Association of Pheochromocytoma and Ganglioneuroma: Unusual Finding in Neurofibromatosis Type 1
Author:
Publisher
Elsevier BV
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Link
http://aace.metapress.com/index/K5417UR17023RX0L.pdf
Reference14 articles.
1. Neurofibromatose: Clínica, Genética e Terapêutica;Geller,2004
2. Medical management of neurofibromatosis 1: a cross-sectional study of 383 patients;Drappier;J Am Acad Dermatol,2003
3. The neurocristopathies: a unifying concept of disease arising in neural crest maldevelopment;Bolande;Hum Pathol,1974
4. A case of von Recklinghausen’s disease with bilateral pheochromocytoma-malignant peripheral nerve sheath tumors of the adrenal and gastrointestinal autonomic nerve tumors;Sakaguchi;Am J Surg Pathol,1996
5. Pheochromocytoma and functional paraganglioma;Roman;Curr Opin Oncol,2004
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1. Abdominal tumors in patients with neurofibromatosis type I: Genotype-phenotype relationships;European Journal of Medical Genetics;2022-11
2. Composite phaeochromocytomas—a systematic review of published literature;Langenbeck's Archives of Surgery;2021-03-02
3. Ganglioneuromas across age groups: Systematic review of individual patient data;Clinical Endocrinology;2020-08-07
4. Surgical treatment of neurofibromatosis type I followed by retroperitoneal tumor;Khirurgiya. Zhurnal im. N.I. Pirogova;2019
5. Pheochromocytoma in Neurofibromatosis Type 1: When Should it Be Suspected;Endocrine Practice;2014-08
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