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

Year Number of Results
1937 1
1940 1
1941 1
1942 2
1944 1
1945 3
1946 12
1947 22
1948 23
1949 36
1950 34
1951 74
1952 47
1953 62
1954 70
1955 69
1956 73
1957 88
1958 86
1959 81
1960 104
1961 83
1962 106
1963 152
1964 208
1965 124
1966 168
1967 183
1968 190
1969 185
1970 173
1971 187
1972 185
1973 187
1974 201
1975 190
1976 187
1977 228
1978 214
1979 256
1980 244
1981 258
1982 324
1983 364
1984 388
1985 398
1986 437
1987 455
1988 442
1989 520
1990 491
1991 468
1992 445
1993 412
1994 421
1995 481
1996 458
1997 449
1998 459
1999 439
2000 488
2001 472
2002 550
2003 435
2004 455
2005 521
2006 542
2007 552
2008 554
2009 556
2010 584
2011 559
2012 631
2013 656
2014 669
2015 641
2016 565
2017 632
2018 605
2019 629
2020 724
2021 775
2022 725
2023 683
2024 228

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25,658 results

Results by year

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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. A considerable number of pheochromocytomas carry germline or somatic gene mutations, which are inherited in the autosomal dominant …
Pheochromocytomas are rare tumors originating in the adrenal medulla. They may be sporadic or in the context of a hereditary syndrome …
Pheochromocytoma: presentation, diagnosis and treatment.
Reisch N, Peczkowska M, Januszewicz A, Neumann HP. Reisch N, et al. J Hypertens. 2006 Dec;24(12):2331-9. doi: 10.1097/01.hjh.0000251887.01885.54. J Hypertens. 2006. PMID: 17082709 Review.
Pheochromocytomas are rare, mostly benign catecholamine-producing tumors of chromaffin cells of the adrenal medulla or of a paraganglion. ...This review provides an update on identification and management of pheochromocytomas, emphasizing current developments in dia …
Pheochromocytomas are rare, mostly benign catecholamine-producing tumors of chromaffin cells of the adrenal medulla or of a paragangl …
Pheochromocytoma.
Bravo EL, Gifford RW Jr. Bravo EL, et al. Endocrinol Metab Clin North Am. 1993 Jun;22(2):329-41. Endocrinol Metab Clin North Am. 1993. PMID: 8325290 Review.
Pheochromocytomas cause the most dramatic life-threatening crises in all of endocrinology. Pheochromocytoma is an explosive clinical syndrome that may be characterized by either severe hypertension associated with cerebral, cardiac, and renal complications or hypote …
Pheochromocytomas cause the most dramatic life-threatening crises in all of endocrinology. Pheochromocytoma is an explosive cl …
Pheochromocytoma.
Manger WM, Gifford RW. Manger WM, et al. J Clin Hypertens (Greenwich). 2002 Jan-Feb;4(1):62-72. doi: 10.1111/j.1524-6175.2002.01452.x. J Clin Hypertens (Greenwich). 2002. PMID: 11821644 Free PMC article. Review.
Pheochromocytoma, a relatively rare (<0.05% of hypertensives), catecholamine-secreting tumor, is almost always lethal unless recognized and appropriately treated. ...All patients with manifestations of hypercatecholaminemia or coexisting neoplasms should be investigated …
Pheochromocytoma, a relatively rare (<0.05% of hypertensives), catecholamine-secreting tumor, is almost always lethal unless recog …
Malignant pheochromocytoma: a review.
Harari A, Inabnet WB 3rd. Harari A, et al. Am J Surg. 2011 May;201(5):700-8. doi: 10.1016/j.amjsurg.2010.04.012. Epub 2010 Sep 27. Am J Surg. 2011. PMID: 20870212 Review.
BACKGROUND: Pheochromocytomas are rare catecholamine-secreting tumors. Approximately 10 percent of pheochromocytomas are malignant. ...In this review, we discuss the current information known of malignant pheochromocytomas. DATA SOURCES: The PubMed database w …
BACKGROUND: Pheochromocytomas are rare catecholamine-secreting tumors. Approximately 10 percent of pheochromocytomas are malig …
Extra-adrenal pheochromocytoma.
Whalen RK, Althausen AF, Daniels GH. Whalen RK, et al. J Urol. 1992 Jan;147(1):1-10. doi: 10.1016/s0022-5347(17)37119-7. J Urol. 1992. PMID: 1729490 Review.
Extra-adrenal pheochromocytomas may arise in any portion of the paraganglion system, although they most commonly occur below the diaphragm. ...Extra-adrenal pheochromocytomas probably represent at least 15% of adult and 30% of childhood pheochromocytomas. ...
Extra-adrenal pheochromocytomas may arise in any portion of the paraganglion system, although they most commonly occur below the diap …
Phaeochromocytoma.
Lenders JW, Eisenhofer G, Mannelli M, Pacak K. Lenders JW, et al. Lancet. 2005 Aug 20-26;366(9486):665-75. doi: 10.1016/S0140-6736(05)67139-5. Lancet. 2005. PMID: 16112304 Review.
Phaeochromocytomas are rare neuroendocrine tumours with a highly variable clinical presentation but most commonly presenting with episodes of headaches, sweating, palpitations, and hypertension. ...After the use of appropriate preoperative treatment to block the effects of …
Phaeochromocytomas are rare neuroendocrine tumours with a highly variable clinical presentation but most commonly presenting with epi …
Pheochromocytoma in Dogs Undergoing Adrenalectomy.
Zini E, Nolli S, Ferri F, Massari F, Gerardi G, Nicoli S, Romanelli G, Montinaro V, Trez D, Cavicchioli L, Ferro S. Zini E, et al. Vet Pathol. 2019 May;56(3):358-368. doi: 10.1177/0300985818819174. Epub 2018 Dec 30. Vet Pathol. 2019. PMID: 30595108 Free article.
The study aim was to investigate PASS and immunohistochemical markers used in humans in 24 dogs with pheochromocytoma that underwent adrenalectomy. Dogs with pheochromocytomas were reviewed and tumors collected. ...Overall, the use of PASS and the present immunohist …
The study aim was to investigate PASS and immunohistochemical markers used in humans in 24 dogs with pheochromocytoma that underwent …
Pheochromocytoma.
Pederson LC, Lee JE. Pederson LC, et al. Curr Treat Options Oncol. 2003 Aug;4(4):329-37. doi: 10.1007/s11864-003-0008-9. Curr Treat Options Oncol. 2003. PMID: 12943613
Pheochromocytoma is a rare tumor, but it represents a potentially curable form of hypertension. In patients with inherited pheochromocytoma, benign and bilateral tumors are more common. The diagnosis of pheochromocytoma rests in biochemical confirmation of ca …
Pheochromocytoma is a rare tumor, but it represents a potentially curable form of hypertension. In patients with inherited pheochr …
The protean manifestations of pheochromocytoma.
Manger WM. Manger WM. Horm Metab Res. 2009 Sep;41(9):658-63. doi: 10.1055/s-0028-1128139. Epub 2009 Feb 25. Horm Metab Res. 2009. PMID: 19242899 Review.
Hypercatecholaminemia manifestations are more common and pronounced when paroxysmal hypertension occurs, but persons with familial pheochromocytoma may be asymptomatic. Protean manifestations of pheochromocytoma may simulate many conditions, some of which may have e …
Hypercatecholaminemia manifestations are more common and pronounced when paroxysmal hypertension occurs, but persons with familial pheoch …
25,658 results
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