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Translational Pediatrics
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February 3, 2016
The evolution of blood-spot newborn screening
Kaustuv Bhattacharya, Tiffany Wotton, Veronica Wiley
JIMD Reports
|
February 23, 2013
Homocysteine measurement in dried blood spot for neonatal detection of homocystinurias
Ahmad N Alodaib, Kevin Carpenter, Veronica Wiley, et al.
Journal of Paediatrics and Child Health
|
December 4, 2024
Challenges in management of abnormal thyroid function tests in unwell infants: A tertiary centre real-world experience
Annabelle Hobbs, Michelle Jack, Paul Benitez-Aguirre, et al.
Children (Basel, Switzerland)
|
November 27, 2024
Newborn Genomic Sequencing Needs Confirmation but Not Repeating
Bruce Bennetts, Gladys Ho, Sarah Shin, et al.
International Journal of Neonatal Screening
|
October 19, 2020
Are We Ready for Fragile X Newborn Screening Testing?-Lessons Learnt from a Feasibility Study
Tiffany Wotton, Veronica Wiley, Bruce Bennetts, et al.
Brain & Development
|
May 8, 2023
Developmental delay and non-phenylketonuria (PKU) hyperphenylalaninemia in DNAJC12 deficiency: Case and approach
Rachel Sze Hui Wong, Shekeeb Mohammad, Bindu Parayil Sankaran, et al.
Molecular Therapy. Methods & Clinical Development
|
April 1, 2024
AAV-delivered hepato-adrenal cooperativity in steroidogenesis: Implications for gene therapy for congenital adrenal hyperplasia
Lara E Graves, Eva B van Dijk, Erhua Zhu, et al.
American Journal of Medical Genetics. Part A
|
January 11, 2013
Maternal attitudes to newborn screening for fragile X syndrome
Louise Christie, Tiffany Wotton, Bruce Bennetts, et al.
Clinical Chemistry and Laboratory Medicine
|
August 23, 2022
Fifty years of newborn screening for congenital hypothyroidism: current status in Australasia and the case for harmonisation
Tony Huynh, Ronda Greaves, Nazha Mawad, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 12, 2025
Targeted editing of the 21-hydroxylase locus confers durable therapeutic effect in a murine model of congenital adrenal hyperplasia
Lara E Graves, Lakshmy Viswanath, Eva B van Dijk, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Translational Pediatrics
|
February 3, 2016
The evolution of blood-spot newborn screening
Kaustuv Bhattacharya, Tiffany Wotton, Veronica Wiley
JIMD Reports
|
February 23, 2013
Homocysteine measurement in dried blood spot for neonatal detection of homocystinurias
Ahmad N Alodaib, Kevin Carpenter, Veronica Wiley, et al.
Journal of Paediatrics and Child Health
|
December 4, 2024
Challenges in management of abnormal thyroid function tests in unwell infants: A tertiary centre real-world experience
Annabelle Hobbs, Michelle Jack, Paul Benitez-Aguirre, et al.
Children (Basel, Switzerland)
|
November 27, 2024
Newborn Genomic Sequencing Needs Confirmation but Not Repeating
Bruce Bennetts, Gladys Ho, Sarah Shin, et al.
International Journal of Neonatal Screening
|
October 19, 2020
Are We Ready for Fragile X Newborn Screening Testing?-Lessons Learnt from a Feasibility Study
Tiffany Wotton, Veronica Wiley, Bruce Bennetts, et al.
Brain & Development
|
May 8, 2023
Developmental delay and non-phenylketonuria (PKU) hyperphenylalaninemia in DNAJC12 deficiency: Case and approach
Rachel Sze Hui Wong, Shekeeb Mohammad, Bindu Parayil Sankaran, et al.
Molecular Therapy. Methods & Clinical Development
|
April 1, 2024
AAV-delivered hepato-adrenal cooperativity in steroidogenesis: Implications for gene therapy for congenital adrenal hyperplasia
Lara E Graves, Eva B van Dijk, Erhua Zhu, et al.
American Journal of Medical Genetics. Part A
|
January 11, 2013
Maternal attitudes to newborn screening for fragile X syndrome
Louise Christie, Tiffany Wotton, Bruce Bennetts, et al.
Clinical Chemistry and Laboratory Medicine
|
August 23, 2022
Fifty years of newborn screening for congenital hypothyroidism: current status in Australasia and the case for harmonisation
Tony Huynh, Ronda Greaves, Nazha Mawad, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 12, 2025
Targeted editing of the 21-hydroxylase locus confers durable therapeutic effect in a murine model of congenital adrenal hyperplasia
Lara E Graves, Lakshmy Viswanath, Eva B van Dijk, et al.
Page
of 2