Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Rod A. Lea"'
Autor:
Neven Maksemous, Claire D. Blayney, Heidi G. Sutherland, Robert A. Smith, Rod A. Lea, Kim Ngan Tran, Omar Ibrahim, Jeffrey R. McArthur, Larisa M. Haupt, M. Zameel Cader, Rocio K. Finol-Urdaneta, David J. Adams, Lyn R. Griffiths
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
Familial hemiplegic migraine (FHM) is a severe neurogenetic disorder for which three causal genes, CACNA1A, SCN1A, and ATP1A2, have been implicated. However, more than 80% of referred diagnostic cases of hemiplegic migraine (HM) are negative for exon
Externí odkaz:
https://doaj.org/article/483ec272a040492885598e5a29002b7f
Autor:
Heidi G. Sutherland, Neven Maksemous, Cassie L. Albury, Omar Ibrahim, Robert A. Smith, Rod A. Lea, Larisa M. Haupt, Bronwyn Jenkins, Benjamin Tsang, Lyn R. Griffiths
Publikováno v:
Cells, Vol 9, Iss 11, p 2368 (2020)
Hemiplegic migraine (HM) is a rare migraine disorder with aura subtype including temporary weakness and visual, sensory, and/or speech symptoms. To date, three main genes—CACNA1A, ATP1A2, and SCN1A—have been found to cause HM. These encode ion ch
Externí odkaz:
https://doaj.org/article/25e3376889694022a9810496bcdda98f
Autor:
Gabrielle Bradshaw, Robbie R. Lualhati, Cassie L. Albury, Neven Maksemous, Deidre Roos-Araujo, Robert A. Smith, Miles C. Benton, David A. Eccles, Rod A. Lea, Heidi G. Sutherland, Larisa M. Haupt, Lyn R. Griffiths
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
BackgroundWe investigated the molecular etiology of a young male proband with confirmed immunodeficiency of unknown cause, presenting with recurrent bacterial and Varicella zoster viral infections in childhood and persistent lymphopenia into early ad
Externí odkaz:
https://doaj.org/article/e148a543bbc64b79b57fc41d5690c2ab
Autor:
Neven, Maksemous, Claire D, Blayney, Heidi G, Sutherland, Robert A, Smith, Rod A, Lea, Kim Ngan, Tran, Omar, Ibrahim, Jeffrey R, McArthur, Larisa M, Haupt, M Zameel, Cader, Rocio K, Finol-Urdaneta, David J, Adams, Lyn R, Griffiths
Publikováno v:
Frontiers in molecular neuroscience. 15
Familial hemiplegic migraine (FHM) is a severe neurogenetic disorder for which three causal genes
Publikováno v:
Journal of Magnetic Resonance Imaging. 50:592-601
BACKGROUND Two-dimensional localized correlation spectroscopy (2D L-COSY) is a research tool that has been applied to evaluate in vivo metabolic activity in many neurological and oncological disorders. Circadian mediators such as brain temperature, h
Autor:
Lauren K. Spriggens, Nesli Avgan, Larisa M. Haupt, Rod A. Lea, Lyn R. Griffiths, Heidi G. Sutherland, David Shum, Omar Ibrahim
Publikováno v:
Neurobiology of Learning and Memory. 155:330-336
The common polymorphism rs17518584, near the cell adhesion molecule 2 gene (CADM2), was previously identified as playing a role in information processing speed in a genome-wide association study of executive functions and processing speed performed i
Autor:
Jameen Arm, Oun Al-iedani, Jeannette Lechner-Scott, Georg Oeltzschner, Saadallah Ramadan, Rod A. Lea
Publikováno v:
Eur J Radiol
Purpose Fatigue is a common symptom in patients with multiple sclerosis (MS) with unknown pathophysiology. Dysfunction of the GABAergic/glutamatergic pathways involving inhibitory and excitatory neurotransmitters such as γ-aminobutyric acid (GABA) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64aee7c6e2f82056369f7454d7daedcc
https://europepmc.org/articles/PMC8900256/
https://europepmc.org/articles/PMC8900256/
Autor:
Oun Al-iedani, Jeannette Lechner-Scott, Rod A. Lea, Jameen Arm, Saadallah Ramadan, Karen Ribbons
Publikováno v:
Journal of neuroimaging : official journal of the American Society of NeuroimagingReferences. 31(3)
BACKGROUND AND PURPOSE Fatigue is the common symptom in patients with multiple sclerosis (MS), yet its pathophysiological mechanism is poorly understood. We investigated the metabolic changes in fatigue in a group of relapsing-remitting MS (RRMS) pat
Autor:
Neven Maksemous, Omar Ibrahim, Rod A. Lea, Cassie L. Albury, Larisa M. Haupt, Bronwyn Jenkins, Benjamin Tsang, Heidi G. Sutherland, Lyn R. Griffiths, Robert A. Smith
Publikováno v:
Cells
Cells, Vol 9, Iss 2368, p 2368 (2020)
Volume 9
Issue 11
Cells, Vol 9, Iss 2368, p 2368 (2020)
Volume 9
Issue 11
Hemiplegic migraine (HM) is a rare migraine disorder with aura subtype including temporary weakness and visual, sensory, and/or speech symptoms. To date, three main genes&mdash
CACNA1A, ATP1A2, and SCN1A&mdash
have been found to cause HM. T
CACNA1A, ATP1A2, and SCN1A&mdash
have been found to cause HM. T
Autor:
Jeannette Lechner-Scott, Scott Quadrelli, Saadallah Ramadan, Jameen Arm, Rod A. Lea, Oun Al-iedani, Karen Ribbons
Publikováno v:
Journal of Magnetic Resonance Imaging. 48:1559-1569
BACKGROUND Two-dimensional localized correlational spectroscopy (2D L-COSY) has been applied in vivo to investigate metabolic profiles in many disorders due to its ability to detect several metabolites simultaneously. Successful application of this t