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      Genotype-Phenotype Correlations and Clinical Outcomes in 155 Cases of Pheochromocytoma and Paraganglioma.

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          Abstract

          Pheochromocytoma and paraganglioma (PPGL) are rare neuroendocrine tumours, often associated with germline mutations that influence the disease biology and clinical course. We aimed to describe the genotypic and phenotypic characteristics of a consecutive series of PPGL patients and correlate mutation status with clinical outcomes.

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          Author and article information

          Journal
          World J Surg
          World journal of surgery
          Springer Science and Business Media LLC
          1432-2323
          0364-2313
          Mar 2023
          : 47
          : 3
          Affiliations
          [1 ] Northern Clinical School, Sydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
          [2 ] Northern Clinical School, Sydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia. alex.papachristos@sydney.edu.au.
          [3 ] Endocrine Surgical Unit, Royal North Shore Hospital, Northern Sydney Local Health District, Sydney, NSW, Australia. alex.papachristos@sydney.edu.au.
          [4 ] NSW Health Pathology, Department of Anatomical Pathology, Royal North Shore Hospital, Northern Sydney Local Health District, Sydney, NSW, Australia.
          [5 ] Cancer Diagnosis and Pathology Group, Kolling Institute of Medical Research, Sydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
          [6 ] Department of Endocrinology, Royal North Shore Hospital, Northern Sydney Local Health District, Sydney, NSW, Australia.
          [7 ] Cancer Genetics Laboratory, Kolling Institute of Medical Research, Sydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
          [8 ] Endocrine Surgical Unit, Royal North Shore Hospital, Northern Sydney Local Health District, Sydney, NSW, Australia.
          Article
          10.1007/s00268-022-06862-w
          10.1007/s00268-022-06862-w
          36550325
          b6f8e297-3528-4712-b52f-da8fc0a0410e
          History

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