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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.
LANDAU–KLEFFNER SYNDROME (ACQUIRED EPILEPTIC APHASIA) WITH A FOCUS ON ELECTROENCEPHALOGRAPHIC CRITERIA
Mukhin K.Y.
MAJOR PRINCIPLES OF EPILEPSY TREATMENT. ALGORITHM OF SELECTION OF ANTIEPILEPTIC DRUGS
Mukhin K.Y., Pylaeva O.A., Glukhova L.Y., Mironov M.B., Bobylova M.Y.
RUFINAMIDE (INOVELON) IN THE TREATMENT OF LENNOX–GASTAUT SYNDROME (A REVIEW OF LITERATURE AND CLINICAL CASE)
Mukhin K.Y., Pylaeva O.A.
RUFINAMIDE IN THE TREATMENT OF LENNOX–GASTAUT SYNDROME: REVIEW OF FOREIGN LITERATURE
Mukhin K.Y., Pylaeva O.A.
Early infantile epileptic encephalopathy in the structure of microcephaly-capillary malformation syndrome: a clinical case
Maslov M.S., Sviridova A.M., Zalevskaya M.A.
Modern approaches in the treatment of Lennox–gastaut syndrome (a review of literature)
Мukhin К.Y., Pylaeva О.A.
Rufinamide (inovelon) in the treatment of Lennox–gastaut syndrome (a review of literature)
Мukhin К.Y., Pylaeva О.A.
FOCAL EPILEPTIC MYOCLONUS IN KOZHEVNIKOV–RASMUSSEN SYNDROME
Kvaskova N.E., Mukhin K.Y.
PSEUDO-LENNOX SYNDROME: CLINICAL AND ELECTROENCEPHALOGRAPHIC CHARACTERISTICS
Mukhin K.Y.
EPILEPTIC SPASMS
Mukhin K.Y., Mironov M.B.
A case of inversion of chromosome 4 and an unbalanced transloca- tion between the short arm of chromosome 4 and long arm of chromosome 18 in a girl: evolution of clinical and electroencephalographic manifestations
Bobylova M.Y., Abramov M.O., Kovalskaya A.V., Alikhanov A.A., Mukhin K.Y.
A rare case of Cohen syndrome and early infantile epileptic encephalopathy (type 52) in two-year-old girl
Olshanskaya A.S., Dyuzhakova A.V., Shnayder N.A., Dmitrenko D.V.
CURRENT APPROACHES TO THERAPY OF RETT’S SYNDROME (A REVIEW OF LITERATURE)
Borovikova N.Y., Bobylova M.Y.
THE DIAGNOSIS AND TREATMENT OF JEAVONS SYNDROME
Kulagin V.N., Mikhailichenko N.V.
CLINICAL AND ENCEPHALOGRAPHIC CHANGES AT LENNOX–GASTAUT SYNDROME
Mukhin K.Y.
Epileptic encephalopathy caused by 1p36 deletion: literature review and case series
Bobylova M.Y., Konurina O.V., Borovikova N.A., Chadaev V.A.
Kleefstra syndrome and epilepsy
Gamirova R.G., Lyukshina N.G., Gamirova R.R., Farnosova M.E.
Modern neurogenetic representations of MELAS syndrome. Clinical cases (the lecture)
Shatalin A.V., Mukhina E.V., Kotov A.S., Amirkhanyan M.G.
EPILEPSY IN 11 PATIENTS WITH TYPICAL RETT SYNDROME CAUSED BY MECP2 MUTATION: CLINICAL AND ELECTROENCEPHALOGRAPHIC CHARACTERISTICS, COURSE, THERAPY (RESULTS OF THE AUTHORS’ OBSERVATIONS)
Bobylova M.Y., Mukhin K.Y., Ivanova I.V., Nekrasova I.V., Pylaeva O.A., Borovikova N.Y., Il’ina E.S.
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