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2. De NovoSCN8A Mutation Identified by Whole-Exome Sequencing in a Boy With Neonatal Epileptic Encephalopathy, Multiple Congenital Anomalies, and Movement Disorders. (December 2014)

5. Long-term neurodevelopmental outcome after perinatal arterial ischemic stroke and periventricular venous infarction. (November 2018)

6. Low Serum IGF-1 in Boys with Recent Onset of Juvenile Idiopathic Arthritis. (28th November 2018)

7. Mutations in GABRB3: From febrile seizures to epileptic encephalopathies. (31st January 2017)

8. Mutations in GABRB3: From febrile seizures to epileptic encephalopathies. (31st January 2017)

9. Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathies. (13th September 2016)