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Caroline Stuart

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The New Zealand Medical Journal|June 21, 2022
Knowledge and management of sport-related concussion in primary care in New ZealandCaroline Stuart, Duncan Reid, Alice Theadom, et al.
Molecular Genetics and Metabolism|April 28, 2004
Renal glucosuria due to SGLT2 mutationsRobert Kleta, Caroline Stuart, Fred A Gill, et al.
BMC Ophthalmology|June 26, 2004
Triple-A syndrome with prominent ophthalmic features and a novel mutation in the AAAS gene: a case reportBrian P Brooks, Robert Kleta, Rafael C Caruso, et al.
Nature Genetics|August 3, 2004
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorderRobert Kleta, Elisa Romeo, Zorica Ristic, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
The New Zealand Medical Journal|June 21, 2022
Knowledge and management of sport-related concussion in primary care in New ZealandCaroline Stuart, Duncan Reid, Alice Theadom, et al.
Molecular Genetics and Metabolism|April 28, 2004
Renal glucosuria due to SGLT2 mutationsRobert Kleta, Caroline Stuart, Fred A Gill, et al.
BMC Ophthalmology|June 26, 2004
Triple-A syndrome with prominent ophthalmic features and a novel mutation in the AAAS gene: a case reportBrian P Brooks, Robert Kleta, Rafael C Caruso, et al.
Nature Genetics|August 3, 2004
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorderRobert Kleta, Elisa Romeo, Zorica Ristic, et al.
Pageof 1