Browsing by Author Walizada, Gina

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Issue DateTitleAuthor(s)Citation
2005Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations.Kennerson, Marina; Nicholson, Garth; Walizada, Gina; Zhu, Danqing; Vance, J. M.; Züchner, Stephan; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Central Clinical School: Medicine; Concord Clinical School: MedicineCharcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations., NEUROLOGY 2005, vol.65,(3),2005,pp 496-497
2010GATA4 Mutations in 357 Unrelated Patients with Congenital Heart MalformationButler, Tanya; Sholler, Gary; Winlaw, David; Blue, Gillian; Cole, Andrew; Costa, Mauro; Esposito, Giorgia; Feneley, Michael; Harvey, Richard P; Kirk, E. P. E.; Waddell, Leigh; Walizada, Gina; Children's Hospital Westmead: Paediatrics & Child Health; Medical Radiation Sciences; Children's Hospital Westmead: Paediatrics & Child HealthGATA4 Mutations in 357 Unrelated Patients with Congenital Heart Malformation, Genetic Testing and Molecular Biomarkers, vol.14, 6,pp 1-6
2005Mild early onset axonal Charcot-Marie-Tooth disease not linked to other axonal Charcot-Marie-Tooth loci.Kennerson, Marina; Nicholson, Garth; Walizada, Gina; Hausmanowa-Petrusewicz, I.; Kawulak, M.; Kochanski, A.; Nowakowski, A.; Rowinska-Marcinska, K.; Ryniewicz, B.; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Central Clinical School: MedicineMild early onset axonal Charcot-Marie-Tooth disease not linked to other axonal Charcot-Marie-Tooth loci., Neurology, vol.64,(3),2005,pp 533-535
2005Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.Kennerson, Marina; Nicholson, Garth; Walizada, Gina; Zhu, Danqing; Claeys, Kristl; De Jonghe, Peter; et, al; Merory, John; Noureddine, Maher; Oliveira, Sofia A.; Speer, Marcy C.; Stenger, Judith E.; Verhoeven, Kristien; Züchner, Stephan; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Central Clinical School: Medicine; Concord Clinical School: MedicineMutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease., Nature Genetics, vol.37,(3),2005,pp 289-294