Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Fiona M. Reid"'
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Pelvic organ prolapse, urinary, bowel and sexual dysfunction, collectively called pelvic floor dysfunction (PFD) affects 1 in 3 women and has a significant public health impact. The causes of PFD are not fully understood but involve injury t
Externí odkaz:
https://doaj.org/article/980223eb37724a3e9b55ecbf11631bd4
Autor:
Fiona M, Reid, Lorna, Aucott, Cathryn M A, Glazener, Andrew, Elders, Christine, Hemming, Kevin G, Cooper, Robert M, Freeman, Anthony R B, Smith, Suzanne, Hagen, Mary, Kilonzo, Dwayne, Boyers, Graeme, MacLennan, John, Norrie, Suzanne, Breeman
Publikováno v:
International urogynecology journal.
Our aim was to compare the mid-term results of native tissue, biological xenograft and polypropylene mesh surgery for women with vaginal wall prolapse.A total of 1348 women undergoing primary transvaginal repair of an anterior and/or posterior prolap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4a53792523a3a5fc87a549a955469b69
https://pubmed.ncbi.nlm.nih.gov/36018353
https://pubmed.ncbi.nlm.nih.gov/36018353
Autor:
Fiona M Reid
Publikováno v:
Obstetrics & Gynaecology ISBN: 9780429162398
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24340900861c6fe83ca45595ecd328ac
https://doi.org/10.1201/b19647-2
https://doi.org/10.1201/b19647-2
Publikováno v:
Human Molecular Genetics. 6:443-449
We have studied mitochondrial gene expression and metabolic function in a human lymphoblastoid cell-line homoplasmic for the np 7445, deafness-associated mitochondrial DNA mutation. The mutation maps to the 3' termini of the oppositely oriented genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48de220dc2df95e248329db3f7c3befd
https://doi.org/10.1093/hmg/6.3.443
https://doi.org/10.1093/hmg/6.3.443
Publikováno v:
Clinical Otolaryngology. 19:314-319
Pure-tone audiometry was carried out on members of a recently described maternal lineage with sensorineural deafness, harbouring a novel mitochondrial mutation in the gene for tRNA-ser(UCN). This revealed a characteristic pattern of symmetrical bilat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60e39815a45946519cb1dd56205e3ae9
https://doi.org/10.1111/j.1365-2273.1994.tb01238.x
https://doi.org/10.1111/j.1365-2273.1994.tb01238.x
Publikováno v:
Human Mutation. 3:243-247
We have detected a novel mitochondrial mutation in a maternal pedigree, at least 13 of whose members have sensorineural hearing loss of varying severity, but who exhibit no other pathological features. The mutation, at np 7445, converts the 3' termin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb180b0f43ae45ad48abab93843c848b
https://doi.org/10.1002/humu.1380030311
https://doi.org/10.1002/humu.1380030311
Autor:
Antonio Toscano, Franco Carrara, Massimo Zeviani, Paolo Girlanda, Francesco Carella, Fiona M. Reid, Patrick Chariot, Paola Soliveri, Valeria Tiranti, Caterina Mariotti, Giovanni Matteo Fratta
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=doi_dedup___::825f5efc1794849c771a9bcba6ad97f8
http://hdl.handle.net/11577/3354580
http://hdl.handle.net/11577/3354580
Publikováno v:
Human Molecular Genetics. 3:1435-1436
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97c0fb28a9615fc1ba0835a62f6b4c5b
https://doi.org/10.1093/hmg/3.8.1435
https://doi.org/10.1093/hmg/3.8.1435
Autor:
B.W. Gurner, Hiro Wakasugi, Z. Meszaros, G.P. Sandilands, R.R.A. Coombs, Yasuhiko Morioka, G.M. Woods, C.R. Zeiss, H. Løwenstein, Thomas F. Smith, Z. Ovary, C. De Vos, Mathias Onsrud, Kazuo Oshimi, Linda K. Remigio, Claes Schalén, K.J. Turner, Anders Grubb, S. Kojima, F. Dessy, P. Eyre, B. Weeke, S.R. Sale, A. Morikawa, Moira G. Peel, A.A. Norris, T.D.G. Lee, R Grubb, T. Breining, R.L. Boyd, J.R. Boot, A. Yano, Marianne Kieffer, Karen Stone, R. Kaji, W.J.F. Sweatman, M. Fiore, G.B. West, T. Plesner, M.J. Barnes, P.G. Holt, P.J. Neveu, Fiona M. Reid, I. Hermecz, P. Prahl, Catriona J. Lewis, Alison H. Rose, D. Bucher, S. Suzuki, Poul Christensen, Michio Miyata, Tadashi Kasahara, G. Oldham, W. Dawson, I. Galbraith, D. Wakelin, R. Patterson, Beverley A. Cox, D. Yawn, K.E. Harris, T. Kuroume
Publikováno v:
International Archives of Allergy and Immunology. 67:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b1d3a87449d25319efbfaeba668cde3
https://doi.org/10.1159/000233035
https://doi.org/10.1159/000233035
Publikováno v:
International archives of allergy and applied immunology. 57(5)
Human blood lymphocytes were tested by an immunofluorescence technique for surface immunoglobulin and by a rosette test with IgG-sensitised red cells for Fc receptors. From combined tests and experiments involving fractionation of lymphocyte populati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abe688b23d5e802e4f4a603d24f50abc
https://pubmed.ncbi.nlm.nih.gov/352967
https://pubmed.ncbi.nlm.nih.gov/352967