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Journal of Neurology
|
January 8, 2018
Movement disorders in mitochondrial disease
Roula Ghaoui, Carolyn M Sue
JAMA Neurology
|
May 22, 2023
Segmental Uniparental Isodisomy Causing an "Inside-to-Outside" Limb-Girdle Muscular Dystrophy Due to a Homozygous Mutation in POGLUT1
Roula Ghaoui, Samuel Curtis, Karin S Kassahn
BMJ Neurology Open
|
March 8, 2021
Progressive cranial neuropathy and uterine involvement in myeloid sarcoma
Anthony Khoo, Thomas Kimber, Penelope Cohen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 27, 2019
Genetic mimics of cerebral palsy
Toni S Pearson, Roser Pons, Roula Ghaoui, et al.
Muscle & Nerve
|
November 11, 2014
Axonal excitability in primary amyloidotic neuropathy
Jessica Hafner, Roula Ghaoui, Luke Coyle, et al.
Chemico-Biological Interactions
|
April 11, 2003
UDP-glucuronosyltransferase-dependent bioactivation of clofibric acid to a DNA-damaging intermediate in mouse hepatocytes
Roula Ghaoui, Benedetta C Sallustio, Philip C Burcham, et al.
Neuromuscular Disorders : NMD
|
March 6, 2026
Congenital skeletal muscle myopathy due to the recently described digenic inheritance of TTN and SRPK3 genetic variants: a case study
Dominic Spicer, Lucas Dejong, Abhi Kulkarni, et al.
Practical Neurology
|
December 14, 2024
Tetrodotoxin toxicity: an increasing threat
Emily Burton, Alastair Ward, Lachlan Tamlin, et al.
Practical Neurology
|
April 24, 2017
A 'limb-girdle muscular dystrophy' responsive to asthma therapy
Eoin Mulroy, Roula Ghaoui, David Hutchinson, et al.
BMJ Neurology Open
|
May 13, 2025
Long-read sequencing for diagnosis of genetic myopathies
Dennis Yeow, Laura Ivete Rudaks, Ryan Davis, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 31) with videos related to
Sort By:
Page
of 4
Journal of Neurology
|
January 8, 2018
Movement disorders in mitochondrial disease
Roula Ghaoui, Carolyn M Sue
JAMA Neurology
|
May 22, 2023
Segmental Uniparental Isodisomy Causing an "Inside-to-Outside" Limb-Girdle Muscular Dystrophy Due to a Homozygous Mutation in POGLUT1
Roula Ghaoui, Samuel Curtis, Karin S Kassahn
BMJ Neurology Open
|
March 8, 2021
Progressive cranial neuropathy and uterine involvement in myeloid sarcoma
Anthony Khoo, Thomas Kimber, Penelope Cohen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 27, 2019
Genetic mimics of cerebral palsy
Toni S Pearson, Roser Pons, Roula Ghaoui, et al.
Muscle & Nerve
|
November 11, 2014
Axonal excitability in primary amyloidotic neuropathy
Jessica Hafner, Roula Ghaoui, Luke Coyle, et al.
Chemico-Biological Interactions
|
April 11, 2003
UDP-glucuronosyltransferase-dependent bioactivation of clofibric acid to a DNA-damaging intermediate in mouse hepatocytes
Roula Ghaoui, Benedetta C Sallustio, Philip C Burcham, et al.
Neuromuscular Disorders : NMD
|
March 6, 2026
Congenital skeletal muscle myopathy due to the recently described digenic inheritance of TTN and SRPK3 genetic variants: a case study
Dominic Spicer, Lucas Dejong, Abhi Kulkarni, et al.
Practical Neurology
|
December 14, 2024
Tetrodotoxin toxicity: an increasing threat
Emily Burton, Alastair Ward, Lachlan Tamlin, et al.
Practical Neurology
|
April 24, 2017
A 'limb-girdle muscular dystrophy' responsive to asthma therapy
Eoin Mulroy, Roula Ghaoui, David Hutchinson, et al.
BMJ Neurology Open
|
May 13, 2025
Long-read sequencing for diagnosis of genetic myopathies
Dennis Yeow, Laura Ivete Rudaks, Ryan Davis, et al.
Page
of 4