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

Year Number of Results
1942 2
1992 1
1994 2
1995 5
1996 1
1997 1
1998 1
1999 1
2000 3
2001 2
2002 1
2003 3
2004 4
2005 1
2006 1
2007 2
2008 4
2010 2
2011 5
2012 2
2013 7
2014 4
2015 4
2016 3
2017 10
2018 8
2019 4
2020 7
2021 1
2022 3
2023 1
2024 3
2025 3

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96 results

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Page 1
Phaeochromocytoma in children.
Armstrong R, Sridhar M, Greenhalgh KL, Howell L, Jones C, Landes C, McPartland JL, Moores C, Losty PD, Didi M. Armstrong R, et al. Among authors: didi m. Arch Dis Child. 2008 Oct;93(10):899-904. doi: 10.1136/adc.2008.139121. Epub 2008 May 22. Arch Dis Child. 2008. PMID: 18499773 Review.
Starting point for benchmarking outcomes and reporting of pituitary adenoma surgery within the European Reference Network on Rare Endocrine Conditions (Endo-ERN): results from a meta-analysis and survey study.
Zamanipoor Najafabadi AH, van der Meulen M, Priego Zurita AL, Faisal Ahmed S, van Furth WR, Charmandari E, Hiort O, Pereira AM, Dattani M, Vitali D, de Graaf JP, Biermasz NR; MTG6 Pituitary of Endo-ERN. Zamanipoor Najafabadi AH, et al. Endocr Connect. 2022 Dec 13;12(1):e220349. doi: 10.1530/EC-22-0349. Print 2023 Jan 1. Endocr Connect. 2022. PMID: 36327151 Free PMC article. Review.
Irradiation-induced growth failure.
Shalet SM, Crowne EC, Didi MA, Ogilvy-Stuart AL, Wallace WH. Shalet SM, et al. Among authors: didi ma. Baillieres Clin Endocrinol Metab. 1992 Jul;6(3):513-26. doi: 10.1016/s0950-351x(05)80109-0. Baillieres Clin Endocrinol Metab. 1992. PMID: 1524549 Review.
Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN).
Eggermann T, Elbracht M, Kurth I, Juul A, Johannsen TH, Netchine I, Mastorakos G, Johannsson G, Musholt TJ, Zenker M, Prawitt D, Pereira AM, Hiort O; European Reference Network on Rare Endocrine Conditions (ENDO-ERN. Eggermann T, et al. Orphanet J Rare Dis. 2020 Jun 8;15(1):144. doi: 10.1186/s13023-020-01420-w. Orphanet J Rare Dis. 2020. PMID: 32513286 Free PMC article. Review.
Congenital hyperinsulinism due to mutations in HNF1A.
Yau D, Colclough K, Natarajan A, Parikh R, Canham N, Didi M, Senniappan S, Banerjee I. Yau D, et al. Among authors: didi m. Eur J Med Genet. 2020 Jun;63(6):103928. doi: 10.1016/j.ejmg.2020.103928. Epub 2020 Apr 20. Eur J Med Genet. 2020. PMID: 32325224
Growth and endocrine function after bone marrow transplantation.
Shalet SM, Didi M, Ogilvy-Stuart AL, Schulga J, Donaldson MD. Shalet SM, et al. Among authors: didi m. Clin Endocrinol (Oxf). 1995 Apr;42(4):333-9. doi: 10.1111/j.1365-2265.1995.tb02640.x. Clin Endocrinol (Oxf). 1995. PMID: 7750186 Review. No abstract available.
Prevention of cisplatin-induced nephrotoxicity by methimazole.
Osman AM, El-Sayed EM, El-Demerdash E, Al-Hyder A, El-Didi M, Attia AS, Hamada FM. Osman AM, et al. Among authors: el didi m. Pharmacol Res. 2000 Jan;41(1):115-21. doi: 10.1006/phrs.1999.0569. Pharmacol Res. 2000. PMID: 10600279
Hyperamylasaemia: pathognomonic to pancreatitis?
Burden S, Poon AS, Masood K, Didi M. Burden S, et al. Among authors: didi m. BMJ Case Rep. 2013 Oct 16;2013:bcr2013009567. doi: 10.1136/bcr-2013-009567. BMJ Case Rep. 2013. PMID: 24132440 Free PMC article.
96 results