Browsing by Author Kurian, Manju

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Issue DateTitleAuthor(s)Citation
2017Not all SCN1A epileptic encephalopathies are Dravet syndromeGill, Deepak; Davis, Suzanne; DeVile, Catherine; et al, Various; Joshi, Charuta; Kurian, Manju; Mandalstem, Simone; Mountier, Emily; Murali, Hema; Nickels, Katherine; Sadleir, Lynette; Wirrell, Elaine; Westmead Clinical School: MedicineNot all SCN1A epileptic encephalopathies are Dravet syndrome, Neurology, vol.89, 10, 2017,pp 1035-1042
2012PRRT2 gene mutations: From paroxysmal dyskinesia to episodic ataxia and hemiplegic migraineDale, Russell; Bhatia, Kailash P; Counihan, Tim; et al, Various; Gardiner, Alice; Kurian, Manju; Schapira, Anthony H V; Schneider, Susanne; Spacey, Sian D.; Stamelou, Maria; Valente, Enza-Maria; Wali, G; Children's Hospital Westmead: Paediatrics & Child HealthPRRT2 gene mutations: From paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine, Neurology, vol.79, 21, 2012,pp 2115-2121
2014A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1Dale, Russell; Gill, Deepak; Brogan, Paul; De Goede, Christian G E L; et al, Various; Falconer, Alistair; Forte, Gabriella M A; Gonzalez-Martinez, Victoria; Kurian, Manju; Lin, Jean-Pierre; Livingston, John H; Munnich, Arnold; Childrens Hospital Westmead: Paediatrics & Child Health; Western Clinical School: Medicine (Westmead)A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1, Journal of Medical Genetics, vol.51, 2, 2014,pp 76-82