Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ronan Walsh"'
Autor:
Rory Gallen, MB, BcH, BAO, Kevin Millar, MB, BcH, BAO, Ronan Walsh, MB, BcH, BAO, Jonathan Lyne, FHRS, Stephen Tuohy, MD, MB, BcH, BAO, MSc
Publikováno v:
HeartRhythm Case Reports, Vol 7, Iss 11, Pp 754-757 (2021)
Externí odkaz:
https://doaj.org/article/5d5d82b912174a68afaca949400705bf
Autor:
Ronan Walsh, BA, MBBS, Jonathan Lyne, MB, BChir, BSc (Hons), MRCP, FHRS, Stephen Tuohy, MB, BCh, BAO, MSc, MD, MRCP
Publikováno v:
HeartRhythm Case Reports, Vol 7, Iss 8, Pp 575- (2021)
Externí odkaz:
https://doaj.org/article/7c96ae7ba11045d4909fa9b961000820
Publikováno v:
HeartRhythm Case Reports
HeartRhythm Case Reports, Vol 7, Iss 11, Pp 754-757 (2021)
HeartRhythm Case Reports, Vol 7, Iss 11, Pp 754-757 (2021)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b3b06efbcd17071302ad9e47061d99d
https://doi.org/10.1016/j.hrcr.2021.08.005
https://doi.org/10.1016/j.hrcr.2021.08.005
Autor:
Ronan Walsh, Sinéad M. Murphy, John Craig, Petya Bogdanova-Mihaylova, Karen Baty, Francesca Brett, Robert W. Taylor, Luke O'Donnell, Michael D Alexander, Emma L. Blakely
Publikováno v:
Journal of Neuromuscular Diseases. 7:355-360
We describe a patient with chronic progressive external ophthalmoplegia (CPEO) due to a rare mitochondrial genetic variant. Muscle biopsy revealed numerous cytochrome c oxidase (COX)-deficient fibres, prompting sequencing of the entire mitochondrial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7425c38226bc00a99dd877de6eacc85
https://doi.org/10.3233/jnd-200486
https://doi.org/10.3233/jnd-200486
Publikováno v:
HeartRhythm Case Reports, Vol 7, Iss 8, Pp 575-(2021)
HeartRhythm Case Reports
HeartRhythm Case Reports
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28dc8062b3bf92ce7459921a9a2eea1b
https://doi.org/10.1016/j.hrcr.2021.05.020
https://doi.org/10.1016/j.hrcr.2021.05.020
Publikováno v:
Lung. 195(2)
Neuralgic Amyotrophy (NA) or Parsonage–Turner syndrome is an idiopathic neuropathy commonly affecting the brachial plexus. Associated phrenic nerve involvement, though recognised, is thought to be very rare. We present a case series of four patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6485d39bed7d6589f3f0c7b2af7829fc
https://pubmed.ncbi.nlm.nih.gov/28260176
https://pubmed.ncbi.nlm.nih.gov/28260176
Publikováno v:
1.13 Clinical Problems - Other.
Neuralgic Amyotrophy (NA) or Parsonage-Turner syndrome is an idiopathic neuropathy commonly affecting the brachial plexus. Associated phrenic nerve involvement, though recognised, is thought to be very rare. We present a case series of four patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49dd050f9766ac07d4962fb756b8ced1
https://doi.org/10.1183/13993003.congress-2015.pa3679
https://doi.org/10.1183/13993003.congress-2015.pa3679