Výsledky vyhledávání

How common are complications following polypropylene mesh, biological xenograft and native tissue surgery for pelvic organ prolapse? A secondary analysis from the PROSPECT trial

Autor: Reid, FM, Elders, A, Breeman, S, Freeman, RM, Glazener, CMA, Hemming, C, Cooper, KG, Smith, ARB, Hagen, S, Montgomery, I, Kilonzo, M, Boyers, D, McDonald, A, McPherson, G, MacLennan, G, Norrie, J

Publikováno v: Reid, FM, Elders, A, Breeman, S, Freeman, RM, Glazener, CMA, Hemming, C, Cooper, KG, Smith, ARB, Hagen, S, Montgomery, I, Kilonzo, M, Boyers, D, McDonald, A, McPherson, G, MacLennan, G & Norrie, J 2021, ' How common are complications following polypropylene mesh, biological xenograft and native tissue surgery for pelvic organ prolapse? A secondary analysis from the PROSPECT trial ', BJOG: An International Journal of Obstetrics & Gynaecology, vol. 128, no. 13, pp. 2180-2189 . https://doi.org/10.1111/1471-0528.16897

Objective: To report complication rates following prolapse surgery using polypropylene mesh inlay, polypropylene mesh kit, biological collagen xenografts and native tissue repairs. Design: Secondary analysis of the PROSPECT randomised controlled tria

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42636f248c4ebf0bac56850ff594ec4c
https://doi.org/10.1111/1471-0528.16897

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Akademický článek

Mesh inlay, mesh kit or native tissue repair for women having repeat anterior or posterior prolapse surgery: randomised controlled trial (PROSPECT).

Publikováno v: BJOG: An International Journal of Obstetrics & Gynaecology; Jul2020, Vol. 127 Issue 8, p1002-1013, 12p, 4 Charts

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From alchemy to epistemology : intuition and private midwifery in Australia

Autor: Reid, FM

University of Technology Sydney. Faculty of Health. Background Intuition entered the lexicon describing midwifery practice as early as the 14th Century and it has remained a component ever since. The Australian College of Midwives (2009) philosophica

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______363::9cf5c830492379d884d0e7647937d268
https://hdl.handle.net/10453/34418

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MATERNALLY INHERITED HEARING-LOSS, ATAXIA AND MYOCLONUS ASSOCIATED WITH A NOVEL POINT MUTATION IN MITOCHONDRIAL TRNA(SER(UCN)) GENE

Autor: TIRANTI, [No Value], CHARIOT, P, CARELLA, F, TOSCANO, A, SOLIVERI, P, GIRLANDA, P, CARRARA, F, FRATTA, GM, REID, FM, MARIOTTI, C, ZEVIANI, M

Publikováno v: Human Molecular Genetics, 4(8), 1421-1427. Oxford University Press

We report on a new maternally-inherited syndrome characterized by a combination of sensorineural hearing loss, ataxia and myoclonus in a large kindred from Sicily, Hearing loss was the most widespread and sometimes the only symptom found in family me

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7a725d8bb85c414adf03bb417777e478
http://hdl.handle.net/11570/15661

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