Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Bryan, Lynch"'
Autor:
Saraswathy Sabanathan, Omar Abdel‐Mannan, Kshitij Mankad, Ata Siddiqui, Krishna Das, Lucinda Carr, Christin Eltze, Michael Eyre, Jon Gadian, Cheryl Hemingway, Marios Kaliakatsos, Rachel Kneen, Deepa Krishnakumar, Bryan Lynch, Amitav Parida, Thomas Rossor, Micheal Taylor, Evangeline Wassmer, Sukhvir Wright, Ming Lim, Yael Hacohen
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 9, Iss 1, Pp 67-78 (2022)
Abstract Objectives To describe the clinical presentation, investigations, management, and disease course in pediatric autoimmune limbic encephalitis (LE). Methods In this retrospective observational study, from the UK Childhood Neuroinflammatory Dis
Externí odkaz:
https://doaj.org/article/682bba95d1374e10ab64b76b766d11d8
Publikováno v:
BMJ Open Quality, Vol 10, Iss 4 (2021)
Background Bronchiolitis is a common reason for infants to present to the emergency department (ED). Clear evidence-based guidelines exist that recommend against routine radiological and laboratory investigations in this cohort. Despite this, preinte
Externí odkaz:
https://doaj.org/article/fbdd8d05a0ad4c82807635416e3ed455
Autor:
Susan, Harvey, Nicholas M, Allen, Mary D, King, Bryan, Lynch, Sally A, Lynch, Mary, O'Regan, Declan, O'Rourke, Amre, Shahwan, David, Webb, Kathleen M, Gorman, S, Tirupathi
Publikováno v:
Developmental Medicine & Child Neurology. 64:780-788
To estimate the prevalence, and evaluate presentation, treatment response, treatment side effects, and long-term seizure outcomes in all known cases of children with Down syndrome and infantile spasms on the island of Ireland.This was a 10-year retro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41c3c2b61cf37bf91e57d99e60366b30
https://doi.org/10.1111/dmcn.15153
https://doi.org/10.1111/dmcn.15153
Autor:
Chia Wei Teoh, Kathleen Mary Gorman, Bryan Lynch, Timothy H. J. Goodship, Niamh Marie Dolan, Mary Waldron, Michael Riordan, Atif Awan
Publikováno v:
Case Reports in Nephrology, Vol 2018 (2018)
Atypical hemolytic uremic syndrome (aHUS) is caused by dysregulation of the complement system. A humanised anti-C5 monoclonal antibody (eculizumab) is available for the treatment of aHUS. We present the first description of atypical HUS in a child wi
Externí odkaz:
https://doaj.org/article/b5d21626363143288dbe2b90b33ed63c
Autor:
Eilish Twomey, Michael Riordan, CS Costigan, Atif Awan, Tara Raftery, Bryan Lynch, Dermot Michael Wildes, Anne G Carroll, Kathleen M. Gorman, M. Waldron, Robert Cunney, Clodagh Sweeney, Amre Shahwan, Niamh Marie Dolan, Claire Reynolds, Maria Stack, Declan O'Rourke, Richard J. Drew
Publikováno v:
European Journal of Pediatrics. 181:501-512
Our objective was to establish the rate of neurological involvement in Shiga toxin-producing Escherichia coli–hemolytic uremic syndrome (STEC-HUS) and describe the clinical presentation, management and outcome. A retrospective chart review of child
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::556f2d8783e515660c347abc4d8aed65
https://doi.org/10.1007/s00431-021-04200-1
https://doi.org/10.1007/s00431-021-04200-1
Autor:
Damien Ferguson, Siobhan O’Malley, Sarah Wrigley, Bryan Lynch, Elaine Purcell, Catherine Crowe, Ben McGinn, Sarah Keane
Publikováno v:
J Clin Sleep Med
STUDY OBJECTIVES: We aimed to describe the clinical features of narcolepsy in patients referred to our sleep center between 2009 and 2016, and to compare these features across age groups and between sporadic vs AS03-adjuvanted H1N1 influenza vaccine-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e946408d5ba12aecca554558f4bcde0
https://doi.org/10.5664/jcsm.9052
https://doi.org/10.5664/jcsm.9052
Autor:
Yvonne Rogers, Joanne Hughes, Kevin Carson, Ina Knerr, Kim Hunter, Atif Awan, Ahmad Monavari, Johannes Häberle, Amre Shahwan, Ingrid Borovickova, Véronique Rüfenacht, Philip Mayne, Bryan Lynch, Ellen Crushell, Daniel O'Reilly, Michael Riordan, Stephanie Ryan, Eileen P. Treacy
Publikováno v:
Journal of Inherited Metabolic Disease. 44:639-655
Since 1972, eighteen patients (10 females/8 males) have been detected by newborn bloodspot screening (NBS) with neonatal-onset Maple Syrup Urine Disease (MSUD) in Ireland. Patients were stratified into three clusters according to clinical outcome at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::103bad65193681a00b024196fe27e3dc
https://doi.org/10.1002/jimd.12337
https://doi.org/10.1002/jimd.12337
Autor:
Abigail Wagle, Elaine Reade, Catherine Crowe, Siobhan O’Malley, Bryan Lynch, Maeve Muldoon, Irwin Gill, Aoife Carey, Aishling Sheils
Publikováno v:
European Journal of Paediatric Neurology. 28:52-57
Aim To describe the population of young people in Ireland diagnosed with narcolepsy with regards to vaccine exposure, symptomatology, investigation results and experience of medical treatment. Method Retrospective review of medical records at the sin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3059f672966d0ee7c1f6762cfae8c4f6
https://doi.org/10.1016/j.ejpn.2020.07.016
https://doi.org/10.1016/j.ejpn.2020.07.016
Autor:
Darach Crimmins, Dominick J. H. McCabe, Peter Boers, David Williams, Sean M. Murphy, Mary O'Regan, Peter J. Kelly, Mohsen Javadpour, Ronan J. Doherty, Desmond O'Neill, Christopher McGuigan, Simon Cronin, Bryan Lynch, Niall Tubridy, John Caird, David Webb, Joan T. Moroney, Mary D. King
Publikováno v:
Irish Journal of Medical Science (1971 -). 190:335-344
There are no previously published reports regarding the epidemiology and characteristics of moyamoya disease or syndrome in Ireland. To examine patient demographics, mode of presentation and the outcomes of extracranial-intracranial bypass surgery in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::497251d5c762c1423568a6589a5f7ab6
https://doi.org/10.1007/s11845-020-02280-w
https://doi.org/10.1007/s11845-020-02280-w
Autor:
Bassett Ds, Kathleen M. Gorman, Colin H. Peters, Peter C. Ruben, Richard E. Rosch, Mary D. King, Bryan Lynch, Laura Jones
Publikováno v:
Brain Communications. 3
Pathogenic variants in the voltage-gated sodium channel gene (SCN1A) are amongst the most common genetic causes of childhood epilepsies. There is considerable heterogeneity in both the types of causative variants and associated phenotypes; a recent e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce658b9c558ab18bf051d74cd13f5e30
https://doi.org/10.1093/braincomms/fcab235
https://doi.org/10.1093/braincomms/fcab235