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Craig Campbell

Showing results (41-50 of 188) with videos related to

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Pediatric Neurology|November 5, 2018
Twinkle-Associated Mitochondrial DNA DepletionSalma Remtulla, Cam-Tu Emilie Nguyen, Chitra Prasad, et al.
Biochemistry and Molecular Biology Education : a Bimonthly Publication of the International Union of Biochemistry and Molecular Biology|July 7, 2021
What biomedical education might learn from real estate toursMatthew Sellwood, Craig Campbell, Jim Cook, et al.
BMC Pediatrics|December 17, 2005
Subacute sclerosing panencephalitis: results of the Canadian Paediatric Surveillance Program and review of the literatureCraig Campbell, Simon Levin, Peter Humphreys, et al.
Journal of Neuromuscular Diseases|July 17, 2018
Prenatal, Neonatal, and Early Childhood Features in Congenital Myotonic DystrophyEugenio Zapata-Aldana, Delia Ceballos-Sáenz, Rhiannon Hicks, et al.
American Journal of Medical Genetics. Part A|April 3, 2019
Distal arthrogryposis type 5 and PIEZO2 novel variant in a Canadian familyEugenio Zapata-Aldana, Sulaiman B Al-Mobarak, Natalya Karp, et al.
Child Neurology Open|May 16, 2017
Seizures Related to Hypomagnesemia: A Case Series and Review of the LiteratureBecky Biqi Chen, Chitra Prasad, Marta Kobrzynski, et al.
Neuropediatrics|May 26, 2023
Duchenne Muscular Dystrophy Fatigue TrajectoriesYi Sally Wei, Mona Hnaini, Basmah ElAloul, et al.
American Journal of Medical Genetics. Part A|September 11, 2017
Treating pediatric neuromuscular disorders: The future is nowJames J Dowling, Hernan D Gonorazky, Ronald D Cohn, et al.
Neurology|February 21, 2020
Drisapersen associated with elevated serum factor VIII levels in Duchenne muscular dystrophyHugh J McMillan, Ali Amid, Hernan Gonorazky, et al.
The Journal of Pediatrics|February 19, 2013
Congenital myotonic dystrophy: Canadian population-based surveillance studyCraig Campbell, Simon Levin, Victoria Mok Siu, et al.
Pageof 19

Showing results (41-50 of 188) with videos related to

Sort By:
Pageof 19
Pediatric Neurology|November 5, 2018
Twinkle-Associated Mitochondrial DNA DepletionSalma Remtulla, Cam-Tu Emilie Nguyen, Chitra Prasad, et al.
Biochemistry and Molecular Biology Education : a Bimonthly Publication of the International Union of Biochemistry and Molecular Biology|July 7, 2021
What biomedical education might learn from real estate toursMatthew Sellwood, Craig Campbell, Jim Cook, et al.
BMC Pediatrics|December 17, 2005
Subacute sclerosing panencephalitis: results of the Canadian Paediatric Surveillance Program and review of the literatureCraig Campbell, Simon Levin, Peter Humphreys, et al.
Journal of Neuromuscular Diseases|July 17, 2018
Prenatal, Neonatal, and Early Childhood Features in Congenital Myotonic DystrophyEugenio Zapata-Aldana, Delia Ceballos-Sáenz, Rhiannon Hicks, et al.
American Journal of Medical Genetics. Part A|April 3, 2019
Distal arthrogryposis type 5 and PIEZO2 novel variant in a Canadian familyEugenio Zapata-Aldana, Sulaiman B Al-Mobarak, Natalya Karp, et al.
Child Neurology Open|May 16, 2017
Seizures Related to Hypomagnesemia: A Case Series and Review of the LiteratureBecky Biqi Chen, Chitra Prasad, Marta Kobrzynski, et al.
Neuropediatrics|May 26, 2023
Duchenne Muscular Dystrophy Fatigue TrajectoriesYi Sally Wei, Mona Hnaini, Basmah ElAloul, et al.
American Journal of Medical Genetics. Part A|September 11, 2017
Treating pediatric neuromuscular disorders: The future is nowJames J Dowling, Hernan D Gonorazky, Ronald D Cohn, et al.
Neurology|February 21, 2020
Drisapersen associated with elevated serum factor VIII levels in Duchenne muscular dystrophyHugh J McMillan, Ali Amid, Hernan Gonorazky, et al.
The Journal of Pediatrics|February 19, 2013
Congenital myotonic dystrophy: Canadian population-based surveillance studyCraig Campbell, Simon Levin, Victoria Mok Siu, et al.
Pageof 19