Add to ORKGphaeochromocytoma and paraganglioma (GAPP). The tumours were scored based on as 5.5G2.6 years. The study Key Words " phaeochromocytoma " paraganglioma " histopathological diagnosis " succinate dehydrogenase gene subunit B " immunohistochemistry " metastasis " survival
Compared to other familial pheochromocytoma/paragangliomas (PHEO/PGLs), the succinate dehydrogenase ...
Context.—Because of the limited number of available primary bladder paraganglioma (PBPG) cases...
Pheochromocytomas and paragangliomas occur sporadi-cally but are commonly associated with the von Hi...
The Grading system for Adrenal Pheochromocytoma and Paraganglioma (GAPP) was proposed for predicting...
OBJECTIVE: Phaeochromocytomas and paragangliomas (PPGL) are rare, but strongly heritable tumours. Va...
Pheochromocytoma (PCC) and sympathetic paraganglioma (PGL) are rare neuroendocrine tumors characteri...
Malignant phaeochromocytomas are rare tumours accounting for ∼10% of all phaeochromocytomas; the pre...
Phaeochromocytomas and paragangliomas (PPGLs) are catecholamine-secreting neuroendocrine tumours cha...
textabstractBackground: Phaeochromocytomas and paragangliomas are neuro-endocrine tumours that occur...
International audienceThe study identifies the importance of positron emission tomographic (PET) and...
Contains fulltext : 80017.pdf (publisher's version ) (Closed access)BACKGROUND: Ph...
Context: Pheochromocytoma-paraganglioma syndrome is caused by mutations in SDHB, SDHC, and SDHD, enc...
Pheochromocytomas (PCCs) and abdominal paragangliomas (PGLs), collectively abbreviated PPGLs, are ne...
Contains fulltext : 71138.pdf (Publisher’s version ) (Open Access)RU Radboud Unive...
Introduction: A substantial proportion of phaeochromocytomas and paragangliomas are associated with ...
Compared to other familial pheochromocytoma/paragangliomas (PHEO/PGLs), the succinate dehydrogenase ...
Context.—Because of the limited number of available primary bladder paraganglioma (PBPG) cases...
Pheochromocytomas and paragangliomas occur sporadi-cally but are commonly associated with the von Hi...
The Grading system for Adrenal Pheochromocytoma and Paraganglioma (GAPP) was proposed for predicting...
OBJECTIVE: Phaeochromocytomas and paragangliomas (PPGL) are rare, but strongly heritable tumours. Va...
Pheochromocytoma (PCC) and sympathetic paraganglioma (PGL) are rare neuroendocrine tumors characteri...
Malignant phaeochromocytomas are rare tumours accounting for ∼10% of all phaeochromocytomas; the pre...
Phaeochromocytomas and paragangliomas (PPGLs) are catecholamine-secreting neuroendocrine tumours cha...
textabstractBackground: Phaeochromocytomas and paragangliomas are neuro-endocrine tumours that occur...
International audienceThe study identifies the importance of positron emission tomographic (PET) and...
Contains fulltext : 80017.pdf (publisher's version ) (Closed access)BACKGROUND: Ph...
Context: Pheochromocytoma-paraganglioma syndrome is caused by mutations in SDHB, SDHC, and SDHD, enc...
Pheochromocytomas (PCCs) and abdominal paragangliomas (PGLs), collectively abbreviated PPGLs, are ne...
Contains fulltext : 71138.pdf (Publisher’s version ) (Open Access)RU Radboud Unive...
Introduction: A substantial proportion of phaeochromocytomas and paragangliomas are associated with ...
Compared to other familial pheochromocytoma/paragangliomas (PHEO/PGLs), the succinate dehydrogenase ...
Context.—Because of the limited number of available primary bladder paraganglioma (PBPG) cases...
Pheochromocytomas and paragangliomas occur sporadi-cally but are commonly associated with the von Hi...