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Treatment of HMG-CoA Lyase Deficiency-Longitudinal Data on Clinical and Nutritional Management of 10 Australian Cases.
Nutrients. 2023 Jan 19;15(3):531. doi: 10.3390/nu15030531.
Nutrients. 2023.
PMID: 36771238
Free PMC article.
Review.
The use of sodium DL-3-Hydroxybutyrate in severe acute neuro-metabolic compromise in patients with inherited ketone body synthetic disorders.
Bhattacharya K, Matar W, Tolun AA, Devanapalli B, Thompson S, Dalkeith T, Lichkus K, Tchan M.
Bhattacharya K, et al. Among authors: dalkeith t.
Orphanet J Rare Dis. 2020 Feb 18;15(1):53. doi: 10.1186/s13023-020-1316-x.
Orphanet J Rare Dis. 2020.
PMID: 32070364
Free PMC article.
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Liver transplantation in children with inborn errors of metabolism: 30 years experience in NSW, Australia.
Elserafy N, Thompson S, Dalkeith T, Stormon M, Thomas G, Shun A, Sawyer J, Balasubramanian S, Bhattacharya K, Badawi N, Ellaway C.
Elserafy N, et al. Among authors: dalkeith t.
JIMD Rep. 2021 May 4;60(1):88-95. doi: 10.1002/jmd2.12219. eCollection 2021 Jul.
JIMD Rep. 2021.
PMID: 34258144
Free PMC article.
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Diagnosis and management of children with McArdle Syndrome (GSD V) in New South Wales.
Adams L, Selvanathan A, Batten KJ, van Doorn N, Thompson S, Mitchell A, Sampaio H, Dalkeith T, Russell J, Ellaway CJ, Farrar M, Broderick C, Bhattacharya K.
Adams L, et al. Among authors: dalkeith t.
JIMD Rep. 2023 Aug 9;64(5):327-336. doi: 10.1002/jmd2.12389. eCollection 2023 Sep.
JIMD Rep. 2023.
PMID: 37701325
Free PMC article.
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Australian children living with rare diseases: experiences of diagnosis and perceived consequences of diagnostic delays.
Zurynski Y, Deverell M, Dalkeith T, Johnson S, Christodoulou J, Leonard H, Elliott EJ; APSU Rare Diseases Impacts on Families Study group.
Zurynski Y, et al. Among authors: dalkeith t.
Orphanet J Rare Dis. 2017 Apr 11;12(1):68. doi: 10.1186/s13023-017-0622-4.
Orphanet J Rare Dis. 2017.
PMID: 28399928
Free PMC article.
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Australian children living with rare diseases: health service use and barriers to accessing care.
Teutsch S, Zurynski Y, Eslick GD, Deverell M, Christodoulou J, Leonard H, Dalkeith T, Johnson SLJ, Elliott EJ.
Teutsch S, et al. Among authors: dalkeith t.
World J Pediatr. 2023 Jul;19(7):701-709. doi: 10.1007/s12519-022-00675-6. Epub 2023 Jan 18.
World J Pediatr. 2023.
PMID: 36653598
Free PMC article.
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Health-related out-of-pocket expenses for children living with rare diseases - tuberous sclerosis and mitochondrial disorders: A prospective pilot study in Australian families.
Deverell M, Phu A, Elliott EJ, Teutsch SM, Eslick GD, Stuart C, Murray S, Davis R, Dalkeith T, Christodoulou J, Zurynski YA.
Deverell M, et al. Among authors: dalkeith t.
J Paediatr Child Health. 2022 Apr;58(4):611-617. doi: 10.1111/jpc.15784. Epub 2021 Oct 27.
J Paediatr Child Health. 2022.
PMID: 34704652
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The first eighteen months of a paediatric ambulatory and community service.
Woolfenden SR, Dalkeith T, Anderson T.
Woolfenden SR, et al. Among authors: dalkeith t.
Aust Health Rev. 2005 Nov;29(4):429-34. doi: 10.1071/ah050429.
Aust Health Rev. 2005.
PMID: 16255707
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