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Title
Authors
Vol 17, No 3 (2022)
Sleep disorder in Angelman syndrome: causes, mechanisms and methods of correction. Literature review
Psyanchin A.A., Bobylova M.Y., Yakupov T.Z.
PDF
(Rus)
Vol 9, No 4 (2014)
DYSTONIA IN CHILDREN (A LECTURE)
Bobylova M.Y., Kakaulina V.S., Ilyina E.S., Nekrasova I.V., Pechatnikova N.L., Mikhailova S.V., Mironov M.B., Mukhin K.Y.
PDF
(Rus)
Vol 17, No 2 (2022)
Epileptic encephalopathy caused by 1p36 deletion: literature review and case series
Bobylova M.Y., Konurina O.V., Borovikova N.A., Chadaev V.A.
PDF
(Rus)
Vol 9, No 4 (2014)
ANALYSIS OF MAIN REASONS FOR MISTAKES IN DIAGNOSTICS OF EPILEPTIC SEIZURES AND EPILEPTIC SYNDROMES (CLINICAL PECULIARITIES OF EPILEPTIC SEIZURES)
Mironov M.B.
PDF
(Rus)
Vol 16, No 4 (2021)
Symptomatic non-convulsive status epilepticus in a patient with acute lymphoblastic leukemia (case report)
Zakharova A.Y., Bobylova M.Y.
PDF
(Rus)
Vol 9, No 3 (2014)
FOCAL EPILEPTIC MYOCLONUS: DIFFERENTIAL DIAGNOSIS AND PROGNOSIS
Kvaskova N.E., Mukhin K.Y., Mironov M.B.
PDF
(Rus)
Vol 16, No 3 (2021)
Mowat-Wilson syndrome: literature review and case series
Bobylova M.Y., Kakaulina V.S., Abramov M.O., Mukhin K.Y.
PDF
(Rus)
Vol 9, No 2 (2014)
THE DIAGNOSIS AND TREATMENT OF JEAVONS SYNDROME
Kulagin V.N., Mikhailichenko N.V.
PDF
(Rus)
Vol 15, No 3-4 (2020)
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.
PDF
(Rus)
Vol 9, No 1 (2014)
AN IMAGINARY WORSENING STATE IN EPILEPSY
Mironov M.B., Okuneva I.V., Mukhin K.Y.
PDF
(Rus)
Vol 11, No 1 (2016)
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.
PDF
(Rus)
Vol 19, No 3 (2024)
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.
PDF
(Rus)
Vol 10, No 4 (2015)
JUVENILE MYOCLONIC EPILEPSY: A FOCUS ON THE EFFICACY OF THERAPY AND THE RATE OF RELAPSES ACCORDING TO LONG-TERM FOLLOW-UP DATA
Mukhin K.Y., Freidkova N.V., Glukhova L.Y., Pylaeva O.A., Mironov M.B., Kvaskova N.E.
PDF
(Rus)
Vol 19, No 2 (2024)
Pontocerebellar hypoplasia caused by the TSEN54 mutation: clinical and electroencephalographic characteristics based on 3 cases
Bobylova M.Y., Abramov M.O., Mukhin K.Y.
PDF
(Rus)
Vol 10, No 3 (2015)
A CLINICAL CASE OF SYNGAP1 GENE MUTATION IN A GIRL WITH EPILEPSY, MENTAL RETARDATION, AUTISM, AND MOTOR DISORDERS
Bobylova M.Y., Mironov M.B., Abramov M.O., Kulikov A.V., Kazakova M.V., Glukhova L.Y., Barletova E.I., Mukhin K.Y.
PDF
(Rus)
1 - 15 of 15 Items

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