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Article

Hereditary pheochromocytoma with the von Hippel-Lindau gene mutation in a child: A case report.

Asian journal of surgery - 1 May 2023

Zheng Shengqi, Yin Guicao, Zhou Ming, Li Yifan

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 36528531
DOI: 10.1016/j.asjsur.2022.11.129

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Hereditary pheochromocytoma with the von Hippel-Lindau gene mutation in a child: A case report.PMID 36528531Read ↗

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Novel gene mutation in von Hippel-Lindau disease - a report of two cases.Semantic proximity Read ↗

Pheochromocytoma in von Hippel-Lindau disease: clinical presentation and mutation analysis in a large, multigenerational kindred.Semantic proximity Read ↗

Novel mutations in the von Hippel-Lindau gene associated with congenital polycythemia.Semantic proximity Read ↗

Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma.Semantic proximity Read ↗

Pheochromocytoma and clear-cell renal carcinoma in a child with von Hippel-Lindau disease: a patient report.Semantic proximity Read ↗

Identification of two sporadically derived mutations in the Von Hippel-Lindau gene.Semantic proximity Read ↗

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