoing endoscopic transsphenoidal surgery for non-functional pituitary adenomas: a single institution study3
Late Night Salivary Cortisol in the diagnosis of neoplastic hypercortisolism (including cyclic Cushing’s syndrome)3
Paltusotine, a novel oral once-daily nonpeptide SST2 receptor agonist, suppresses GH and IGF-1 in healthy volunteers3
Impact of nasal septal deviation on surgical outcomes in endoscopic transsphenoidal surgery: a population-based study3
Correlates of prolonged length of stay after endoscopic transsphenoidal surgery for pituitary adenomas: varying definitions and non-clinical factors3
Repeat endoscopic endonasal transsphenoidal surgery for residual or recurrent Cushing’s disease: safety, feasibility, and success3
Evaluation of acromegaly treatment direct costs with respect to biochemical control and follow-up length3
Clinical characteristics and therapeutic outcomes of acromegalic patients with giant growth hormone-secreting pituitary adenomas: a single-center study of 67 cases2
Pituitary hypophysitis in granulomatosis with polyangiitis (GPA): a case series2
Delayed postoperative hyponatremia in patients with acromegaly: incidence and predictive factors2
Postsurgical outcomes of nonfunctioning pituitary adenomas: a patient-level meta-analysis2
Neuropathic foot ulcers in the tallest patients with acromegalic gigantism: a common and significant problem. Historical overview2
Pituitary stalk interruption syndrome: phenotype, predictors, and pathophysiology of perinatal events2
Colonoscopy in acromegaly: when and why2
Typing of inflammatory lesions of the pituitary2
Pilot study to define criteria for Pituitary Tumors Centers of Excellence (PTCOE): results of an audit of leading international centers2
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)2
Contemporary radiotherapy and radiosurgery techniques for refractory pituitary adenomas2
Neuroendocrine challenges and clinical outcomes in men with chronic traumatic brain injury: a cross-sectional study2
Role of biological effective dose for prediction of endocrine remission in acromegaly patients treated with stereotactic radiosurgery2
Correction to: Oral octreotide capsules for the treatment of acromegaly: comparison of 2 phase 3 trial results2
Inflammation of adenohypophysis is commonly associated with headache in surgically managed Rathke’s cleft cysts2
Cytokines and chemokines modulate the growth of pituitary adenoma/neuroendocrine tumors: preliminary results of a monocenter prospective pilot study2
Effects of growth hormone replacement therapy in childhood-onset craniopharyngioma: an updated systematic review and meta-analysis2
Symptoms and steroid dose adjustments following the Covid-19 vaccine in patients with adrenal insufficiency2
Cushing’s disease: risk of recurrence following trans-sphenoidal surgery, timing and methods for evaluation2
Pituitary apoplexy score, toward standardized decision-making: a descriptive study2
Newer parameters of the octreotide test in patients with acromegaly2
Growth hormone secreting pituitary adenomas show distinct extrasellar extension patterns compared to nonfunctional pituitary adenomas2
Diagnostic, therapeutic, and prognostic characteristics of patients with acromegaly according to tumor size at diagnosis2
Good response rates and predictors during the first year of cabergoline treatment in large invasive prolactinomas2
Anterior-posterior diameter is a key driver of resectability and complications for pituitary adenomas with suprasellar extension in endoscopic transsphenoidal surgery2
Lateral orientation of Rathke cleft cysts may be associated with high rates of recurrence after surgery2
Advances in surgical approaches for refractory pituitary adenomas2
Venous thromboembolism chemical prophylaxis after endoscopic trans-sphenoidal pituitary surgery2
Frailty and pituitary surgery: a systematic review2
Treatment of acromegaly-induced diabetes: an updated proposal2
Cushing’s disease: role of bilateral adrenalectomy2
The spectrum of cardiac abnormalities in patients with acromegaly: results from a case-control cardiac magnetic resonance study2
Evaluating the burden of endogenous Cushing’s syndrome using a web-based questionnaire and validated patient-reported outcome measures2
Surgical outcomes and quality of life in Rathke’s cleft cysts undergoing endoscopic transsphenoidal resection: a multicentre study and systematic review of the literature2
Pituitary and COVID-19 vaccination: a systematic review2
Temporal and masseter muscle evaluation by MRI provides information on muscle mass and quality in acromegaly patients2
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