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Pediatric Neurology
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November 5, 2018
Twinkle-Associated Mitochondrial DNA Depletion
Salma 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 tours
Matthew 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 literature
Craig Campbell, Simon Levin, Peter Humphreys, et al.
Journal of Neuromuscular Diseases
|
July 17, 2018
Prenatal, Neonatal, and Early Childhood Features in Congenital Myotonic Dystrophy
Eugenio 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 family
Eugenio 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 Literature
Becky Biqi Chen, Chitra Prasad, Marta Kobrzynski, et al.
Neuropediatrics
|
May 26, 2023
Duchenne Muscular Dystrophy Fatigue Trajectories
Yi 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 now
James 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 dystrophy
Hugh J McMillan, Ali Amid, Hernan Gonorazky, et al.
The Journal of Pediatrics
|
February 19, 2013
Congenital myotonic dystrophy: Canadian population-based surveillance study
Craig Campbell, Simon Levin, Victoria Mok Siu, et al.
Page
of 19
Search research articles
Search
Showing results (41-50 of 188) with videos related to
Sort By:
Page
of 19
Pediatric Neurology
|
November 5, 2018
Twinkle-Associated Mitochondrial DNA Depletion
Salma 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 tours
Matthew 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 literature
Craig Campbell, Simon Levin, Peter Humphreys, et al.
Journal of Neuromuscular Diseases
|
July 17, 2018
Prenatal, Neonatal, and Early Childhood Features in Congenital Myotonic Dystrophy
Eugenio 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 family
Eugenio 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 Literature
Becky Biqi Chen, Chitra Prasad, Marta Kobrzynski, et al.
Neuropediatrics
|
May 26, 2023
Duchenne Muscular Dystrophy Fatigue Trajectories
Yi 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 now
James 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 dystrophy
Hugh J McMillan, Ali Amid, Hernan Gonorazky, et al.
The Journal of Pediatrics
|
February 19, 2013
Congenital myotonic dystrophy: Canadian population-based surveillance study
Craig Campbell, Simon Levin, Victoria Mok Siu, et al.
Page
of 19