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

Year Number of Results
1999 1
2000 1
2002 1
2004 1
2005 1
2006 1
2007 3
2008 5
2009 1
2010 1
2011 1
2012 2
2013 1
2014 1
2016 1
2019 2
2020 3
2021 1
2023 2
2024 1

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25 results

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Page 1
Renin-angiotensin systems and reproduction.
Vinson GP, Saridogan E, Puddefoot JR, O'Mahony OA, Mahmood T, Djahanbakhch O. Vinson GP, et al. Among authors: o mahony oa. Gynecol Endocrinol. 1999 Feb;13(1):56-70. doi: 10.1080/09513599909167532. Gynecol Endocrinol. 1999. PMID: 10368799 Free article. Review. No abstract available.
Late-Onset Tay-Sachs Disease in an Irish Family.
Lefter S, O' Mahony O, Sweeney B, Ryan AM. Lefter S, et al. Among authors: o mahony o. Mov Disord Clin Pract. 2020 Oct 28;8(1):106-110. doi: 10.1002/mdc3.13096. eCollection 2021 Jan. Mov Disord Clin Pract. 2020. PMID: 33426165 Free PMC article.
Paediatric neuro-disability end-of-life care: symptom burden and management.
Stephens C, Coghlan Z, Gibson L, McSweeney N, O'Mahony O, O'Leary MJ. Stephens C, et al. Among authors: o mahony o. BMJ Support Palliat Care. 2024 Jan 8;13(e3):e731-e732. doi: 10.1136/bmjspcare-2021-003486. BMJ Support Palliat Care. 2024. PMID: 34952864 No abstract available.
Your diagnosis? Congenital foot drop.
Hawkes CP, McNamara B, O'Mahony O, Dempsey EM. Hawkes CP, et al. Among authors: o mahony o. Eur J Pediatr. 2013 Aug;172(8):1145-7. doi: 10.1007/s00431-012-1837-y. Epub 2012 Sep 28. Eur J Pediatr. 2013. PMID: 23052613
Pathogenic mtDNA mutations causing mitochondrial myopathy: The need for muscle biopsy.
Hardy SA, Blakely EL, Purvis AI, Rocha MC, Ahmed S, Falkous G, Poulton J, Rose MR, O'Mahony O, Bermingham N, Dougan CF, Ng YS, Horvath R, Turnbull DM, Gorman GS, Taylor RW. Hardy SA, et al. Among authors: o mahony o. Neurol Genet. 2016 Jun 23;2(4):e82. doi: 10.1212/NXG.0000000000000082. eCollection 2016 Aug. Neurol Genet. 2016. PMID: 27536729 Free PMC article.
Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations.
Geranmayeh F, Clement E, Feng LH, Sewry C, Pagan J, Mein R, Abbs S, Brueton L, Childs AM, Jungbluth H, De Goede CG, Lynch B, Lin JP, Chow G, Sousa Cd, O'Mahony O, Majumdar A, Straub V, Bushby K, Muntoni F. Geranmayeh F, et al. Among authors: o mahony o. Neuromuscul Disord. 2010 Apr;20(4):241-50. doi: 10.1016/j.nmd.2010.02.001. Epub 2010 Mar 6. Neuromuscul Disord. 2010. PMID: 20207543
25 results