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Clinical case of the late diagnosis of neurolipomatosis (Dercum’s disease)
Shnayder N.A., Kiselev I.A., Dmitrenko D.V.
Glutaric aciduria type 1 in children. Clinical presentation of 46 cases in Russian families
Mikhailova S.V., Saifullina E.V., Baranova P.V., Vorontsova V.P., Gribov D. ., Zhivihina M.V., Slatetskaya A.N., Magzhanov R. ., Samokhvalov V.A.,  Virtseva M. ., Borscheva L.P.,  Koh E. .,  Novikova M.V., Abrukova A.V., Belyashova E.Y., Gerasimenko N. ., Guseva L.V., Yukhimenko Z.V., Nikitina N.V., Belyaeva T. .,  Shkurko T.A.,  Pichkur N.A., Kakaulina V.S., Pechatnikova N.L., Polyakova N. ., Korostelev S.A., Pyankov D. ., Kanivets I. .,  Demina N.A., Pyrkova E.Y., Baidakova G.V., Kurkina M. .,  Zakharova E.Y.
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): literature review
Nuzhnyi E.P., Illarioshkin S.N.
Amyotrophic lateral sclerosis: pathogenetic mechanisms and new approaches to pharmacotherapy (literature review)
Alekseeva T.M., Stuchevskaya T.R., Demeshonok V.S.
Study of tactile sensitivity by Semmes–Weinstein monofilaments in patients with carpal tunnel syndrome and healthy individuals
Mikhailyuk I.G., Spirin N.N., Salnikov E.V.
Amyotrophic lateral sclerosis: Clinical heterogeneity and approaches to classification
Bakulin I.S., Zakroyschikova I.V., Suponeva N.A., Zakharova M.N.
Juvenile amyotrophic lateral sclerosis type 4: case report and review
Rudenskaya G.E., Nikitin S.S., Shatokhina O.L., Shchagina O.A.
Clinical heterogeneity in Fabry disease
Salogub G.N.
The first family case of spinocerebellar ataxia type 14 in Russia
Nuzhnyy E.P., Abramycheva N.Y., Klyushnikov S.A., Illarioshkin S.N.
Positive experience of the usage of Rituximab in management of refractory myasthenia gravis in Russia
Shcherbakova N.I., Suponeva N.A., Shvedkov V.V., Shabalina A.A., Kostyreva M.V., Rudnichenko V.A., Galkina O.I.
The concept of “ambulatory” and “non-ambulatory” in patients with Duchenne muscular dystrophy: definitions and criteria
Gremyakova T.A., Artemyeva S.V., Vashakmadze N.D., Vitkovskaya I.P., Guzeva V.I., Guzeva O.V., Kuzenkova L.M., Mikhailova S.V., Nazarenko L.P., Pervunina T.M., Pechatnikova N.L., Podkletnova T.V., Sakbaeva G.E., Stepanov A.A., Suslov V.M., Gremyakova O.I., Shakhovskaya N.I., Nikitin S.S.
Role of the peripheral neuromuscular disturbances in the development of severe movement disorders in patients with cerebral palsy
Kurenkov A.L., Artemenko A.R.
Organization experience of diagnostic and medicosocial services for patients with Charcot—Marie—Tooth disease in Krasnoyarsk region
Glushchenko E.V., Shnayder N.A., Kantimirova E.A., Kozulina E.A., Voevoda M.I., Maksimov V.N., Allakhverdyan A.A.
Clinical and genetic characteristics of 2 patients from Russia with autosomal-recessive microcephaly type 2, due to mutations of the WDR62 gene (OMIM: 604317)
Guseva D.M., Dadali E.L.
Genetic heterogeneity of hereditary diseases of nervous system: problems and solutions
Dadali E.L., Ginter E.K., Polyakov A.B.
1 - 15 of 15 Items

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