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American Journal of Medical Genetics. Part A
|
August 7, 2013
A distinct mitochondrial myopathy, lactic acidosis and sideroblastic anemia (MLASA) phenotype associates with YARS2 mutations
Rojeen Shahni, Yehani Wedatilake, Maureen A Cleary, et al.
BMJ Case Reports
|
October 9, 2013
Treatable Leigh-like encephalopathy presenting in adolescence
Elisa Fassone, Yehani Wedatilake, Catherine J DeVile, et al.
Journal of Inherited Metabolic Disease
|
September 28, 2011
Pregnancy and its management in women with GSD type III - a single centre experience
Radha Ramachandran, Yehani Wedatilake, Caroline Coats, et al.
Frontiers in Aging Neuroscience
|
October 3, 2022
Blood pressure trajectories over 35 years and dementia risk: A retrospective study: The HUNT study
Geir Selbaek, Josephine Stuebs, Knut Engedal, et al.
Journal of Inherited Metabolic Disease
|
February 21, 2018
Outcome of adult patients with X-linked hypophosphatemia caused by PHEX gene mutations
Douglas Chesher, Michael Oddy, Ulpee Darbar, et al.
Mitochondrion
|
August 1, 2016
Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial disease
Manoj P Menezes, Shamima Rahman, Kaustuv Bhattacharya, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
February 12, 2025
A brain DNA co-methylation network analysis of psychosis in Alzheimer's disease
Morteza Kouhsar, Luke Weymouth, Adam R Smith, et al.
Orphanet Journal of Rare Diseases
|
July 3, 2016
TRNT1 deficiency: clinical, biochemical and molecular genetic features
Yehani Wedatilake, Rojeen Niazi, Elisa Fassone, et al.
Acta Pharmaceutica Sinica. B
|
October 6, 2025
Artificial intelligence in drug development for delirium and Alzheimer's disease
Ruixue Ai, Xianglu Xiao, Shenglong Deng, et al.
Brain : a Journal of Neurology
|
July 1, 2015
Signal transducer and activator of transcription 2 deficiency is a novel disorder of mitochondrial fission
Rojeen Shahni, Catherine M Cale, Glenn Anderson, et al.
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of 2
Search research articles
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Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
American Journal of Medical Genetics. Part A
|
August 7, 2013
A distinct mitochondrial myopathy, lactic acidosis and sideroblastic anemia (MLASA) phenotype associates with YARS2 mutations
Rojeen Shahni, Yehani Wedatilake, Maureen A Cleary, et al.
BMJ Case Reports
|
October 9, 2013
Treatable Leigh-like encephalopathy presenting in adolescence
Elisa Fassone, Yehani Wedatilake, Catherine J DeVile, et al.
Journal of Inherited Metabolic Disease
|
September 28, 2011
Pregnancy and its management in women with GSD type III - a single centre experience
Radha Ramachandran, Yehani Wedatilake, Caroline Coats, et al.
Frontiers in Aging Neuroscience
|
October 3, 2022
Blood pressure trajectories over 35 years and dementia risk: A retrospective study: The HUNT study
Geir Selbaek, Josephine Stuebs, Knut Engedal, et al.
Journal of Inherited Metabolic Disease
|
February 21, 2018
Outcome of adult patients with X-linked hypophosphatemia caused by PHEX gene mutations
Douglas Chesher, Michael Oddy, Ulpee Darbar, et al.
Mitochondrion
|
August 1, 2016
Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial disease
Manoj P Menezes, Shamima Rahman, Kaustuv Bhattacharya, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
February 12, 2025
A brain DNA co-methylation network analysis of psychosis in Alzheimer's disease
Morteza Kouhsar, Luke Weymouth, Adam R Smith, et al.
Orphanet Journal of Rare Diseases
|
July 3, 2016
TRNT1 deficiency: clinical, biochemical and molecular genetic features
Yehani Wedatilake, Rojeen Niazi, Elisa Fassone, et al.
Acta Pharmaceutica Sinica. B
|
October 6, 2025
Artificial intelligence in drug development for delirium and Alzheimer's disease
Ruixue Ai, Xianglu Xiao, Shenglong Deng, et al.
Brain : a Journal of Neurology
|
July 1, 2015
Signal transducer and activator of transcription 2 deficiency is a novel disorder of mitochondrial fission
Rojeen Shahni, Catherine M Cale, Glenn Anderson, et al.
Page
of 2