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A Reghan Foley

Showing results (11-20 of 114) with videos related to

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Journal of Neuromuscular Diseases|August 23, 2024
An international retrospective early natural history study of LAMA2-related dystrophiesLauren Hinkley, Rotem Orbach, Justin Park, et al.
Neuromuscular Disorders : NMD|June 25, 2014
Limb girdle muscular dystrophy due to LAMA2 mutations: diagnostic difficulties due to associated peripheral neuropathySophelia H S Chan, A Reghan Foley, Rahul Phadke, et al.
Muscle & Nerve|January 10, 2017
Anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase necrotizing myopathy masquerading as a muscular dystrophy in a childPayam Mohassel, A Reghan Foley, Sandra Donkervoort, et al.
Journal of Neurosurgery. Pediatrics|August 2, 2008
Anatomic hemispherectomy for intractable epilepsy in a patient with unilateral schizencephalyGregory G Heuer, Douglas A Hardesty, Kareem A Zaghloul, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 8, 2014
Whole-genome sequencing and the clinician: a tale of two citiesA Reghan Foley, Robert D S Pitceathly, Jie He, et al.
Journal of Child Neurology|May 29, 2012
A novel mutation in the mitochondrial DNA cytochrome b gene (MTCYB) in a patient with mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes syndromeValentina Emmanuele, Evangelia Sotiriou, Purificación Gutierrez Rios, et al.
Neuromuscular Disorders : NMD|November 4, 2009
Autosomal recessive inheritance of classic Bethlem myopathyA Reghan Foley, Ying Hu, Yaqun Zou, et al.
ERJ Open Research|June 30, 2017
Pneumothoraces in collagen VI-related dystrophy: a case series and recommendations for managementKristin L Fraser, Scott Wong, A Reghan Foley, et al.
European Journal of Neurology|January 23, 2018
Congenital myasthenic syndrome due to DPAGT1 mutations mimicking congenital myopathy in an Irish familyP Bogdanova-Mihaylova, R P J Murphy, M D Alexander, et al.
The Journal of Rheumatology|June 3, 2015
Infantile-onset LMNA-associated Muscular Dystrophy Mimicking Juvenile Idiopathic Inflammatory MyopathyElena Moraitis, A Reghan Foley, Clarissa A Pilkington, et al.
Pageof 12

Showing results (11-20 of 114) with videos related to

Sort By:
Pageof 12
Journal of Neuromuscular Diseases|August 23, 2024
An international retrospective early natural history study of LAMA2-related dystrophiesLauren Hinkley, Rotem Orbach, Justin Park, et al.
Neuromuscular Disorders : NMD|June 25, 2014
Limb girdle muscular dystrophy due to LAMA2 mutations: diagnostic difficulties due to associated peripheral neuropathySophelia H S Chan, A Reghan Foley, Rahul Phadke, et al.
Muscle & Nerve|January 10, 2017
Anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase necrotizing myopathy masquerading as a muscular dystrophy in a childPayam Mohassel, A Reghan Foley, Sandra Donkervoort, et al.
Journal of Neurosurgery. Pediatrics|August 2, 2008
Anatomic hemispherectomy for intractable epilepsy in a patient with unilateral schizencephalyGregory G Heuer, Douglas A Hardesty, Kareem A Zaghloul, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 8, 2014
Whole-genome sequencing and the clinician: a tale of two citiesA Reghan Foley, Robert D S Pitceathly, Jie He, et al.
Journal of Child Neurology|May 29, 2012
A novel mutation in the mitochondrial DNA cytochrome b gene (MTCYB) in a patient with mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes syndromeValentina Emmanuele, Evangelia Sotiriou, Purificación Gutierrez Rios, et al.
Neuromuscular Disorders : NMD|November 4, 2009
Autosomal recessive inheritance of classic Bethlem myopathyA Reghan Foley, Ying Hu, Yaqun Zou, et al.
ERJ Open Research|June 30, 2017
Pneumothoraces in collagen VI-related dystrophy: a case series and recommendations for managementKristin L Fraser, Scott Wong, A Reghan Foley, et al.
European Journal of Neurology|January 23, 2018
Congenital myasthenic syndrome due to DPAGT1 mutations mimicking congenital myopathy in an Irish familyP Bogdanova-Mihaylova, R P J Murphy, M D Alexander, et al.
The Journal of Rheumatology|June 3, 2015
Infantile-onset LMNA-associated Muscular Dystrophy Mimicking Juvenile Idiopathic Inflammatory MyopathyElena Moraitis, A Reghan Foley, Clarissa A Pilkington, et al.
Pageof 12