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Declan O'Rourke

Showing results (11-20 of 47) with videos related to

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Veterinary Record Open|August 30, 2017
Veterinary pharmacovigilance in Europe: a survey of veterinary practitionersNancy De Briyne, Raquel Gopal, Gillian Diesel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 16, 2022
Room to improve: The diagnostic journey of Spinal Muscular AtrophyMichael Carter, Andrea Tobin, Lucy Coy, et al.
British Journal of Hospital Medicine (London, England : 2005)|October 26, 2013
Haemoptysis and liver dysfunctionGaurav Manikpure, Inder Mainie, John H Brown, et al.
Neuromuscular Disorders : NMD|January 15, 2020
X-linked infantile spinal muscular atrophy (SMAX2) caused by novel c.1681G>A substitution in the UBA1 gene, expanding the phenotypeNiamh Shaughnessy, Eva B Forman, Declan O'Rourke, et al.
Epilepsy & Behavior Case Reports|June 14, 2019
Compound heterozygosity with <i>PRRT2</i>: Pushing the phenotypic envelope in genetic epilepsiesChristelle Moufawad El Achkar, Beth Rosen Sheidley, Declan O'Rourke, et al.
Leukemia & Lymphoma|July 15, 2006
Urinary bladder infiltration with chronic B-lymphocytic leukemia: two cases with unusual presentationKhaled M A Ramadan, Ann Kyle, Damian McManus, et al.
British Journal of Clinical Pharmacology|November 9, 2021
Challenging times: Delivering gene therapies and an opportunity for shared learningCormac Kennedy, Edel O'Dea, Derval Reidy, et al.
JIMD Reports|March 6, 2023
Autonomic instability, arrhythmia and visual impairment in a new presentation of <i>MTFMT</i>-related mitochondrial diseaseCaoimhe Howard, Arundhati Dev-Borman, John Stokes, et al.
Journal of Neurosurgery. Pediatrics|December 10, 2016
Possible toxicity following embolization of congenital giant vertex hemangioma: case reportIngrid Kieran, Zaitun Zakaria, Chandrasekaran Kaliaperumal, et al.
Neuromuscular Disorders : NMD|March 7, 2022
Troponin-T type 1 (TNNT1)-related nemaline myopathy: unique respiratory phenotype and muscle pathology findingsAlberto A Zambon, François Abel, Barry Linnane, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Veterinary Record Open|August 30, 2017
Veterinary pharmacovigilance in Europe: a survey of veterinary practitionersNancy De Briyne, Raquel Gopal, Gillian Diesel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 16, 2022
Room to improve: The diagnostic journey of Spinal Muscular AtrophyMichael Carter, Andrea Tobin, Lucy Coy, et al.
British Journal of Hospital Medicine (London, England : 2005)|October 26, 2013
Haemoptysis and liver dysfunctionGaurav Manikpure, Inder Mainie, John H Brown, et al.
Neuromuscular Disorders : NMD|January 15, 2020
X-linked infantile spinal muscular atrophy (SMAX2) caused by novel c.1681G>A substitution in the UBA1 gene, expanding the phenotypeNiamh Shaughnessy, Eva B Forman, Declan O'Rourke, et al.
Epilepsy & Behavior Case Reports|June 14, 2019
Compound heterozygosity with <i>PRRT2</i>: Pushing the phenotypic envelope in genetic epilepsiesChristelle Moufawad El Achkar, Beth Rosen Sheidley, Declan O'Rourke, et al.
Leukemia & Lymphoma|July 15, 2006
Urinary bladder infiltration with chronic B-lymphocytic leukemia: two cases with unusual presentationKhaled M A Ramadan, Ann Kyle, Damian McManus, et al.
British Journal of Clinical Pharmacology|November 9, 2021
Challenging times: Delivering gene therapies and an opportunity for shared learningCormac Kennedy, Edel O'Dea, Derval Reidy, et al.
JIMD Reports|March 6, 2023
Autonomic instability, arrhythmia and visual impairment in a new presentation of <i>MTFMT</i>-related mitochondrial diseaseCaoimhe Howard, Arundhati Dev-Borman, John Stokes, et al.
Journal of Neurosurgery. Pediatrics|December 10, 2016
Possible toxicity following embolization of congenital giant vertex hemangioma: case reportIngrid Kieran, Zaitun Zakaria, Chandrasekaran Kaliaperumal, et al.
Neuromuscular Disorders : NMD|March 7, 2022
Troponin-T type 1 (TNNT1)-related nemaline myopathy: unique respiratory phenotype and muscle pathology findingsAlberto A Zambon, François Abel, Barry Linnane, et al.
Pageof 5