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Alan Ma

Showing results (1-10 of 40) with videos related to

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Journal of Paediatrics and Child Health|March 16, 2012
A life without pain: congenital insensitivity to pain due to compound heterozygous SCN9A mutationAlan Ma, Anne Turner
The Medical Journal of Australia|March 16, 2023
Precision medicine in Australia: now is the time to get it rightRosie O'Shea, Alan Ma, Robyn Jamieson, et al.
Seizure|March 21, 2020
Vaccination management in an asymptomatic child with a novel SCN1A variant and family history of status epilepticus following vaccination: A case report on a potential new direction in personalised medicineLucy Deng, Alan Ma, Nicholas Wood, et al.
European Journal of Human Genetics : EJHG|February 20, 2024
What is the power of a genomic multidisciplinary team approach? A systematic review of implementation and sustainabilityAlan Ma, Rosie O'Shea, Laura Wedd, et al.
Journal of Paediatrics and Child Health|February 20, 2014
CHARGE syndrome: a reviewPeter Hsu, Alan Ma, Meredith Wilson, et al.
Journal of Paediatrics and Child Health|August 6, 2025
A Practical Guide to Genetic Eye Conditions for PaediatriciansRichard Lin, Alan Ma, Benjamin M Nash, et al.
Ophthalmic Genetics|June 10, 2025
Longitudinal study in autosomal recessive <i>PROM1</i> inherited retinal diseaseWilliam B Yates, John R Grigg, Benjamin M Nash, et al.
Ophthalmology Science|October 17, 2022
Patient-Reported Health-Related Quality of Life in Individuals with Inherited Retinal DiseasesDeborah Schofield, Joshua Kraindler, Owen Tan, et al.
The Journal of Allergy and Clinical Immunology. in Practice|November 14, 2015
The Immune Phenotype of Patients with CHARGE SyndromePeter Hsu, Alan Ma, Elizabeth H Barnes, et al.
The Medical Journal of Australia|June 10, 2023
The health care and societal costs of inherited retinal diseases in Australia: a microsimulation modelling studyDeborah Schofield, Joshua Kraindler, Owen Tan, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Journal of Paediatrics and Child Health|March 16, 2012
A life without pain: congenital insensitivity to pain due to compound heterozygous SCN9A mutationAlan Ma, Anne Turner
The Medical Journal of Australia|March 16, 2023
Precision medicine in Australia: now is the time to get it rightRosie O'Shea, Alan Ma, Robyn Jamieson, et al.
Seizure|March 21, 2020
Vaccination management in an asymptomatic child with a novel SCN1A variant and family history of status epilepticus following vaccination: A case report on a potential new direction in personalised medicineLucy Deng, Alan Ma, Nicholas Wood, et al.
European Journal of Human Genetics : EJHG|February 20, 2024
What is the power of a genomic multidisciplinary team approach? A systematic review of implementation and sustainabilityAlan Ma, Rosie O'Shea, Laura Wedd, et al.
Journal of Paediatrics and Child Health|February 20, 2014
CHARGE syndrome: a reviewPeter Hsu, Alan Ma, Meredith Wilson, et al.
Journal of Paediatrics and Child Health|August 6, 2025
A Practical Guide to Genetic Eye Conditions for PaediatriciansRichard Lin, Alan Ma, Benjamin M Nash, et al.
Ophthalmic Genetics|June 10, 2025
Longitudinal study in autosomal recessive <i>PROM1</i> inherited retinal diseaseWilliam B Yates, John R Grigg, Benjamin M Nash, et al.
Ophthalmology Science|October 17, 2022
Patient-Reported Health-Related Quality of Life in Individuals with Inherited Retinal DiseasesDeborah Schofield, Joshua Kraindler, Owen Tan, et al.
The Journal of Allergy and Clinical Immunology. in Practice|November 14, 2015
The Immune Phenotype of Patients with CHARGE SyndromePeter Hsu, Alan Ma, Elizabeth H Barnes, et al.
The Medical Journal of Australia|June 10, 2023
The health care and societal costs of inherited retinal diseases in Australia: a microsimulation modelling studyDeborah Schofield, Joshua Kraindler, Owen Tan, et al.
Pageof 4