Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1964 1
1965 1
1967 2
1970 2
1971 3
1972 2
1973 1
1974 2
1976 1
1977 4
1978 1
1979 2
1981 1
1983 2
1984 4
1985 2
1986 2
1987 1
1988 4
1989 5
1990 3
1991 6
1992 4
1993 1
1994 2
1995 8
1996 4
1997 13
1998 4
1999 8
2000 8
2001 10
2002 4
2003 10
2004 6
2005 6
2006 12
2007 5
2008 7
2009 6
2010 10
2011 5
2012 8
2013 13
2014 12
2015 9
2016 8
2017 11
2018 14
2019 12
2020 9
2021 7
2022 8
2023 12
2024 4

Text availability

Article attribute

Article type

Publication date

Search Results

287 results

Results by year

Filters applied: . Clear all
Page 1
Pheochromocytoma.
Farrugia FA, Charalampopoulos A. Farrugia FA, et al. Endocr Regul. 2019 Jul 1;53(3):191-212. doi: 10.2478/enr-2019-0020. Endocr Regul. 2019. PMID: 31517632 Free article. Review.
Pheochromocytomas are rare tumors originating in the adrenal medulla. They may be sporadic or in the context of a hereditary syndrome. ...
Pheochromocytomas are rare tumors originating in the adrenal medulla. They may be sporadic or in the context of a hereditary s …
Pheochromocytomas and Hypertension.
Pappachan JM, Tun NN, Arunagirinathan G, Sodi R, Hanna FWF. Pappachan JM, et al. Curr Hypertens Rep. 2018 Jan 22;20(1):3. doi: 10.1007/s11906-018-0804-z. Curr Hypertens Rep. 2018. PMID: 29356966 Review.
PURPOSE OF REVIEW: Pheochromocytomas and paragangliomas (PPGLs) are uncommon catecholamine-producing neuroendocrine neoplasms that usually present with secondary hypertension. This review is to update the current knowledge about these neoplasms, the pathophysiology, …
PURPOSE OF REVIEW: Pheochromocytomas and paragangliomas (PPGLs) are uncommon catecholamine-producing neuroendocrine neoplasms that us …
Overview of the 2022 WHO Classification of Paragangliomas and Pheochromocytomas.
Mete O, Asa SL, Gill AJ, Kimura N, de Krijger RR, Tischler A. Mete O, et al. Endocr Pathol. 2022 Mar;33(1):90-114. doi: 10.1007/s12022-022-09704-6. Epub 2022 Mar 13. Endocr Pathol. 2022. PMID: 35285002 Review.
This review summarizes the classification of tumors of the adrenal medulla and extra-adrenal paraganglia as outlined in the 5th series of the WHO Classification of Endocrine and Neuroendocrine Tumors. ...This review adopts a practical question-answer framewor …
This review summarizes the classification of tumors of the adrenal medulla and extra-adrenal paraganglia as outlined in …
[Phaeochromocytoma and paraganglioma].
Cornu E, Belmihoub I, Burnichon N, Grataloup C, Zinzindohoué F, Baron S, Billaud E, Azizi M, Gimenez-Roqueplo AP, Amar L. Cornu E, et al. Rev Med Interne. 2019 Nov;40(11):733-741. doi: 10.1016/j.revmed.2019.07.008. Epub 2019 Sep 4. Rev Med Interne. 2019. PMID: 31493938 Review. French.
Phaeochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumors that arise from the adrenal medulla or sympathetic and parasympathetic ganglia. These tumors produce most often catecholamines in excess, causing hypertension and sometimes severe acute card …
Phaeochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumors that arise from the adrenal medulla or sympathetic …
E-Cigarettes and Cancer Risk.
Mravec B, Tibensky M, Horvathova L, Babal P. Mravec B, et al. Cancer Prev Res (Phila). 2020 Feb;13(2):137-144. doi: 10.1158/1940-6207.CAPR-19-0346. Epub 2019 Oct 16. Cancer Prev Res (Phila). 2020. PMID: 31619443 Review.
Mediastinal neuroblastoma, ganglioneuroblastoma, and ganglioneuroma: Pathology review and diagnostic approach.
Choi JH, Ro JY. Choi JH, et al. Semin Diagn Pathol. 2022 Mar;39(2):120-130. doi: 10.1053/j.semdp.2021.06.007. Epub 2021 Jun 15. Semin Diagn Pathol. 2022. PMID: 34167847 Review.
Neuroblastic tumors are a group of tumors of the sympathetic ganglia and adrenal medulla that derive from primordial neural crest cells. These tumors include neuroblastoma, intermixed ganglioneuroblastoma, nodular ganglioneuroblastoma, and ganglioneuroma. ...
Neuroblastic tumors are a group of tumors of the sympathetic ganglia and adrenal medulla that derive from primordial neural cr …
Robot-assisted adrenalectomy: indications and drawbacks.
Nomine-Criqui C, Germain A, Ayav A, Bresler L, Brunaud L. Nomine-Criqui C, et al. Updates Surg. 2017 Jun;69(2):127-133. doi: 10.1007/s13304-017-0448-6. Epub 2017 May 12. Updates Surg. 2017. PMID: 28497219 Review.
Adrenal tumors can vary from a benign adrenocortical adenoma with no hormonal secretion to a secretory adrenocortical malignancy (adrenocortical carcinoma) or a hormone-secreting tumor of the adrenal medulla (pheochromocytoma). Currently, laparoscopic
Adrenal tumors can vary from a benign adrenocortical adenoma with no hormonal secretion to a secretory adrenocortical malignan
Familial pheochromocytomas and paragangliomas.
King KS, Pacak K. King KS, et al. Mol Cell Endocrinol. 2014 Apr 5;386(1-2):92-100. doi: 10.1016/j.mce.2013.07.032. Epub 2013 Aug 7. Mol Cell Endocrinol. 2014. PMID: 23933153 Free PMC article. Review.
Pheochromocytomas and paragangliomas are neural crest cell tumors of the adrenal medulla and parasympathetic/sympathetic ganglia, respectively, that are often associated with catecholamine production. ...Most of the susceptibility genes are now associated with speci …
Pheochromocytomas and paragangliomas are neural crest cell tumors of the adrenal medulla and parasympathetic/sympathetic gangl …
Diagnosis and Management of Pheochromocytomas and Paragangliomas: A Guide for the Clinician.
Sharma S, Fishbein L. Sharma S, et al. Endocr Pract. 2023 Dec;29(12):999-1006. doi: 10.1016/j.eprac.2023.07.027. Epub 2023 Aug 15. Endocr Pract. 2023. PMID: 37586639 Review.
RESULTS: PPGL are neuroendocrine tumors arising from the chromaffin cells of adrenal medulla and sympathetic and parasympathetic ganglia, respectively. ...
RESULTS: PPGL are neuroendocrine tumors arising from the chromaffin cells of adrenal medulla and sympathetic and parasympathet …
Pheochromocytoma: An approach to diagnosis.
Sbardella E, Grossman AB. Sbardella E, et al. Best Pract Res Clin Endocrinol Metab. 2020 Mar;34(2):101346. doi: 10.1016/j.beem.2019.101346. Epub 2019 Oct 22. Best Pract Res Clin Endocrinol Metab. 2020. PMID: 31708376 Review.
Pheochromocytomas are rare neuroendocrine chromaffin-derived tumors that arise within the adrenal medulla. They are usually benign, but if not diagnosed or if left untreated, they can have devastating consequences. ...
Pheochromocytomas are rare neuroendocrine chromaffin-derived tumors that arise within the adrenal medulla. They are usually …
287 results