Rare complications of neurofibromatosis 1 diagnosed incidentally in two children

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Rare complications of neurofibromatosis 1 diagnosed incidentally in two children

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wetenschappelijk artikel

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наукова стаття, опублікована у 2018

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Rare complications of neurofibromatosis 1 diagnosed incidentally in two children

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Rare complications of neurofibromatosis 1 diagnosed incidentally in two children

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Rare complications of neurofibromatosis 1 diagnosed incidentally in two children

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Rare complications of neurofibromatosis 1 diagnosed incidentally in two children

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Rare complications of neurofibromatosis 1 diagnosed incidentally in two children

@en

Rare complications of neurofibromatosis 1 diagnosed incidentally in two children

@nl

P1476

Rare complications of neurofibromatosis 1 diagnosed incidentally in two children

@en

P2093

Camelia Al-Khzouz

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Carmen Asavoaie

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Cecilia Lazea

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Lenuta Popa

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P2860

Pheochromocytomas and Paragangliomas: Clinical and Genetic Approaches

Pheochromocytoma: implications in tumorigenesis and the actual management

Insights into the pathogenesis of neurofibromatosis 1 vasculopathy

von Recklinghausen's disease and pheochromocytomas.

Age at diagnosis of pheochromocytoma differs according to catecholamine phenotype and tumor location.

Von Recklinghausen's neurofibromatosis: neurofibromatosis type 1.

Disease Beyond the Arch: A Systematic Review of Middle Aortic Syndrome in Childhood.

Guidelines for the diagnosis and management of individuals with neurofibromatosis 1

Vascular abnormalities in patients with neurofibromatosis syndrome type I: clinical spectrum, management, and results.

Midaortic syndrome: 30 years of experience with medical, endovascular and surgical management.

P304

1547-1552

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P31

scholarly article

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10.2147/TCRM.S173237

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P407

English

P478

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P577

2018-01-01T00:00:00Z

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P698

30214218

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P932

6124468

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