Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Jashelle Caga"'
Autor:
Jashelle Caga-Meller
Publikováno v:
The Lancet Regional Health. Western Pacific, Vol 41, Iss , Pp 100997- (2023)
Externí odkaz:
https://doaj.org/article/58b9c453ad7e4f17893a7c8aae0bac37
Autor:
Jashelle Caga-Meller
Publikováno v:
The Lancet Regional Health. Western Pacific, Vol 39, Iss , Pp 100929- (2023)
Externí odkaz:
https://doaj.org/article/44bce6e8d2da4020a7eacbf73777375f
Autor:
Nga Yan Tse, Martina Bocchetta, Emily G. Todd, Emma M. Devenney, Sicong Tu, Jashelle Caga, John R. Hodges, Glenda M. Halliday, Muireann Irish, Matthew C. Kiernan, Olivier Piguet, Jonathan D. Rohrer, Rebekah M. Ahmed
Publikováno v:
NeuroImage: Clinical, Vol 37, Iss , Pp 103281- (2023)
Background: Hypothalamic dysregulation plays an established role in eating abnormalities in behavioural variant frontotemporal dementia (bvFTD) and amyotrophic lateral sclerosis (ALS). Its contribution to cognitive and behavioural impairments, howeve
Externí odkaz:
https://doaj.org/article/14034e5d4dcf46dab7658ad2311c9390
Autor:
Emma M. Devenney, Sicong Tu, Jashelle Caga, Rebekah M. Ahmed, Eleanor Ramsey, Margie Zoing, John Kwok, Glenda M. Halliday, Olivier Piguet, John R. Hodges, Matthew C. Kiernan
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 8, Iss 8, Pp 1576-1591 (2021)
Abstract Objective The aims of this study were to (i) explore psychotic experiences across the entire amyotrophic lateral sclerosis‐frontotemporal dementia (ALS‐FTD) spectrum from a clinical and genetic perspective, (ii) determine the rate of abn
Externí odkaz:
https://doaj.org/article/de543270f71c4bb789b027bba51a6e35
Autor:
Smriti Agarwal, Elizabeth Highton-Williamson, Jashelle Caga, James Howells, Thanuja Dharmadasa, José M. Matamala, Yan Ma, Kazumoto Shibuya, John R. Hodges, Rebekah M. Ahmed, Steve Vucic, Matthew C. Kiernan
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are well-recognised as an extended disease spectrum. This study hypothesised that cortical hyperexcitability, an early pathophysiological abnormality in ALS, would disting
Externí odkaz:
https://doaj.org/article/f078d7f7bedc4ed1b7dc8b9ca05c2cf6
Autor:
Emma M. Devenney, Kate McErlean, Nga Yan Tse, Jashelle Caga, Thanuja Dharmadasa, William Huynh, Colin J. Mahoney, Margaret Zoing, Srestha Mazumder, Carol Dobson-Stone, John B. Kwok, Glenda M. Halliday, John R. Hodges, Olivier Piguet, Rebekah M. Ahmed, Matthew C. Kiernan
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Objective: This study aimed to establish (1) the pattern and severity of neuropsychiatric symptoms and other non-motor symptoms of sleep and mood, across ALS phenotypes in comparison to bvFTD and (2) the contribution of non-modifiable factors includi
Externí odkaz:
https://doaj.org/article/699516c0614b4b02a87827e30181fbbd
Autor:
Jashelle Caga, Emma Devenney, William Huynh, Margaret C. Zoing, Rebekah M. Ahmed, Matthew C. Kiernan
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Timely management of frontotemporal dysfunction associated with amyotrophic lateral sclerosis (ALS) has important prognostic and therapeutic implications. However, there remains a paucity of research on best practise recommendations to guide the deve
Externí odkaz:
https://doaj.org/article/31828709c962421b9c5669b0fbbffeef
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Pseudobulbar affect is a disorder of emotional expression commonly observed in amyotrophic lateral sclerosis (ALS), presenting as episodes of involuntary laughter, or crying. The objective of the current study was to determine the association between
Externí odkaz:
https://doaj.org/article/7101e8682a804f288898984b33995c4a
Autor:
Martina Bocchetta, Emily G. Todd, Nga Yan Tse, Emma M. Devenney, Sicong Tu, Jashelle Caga, John R. Hodges, Glenda M. Halliday, Muireann Irish, Olivier Piguet, Matthew C. Kiernan, Jonathan D. Rohrer, Rebekah M. Ahmed
Publikováno v:
Brain Sciences, Vol 12, Iss 3, p 336 (2022)
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are part of the same disease spectrum. While thalamic–cerebellar degeneration has been observed in C9orf72 expansion carriers, the exact subregions involved across the clinical p
Externí odkaz:
https://doaj.org/article/b4234d304d8f4ab1a1fb9af5cd53925b
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Previously thought to be a pure motor disease, amyotrophic lateral sclerosis (ALS) is now established as multisystem neurodegenerative disorder that lies on a continuum with frontotemporal dementia (FTD). Cognitive and behavioral symptoms primarily e
Externí odkaz:
https://doaj.org/article/bd0fb32566ed47eda1444d37f7a82c58