Zobrazeno 1 - 10
of 13
pro vyhledávání: '"David McGibbon"'
Autor:
Yih Jia Poh, Abdulrahman Alrashid, Shirish R Sangle, Eleanor Higgins, Emma Benton, David McGibbon, David P D’Cruz
Publikováno v:
Lupus. 31:1078-1083
Background There is a growing literature reporting the association between proton pump inhibitor (PPI) use and subacute cutaneous lupus erythematosus (SCLE). Aims To compare the clinical characteristics of a cohort of patients with PPI-induced SCLE,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71e4d3b8f694a348a38644def1a61944
https://doi.org/10.1177/09612033221104237
https://doi.org/10.1177/09612033221104237
Autor:
David McGibbon
Publikováno v:
Rheumatology. 58
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa052a2c5ba18be5c3db711d792df1d1
https://doi.org/10.1093/rheumatology/kez109.099
https://doi.org/10.1093/rheumatology/kez109.099
Autor:
David, McGibbon
Publikováno v:
Transactions of the Medical Society of London. 129
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ec247020cc31121526c6c5ccfc17c3af
https://pubmed.ncbi.nlm.nih.gov/26021008
https://pubmed.ncbi.nlm.nih.gov/26021008
Publikováno v:
Medical Education. 35:326-330
BACKGROUND: Clinical examinations increasingly consist of composite tests to assess all aspects of the curriculum recommended by the General Medical Council. SETTING: A final undergraduate medical school examination for 214 students. AIM: To estimate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7d1343a4b161c7f3c6628d9f46ab214
https://doi.org/10.1046/j.1365-2923.2001.00929.x
https://doi.org/10.1046/j.1365-2923.2001.00929.x
Autor:
A.H. O'Hagan, David McGibbon, Kevin McKenna, C. Buckley, M.Y. Walsh, E.A. Bingham, Anne E. Hughes, F. Maloney
Publikováno v:
British Journal of Dermatology. 154:450-452
Summary Background Glomuvenous malformations (GVMs) are rare bluish lesions that can affect the skin and mucosal surfaces. They represent defects in vasculogenesis. Lesions can occur sporadically or in an autosomal dominant mode of inheritance. Recen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76c439748ea2d714ec71522723aa081c
https://doi.org/10.1111/j.1365-2133.2005.07041.x
https://doi.org/10.1111/j.1365-2133.2005.07041.x
Publikováno v:
American Journal of Medical Genetics. 75:1-3
A 37-year-old woman was referred for genetic counseling after termination of her probable seventh pregnancy. Ultrasound examination at 13 weeks of gestation had shown a fetus with bilateral cystic hygromas. A transabdominal amniocentesis confirmed 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5844a60ec28bc65fb27e7ddc6435b4de
https://doi.org/10.1002/(sici)1096-8628(19980106)75:1<1::aid-ajmg1>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19980106)75:1<1::aid-ajmg1>3.0.co
Autor:
Ryan Graydon, Ian S. Young, Stuart J. McGimpsey, Jayne V. Woodside, David McGibbon, Gareth C. McKeeman, Dermot O'Reilly, Sarah Gilchrist, Louise Bamford, Anne E. Hughes, Christopher Patterson, Usha Chakravarthy
Publikováno v:
Investigative ophthalmologyvisual science. 46(12)
PURPOSE. The aim of this case- control study was to investigate the relationship between homocysteine (tHcy), 5,10 methylene tetrahydrofolate reductase (MTHFR) C677T genotype, folate and vitamin B12 status, and retinal vein occlusion (RVO). METHODS.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aadc600a4e69ccaa3341e2c0d9c3fb82
https://pubmed.ncbi.nlm.nih.gov/16303969
https://pubmed.ncbi.nlm.nih.gov/16303969
Publikováno v:
Cytogenetics and cell genetics. 93(1-2)
Central areolar choroidal dystrophy (CACD) causes bilateral irreversible central visual loss in the 5th to 7th decades. The authors previously described a large pedigree with the disorder, which showed linkage to chromosome 17p13.2→p13.1 between mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4c09e38a07183165d825349f96b87b0
https://pubmed.ncbi.nlm.nih.gov/11474177
https://pubmed.ncbi.nlm.nih.gov/11474177
Publikováno v:
Human molecular genetics. 4(7)
Chondrocalcinosis is a common disorder which may associate with acute and chronic arthritis. A familial form, inherited as an autosomal dominant trait, has been mapped in a large family in which affected members also suffer recurrent fits in childhoo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0e8f2de20d05b6945349483786ed132
https://pubmed.ncbi.nlm.nih.gov/8528213
https://pubmed.ncbi.nlm.nih.gov/8528213
Autor:
Gary K. Meenagh, David McGibbon, James Nixon, Gary D. Wright, Michael Doherty, Anne E. Hughes
Publikováno v:
Arthritis & Rheumatism; Jul2005, Vol. 52 Issue 7, p2040-2043, 4p