Pheochromocytoma, paraganglioma and neuroblastoma are the most common neural crest-derived tumors in adults and children, respectively. These neoplasms are associated with significant morbidity and mortality. Some international studies currently underway are researching and evaluating the presence of any similarities and differences between these tumors. Hopefully, future results will reveal several potential novel genes and pathways that might have major roles in the pathogenesis and progression of these neoplasms. This book discusses epidemiology, genetics, and treatment of these malignancies
Pheochromocytomas and paragangliomas are rare neuroendocrine tumors, with genetic background in abou...
This work summarizes the results of a research inquiring into relatively rare neuroendocrine tumors ...
Pheochromocytomas and paragangliomas are rare tumors of neural crest origin. Their remarkable geneti...
Pheochromocytomas (PCC) and paragangliomas (PGL) are rare neuroendocrine tumors that arise in the ad...
The familial forms of pheochromocytoma have recently been demonstrated to be more frequent than beli...
The familial forms of pheochromocytoma have recently been demonstrated to be more frequent than beli...
textabstractPheochromocytomas (PCC) are rare tumours of the adrenal medulla. These tumours are deriv...
Pheochromocytomas and paragangliomas are the most heritable endocrine tumors. In addition to the inh...
Pheochromocytomas and paragangliomas are neuroendocrine tumors that arise from neural crest-derived ...
Paragangliomas and pheochromocytomas are rare tumors of the autonomic nervous system that represent ...
Pheochromocytoma and paraganglioma are tumors of the sympathetic or parasympathetic paraganglia. Phe...
Pheochromocytoma and paraganglioma are tumors of the sympathetic or parasympathetic paraganglia. Phe...
Pheochromocytomas and paragangliomas are rare tumors, characterized by catecholamine synthesis, rele...
This work summarizes the results of a research inquiring into relatively rare neuroendocrine tumors ...
Pheochromocytoma and paraganglioma are rare neuroendocrine tumors. Knowledge about such neoplasms am...
Pheochromocytomas and paragangliomas are rare neuroendocrine tumors, with genetic background in abou...
This work summarizes the results of a research inquiring into relatively rare neuroendocrine tumors ...
Pheochromocytomas and paragangliomas are rare tumors of neural crest origin. Their remarkable geneti...
Pheochromocytomas (PCC) and paragangliomas (PGL) are rare neuroendocrine tumors that arise in the ad...
The familial forms of pheochromocytoma have recently been demonstrated to be more frequent than beli...
The familial forms of pheochromocytoma have recently been demonstrated to be more frequent than beli...
textabstractPheochromocytomas (PCC) are rare tumours of the adrenal medulla. These tumours are deriv...
Pheochromocytomas and paragangliomas are the most heritable endocrine tumors. In addition to the inh...
Pheochromocytomas and paragangliomas are neuroendocrine tumors that arise from neural crest-derived ...
Paragangliomas and pheochromocytomas are rare tumors of the autonomic nervous system that represent ...
Pheochromocytoma and paraganglioma are tumors of the sympathetic or parasympathetic paraganglia. Phe...
Pheochromocytoma and paraganglioma are tumors of the sympathetic or parasympathetic paraganglia. Phe...
Pheochromocytomas and paragangliomas are rare tumors, characterized by catecholamine synthesis, rele...
This work summarizes the results of a research inquiring into relatively rare neuroendocrine tumors ...
Pheochromocytoma and paraganglioma are rare neuroendocrine tumors. Knowledge about such neoplasms am...
Pheochromocytomas and paragangliomas are rare neuroendocrine tumors, with genetic background in abou...
This work summarizes the results of a research inquiring into relatively rare neuroendocrine tumors ...
Pheochromocytomas and paragangliomas are rare tumors of neural crest origin. Their remarkable geneti...