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Current views on paediatric phaeochromocytoma and paraganglioma with a focus on newest guidelines
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Recent advances in algorithms predicting hemodynamic instability undergoing surgery for phaeochromocytoma and paraganglioma
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Current views on the role of HIF-2α in the pathogenesis and syndromic presentation of pheochromocytoma and paraganglioma
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Progress in surgical approaches and outcomes of patients with pheochromocytoma and paraganglioma
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Update on clinical characteristics in the evaluation of phaeochromocytoma and paraganglioma
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Metabolomics and proteomics in pheochromocytoma and paraganglioma: Translating biochemistry and biology to bedside
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Head and neck paragangliomas: recent advances in translational and clinical research and guidelines for patient care
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Role of B cells in intratumoral MBTA immunotherapy of murine pheochromocytoma model
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Overview of recent guidelines and consensus statements on initial screening and management of phaeochromocytoma and paraganglioma in SDHx pathogenic variant carriers and patients
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Recent progress in molecular classification of phaeochromocytoma and paraganglioma
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Gender-affirming hormone treatment modalities for transfemale & non-binary transfeminine individuals: A UK perspective
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Personalized management for phaeochromocytomas and paragangliomas in Latin America: a genetic perspective
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The current and upcoming era of radiomics in phaeochromocytoma and paraganglioma
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SDH-related head and neck paragangliomas: Unraveling PET radiomics beyond 18F-FDG
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Recent discoveries of Sino-Caucasian differences in the genetics of phaeochromocytomas and paragangliomas
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Testosterone-induced erythrocytosis in transgender males: Challenges arising from an increasing prevalence of metabolic syndrome and wider therapeutic indications for prescribing SGLT2 inhibitor drugs
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Transgender
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MAML3-fusions modulate vascular and immune tumour microenvironment and confer high metastatic risk in pheochromocytoma and paraganglioma
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Clinical considerations and endocrinological implications in the detransition process
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Metabolomics and proteomics in pheochromocytoma/paraganglioma: translating biochemistry and biology to bedside
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Best practice and research, clinical endocrinology and metabolism preface to the special issue: Diagnosis and treatment of acromegaly acromegaly, a paradigmatic disease second part: Treatment
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Pre-clinical phaeochromocytoma and paraganglioma models: Cell lines, animal models, and a human primary culture model
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Best Practice and Research, Clinical Endocrinology and Metabolism Preface to the Special issue: Diagnosis and Treatment of Acromegaly Acromegaly, a paradigmatic disease Second part: Treatment
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Growth hormone receptor antagonist pegvisomant and its role in the medical therapy of growth hormone excess
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Testosterone and other treatments for transgender males and non-binary trans masculine individuals
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The implications of hormone treatment for cancer risk, screening and treatment in transgender individuals
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Metabolic and cardiovascular risks of hormone treatment for transgender individuals
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Treatment of acromegaly with the nonpeptide, highly selective somatostatin receptor type 2 agonist paltusotine
Treatment of acromegaly with the nonpeptide, highly selective somatostatin receptor type 2 agonist paltusotine
Acromegaly is a chronic, systemic disease characterized by high levels of growth hormone (GH) and insulin-like growth fact...
Efficacy and safety of radiosurgery in acromegaly
Efficacy and safety of radiosurgery in acromegaly
Pituitary adenomas originate from the endocrine tissue of the adenohypophysis and are the most common sellar lesions (acco...
Preface to the Special issue: Diagnosis and treatment of acromegaly, a paradigmatic disease
Preface to the Special issue: Diagnosis and treatment of acromegaly, a paradigmatic disease
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