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Roula Ghaoui

Showing results (1-10 of 31) with videos related to

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Journal of Neurology|January 8, 2018
Movement disorders in mitochondrial diseaseRoula 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 POGLUT1Roula Ghaoui, Samuel Curtis, Karin S Kassahn
BMJ Neurology Open|March 8, 2021
Progressive cranial neuropathy and uterine involvement in myeloid sarcomaAnthony Khoo, Thomas Kimber, Penelope Cohen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 27, 2019
Genetic mimics of cerebral palsyToni S Pearson, Roser Pons, Roula Ghaoui, et al.
Muscle & Nerve|November 11, 2014
Axonal excitability in primary amyloidotic neuropathyJessica 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 hepatocytesRoula 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 studyDominic Spicer, Lucas Dejong, Abhi Kulkarni, et al.
Practical Neurology|December 14, 2024
Tetrodotoxin toxicity: an increasing threatEmily Burton, Alastair Ward, Lachlan Tamlin, et al.
Practical Neurology|April 24, 2017
A 'limb-girdle muscular dystrophy' responsive to asthma therapyEoin Mulroy, Roula Ghaoui, David Hutchinson, et al.
BMJ Neurology Open|May 13, 2025
Long-read sequencing for diagnosis of genetic myopathiesDennis Yeow, Laura Ivete Rudaks, Ryan Davis, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Journal of Neurology|January 8, 2018
Movement disorders in mitochondrial diseaseRoula 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 POGLUT1Roula Ghaoui, Samuel Curtis, Karin S Kassahn
BMJ Neurology Open|March 8, 2021
Progressive cranial neuropathy and uterine involvement in myeloid sarcomaAnthony Khoo, Thomas Kimber, Penelope Cohen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 27, 2019
Genetic mimics of cerebral palsyToni S Pearson, Roser Pons, Roula Ghaoui, et al.
Muscle & Nerve|November 11, 2014
Axonal excitability in primary amyloidotic neuropathyJessica 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 hepatocytesRoula 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 studyDominic Spicer, Lucas Dejong, Abhi Kulkarni, et al.
Practical Neurology|December 14, 2024
Tetrodotoxin toxicity: an increasing threatEmily Burton, Alastair Ward, Lachlan Tamlin, et al.
Practical Neurology|April 24, 2017
A 'limb-girdle muscular dystrophy' responsive to asthma therapyEoin Mulroy, Roula Ghaoui, David Hutchinson, et al.
BMJ Neurology Open|May 13, 2025
Long-read sequencing for diagnosis of genetic myopathiesDennis Yeow, Laura Ivete Rudaks, Ryan Davis, et al.
Pageof 4