Disease: Pheochromocytoma as part of Neurofibromatosis
- A rare case of Von Hippel Lindau disease
- Bilateral pheochromocytomas
- Case Report: Composite pheochromocytoma with ganglioneuroma component: A report of three cases
- Clinical Presentation and Outcomes of Phaeochromocytomas/Paragangliomas in Neurofibromatosis Type 1
- Echocardiographic features of genetic diseases: part 5. Tumors
- Epithelial and neuroendocrine tumors of the duodenum
- Exposure of newborn mice to adenosine causes neural crest dysplasia and tumor formation
- Gastrointestinal and retroperitoneal manifestations of type 1 neurofibromatosis
- Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas
- Germinal mutations of RET, SDHB, SDHD, and VHL genes in patients with apparently sporadic pheochromocytomas and paragangliomas
- Hereditary Pheochromocytoma
- Hereditary pheochromocytoma and paraganglioma
- Incidence of pheochromocytoma in South Galicia, Spain
- Inflammatory rhabdomyoblastic tumor, pheochromocytoma, and pulmonary hamartoma in a patient with neurofibromatosis type 1: a case report
- Isolated familial pheochromocytoma as a variant of von Hippel-Lindau disease
- Malignant and benign tumors in patients with neurofibromatosis type 1 in a defined Swedish population
- Malignant peripheral nerve sheath tumor of adrenal gland with heterologus osseous differentiation in a case of Von Recklinghausen's disease
- Multiple gastrointestinal stromal tumors and pheochromocytoma in a patient with von Recklinghausen's disease
- Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas
- Neuroendocrine tumors and tumor syndromes in childhood
- New insights into the genetics of familial chromaffin cell tumors
- Oncogene and growth factor expression in MEN 2 and related tumors
- Pheochromocytoma and paraganglioma in children and adolescents
- Pheochromocytoma and Recklinghausen's cutaneous neurofibromatosis. Localizing value of abdominal reflexes in a case
- Pheochromocytomas and secreting paragangliomas
- Rare forms of pheochromocytoma in children
- Skull metastasis from papillary thyroid carcinoma accompanied by neurofibromatosis type 1 and pheochromocytoma: report of a case
- Somatostatinoma
- Surgical management of abdominal manifestations of type 1 neurofibromatosis: experience of a single center
- The association of neurofibromatosis, pheochromocytoma, and somatostatin-rich duodenal carcinoid tumor
- The clinical genetics of phaeochromocytoma and paraganglioma
- Tumours of familial origin in the head and neck
- Update on Pheochromocytoma and Paraganglioma from the SSO Endocrine/Head and Neck Disease-Site Work Group. Part 1 of 2: Advances in Pathogenesis and Diagnosis of Pheochromocytoma and Paraganglioma
- Usefulness of Succinate dehydrogenase B (SDHB) immunohistochemistry in guiding mutational screening among patients with pheochromocytoma-paraganglioma syndromes
- Von Recklinghausen's disease: experimental models and comparative aspects