Browsing by Author Hammans, Simon

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Issue DateTitleAuthor(s)Citation
2015Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathySue, Carolyn; Accarino, Anna; Bakker, Jaap A.; Barba, Pere; Beguin, Yves; Boelens, Jaap; Casali, C; Chinnery, Patrick F; Collin, Matthew; de Coo, Irenaeus F. M.; Dotti, Maria T.; Elhasid, R; Fay, Keith; Ferra, Chrristelle; Filosto, Massimiliano; Gratwohl, A.; Halter, Jörg; Hammans, Simon; Hirano, M; Illa, Isabel; M Sue, C; Mandel, Hanna; Marotta, Giuseppe; Marti, Ramon; Nachbaur, David; Orchard, Kim; Pinto Simoes, Belinda; Pintos, Guillem; Rovelli, Attilio; Savage, David; Schupbach, W. Michael M.; Sobreira, Claudia; Valcarel, David; Zoller, Heinz; Northern Clinical School: MedicineAllogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy, Brain, vol.138, 10, 2015,pp 2847-2858
2011Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing lossNicholson, Garth; Botuyan, Maria-Victoria; et al, various; Hammans, Simon; Hojo, Kaori; Karpf, Adam; Klein, Christopher; Simon, Mariella; Wallace, Douglas; Ward, Christopher; Wu, Yanhong; Yamanishi, Hiromitch; Concord Clinical School: ANZAC Research InstituteMutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss, Nature Genetics, vol.43, 6, 2011,pp 595-600
2014Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutationsClarke, Nigel; Waddell, Leigh Brook; et al, Various; Fellig, Yakov; Foulds, Nicola; Hammans, Simon; Katifi, Haider; Lindberg, Christopher; Lossos, Alexander; Mazanti, Ingrid; Tajsharghi, Homa; Webster, Richard; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthRecessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutations, European Journal of Human Genetics, vol.22, 6, 2014,pp 801-806