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SCI Abstract
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Long-term metabolic effectiveness and safety of growth hormone replacement therapy in patients with adult growth hormone deficiency: a single-institution study in Japan
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Approach to the patient with controlled acromegaly and acromegalic arthropathy: clinical diagnosis and management
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Standards of care for medical management of acromegaly in pituitary tumor centers of excellence (PTCOE)
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The spectrum of cardiac abnormalities in patients with acromegaly: results from a case-control cardiac magnetic resonance study
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Utility of copeptin in predicting non-pathological postoperative polyuria in patients affected by acromegaly undergoing pituitary neurosurgery
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Pituitary apoplexy in cushing’s disease: a single center study and systematic literature review
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The conundrum of differentiating Cushing’s syndrome from non-neoplastic hypercortisolism: a systematic review and meta-analysis
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Clinicopathological analysis of non-functioning pituitary adenomas (PAs) according to the 2022 WHO classification
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Growth hormone increase by luteinizing hormone-releasing hormone reflects gonadotroph-related characteristics in acromegaly
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Pituitary apoplexy: a systematic review of non-gestational risk factors
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Glucose metabolism outcomes after pituitary surgery in patients with acromegaly
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Decreased β-cell volume and insulin secretion but preserved glucose tolerance in a growth hormone insensitive pig model
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Temporal and masseter muscle evaluation by MRI provides information on muscle mass and quality in acromegaly patients
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Pituitary surgery and COVID
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Development and validation of a novel treatment adherence, satisfaction and knowledge questionnaire (TASK-Q) for adult patients with hypothalamic-pituitary disorders
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Outcome of non-functioning ACTH pituitary tumors: silent does not mean indolent
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Idiopathic isolated adrenocorticotropic hormone deficiency: a systematic review of a heterogeneous and underreported disease
Isolated adrenocorticotropic hormone deficiency (IAD) is considered to be a rare disease. Due to the nonspecific clinical ...
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Pituitary apoplexy score, toward standardized decision-making: a descriptive study
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Correction: incidence of postoperative hyponatremia after endoscopic endonasal pituitary transposition for skull base pathologies
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Different patient versus provider perspectives on living with Cushing’s disease
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Glucose intolerance in acromegaly is driven by low insulin secretion; results from an intravenous glucose tolerance test
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Pituitary tumours without distinct lineage differentiation express stem cell marker SOX2
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The prevalence and associated risk factors of detectable renal morphological abnormalities in acromegaly
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