Pheochromocytoma–Paraganglioma Syndrome: A Multiform Disease with Different Genotype and Phenotype Features - Giacché, Mara; Tacchetti, Maria Chiara; Agabiti-Rosei, Claudia; Torlone, Francesco; Bandera, Francesco; Izzi, Claudia; Agabiti-Rosei, Enrico (Biomedicines, 2024)
Keywords: Acute coronary syndromes; Adrenal medulla; Analysis; Asymptomatic; Blood pressure; Cardiac arrhythmia; Cardiomyopathy; Care and treatment; Catecholamines; Chromaffin cells; Diagnosis; Disease; Disease susceptibility; Ejection fraction; Gene frequency; Gene mutations; Genetic aspects; genetics; Genotype & phenotype; Genotypes; Health aspects; Heart failure; Hemodynamics; Hypertension; Hypoxia; Kinases; Malignancy; Metabolites; Multiple endocrine neoplasia; Mutation; Neurofibromatosis; Neurofibromin 1; NF1; Orthostatic hypotension; Paraganglioma; Patients; Phenotypes; Pheochromocytoma; Plasma; Recklinghausen's disease; RET; Ret protein; Review; Surveillance; Transcription activation; Transcriptomics; Tumorigenesis; Tumors; VHL; VHL protein; Wnt protein; Italy; RET; FH; genetics; MAX; TMEM; SDHX; NF1; pheochromocytoma; VHL; paraganglioma