Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1993 2
1994 3
1995 3
1996 1
1997 1
1998 4
1999 1
2000 2
2001 2
2002 1
2003 5
2004 4
2005 2
2006 2
2007 3
2008 2
2009 5
2010 4
2011 1
2012 1
2013 4
2014 1
2015 5
2016 4
2018 1
2019 2
2020 3
2021 6
2022 4
Text availability
Article attribute
Article type
Publication date

Search Results

73 results
Results by year
Filters applied: . Clear all
Page 1
New Therapeutic Horizons for Graves' Hyperthyroidism.
Lane LC, Cheetham TD, Perros P, Pearce SHS. Lane LC, et al. Among authors: cheetham td. Endocr Rev. 2020 Dec 1;41(6):873-84. doi: 10.1210/endrev/bnaa022. Endocr Rev. 2020. PMID: 32845332 Free PMC article. Review.
Prevention and treatment of vitamin D deficiency.
Sinha A, Cheetham TD, Pearce SH. Sinha A, et al. Among authors: cheetham td. Calcif Tissue Int. 2013 Feb;92(2):207-15. doi: 10.1007/s00223-012-9663-9. Epub 2012 Nov 3. Calcif Tissue Int. 2013. PMID: 23124916 Review.
Diagnosis and management of polyendocrinopathy syndromes.
Owen CJ, Cheetham TD. Owen CJ, et al. Among authors: cheetham td. Endocrinol Metab Clin North Am. 2009 Jun;38(2):419-36, x. doi: 10.1016/j.ecl.2009.01.007. Endocrinol Metab Clin North Am. 2009. PMID: 19328420 Review.
Diagnosis and management of vitamin D deficiency.
Pearce SH, Cheetham TD. Pearce SH, et al. Among authors: cheetham td. BMJ. 2010 Jan 11;340:b5664. doi: 10.1136/bmj.b5664. BMJ. 2010. PMID: 20064851 Review. No abstract available.
The broad phenotypic spectrum of 17α-hydroxylase/17,20-lyase (CYP17A1) deficiency: a case series.
Sun M, Mueller JW, Gilligan LC, Taylor AE, Shaheen F, Noczyńska A, T'Sjoen G, Denvir L, Shenoy S, Fulton P, Cheetham TD, Gleeson H, Rahman M, Krone NP, Taylor NF, Shackleton CHL, Arlt W, Idkowiak J. Sun M, et al. Among authors: cheetham td. Eur J Endocrinol. 2021 Oct 11;185(5):729-741. doi: 10.1530/EJE-21-0152. Eur J Endocrinol. 2021. PMID: 34524979 Free PMC article.
Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years' Experience in the UK.
Buonocore F, Maharaj A, Qamar Y, Koehler K, Suntharalingham JP, Chan LF, Ferraz-de-Souza B, Hughes CR, Lin L, Prasad R, Allgrove J, Andrews ET, Buchanan CR, Cheetham TD, Crowne EC, Davies JH, Gregory JW, Hindmarsh PC, Hulse T, Krone NP, Shah P, Shaikh MG, Roberts C, Clayton PE, Dattani MT, Thomas NS, Huebner A, Clark AJ, Metherell LA, Achermann JC. Buonocore F, et al. Among authors: cheetham td. J Endocr Soc. 2021 May 11;5(8):bvab086. doi: 10.1210/jendso/bvab086. eCollection 2021 Aug 1. J Endocr Soc. 2021. PMID: 34258490 Free PMC article.
73 results