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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 mutation
Alan Ma, Anne Turner
The Medical Journal of Australia
|
March 16, 2023
Precision medicine in Australia: now is the time to get it right
Rosie 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 medicine
Lucy 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 sustainability
Alan Ma, Rosie O'Shea, Laura Wedd, et al.
Journal of Paediatrics and Child Health
|
February 20, 2014
CHARGE syndrome: a review
Peter Hsu, Alan Ma, Meredith Wilson, et al.
Journal of Paediatrics and Child Health
|
August 6, 2025
A Practical Guide to Genetic Eye Conditions for Paediatricians
Richard Lin, Alan Ma, Benjamin M Nash, et al.
Ophthalmic Genetics
|
June 10, 2025
Longitudinal study in autosomal recessive <i>PROM1</i> inherited retinal disease
William 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 Diseases
Deborah 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 Syndrome
Peter 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 study
Deborah Schofield, Joshua Kraindler, Owen Tan, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 40) with videos related to
Sort By:
Page
of 4
Journal of Paediatrics and Child Health
|
March 16, 2012
A life without pain: congenital insensitivity to pain due to compound heterozygous SCN9A mutation
Alan Ma, Anne Turner
The Medical Journal of Australia
|
March 16, 2023
Precision medicine in Australia: now is the time to get it right
Rosie 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 medicine
Lucy 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 sustainability
Alan Ma, Rosie O'Shea, Laura Wedd, et al.
Journal of Paediatrics and Child Health
|
February 20, 2014
CHARGE syndrome: a review
Peter Hsu, Alan Ma, Meredith Wilson, et al.
Journal of Paediatrics and Child Health
|
August 6, 2025
A Practical Guide to Genetic Eye Conditions for Paediatricians
Richard Lin, Alan Ma, Benjamin M Nash, et al.
Ophthalmic Genetics
|
June 10, 2025
Longitudinal study in autosomal recessive <i>PROM1</i> inherited retinal disease
William 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 Diseases
Deborah 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 Syndrome
Peter 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 study
Deborah Schofield, Joshua Kraindler, Owen Tan, et al.
Page
of 4