Browsing by Author Nishino, Ichizo

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Issue DateTitleAuthor(s)Citation
2004Actin Mutations Are One Cause Of Congenital Fibre Type Disproportion.Clarke, Nigel; North, Kathryn; Ouvrier, Robert; Dye, Danielle E; Hagiwara, Tohru; Kobayashi, Yasuaki; Laing, Nigel G; Liyanage, Khema; Nishino, Ichizo; Nonaka, Ikuya; Shimakawa, Shuichi; Sparrow, John C; Walker, Kendall R; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthActin Mutations Are One Cause Of Congenital Fibre Type Disproportion., Annals of Neurology, vol.56,(5),2004,pp 689-694
2012Clinical utility gene card for: Centronuclear and myotubular myopathiesNorth, Kathryn; Beggs, Alan H.; Biancalana, Valerie; Das, Soma; Jungbluth, Heinz; Kress, Wolfram; Laporte, Jocelyn; Nishino, Ichizo; Romero, Norma; Children's Hospital Westmead: Paediatrics & Child HealthClinical utility gene card for: Centronuclear and myotubular myopathies, European Journal of Human Genetics, vol.20, 10, 2012,pp 1-5
2007Distinctive patterns of microRNA expression in primary muscular disorders.North, Kathryn; Amato, Anthony; Beggs, Alan H.; Eisenberg, Iris; Eran, Alal; Flanigan, Kevin M.; Kang, Peter; Kohane, Isaac S.; Kunkel, Louis M.; Lamperti, Costanza; Lidov, Hart; Mitrani-Rosenbaum, Stella; Moggio, Maurizio; Neely, Lori A.; Nishino, Ichizo; Whitney, Duncan; Children's Hospital Westmead: Paediatrics & Child HealthDistinctive patterns of microRNA expression in primary muscular disorders., National Academy of Sciences 2005, vol.104,(43),2007,pp 17016-17021