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

Year Number of Results
1892 1
1893 1
1895 2
1901 1
1903 1
1904 2
1905 1
1907 2
1908 4
1909 1
1910 3
1913 3
1914 3
1916 1
1917 2
1919 2
1920 2
1921 3
1922 5
1923 1
1924 2
1925 7
1926 4
1927 1
1928 1
1929 1
1930 5
1931 7
1932 2
1933 9
1934 2
1935 3
1936 3
1937 4
1938 6
1939 9
1940 2
1941 6
1942 3
1943 3
1944 3
1945 53
1946 200
1947 221
1948 254
1949 274
1950 408
1951 493
1952 525
1953 515
1954 592
1955 649
1956 687
1957 690
1958 687
1959 598
1960 526
1961 558
1962 589
1963 688
1964 866
1965 715
1966 674
1967 804
1968 913
1969 1009
1970 1080
1971 1145
1972 1140
1973 1219
1974 1316
1975 1319
1976 1340
1977 1389
1978 1358
1979 1525
1980 1403
1981 1534
1982 1700
1983 1860
1984 1996
1985 2111
1986 1988
1987 2157
1988 2062
1989 2358
1990 2101
1991 2071
1992 2005
1993 1982
1994 1939
1995 2003
1996 2098
1997 2076
1998 2137
1999 2197
2000 2336
2001 2414
2002 2532
2003 2525
2004 2642
2005 2851
2006 3091
2007 3239
2008 3399
2009 3442
2010 3719
2011 4123
2012 4666
2013 5046
2014 5352
2015 5341
2016 5576
2017 5642
2018 5709
2019 6139
2020 6801
2021 7091
2022 6877
2023 6684
2024 1771

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163,010 results

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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
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
Phaeochromocytoma and Paraganglioma.
Gunawardane PTK, Grossman A. Gunawardane PTK, et al. Adv Exp Med Biol. 2017;956:239-259. doi: 10.1007/5584_2016_76. Adv Exp Med Biol. 2017. PMID: 27888488 Review.
Phaeochromocytomas and paragangliomas are relatively uncommon tumours which may be manifest in many ways, specifically as sustained or paroxysmal hypertension, episodes of palpitations, sweating, headache and anxiety, or increasingly as an incidental finding. ...
Phaeochromocytomas and paragangliomas are relatively uncommon tumours which may be manifest in many ways, specifically as sustained o
Phaeochromocytoma: state-of-the-art.
Donckier JE, Michel L. Donckier JE, et al. Acta Chir Belg. 2010 Mar-Apr;110(2):140-8. doi: 10.1080/00015458.2010.11680587. Acta Chir Belg. 2010. PMID: 20514823 Review.
Extra-adrenal phaeochromocytomas are called paragangliomas. A diagnosis of phaeochromocytoma is suspected by typical paroxysmal symptoms, unusual or refractory hypertension, discovery of an adrenal incidentaloma or a family history of phaeochromocytoma or par …
Extra-adrenal phaeochromocytomas are called paragangliomas. A diagnosis of phaeochromocytoma is suspected by typical paroxysma …
Subclinical phaeochromocytoma.
Mannelli M, Lenders JW, Pacak K, Parenti G, Eisenhofer G. Mannelli M, et al. Best Pract Res Clin Endocrinol Metab. 2012 Aug;26(4):507-15. doi: 10.1016/j.beem.2011.10.008. Epub 2012 May 22. Best Pract Res Clin Endocrinol Metab. 2012. PMID: 22863392 Free PMC article. Review.
Phaeochromocytomas and paragangliomas are neural crest-derived tumours. ...Adrenoceptor desensitization can result in a subclinical presentation, even when catecholamine levels are high. Subclinical phaeochromocytomas are often discovered as incidentalomas during ra
Phaeochromocytomas and paragangliomas are neural crest-derived tumours. ...Adrenoceptor desensitization can result in a subclinical p
[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. ...Therapeutic management consists mostly of surgical excision, after drug preparation, and should be done in referra
Phaeochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumors that arise from the adrenal medulla or sympathetic and pa
Deconjugated urinary metanephrine, normetanephrine and 3-methoxytyramine in laboratory diagnosis of pheochromocytoma and paraganglioma.
Bílek R, Zelinka T, Vlček P, Dušková J, Michalský D, Novák K, Bešťák J, Widimský J Jr. Bílek R, et al. Physiol Res. 2015;64(Suppl 2):S313-22. doi: 10.33549/physiolres.933109. Physiol Res. 2015. PMID: 26680494 Free article.
This work discusses the clinical performance of deconjugated metanephrine (MN), normetanephrine (NMN) and 3-methoxytyramine (3MT) determined in the basal first morning urine using a chromatographic method with electrochemical detection for the clinical diagnosis of pheo
This work discusses the clinical performance of deconjugated metanephrine (MN), normetanephrine (NMN) and 3-methoxytyramine (3MT) det …
Plasma and urinary metanephrine and normetanephrine concentrations using liquid chromatography with tandem mass spectrometry in healthy cats and in a cat with pheochromocytoma.
Prego MT, Dias MJ, Ferreira RL, Gonçalves S, Dias Domingues T, Junius G, Van den Steen E, Galac S, Leal RO. Prego MT, et al. J Vet Intern Med. 2023 May-Jun;37(3):910-914. doi: 10.1111/jvim.16648. Epub 2023 Apr 13. J Vet Intern Med. 2023. PMID: 37057306 Free PMC article.
BACKGROUND: Pheochromocytoma (PCC) is rare in cats and plasma (PL) and urinary (U) metanephrines (metanephrine [MN]; normetanephrine [NMN]) measurement is rarely described in cats. OBJECTIVES: We evaluated the utility of PL and U MNs measurement in 10 healthy …
BACKGROUND: Pheochromocytoma (PCC) is rare in cats and plasma (PL) and urinary (U) metanephrines (metanephrine [MN]; normet
Hereditary and Sporadic Pheochromocytoma: Comparison of Imaging, Clinical, and Laboratory Features.
Chung R, O'Shea A, Sweeney AT, Mercaldo ND, McDermott S, Blake MA. Chung R, et al. AJR Am J Roentgenol. 2022 Jul;219(1):97-109. doi: 10.2214/AJR.21.26918. Epub 2022 Jan 26. AJR Am J Roentgenol. 2022. PMID: 35080458
When combining CT and MRI, cystic change/necrosis was observed in 35% of hereditary versus 67% of sporadic pheochromocytomas (p = .10). Hereditary pheochromocytoma, compared with sporadic, had lower frequency of symptoms (31% vs 74%; p = .004) and lower 24-hour u
When combining CT and MRI, cystic change/necrosis was observed in 35% of hereditary versus 67% of sporadic pheochromocytomas (p = .10 …
Phaeochromocytoma: current concepts.
Alderazi Y, Yeh MW, Robinson BG, Benn DE, Sywak MS, Learoyd DL, Delbridge LW, Sidhu SB. Alderazi Y, et al. Med J Aust. 2005 Aug 15;183(4):201-4. doi: 10.5694/j.1326-5377.2005.tb06997.x. Med J Aust. 2005. PMID: 16097921 Review.
The discovery of novel mutations in genes encoding succinate dehydrogenase subunits has revealed that familial phaeochromocytomas are much more common than previously thought. Genetic screening should be offered to patients with apparently sporadic phaeochromocytomas
The discovery of novel mutations in genes encoding succinate dehydrogenase subunits has revealed that familial phaeochromocytomas are …
163,010 results
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