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Developmental encephalopathy and epilepsy associated with a heterozygous de novo mutation in the IRF2BPL gene: a case report
Lyukshina N.G., Sharkov A.A., Tolmacheva E.N.
Genetic epilepsy caused by CDKL5 gene mutations as an example of epileptic encephalopathy and developmental encephalopathy: literature review and own observations
Mukhin K.Y., Pylaeva O.A., Bobylova M.Y., Chadaev V.A.
Experience with the use of a ketogenic diet with type 1 glucose transporter deficiency (De Vivo disease)
Lyukshina N.G.
Epileptic encephalopathy caused by 1p36 deletion: literature review and case series
Bobylova M.Y., Konurina O.V., Borovikova N.A., Chadaev V.A.
Pontocerebellar hypoplasia caused by the TSEN54 mutation: clinical and electroencephalographic characteristics based on 3 cases
Bobylova M.Y., Abramov M.O., Mukhin K.Y.
Comorbidity of cerebral palsy and epilepsy with autism in children
Abusueva B.A., Askevova M.A., Shanavazova M.D., Nasrutdinova B.M., Bobylova M.Y., Gadzhieva A.S.
Dynamics of management of monogenic epilepsies, developmental and epileptic encephalopathies in routine clinical practice
Rakhmanina О.A., Volkov I.V., Tomenko Т.R., Shestakova O.I., Volkova О.К.
The case of development and epileptic encephalopathy with spike-wave activation in sleep in a boy with Smith–Magenis syndrome
Bobylova M.Y., Аbramov M.O., Pylaeva O.A., Мukhin K.Y., Petrukhin A.S.
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