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Vol 14, No 2 (2019)

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.

(Rus)

Vol 11, No 1 (2016)

ORNITHINE TRANSCARBAMYLASE DEFICIENCY – THE REAL CAUSE OF “FAMILY CURSE”. A CASE REPORT

Bagomedova Z.S., Kotov A.S., Borisova M.N., Panteleeva M.V., Zhurkova N.V., Byome A.A., Kotalevskaya Y.Y., Mironova O.S., Razheva I.V.

(Rus)

Vol 7, No 1 (2012)

COGNITIVE EPILEPTIFORM DISINTEGRATION: DEFINITION, DIAGNOSIS, THERAPY

Mukhin K.Y.

(Rus)

Vol 9, No 2 (2014)

THE CLINICAL, ELECTROENCEPHALOGRAPHIC, AND NEUROIMAGING CHARACTERISTICS OF PATIENTS WITH EPILEPTIC EYELID MYOCLONIA

Mironov M.B., Mukhin K.Y.

(Rus)

Vol 20, No 2 (2025)

Balo’s concentric sclerosis. A lecture describing six clinical cases

Benidze А.А., Kotov А.S., Ovchinnikova E.O., Syanov S.A., Peshkin A.N.

(Rus)

Vol 14, No 2 (2019)

Difficulties of diagnostics of epilepsy due to molybdenum cofactor deficiency: a case report

Malov A.G., Karakulova Y.V., Severino M., Kravtsov Y.I.

(Rus)

Vol 11, No 1 (2016)

PSEUDO-LENNOX SYNDROME: CLINICAL AND ELECTROENCEPHALOGRAPHIC CHARACTERISTICS

Mukhin K.Y.

(Rus)

Vol 10, No 2 (2015)

ATTENTION DEFICIT HYPERACTIVITY DISORDER: COMORBIDITIES, EMPHASIS ON CONCURRENCE WITH EPILEPSY

Pylaeva O.A., Shatenshtein A.A., Dorofeeva M.Y., Mukhin K.Y.

(Rus)

Vol 19, No 4 (2024)

Cerebral palsy: current status of the problem (review of literature)

Kolesnikova E.V., Vyshlova I.A., Karpov S.M., Soboleva O.A.

(Rus)

Vol 13, No 3 (2018)

Attention deficit hyperactivity disorder: concomitant diseases with an emphasis on epilepsy

Pylaeva O.A., Shatenshtein A.A., Mukhin K.Y.

(Rus)

Vol 10, No 4 (2015)

PSEUDOTUMORAL FORM OF MULTIPLE SCLEROSIS WITH SYMPTOMATIC CONVULSIVE SEIZURES (A CLINICAL CASE)

Belova Y.A., Yakushina T.I., Rudakova I.G.

(Rus)

Vol 10, No 2 (2015)

THE INCIDENCE OF JUVENILE MYOCLONIC EPILEPSY AND ANALYSIS OF ITS THERAPY ACCORDING TO THE DATA OF THE “EPICENTER” (VOLGOGRAD)

Belyaev O.V., Volkova E.A.

(Rus)

Vol 19, No 3 (2024)

Balo’s concentric sclerosis: nosological affiliation, diagnostic criteria and treatment approaches Lecture with a description of a clinical case

Benidze A.A., Kotov A.S.

(Rus)

Vol 13, No 1 (2018)

Problems of differential diagnosis of myoclon us-epilepsy associated with the mutation of the POLG gene and juvenile myoclonic epilepsy: a clinical case

Shilkina O.S., Shnayder N.A., Artyukhov I.P., Moskaleva P.V., Panina Y.S.

(Rus)

Vol 7, No 4 (2012)

OUTCOME AND TRANSFORMATION OF FEBRILE SEIZURES IN CHILDREN (DATA OF SVT. LUKA'S INSTITUTE OF CHILD NEUROLOGY & EPILEPSY)

Mironov M.B., Mukhin K.Y.

(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.

(Rus)

Vol 19, No 1 (2024)

Identification of patients with orfan pathology as a result of routine creatine phosphokinase level analysis. The experience of the Krasnoyarsk Territory

Shishkina E.V.

(Rus)

Vol 12, No 2 (2017)

NEUROFIBROMATOSIS TYPE 1 OR GIANT MELANOCYTIC NEVUS: PROBLEMS OF DIAGNOSTIC

Ol’shanskaya A.S., Dyuzhakova A.V., Artyukhov I.P., Shnayder N.A., Dmitrenko D.V., Karacheva Y.V.

(Rus)

Vol 7, No 3 (2012)

ARTIFACTS ON EEG: IDENTIFICATION AND DIFFERENTIAL DIAGNOSIS

Guljaev S.A., Arkhipenko I.V.

(Rus)

Vol 9, No 4 (2014)

EPILEPTIC SPASMS

Mukhin K.Y., Mironov M.B.

(Rus)

Vol 18, No 4 (2023)

The modern approaches to the diagnostics and treatment of Lennox–Gastaut syndrome (literature review)

Mukhin K.Y., Pylaeva O.A.

(Rus)

Vol 11, No 3 (2016)

THE MITOCHONDRIAL DISEASE NARP SYNDROME IN THE PRACTICE OF A PEDIATRIC NEUROLOGIST

Shishkina E.V., Barkhatov M.V., Borisova E.V., Falalaleeva S.O., Shchekaleva N.A., Makarevskaya N.Y., Chubko M.A.

(Rus)

Vol 8, No 1 (2013)

EVOLUTION OF HYPERKINESIS DURING THE COURSE OF DISEASES IN CHILDREN (A REVIEW, OWN RESULTS)

Bobylova M.Y.

(Rus)

Vol 9, No 4 (2014)

ELECTROENCEPHALOGRAPHIC CHANGES WITH DRAVET SYNDROME

Mukhin K.Y., Pylaeva O.A., Mironov M.B., Dolinina A.F., Morozov D.V., Nikitina M.A.

(Rus)

Vol 16, No 1-2 (2021)

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.

(Rus)

Vol 11, No 3 (2016)

MODERN TECHNOLOGIES IN THE DIAGNOSIS OF THE VISION ORGAN PATHOLOGY IN PATIENTS WITH NEUROFIBROMATOSIS TYPE I (REVIEW OF LITERATURE)

Ol’shanskaya A.S., Shnayder N.A., Dmitrenko D.V., Kozina E.V., Chesheyko E.Y., Dyuzhakova A.V.

(Rus)

Vol 7, No 1 (2012)

AUTISTIC EPILEPTIFORM REGRESSION (A REVIEW)

Glukhova L.Y.

(Rus)

Vol 9, No 3 (2014)

EATING EPILEPSY

Rudakova I.G., Mukhin K.Y., Mironov M.B., Abramov M.O.

(Rus)

Vol 15, No 1 (2020)

Febrile infection-related epilepsy syndrome: long-term consequences (own observations)

Drobitova A.V., Karas A.Y., Maslova N.V., Mukhin K.Y.

(Rus)

Vol 11, No 3 (2016)

LANDAU–KLEFFNER SYNDROME (ACQUIRED EPILEPTIC APHASIA) WITH A FOCUS ON ELECTROENCEPHALOGRAPHIC CRITERIA

Mukhin K.Y.

(Rus)

Vol 7, No 1 (2012)

EPILEPTIC ENCEPHALOPATHY WITH CONTINUOUS SPIKES-WAVES ACTIVITY DURING SLEEP

Belousova E.D.

(Rus)

Vol 9, No 3 (2014)

CLINICAL AND ELECTROENCEPHALOGRAPHIC CHANGES IN JUVENILE MYOCLONIC EPILEPSY (A LECTURE)

Mukhin K.Y., Mironov M.B., Glukhova L.Y.

(Rus)

1 - 32 of 32 Items

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