Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Simone Ardern-Holmes"'
Autor:
Russell C. Dale, Terrence Thomas, Shrujna Patel, Velda X. Han, Kavitha Kothur, Christopher Troedson, Sachin Gupta, Deepak Gill, Stephen Malone, Michaela Waak, Sophie Calvert, Gopinath Subramanian, P. Ian Andrews, Tejaswi Kandula, Manoj P. Menezes, Simone Ardern‐Holmes, Shekeeb Mohammad, Sushil Bandodkar, Jingya Yan
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 8, Pp 1417-1432 (2023)
Abstract Objective Infection‐triggered encephalopathy syndromes (ITES) are potentially devastating neuroinflammatory conditions. Although some ITES syndromes have recognisable MRI neuroimaging phenotypes, there are otherwise few biomarkers of disea
Externí odkaz:
https://doaj.org/article/1c41c2d648974bcc8a098e644408d090
Autor:
Jingya Yan, Kavitha Kothur, Shekeeb Mohammad, Jason Chung, Shrujna Patel, Hannah F. Jones, Brooke A. Keating, Velda X. Han, Richard Webster, Simone Ardern-Holmes, Jayne Antony, Manoj P. Menezes, Esther Tantsis, Deepak Gill, Sachin Gupta, Tejaswi Kandula, Hugo Sampaio, Michelle A. Farrar, Christopher Troedson, P Ian Andrews, Sekhar C. Pillai, Benjamin Heng, Gilles J. Guillemin, Anna Guller, Sushil Bandodkar, Russell C. Dale
Publikováno v:
EBioMedicine, Vol 91, Iss , Pp 104589- (2023)
Summary: Background: Defining the presence of acute and chronic brain inflammation remains a challenge to clinicians due to the heterogeneity of clinical presentations and aetiologies. However, defining the presence of neuroinflammation, and monitori
Externí odkaz:
https://doaj.org/article/f3f98b36f0cb49b9aa7418bacef1fbf5
Autor:
Géza Berecki, Katherine B. Howell, Jacqueline Heighway, Nelson Olivier, Jill Rodda, Isabella Overmars, Danique R. M. Vlaskamp, Tyson L. Ware, Simone Ardern-Holmes, Gaetan Lesca, Michael Alber, Pierangelo Veggiotti, Ingrid E. Scheffer, Samuel F. Berkovic, Markus Wolff, Steven Petrou
Publikováno v:
Communications Biology, Vol 5, Iss 1, Pp 1-13 (2022)
A comprehensive biophysical analysis of disease-associated mutations in the voltage-gated sodium channel gene, SCN2A, suggests that dynamic action potential clamp may be a better predictor than voltage clamp of how these mutations alter neuronal exci
Externí odkaz:
https://doaj.org/article/7e36edaad8f740ddbb8634f082580efc
Autor:
Jingya Yan, Kavitha Kothur, Emily A. Innes, Velda X. Han, Hannah F. Jones, Shrujna Patel, Erica Tsang, Richard Webster, Sachin Gupta, Christopher Troedson, Manoj P. Menezes, Jayne Antony, Simone Ardern-Holmes, Esther Tantsis, Shekeeb Mohammad, Louise Wienholt, Ananda S. Pires, Benjamin Heng, Gilles J. Guillemin, Anna Guller, Deepak Gill, Sushil Bandodkar, Russell C. Dale
Publikováno v:
EBioMedicine, Vol 84, Iss , Pp 104280- (2022)
Summary: Background: Epileptic (previously infantile) spasms is the most common epileptic encephalopathy occurring during infancy and is frequently associated with abnormal neurodevelopmental outcomes. Epileptic spasms have a diverse range of known (
Externí odkaz:
https://doaj.org/article/a996c30a8b944c29b682c22fe3ffea37
Autor:
Simone Ardern-Holmes, Mark Wong, Simon So, Sarita Bahure, Paul de Souza, Elizabeth Hovey, Geoff McCowage, Michael Slancar, Mark Dexter, Simon Troon, Cassandra White, John Simes
Publikováno v:
Australasian Journal of Neuroscience, Vol 31, Iss 1 (2021)
Introduction: We describe an Australian experience of infusional bevacizumab for vestibular schwannoma (VS) in neurofibromatosis type 2 patients, with specific focus on 3-dimensional tumour volume and audiometry. Method: Data was pooled from patients
Autor:
Simone Ardern-Holmes
Publikováno v:
Pediatric Medicine. 3:AB008-AB008
Publikováno v:
Journal of Pediatric Neurology. :109-113
Back pain is often reported in children undergoing cancer treatment, but is not typically a presenting symptom. Spinal cord compression secondary to myeloid sarcoma (chloroma) has been described, although is rare in children. We describe a 10-year-ol
Publikováno v:
Journal of child neurology. 32(1)
Neurofibromatosis type 2 (NF2) is a rare autosomal dominant disorder (incidence 1:33 000-40 000) characterized by formation of central nervous system tumors, due to mutation in the NF2 gene on chromosome 22q12. Vestibular schwannomas are the hallmark
Autor:
Alison M. Kesson, Nikola J. Morton, Ella Sugo, Pamela Palasanthiran, Ann M. E. Bye, Tom Snelling, Philip N Britton, Simone Ardern-Holmes
Publikováno v:
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America. 57(8)
Angiostrongylus cantonensis is the most common cause of eosinophilic meningitis worldwide. We describe 2 cases among young children from Sydney, Australia, where locally acquired infection of children has not been reported previously. Both cases mani