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Epilepsy and paroxysmal conditions

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Vol 7, No 1 (2015) SEVERE EPILEPTIC ENCEPHALOPATHY OF EARLY CHILDHOOD DUE TO SCN2A MUTATION Abstract  similar documents
I. S. Bachtin, E. D. Belousova, P. A. Shatalov, S. O. Ayvazyan
"... SCN2A mutations are traditionally described in benign infantile seizures. We are describing rather ..."
 
Vol 7, No 2 (2015) NEUROLOGICAL PAROXYSMAL DISORDERS IN CHILDREN WITH HYPOGLYCEMIA IN CONGENITAL HYPERINSULINISM: POLYMORPHISM OF CLINICAL IMPLICATIONS Abstract  similar documents
I. O. Shchederkina, M. A. Melikyan, A. N. Zavadenko, E. V. Kozlova, N. N. Zavadenko
"... . Children with ABCC8 gene mutations have more complicated for CHI and more prominent developmental delay.  ..."
 
Vol 8, No 2 (2016) CLINICAL AND GENETIC HETEROGENITY OF JUVENILE MYOCLONIC EPILEPSY Abstract  similar documents
N. A. Shnayder, O. S. Shilkina, K. V. Petrov, I. A. Chernykh, A. V. Diuzhakova
 
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