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Treatment of an infant with X-linked severe combined immunodeficiency (SCID-X1) by gene therapy in Australia.
Ginn SL, Curtin JA, Kramer B, Smyth CM, Wong M, Kakakios A, McCowage GB, Watson D, Alexander SI, Latham M, Cunningham SC, Zheng M, Hobson L, Rowe PB, Fischer A, Cavazzana-Calvo M, Hacein-Bey-Abina S, Alexander IE. Ginn SL, et al. Among authors: curtin ja. Med J Aust. 2005 May 2;182(9):458-63. doi: 10.5694/j.1326-5377.2005.tb06785.x. Med J Aust. 2005. PMID: 15865589
ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder.
Williams LB, Javed A, Sabri A, Morgan DJ, Huff CD, Grigg JR, Heng XT, Khng AJ, Hollink IHIM, Morrison MA, Owen LA, Anderson K, Kinard K, Greenlees R, Novacic D, Nida Sen H, Zein WM, Rodgers GM, Vitale AT, Haider NB, Hillmer AM, Ng PC, Shankaracharya, Cheng A, Zheng L, Gillies MC, van Slegtenhorst M, van Hagen PM, Missotten TOAR, Farley GL, Polo M, Malatack J, Curtin J, Martin F, Arbuckle S, Alexander SI, Chircop M, Davila S, Digre KB, Jamieson RV, DeAngelis MM. Williams LB, et al. Genet Med. 2019 Sep;21(9):2103-2115. doi: 10.1038/s41436-019-0476-3. Epub 2019 Apr 10. Genet Med. 2019. PMID: 30967659 Free PMC article.
Immune tolerance induction using a factor VIII/von Willebrand factor concentrate (BIOSTATE), with or without immunosuppression, in Australian paediatric severe haemophilia A patients with high titre inhibitors: a multicentre, retrospective study.
Robertson JD, Higgins P, Price J, Dunkley S, Barrese G, Curtin J. Robertson JD, et al. Thromb Res. 2014 Nov;134(5):1046-51. doi: 10.1016/j.thromres.2014.09.010. Epub 2014 Sep 21. Thromb Res. 2014. PMID: 25267706 Free article.
Challenges in hemophilia care in Australia and New Zealand.
Brown SA, Phillips J, Barnes C, Curtin J, McRae S, Ockelford P, Rowell J, Smith MP, Dunkley S. Brown SA, et al. Curr Med Res Opin. 2015 Nov;31(11):1985-91. doi: 10.1185/03007995.2015.1082990. Epub 2015 Oct 2. Curr Med Res Opin. 2015. PMID: 26296234
110 results