Browsing by Author Kornberg, Andrew J.

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 5 of 5
Issue DateTitleAuthor(s)Citation
2009Ascorbic acid for Charcot-Marie-Tooth disease type 1A in children: a randomised, double-blind, placebo-controlled, safety and efficacy trialBurns, Joshua; Ouvrier, Robert; Fahey, Michael; Joseph, Pathma; Kornberg, Andrew J.; Ryan, Monique; Yiu, Eppie M.; Clinical and Rehabilitation Sciences; Children's Hospital Westmead: Paediatrics & Child HealthAscorbic acid for Charcot-Marie-Tooth disease type 1A in children: a randomised, double-blind, placebo-controlled, safety and efficacy trial, Lancet Neurology, vol.8, 6, 2009,pp 537-544
2009Cap disease due to mutation of the beta-tropomyosin gene (TPM2)Clarke, Nigel; Domazetovska, Ana; North, Kathryn; Waddell, Leigh; Kornberg, Andrew J.; McLean, Catriona A.; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthCap disease due to mutation of the beta-tropomyosin gene (TPM2), Neuromuscular Disorders, vol.19, 5,pp 348-351
2006A clinical and pathological study of congenital fibre type disproportionArbuckle, Susan; Clarke, Nigel; North, Kathryn; Beggs, A; Dennett, X; Ferreiro, Ana; Gonzalez, V; Guicheney, Pascale; Kornberg, Andrew J.; Manson, James I.; Nonaka, I; Shield, Lloyd K.; Smith, R; Children's Hospital Westmead: Medicine; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthA clinical and pathological study of congenital fibre type disproportion, Neuromuscular Disorders, vol.16,(9-10),2006,pp 646-646
2010Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3Clarke, Nigel; North, Kathryn; Waddell, Leigh; Kennedy, Paul; Kornberg, Andrew J.; Kreissl, Michaela; Labarre-Vila, Annick; McLean, Catriona A.; Monnier, Nicole; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthEvidence for a dominant negative disease mechanism in cap myopathy due to TPM3, Neuromuscular Disorders, vol.20, N/A,pp 464-466
2006SEPN1: associated with congenital fiber-type disproportion and insulin resistance.Clarke, Nigel; North, Kathryn; Estournet, Brigitte; Ferreiro, Ana; Guicheney, Pascale; Kidson, Warren; Kornberg, Andrew J.; Manson, James I.; Quijano-Roy, Susana; Shield, Lloyd K.; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthSEPN1: associated with congenital fiber-type disproportion and insulin resistance., Annals of Neurology, vol.59,(3),2006,pp 546-552