FOCAL CORTICAL DYSPLASIA: ALGORITHM OF PREOPERATIVE EXAMINATION

Por S. O. Ayvazyan
Publicado em 2016-09-01

COMORBIDITY IN HEMICONVULSION-HEMIPLEGIA-EPILEPSY SYNDROME IN CHILDREN

Por S. O. Ayvazyan
Publicado em 2018-05-01

MODERN TREATMENT OF DRUG-RESISTANT EPILEPSY, AVAILABLE IN RUSSIAN

Por S. O. Ayvazyan, Yu. S. Shiryaev
Publicado em 2016-06-01

SEVERE EPILEPTIC ENCEPHALOPATHY OF EARLY CHILDHOOD DUE TO SCN2A MUTATION

Por I. S. Bachtin, E. D. Belousova, P. A. Shatalov, S. O. Ayvazyan
Publicado em 2016-05-01

Significance of exome sequencing for diagnosis of epilepsy in children

Por T. V. Kozhanova, S. S. Zhilina, T. I. Meshheryakova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko
Publicado em 2020-01-01

EFFECT OF KETOGENIC DIET ON COGNITIVE AND MOTOR FUNCTIONS IN CHILDREN WITH DRUG-RESISTANT EPILEPSY

Por E. G. Lukyanova, S. O. Ayvazyan, K. V. Osipova, T. N. Sorvacheva, E. A. Pyreva
Publicado em 2016-06-01

Mutation of the ALDH7A1 gene in a patient with pyridoxal phosphate-dependent neonatal epileptic encephalopathy: a clinical case

Por T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, E. G. Lukyanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko
Publicado em 2019-04-01

Helsmoortel-van der Aa syndrome syndrome in a patient with epilepsy, developmental delay, intellectual disability, and autism spectrum disorder

Por T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, E. G. Luk`yanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko
Publicado em 2020-04-01

Clinical case of epilepsy, hearing loss and mental retardation syndrome associated with mutations in SPATA5 gene

Por T. V. Kozhanova, S. S. Zhilina, T. I. Meshcheryakova, E. G. Luk’yanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko, N. N. Zavadenko
Publicado em 2021-04-01

Epilepsy combined with Wolf-Hirschhorn syndrome: a literature review and description of clinical cases

Por M. B. Mironov, N. V. Chebanenko, S. O. Ayvazyan, S. A. Vladimirova, K. V. Osipova, S. G. Burd, Yu. V. Rubleva, T. M. Krasilshchikova, V. G. Bychenko
Publicado em 2019-03-01