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

Year Number of Results
1963 1
1964 1
1966 3
1967 5
1968 6
1969 6
1970 3
1971 8
1972 8
1973 8
1974 6
1975 7
1976 2
1977 4
1978 3
1979 6
1980 3
1981 3
1982 1
1983 6
1984 12
1985 4
1986 3
1987 4
1988 6
1989 6
1990 12
1991 7
1992 11
1993 17
1994 11
1995 20
1996 14
1997 16
1998 8
1999 17
2000 16
2001 16
2002 18
2003 17
2004 20
2005 16
2006 12
2007 7
2008 17
2009 26
2010 21
2011 23
2012 29
2013 26
2014 27
2015 26
2016 24
2017 33
2018 21
2019 23
2020 31
2021 36
2022 34
2023 33
2024 3

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Search Results

751 results

Results by year

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Page 1
Glioblastoma and other malignant gliomas: a clinical review.
Omuro A, DeAngelis LM. Omuro A, et al. JAMA. 2013 Nov 6;310(17):1842-50. doi: 10.1001/jama.2013.280319. JAMA. 2013. PMID: 24193082 Review.
IMPORTANCE: Glioblastomas and malignant gliomas are the most common primary malignant brain tumors, with an annual incidence of 5.26 per 100,000 population or 17,000 new diagnoses per year. ...Articles were also identified through searches of the authors' own files. …
IMPORTANCE: Glioblastomas and malignant gliomas are the most common primary malignant brain tumors, with an annual incidence o …
Carcinoid-syndrome: recent advances, current status and controversies.
Ito T, Lee L, Jensen RT. Ito T, et al. Curr Opin Endocrinol Diabetes Obes. 2018 Feb;25(1):22-35. doi: 10.1097/MED.0000000000000376. Curr Opin Endocrinol Diabetes Obes. 2018. PMID: 29120923 Free PMC article. Review.
These include new studies on its epidemiology which demonstrate it is increasing in frequency; increasing insights into the pathogenesis of its various clinical manifestations and into its natural history: definition of prognostic factors; new methods to verify its presence; the …
These include new studies on its epidemiology which demonstrate it is increasing in frequency; increasing insights into the pathogenesis of …
The 2021 WHO Classification of Tumors of the Thymus and Mediastinum: What Is New in Thymic Epithelial, Germ Cell, and Mesenchymal Tumors?
Marx A, Chan JKC, Chalabreysse L, Dacic S, Detterbeck F, French CA, Hornick JL, Inagaki H, Jain D, Lazar AJ, Marino M, Marom EM, Moreira AL, Nicholson AG, Noguchi M, Nonaka D, Papotti MG, Porubsky S, Sholl LM, Tateyama H, Thomas de Montpréville V, Travis WD, Rajan A, Roden AC, Ströbel P. Marx A, et al. J Thorac Oncol. 2022 Feb;17(2):200-213. doi: 10.1016/j.jtho.2021.10.010. Epub 2021 Oct 22. J Thorac Oncol. 2022. PMID: 34695605 Free article. Review.
This overview of the fifth edition of the WHO classification of thymic epithelial tumors (including thymomas, thymic carcinomas, and thymic neuroendocrine tumors [NETs]), mediastinal germ cell tumors, and mesenchymal neoplasms aims to (1) list established and …
This overview of the fifth edition of the WHO classification of thymic epithelial tumors (including thymomas, thymic carcinomas, and thymic …
Lentigo maligna: diagnosis and treatment.
De Luca EV, Perino F, Di Stefani A, Coco V, Fossati B, Peris K. De Luca EV, et al. G Ital Dermatol Venereol. 2020 Apr;155(2):179-189. doi: 10.23736/S0392-0488.18.06003-0. Epub 2018 Apr 19. G Ital Dermatol Venereol. 2020. PMID: 29683288 Free article. Review.
Carcinoid Heart Disease: Pathophysiology, Pathology, Clinical Manifestations, and Management.
Jin C, Sharma AN, Thevakumar B, Majid M, Al Chalaby S, Takahashi N, Tanious A, Arockiam AD, Beri N, Amsterdam EA. Jin C, et al. Cardiology. 2021;146(1):65-73. doi: 10.1159/000507847. Epub 2020 Oct 16. Cardiology. 2021. PMID: 33070143 Free article. Review.
Carcinoid heart disease (CHD) is a rare and potentially lethal manifestation of an advanced carcinoid (neuroendocrine) tumor. ...Serotonin stimulates fibroblast growth and fibrogenesis, which can lead to cardiac valvular fibrosis. CHD primarily affects right …
Carcinoid heart disease (CHD) is a rare and potentially lethal manifestation of an advanced carcinoid (neuroendocrine) tumor. …
Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variants.
Taïeb D, Wanna GB, Ahmad M, Lussey-Lepoutre C, Perrier ND, Nölting S, Amar L, Timmers HJLM, Schwam ZG, Estrera AL, Lim M, Pollom EL, Vitzthum L, Bourdeau I, Casey RT, Castinetti F, Clifton-Bligh R, Corssmit EPM, de Krijger RR, Del Rivero J, Eisenhofer G, Ghayee HK, Gimenez-Roqueplo AP, Grossman A, Imperiale A, Jansen JC, Jha A, Kerstens MN, Kunst HPM, Liu JK, Maher ER, Marchioni D, Mercado-Asis LB, Mete O, Naruse M, Nilubol N, Pandit-Taskar N, Sebag F, Tanabe A, Widimsky J, Meuter L, Lenders JWM, Pacak K. Taïeb D, et al. Lancet Diabetes Endocrinol. 2023 May;11(5):345-361. doi: 10.1016/S2213-8587(23)00038-4. Epub 2023 Mar 31. Lancet Diabetes Endocrinol. 2023. PMID: 37011647 Review.
Patients with germline SDHD pathogenic variants (encoding succinate dehydrogenase subunit D; ie, paraganglioma 1 syndrome) are predominantly affected by head and neck paragangliomas, which, in almost 20% of patients, might coexist with paragangliomas arising from other locations …
Patients with germline SDHD pathogenic variants (encoding succinate dehydrogenase subunit D; ie, paraganglioma 1 syndrome) are predominantly …
Pheochromocytoma/paraganglioma-associated cardiomyopathy.
Szatko A, Glinicki P, Gietka-Czernel M. Szatko A, et al. Front Endocrinol (Lausanne). 2023 Jul 13;14:1204851. doi: 10.3389/fendo.2023.1204851. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37522121 Free PMC article. Review.
This mini-review summarizes current data on pathophysiological pathways of cardiac damage caused by catecholamines, the clinical presentation of PPGL-induced cardiomyopathies, and discusses treatment options....
This mini-review summarizes current data on pathophysiological pathways of cardiac damage caused by catecholamines, the clinical pres …
Pseudopheochromocytoma.
Mamilla D, Gonzales MK, Esler MD, Pacak K. Mamilla D, et al. Endocrinol Metab Clin North Am. 2019 Dec;48(4):751-764. doi: 10.1016/j.ecl.2019.08.004. Epub 2019 Sep 18. Endocrinol Metab Clin North Am. 2019. PMID: 31655774 Free PMC article. Review.
Pseudopheochromocytoma manifests as severe, symptomatic paroxysmal hypertension without significant elevation in catecholamine and metanephrine levels and lack of evidence of tumor in the adrenal gland. The clinical manifestations are similar but not identical to those in …
Pseudopheochromocytoma manifests as severe, symptomatic paroxysmal hypertension without significant elevation in catecholamine and metanephr …
Fetal intrapericardial teratomas.
Yuan SM, Lin H. Yuan SM, et al. Turk J Pediatr. 2019;61(2):153-158. doi: 10.24953/turkjped.2019.02.001. Turk J Pediatr. 2019. PMID: 31951327 Free article. Review.
A growing trend of tumors was observed in more than half of the cases. Prenatal centesis and postnatal tumor resection were required in most of the cases. Fetoneonatal deaths (including fetal demise, termination of pregnancy and neonatal death) occurred in one-third of the …
A growing trend of tumors was observed in more than half of the cases. Prenatal centesis and postnatal tumor resection were required …
[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.
The diagnosis of PPGL cannot be made without visualization of a tumor. Therapeutic management consists mostly of surgical excision, after drug preparation, and should be done in referral centers. ...
The diagnosis of PPGL cannot be made without visualization of a tumor. Therapeutic management consists mostly of surgical excision, a …
751 results