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Articles Published Processes
9/10/2014 7:57:00 PM | Browse: 1133 | Download: 1156
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Received |
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2013-01-29 14:06 |
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Peer-Review Started |
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2013-01-30 16:54 |
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First Decision by Editorial Office Director |
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Return for Revision |
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2013-03-08 11:04 |
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Revised |
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2013-03-11 14:56 |
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Publication Fee Transferred |
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Second Decision by Editor |
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2013-05-09 14:14 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2013-05-10 07:04 |
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Articles in Press |
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Edit the Manuscript by Language Editor |
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2013-05-30 04:19 |
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Typeset the Manuscript |
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2013-06-09 20:09 |
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Publish the Manuscript Online |
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2013-07-19 16:11 |
| Category |
Medicine, General & Internal |
| Manuscript Type |
Autobiography |
| Article Title |
Malignant pheochromocytoma in neurofibromatosis; mutation screening of RET proto-oncogene, VHL and SDH gene
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| Manuscript Source |
Invited Manuscript |
| All Author List |
Shirin Hasani-Ranjbar, Mahsa M Amoli, Maasumeh Noorani and Mohsen Ghadami |
| Funding Agency and Grant Number |
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| Corresponding Author |
Shirin Hasani-Ranjbar, Endocrinologist, Obesity and Eating Habits Research Center, Endocrinology and Metabolism Cellular and Molecular Sciences Institute, Shariati Hospital, Tehran University of Medical Sciences, North Kargar Ave., Tehran 14114, Iran. sh_hasani@sina.tums.ac.ir
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| Key Words |
Neurofibromatosis; Familial pheochromocytoma; Malignant pheochromocytoma; Metastatic pheochromocytoma; RET proto-oncogene; von Hippel-Lindau; Succinate dehydrogenase complex subunits |
| Core Tip |
Malignant pheochromocytoma associated with neurofibromatosis (NF) is very rare. We screened for all possible mutations related to pheochromocytoma in a patient with NF and malignant pheochromocytoma but found no mutations. This negative result shows that the NF1 gene is responsible for this rare presentation.
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| Publish Date |
2013-07-19 16:11 |
| Citation |
Hasani-Ranjbar S, Amoli MM, Noorani M, Ghadami M. Malignant pheochromocytoma in neurofibromatosis; mutation screening of RET proto-oncogene, VHL and SDH gene. World J Med Genet 2013; 3(1): 1-4
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| URL |
http://www.wjgnet.com/2220-3184/full/v3/i1/1.htm |
| DOI |
http://dx.doi.org/10.5496/wjmg.v3.i1.1 |
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