Martin B Delatycki

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Credit Name
Martin B Delatycki
Full Name
Delatycki, Martin B
 
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Publications

Results 61-70 of 70 (Search time: 0.01 seconds).

Publication YearTitleAuthor(s)
6128-Sep-2014Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features.Lessel, Davor; Vaz, Bruno; Halder, Swagata; Lockhart, Paul J; Marinovic-Terzic, Ivana; Lopez-Mosqueda, Jaime; Philipp, Melanie; Sim, Joe C H; Smith, Katherine R; Oehler, Judith; Cabrera, Elisa; Freire, Raimundo; Pope, Kate; Nahid, Amsha; Norris, Fiona; Leventer, Richard J; Delatycki, Martin B ; Barbi, Gotthold; von Ameln, Simon; Högel, Josef; Degoricija, Marina; Fertig, Regina; Burkhalter, Martin D; Hofmann, Kay; Thiele, Holger; Altmüller, Janine; Nürnberg, Gudrun; Nürnberg, Peter; Bahlo, Melanie; Martin, George M; Aalfs, Cora M; Oshima, Junko; Terzic, Janos; Amor, David John; Dikic, Ivan; Ramadan, Kristijan; Kubisch, Christian
6211-Aug-2014A study of up to 12 years of follow-up of Friedreich ataxia utilising four measurement tools.Tai, Geneieve; Corben, Louise A; Gurrin, Lyle; Yiu, Eppie M; Churchyard, Andrew; Fahey, Michael; Hoare, Brian; Downie, Sharon; Delatycki, Martin B 
632-Jun-2014Myelin paucity of the superior cerebellar peduncle in individuals with Friedreich ataxia: an MRI magnetization transfer imaging study.Corben, Louise A; Kashuk, Saman R; Akhlaghi, Hamed; Jamadar, Sharna; Delatycki, Martin B ; Fielding, Joanne; Johnson, Beth; Georgiou-Karistianis, Nellie; Egan, Gary F
6419-Apr-2014Saccade reprogramming in Friedreich ataxia reveals impairments in the cognitive control of saccadic eye movement.Hocking, Darren R; Corben, Louise A; Fielding, Joanne; Cremer, Phillip D; Millist, Lynette; White, Owen B; Delatycki, Martin B 
653-Jan-2014HFE p.C282Y heterozygosity is associated with earlier disease onset in Friedreich ataxia.Delatycki, Martin B ; Tai, Geneieve; Corben, Louise A; Yiu, Eppie M; Evans-Galea, Marguerite V; Stephenson, Sarah E M; Gurrin, Lyle; Allen, Katrina J; Lynch, David; Lockhart, Paul J
6620-Nov-2013Attitudes and opinions of pregnant women who are not offered cystic fibrosis carrier screening.Ioannou, Liane; Massie, John; Lewis, Sharon; Collins, Veronica; McClaren, Belinda; Delatycki, Martin B 
679-Oct-2013Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome.Wilson, Gabrielle R; Sunley, Jasmine; Smith, Katherine R; Pope, Kate; Bromhead, Catherine J; Fitzpatrick, Elizabeth; Di Rocco, Maja; van Steensel, Maurice; Coman, David J; Leventer, Richard J; Delatycki, Martin B ; Amor, David John; Bahlo, Melanie; Lockhart, Paul J
6812-Sep-2013Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research.Ioannou, Liane; McClaren, Belinda J; Massie, John; Lewis, Sharon; Metcalfe, Sylvia A; Forrest, Laura; Delatycki, Martin B 
691-Feb-2012The ethics of screening for disease.Delatycki, Martin B 
702-Aug-2010Ethical considerations in choosing a model for population-based cystic fibrosis carrier screening.Modra, Lucy J ; Massie, R John; Delatycki, Martin B