Shenton A[au] - Search Results

Year	Number of Results
1972	1
1973	2
1987	1
1998	1
2000	2
2001	3
2002	1
2003	3
2004	2
2005	4
2006	6
2007	6
2008	9
2009	8
2010	3
2011	3
2021	1
2022	1
2023	0

1

De Garengeot's hernia in an elderly woman as a diagnostic challenge: a review of literature.

Ahmed ZS, Azam S, Shenton A, Akingboye AA. Ahmed ZS, et al. Among authors: shenton a. BMJ Case Rep. 2021 Jan 28;14(1):e237526. doi: 10.1136/bcr-2020-237526. BMJ Case Rep. 2021. PMID: 33509866 Free PMC article. Review.

2

A case report and review of the locked metacarpophalangeal joint.

Gilligan P, Hegarty D, Bradley P, Todd F, Shenton AF. Gilligan P, et al. Among authors: shenton af. Accid Emerg Nurs. 2003 Apr;11(2):103-5. doi: 10.1016/s0965-2302(02)00167-4. Accid Emerg Nurs. 2003. PMID: 12633628 Review.

3

What are the implications in individuals with unilateral vestibular schwannoma and other neurogenic tumors?

Evans DG, Ramsden RT, Shenton A, Gokhale C, Bowers N, Huson SM, Wallace AJ. Evans DG, et al. Among authors: shenton a. J Neurosurg. 2008 Jan;108(1):92-6. doi: 10.3171/JNS/2008/108/01/0092. J Neurosurg. 2008. PMID: 18173316

4

Rosai-Dorfman disease manifesting as subglottic stenosis and skin rash mimicking granulomatosis with polyangiitis.

Ho GN, Cundell D, Shenton A, Klocke R. Ho GN, et al. Among authors: shenton a. Rheumatol Adv Pract. 2022 Oct 29;6(3):rkac089. doi: 10.1093/rap/rkac089. eCollection 2022. Rheumatol Adv Pract. 2022. PMID: 36382266 Free PMC article. No abstract available.

5

Further genotype--phenotype correlations in neurofibromatosis 2.

Selvanathan SK, Shenton A, Ferner R, Wallace AJ, Huson SM, Ramsden RT, Evans DG. Selvanathan SK, et al. Among authors: shenton a. Clin Genet. 2010 Feb;77(2):163-70. doi: 10.1111/j.1399-0004.2009.01315.x. Epub 2009 Nov 23. Clin Genet. 2010. PMID: 19968670

6

A molecular analysis of individuals with neurofibromatosis type 1 (NF1) and optic pathway gliomas (OPGs), and an assessment of genotype-phenotype correlations.

Sharif S, Upadhyaya M, Ferner R, Majounie E, Shenton A, Baser M, Thakker N, Evans DG. Sharif S, et al. Among authors: shenton a. J Med Genet. 2011 Apr;48(4):256-60. doi: 10.1136/jmg.2010.081760. Epub 2011 Jan 28. J Med Genet. 2011. PMID: 21278392

7

A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO.

Evans DG, Eccles DM, Rahman N, Young K, Bulman M, Amir E, Shenton A, Howell A, Lalloo F. Evans DG, et al. Among authors: shenton a. J Med Genet. 2004 Jun;41(6):474-80. doi: 10.1136/jmg.2003.017996. J Med Genet. 2004. PMID: 15173236 Free PMC article.

8

Breast cancer susceptibility variants alter risks in familial disease.

Latif A, Hadfield KD, Roberts SA, Shenton A, Lalloo F, Black GC, Howell A, Evans DG, Newman WG. Latif A, et al. Among authors: shenton a. J Med Genet. 2010 Feb;47(2):126-31. doi: 10.1136/jmg.2009.067256. Epub 2009 Jul 16. J Med Genet. 2010. PMID: 19617217

9

Women with neurofibromatosis 1 are at a moderately increased risk of developing breast cancer and should be considered for early screening.

Sharif S, Moran A, Huson SM, Iddenden R, Shenton A, Howard E, Evans DG. Sharif S, et al. Among authors: shenton a. J Med Genet. 2007 Aug;44(8):481-4. doi: 10.1136/jmg.2007.049346. Epub 2007 Mar 16. J Med Genet. 2007. PMID: 17369502 Free PMC article.

10

Screening by mammography, women with a family history of breast cancer.

Lalloo F, Boggis CR, Evans DG, Shenton A, Threlfall AG, Howell A. Lalloo F, et al. Among authors: shenton a. Eur J Cancer. 1998 May;34(6):937-40. doi: 10.1016/s0959-8049(98)00005-7. Eur J Cancer. 1998. PMID: 9797712

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