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

Year Number of Results
1976 1
1981 2
1987 1
1993 1
1994 2
1996 1
1997 1
2002 1
2004 1
2005 1
2006 1
2007 1
2008 3
2011 1
2012 1
2015 1
2016 2
2020 1
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2024 1

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Page 1
Pediatric adrenocortical tumours.
Pinto EM, Zambetti GP, Rodriguez-Galindo C. Pinto EM, et al. Best Pract Res Clin Endocrinol Metab. 2020 May;34(3):101448. doi: 10.1016/j.beem.2020.101448. Epub 2020 Jul 3. Best Pract Res Clin Endocrinol Metab. 2020. PMID: 32636100 Review.
For patients undergoing complete tumor resection, favorable prognostic factors include young age, small tumor size, virilization, and adenoma histology. ...
For patients undergoing complete tumor resection, favorable prognostic factors include young age, small tumor size, virilization, and …
Historical background and natural history of carcinoids.
Creutzfeldt W. Creutzfeldt W. Digestion. 1994;55 Suppl 3:3-10. doi: 10.1159/000201195. Digestion. 1994. PMID: 7698535 Review.
For the natural history of carcinoid tumors, several independent predictive parameters can be defined: size, site of origin, growth pattern, and hormone dependence. The number of neuropeptides and amines expressed by a carcinoid or the amount of biologically active neuroho …
For the natural history of carcinoid tumors, several independent predictive parameters can be defined: size, site of origin, growth p …
Clinical Factors Predicting Multiple Endocrine Neoplasia Type 1 and Type 4 in Patients with Neuroendocrine Tumors.
Faggiano A, Fazzalari B, Mikovic N, Russo F, Zamponi V, Mazzilli R, Guarnieri V, Piane M, Visco V, Petrucci S. Faggiano A, et al. Genes (Basel). 2023 Sep 10;14(9):1782. doi: 10.3390/genes14091782. Genes (Basel). 2023. PMID: 37761922 Free PMC article.
The aim of this study is to evaluate the predictive role of specific clinical factors for the diagnosis of Multiple Endocrine Neoplasia type-1 (MEN1) and type-4 (MEN4) in patients with an initial diagnosis of gastrointestinal, bronchial, or thymic neuroendocrine tumor (NET …
The aim of this study is to evaluate the predictive role of specific clinical factors for the diagnosis of Multiple Endocrine Neoplas …
Childhood adrenocortical tumours.
Ribeiro RC, Figueiredo B. Ribeiro RC, et al. Eur J Cancer. 2004 May;40(8):1117-26. doi: 10.1016/j.ejca.2004.01.031. Eur J Cancer. 2004. PMID: 15110875 Review.
Among patients who undergo complete tumour resection, favourable prognostic factors include age <4 years, smaller tumour size, signs of virilisation alone at presentation, and adenomatous tumour histology. ...
Among patients who undergo complete tumour resection, favourable prognostic factors include age <4 years, smaller tumour size, sig …
ASO Practice Guidelines Series: Surgical Management of Gastrointestinal (Midgut) Neuroendocrine Neoplasms.
Hallet J, Clarke CN. Hallet J, et al. Ann Surg Oncol. 2024 Mar;31(3):1704-1713. doi: 10.1245/s10434-023-14802-8. Epub 2024 Jan 2. Ann Surg Oncol. 2024. PMID: 38167813 Review.
Because of heterogeneous tumor behaviour, association with endocrine syndrome, and prognosis, the management of NETs must be individualized to all these factors in addition to the primary site. ...
Because of heterogeneous tumor behaviour, association with endocrine syndrome, and prognosis, the management of NETs must be individu …
Surgical management of gastrointestinal endocrine tumours.
Goldstone AP, Scott-Coombes DM, Lynn JA. Goldstone AP, et al. Baillieres Clin Gastroenterol. 1996 Dec;10(4):707-36. doi: 10.1016/s0950-3528(96)90020-2. Baillieres Clin Gastroenterol. 1996. PMID: 9113319 Review.
Cholestasis Reveals Severe Cortisol Deficiency in Neonatal Pituitary Stalk Interruption Syndrome.
Mauvais FX, Gonzales E, Davit-Spraul A, Jacquemin E, Brauner R. Mauvais FX, et al. PLoS One. 2016 Feb 1;11(2):e0147750. doi: 10.1371/journal.pone.0147750. eCollection 2016. PLoS One. 2016. PMID: 26829045 Free PMC article.
OBJECTIVES: Cholestasis has been reported during the course of congenital hypothalamic-pituitary deficiency, but crucial information is lacking regarding both its origin and prognosis. We aimed to characterize the course of cholestasis and factors contributin …
OBJECTIVES: Cholestasis has been reported during the course of congenital hypothalamic-pituitary deficiency, but crucial information …
Untargeted metabolomic approach to study the serum metabolites in women with polycystic ovary syndrome.
Yu Y, Tan P, Zhuang Z, Wang Z, Zhu L, Qiu R, Xu H. Yu Y, et al. BMC Med Genomics. 2021 Aug 20;14(1):206. doi: 10.1186/s12920-021-01058-y. BMC Med Genomics. 2021. PMID: 34416878 Free PMC article.
CONCLUSION: The present study characterized the difference of serum metabolites and related pathway profiles in PCOS patients, this finding hopes to provide potential metabolic markers for the prognosis and diagnosis of this disease....
CONCLUSION: The present study characterized the difference of serum metabolites and related pathway profiles in PCOS patients, this finding …
24 results