| Issue |
Title |
File |
| Vol 6, No 3 (2016) |
. |
(Rus)
|
|
Zoltan L., Nieves Cobos P., Wenninger S., Willis T.A., Guglieri M., Roberts M., Quinlivan R., Hilton-Jones D., Evangelista T., Zierz S., Schlotter-Weigel B., Walter M.C., Reilich P., Klopstock T., Deschauer M., Straub V., Müller-Felber W., Schoser B.
|
| Vol 13, No 4 (2023) |
Безопасность и эффективность авалглюкозидазы альфа по сравнению с алглюкозидазой альфа у пациентов с болезнью Помпе с поздним началом: рандомизированное многоцентровое исследование III фазы COMET |
(Rus)
|
|
., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., ., .
|
| Vol 2, No 4 (2012) |
2 cases transformation myasthenia gravis to amyotrophic lateral sclerosis |
(Rus)
|
|
Sanadze A.G., Kasatkina L.F.
|
| Vol 6, No 1 (2016) |
A case of Becker myotonia with pseudodominant inheritance: сurrent approaches to the differential diagnosis of Thomsen’s and Becker's myotonia congenita |
(Rus)
|
|
Kurbatov S.A., Nikitin S.S., Illarioshkin S.N., Gundorova P., Polyakov A.V.
|
| Vol 8, No 2 (2018) |
A case of hereditary motor and sensory neuropathy type IVA with unusual genealogy |
(Rus)
|
|
Kurbatov S.A., Milovidova T.B., Fedotov V.P., Murtazina A.F., Rudenskaya G.E., Shchagina O.A., Polyakov A.V.
|
| Vol 3, No 4 (2013) |
A case of Pompe disease in infant |
(Rus)
|
|
Sudorgina E.F., Choloyan S.B., Sheenkova M.V., Kolesnikova L.P.
|
| Vol 13, No 4 (2023) |
A clinical case of severe aromatic L-amino acid decarboxylase deficiency |
(Rus)
|
|
Shidlovskaya O.A., Artemyeva S.B., Belousova E.D., Gorchkhanova Z.K.
|
| Vol 5, No 1 (2015) |
A familial case of segregation of motor sensory neuropathy type 1B with multiple exostoses in monozygous twins |
(Rus)
|
|
Fedotov V.P., Kurbatov S.A., Nikitin S.S., Milovidova T.B., Galeeva N.M., Polyakov A.V.
|
| Vol 12, No 4 (2022) |
A new mutation in the TYMP-gene: clinical and morphological characteristics of a patient with MNGIE syndrome |
(Rus)
|
|
Bardakov S.N., Limaev I.S., Emelin A.M., Nikitins V., Presnyakov E.V., Kurbatov S.A., Tsygankova P.G., Tsargush V.A., Chekmareva I.A., Kolmakova E.V., Bakulina N.V., Deev R.V.
|
| Vol 3, No 2 (2013) |
A patient with back pain: therapy possibilities |
(Rus)
|
|
Kamchatnov P.R., Chugunov A.V., Trubetskaya E.A.
|
| Vol 4, No 3 (2014) |
Acetyl-L-carnitine improves pain, nerve regeneration, and vibratory perception in patients with chronic diabetic neuropathy |
(Rus)
|
|
A.F. Sima A., Calvani M., Mehra M., Amato A.
|
| Vol 5, No 4 (2015) |
Actovegin in the treatment of patients with cognitive impairments in the chronic cerebral ischemia |
(Rus)
|
|
Boriskina L.M.
|
| Vol 11, No 2 (2021) |
Acute and chronic dysimmune polyneuropathies in the context of the COVID-19 pandemic: pathogenesis, features of the clinical picture, diagnosis and therapy (literature review) |
(Rus)
|
|
Khrulev A.E., Shiyanova N.A., Sorokoumova S.N., Kasatkin D.S., Grigoryeva V. ., Belyakov K. ., Romanova E.S., Yankevich D.S.
|
| Vol 5, No 1 (2015) |
Acute rhabdomyolysis |
(Rus)
|
|
de Lonlay P., Mamoune A., Hamel Y., Bahuau M., Vergnaud S., Piraud M., Lallemand L., Nguyen More M., Vio M., Romero N.
|
| Vol 4, No 3 (2014) |
Adequate managment of patients with dystrophinopathies (muscular dystrophy Duchenne/Becker): objective scales and additional diagnostic methods |
(Rus)
|
|
Nosko A.S., Kurenkov A.L., Nikitin S.S., Zykov V.P.
|
| Vol 12, No 4 (2022) |
Adult spinal muscular atrophy: problems of early diagnosis |
(Rus)
|
|
Shpilyukova Y.A., Illarioshkin S.N.
|
| Vol 7, No 3 (2017) |
Amyotrophic lateral sclerosis: Clinical heterogeneity and approaches to classification |
(Rus)
|
|
Bakulin I.S., Zakroyschikova I.V., Suponeva N.A., Zakharova M.N.
|
| Vol 8, No 4 (2018) |
Amyotrophic lateral sclerosis: pathogenetic mechanisms and new approaches to pharmacotherapy (literature review) |
(Rus)
|
|
Alekseeva T.M., Stuchevskaya T.R., Demeshonok V.S.
|
| Vol 10, No 1 (2020) |
Analysis of clinical manifestations and diagnosis of late-onset myasthenia gravis |
(Rus)
|
|
Khalmurzina A.N., Alekseeva T.M., Lobzin S.V., Rudenko D.I., Kryuchkova V.V.
|
| Vol 7, No 1 (2017) |
Analysis of primary diagnostics of hereditary motor and sensory neuropathies in the Republic of Bashkortostan |
(Rus)
|
|
Saifullina E.V., Magzhanov R.V., Khidiiatova I.M., Khusnutdinova E.K.
|
| Vol 4, No 3 (2014) |
Analyzing the diagnostic accuracy of the causes of spinal pain at neurology hospital in accordance with the International Classification of Diseases |
(Rus)
|
|
Mikhailyuk I.G.
|
| Vol 12, No 4 (2022) |
Anemia in patients with inflammatory bowel disease as a risk factor for restless legs syndrome. Literature review |
(Rus)
|
|
Zakharova S.A., Kalinkin A.L.
|
| Vol 6, No 2 (2016) |
Anomalous innervations: variations and typical electromyography pattern |
(Rus)
|
|
Grishina D.A., Suponeva N.A., Pavlov E.V., Savitskaya N.G.
|
| Vol 4, No 2 (2014) |
Antibodies to autoantigen targets in myasthenia and their value in clinical practice |
(Rus)
|
|
Dedaev S.I.
|
| Vol 13, No 2 (2023) |
Anti-SRP antibody-associated necrotizing myopathy: 2 clinical cases |
(Rus)
|
|
Abbasov F.A., Zemtsova G.V., Popov P.A., Chekhonatskaya K.I., Kukhno D.V., Severova M.M., Shmyreva M.V., Kindarova A.A., Schekochikhin D.Y.
|
| Vol 7, No 1 (2017) |
Applied research conference with international participation “Autoimmune disorders affecting peripheral nerves and muscles” |
(Rus)
|
|
Boriskina L.M.
|
| Vol 14, No 1 (2024) |
Approaches to pathogenetic therapy of spinal muscular atrophy in children and newborns |
(Rus)
|
|
Artemyeva S.B., Shidlovskaya O.A., Papina Y.O., Monakhova A.V., Shulyakova I.V., Belousova E.D., Germanenko O.Y., Vlodavets D.V.
|
| Vol 14, No 2 (2024) |
Aromatic L-amino acid decarboxylase deficiency – disease under the masks of cerebral palsy and epilepsy |
(Rus)
|
|
Chebanenko N.V.
|
| Vol 15, No 1 (2025) |
Assessment of social emotional, cognitive and communicative development and adaptive behavior in children with spinal muscular atrophy 5q |
(Rus)
|
|
Papina Y.O., Zavadenko N.N., Melnik E.A., Artemyeva S.B., Berdalina I.A., Vlodavets D.V.
|
| Vol 15, No 1 (2025) |
Assessment of walking in patients with Duchenne muscular dystrophy receiving ataluren in real clinical practice |
(Rus)
|
|
Aizatulina D.V., Nikitin S.S.
|
| Vol 10, No 2 (2020) |
Atypical variants of chronic inflammatory demyelinating polyneuropathy with benign course: a clinical observation for 8 patients without pathogenic therapy |
(Rus)
|
|
Grishina D.A., Suponeva N.A., Rizvanova A.S.
|
| Vol 3, No 1 (2013) |
Autosomal dominant limb-girdle muscular dystrophy: Leyden–Möbius pelvifemoral form |
(Rus)
|
|
Shnayder N.A., Nikolayeva T.Y., Boroeva E.N., Pshennikova G.M., Luginov N.V., Panina Y.S.
|
| Vol 11, No 3 (2021) |
Aymé–Gripp syndrome in a Russian patient with a newly detected mutation in the MAF gene |
(Rus)
|
|
Dadali E.L., Markova T.V., Ryzhkova O.P.
|
| Vol 10, No 1 (2020) |
Basic principles for the management of neurological patients during the COVID-19 pandemic |
(Rus)
|
|
Kopishinskaya S.V., Zharinova N.O., Velichko I.A., Zhukova N.G., Bucev V.V., Korobejnikov I.V., Gasanova A.A., Arakelyan A.S., Petruchik O.V., Payudis A.N.
|
| Vol 7, No 3 (2017) |
Bickerstaff brainstem encephalitis, acute transverse myelitis, and acute motor axonal neuropathy: diagnostic and treatment challenges in patients with concomitant syndromes. Clinical observation |
(Rus)
|
|
Murtazina A.F., Naumova E.S., Nikitin S.S., Boriskina L.M., Lagutin A.V.
|
| Vol 3, No 4 (2013) |
Botulinum neurotoxin and chronic migraine: muscle fiber chemodenervation or nociceptic system modulation? |
(Rus)
|
|
Artemenko A.R., Kurenkov A.L., Nikitin S.S., Belomestova K.B.
|
| Vol 4, No 3 (2014) |
Botulinum therapy for poststroke spasticity of the lower extremity (clinical cases) |
(Rus)
|
|
Krylova L.V., Khasanova D.R.
|
| Vol 10, No 1 (2020) |
Botulinum therapy using in the complex treatment of children with the result of the brachial plexus intranatal injury (literature review) |
(Rus)
|
|
Agranovich O.E.
|
| Vol 7, No 3 (2017) |
Botulinum toxin treatment of lower extremity spasticity |
(Rus)
|
|
Khat’kova S.E., Akulov M.A., Orlova O.R., Usachev D.Y., Orlova A.S., Krylova L.V.
|
| Vol 3, No 3 (2013) |
Botulinum toxin type A chemodenervation treatment in spastic forms of cerebral palsy |
(Rus)
|
|
Kurenkov A.L., Nikitin S.S., Artemenko A.R., Bursagova B.I., Kuzenkova L.M., Petrova S.A., Klochkova O.A., Mamedyarov A.M.
|
| Vol 3, No 2 (2013) |
Botulinum toxin: yesterday, today, tomorrow |
(Rus)
|
|
Artemenko A.R., Kurenkov A.L.
|
| Vol 9, No 3 (2019) |
Brachialgia: possible causes of pain (literature review) |
(Rus)
|
|
Grishina D.A., Suponeva N.A., Belova N.V., Grozova D.A.
|
| Vol 8, No 1 (2018) |
Bruxism as a neurological problem (literature review) |
(Rus)
|
|
Orlova O.R., Alekseeva A.Y., Mingazova L.R., Konovalova Z.N.
|
| Vol 9, No 2 (2019) |
Bruxism: methods of application and results of treatment with botulinum neuroprotein (Relatox) |
(Rus)
|
|
Orlova O.R., Soykher M.I., Soykher M.G., Mingazova L.R., Medovnikova D.V., Soykher E.M., Konovalova Z.N., Alekseeva A.Y.
|
| Vol 14, No 2 (2024) |
Calculating pain sensation in neuropathies |
(Eng)
|
|
Soufla A., Schmelz M., Rukwied R., Kokotis P.
|
| Vol 10, No 3 (2020) |
Candidate genes involved in the development of antipsychotic-induced tardive dyskinesia in patients with schizophrenia |
(Rus)
|
|
Vaiman E.E., Shnayder N.A., Neznanov N.G., Nasyrova R.F.
|
| Vol 5, No 4 (2015) |
Cardiac involvement in children with neuro-muscular disorders |
(Rus)
|
|
Arkhipova E.N.
|
| Vol 8, No 4 (2018) |
Cardiofaciocutaneus syndrome: literature review and case report |
(Rus)
|
|
Umnov V.V., Nikitina N.V., Khodorovskaya A.M., Barlova O.V.
|
| Vol 4, No 2 (2014) |
Carpal tunnel syndrome in rheumatic diseases |
(Rus)
|
|
Filatova E.S.
|
| Vol 9, No 4 (2019) |
Carpal tunnel syndrome: assessment of the need for rehabilitation and recovery treatment after endoscopic decompression of the median nerve in the late and long-term postoperative periods |
(Rus)
|
|
Yusupova D.G., Zimin A.A., Grishina D.A., Belova N.V., Vershinin A.V., Arestov S.О., Kozlova A.V., Druina L.D., Chechetkin A.O., Gouscha A.O., Suponeva N.A., Piradov M.A.
|
| Vol 9, No 4 (2019) |
Case of hypokalemic paralysis due to use of drug containing therapeutic doses liquorice root |
(Rus)
|
|
Vasilenko A.F., Karpova M.I., Sergeitsev A.N., Zaliautdinova R.I.
|
| Vol 4, No 1 (2014) |
Case report of a child with combined genetic pathology: cystic fibrosis and facioscapulohumeral progressive muscular dystrophy |
(Rus)
|
|
Klochkova O.A., Kurenkov A.L., Mamedyarov A.M., Karimova H.M.
|
| Vol 10, No 3 (2020) |
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): literature review |
(Rus)
|
|
Nuzhnyi E.P., Illarioshkin S.N.
|
| Vol 13, No 1 (2023) |
Change in the spectrum of detected mutations in the DMD gene depending on the methodological capabilities of the laboratory |
(Rus)
|
|
Zinina E.V., Bulakh M.V., Ryzhkova O.P., Shchagina O.A., Polyakov A.V.
|
| Vol 8, No 2 (2018) |
Characteristics of electrophysiological activity of the cerebral cortex in children with arthrogryposis |
(Rus)
|
|
Blagoveschenskiy E.D., Agranovich O.E., Kononova E.L., Baindurashvili A.G., Nazarova M.A., Shestokova A.N., Gabbasova E.L., Nikulin V.V.
|
| Vol 12, No 3 (2022) |
Characteristics of genetic changes in the SMN1 gene in spinal muscular atrophy 5q |
(Rus)
|
|
Dil A.V., Nazarov V.D., Sidorenko D.V., Lapin S.V., Emanuel V.L.
|
| Vol 9, No 1 (2019) |
Characteristics of short-patent auditory evoked potentials in children with cerebral palsy |
(Rus)
|
|
Dulnev V.V., Slyusar’ Т.A.
|
| Vol 7, No 1 (2017) |
Characteristics of soft tissues at the apex of the deformity in patients with kyphoscoliosis with underlying type 1 neurofibromatosis |
(Rus)
|
|
Shchurova E.N., Gorbach E.N., Filimonova G.N., Ryabykh S.O., Ochirova E.N.
|
| Vol 8, No 4 (2018) |
Christianic–Weber panniculitis in a young patient with myasthenia (description of clinical case) |
(Rus)
|
|
Torgashova A.N., Barabanova M.A., Porkhanov V.A., Timchenko L.V., Zhadan O.N., Baryshev A.G., Petropavlovskaya T.A., Stoyanova O.V., Triandafilov K.G., Terman E.A., Aliev K.B., Bondarovich K.A., Nevyantsev O.M., Golovko E.N., Elizbaryan I.S.
|
| Vol 6, No 1 (2016) |
Chronic inflammatory demyelinating polyneuropathy in adults: diagnostic approaches and first line therapy |
(Rus)
|
|
Suponevа N.А., Naumovа E.S., Gnedovskaya E.V.
|
| Vol 6, No 4 (2016) |
CHRONIC INTOXICATION WITH “LAUGHING GAS” (NITROUS OXIDE) AS A CAUSE OF B12 DEFICIENCY MYELOPOLYNEUROPATHY IN YOUNG ADULTS |
(Rus)
|
|
Suponeva N.A., Grishina D.A., Legostaeva L.A., Mochalova E.G.
|
| Vol 3, No 3 (2013) |
Chronic low back pain: possibilities for prevention and treatment |
(Rus)
|
|
Kamchatnov P.R., Umarova K.Y., Kazakov A.Y.
|
| Vol 8, No 3 (2018) |
Chronic pain, depression and cognitive impairment: a close relationship |
(Rus)
|
|
Latysheva N.V., Filatova E.G., Osipova D.V.
|
| Vol 3, No 1 (2013) |
Clinical and diagnostic role of autoantibodies to gangliosides of peripheral nerves: literature review and own expirience |
(Rus)
|
|
Suponeva N.A.
|
| Vol 2, No 3 (2012) |
Clinical and electromyographic criteria for the diagnosis of hereditary myotonic syndromes |
(Rus)
|
|
Fedotov V.P., Kurbatov S.A., Ivanova E.A., Galeeva N.M., Polyakov A.V.
|
| Vol 13, No 3 (2023) |
Clinical and epidemiological characteristics of acute flaccid myelitis cases in children registered in the Russian Federation in 2015–2019 |
(Rus)
|
|
Shakaryan A.K., Belyaletdinova I.K., Shakhgildyan S.V., Ivanova O.E., Eremeeva T.P., Gmyl A.P., Baykova O.Y., Mustafina A.N., Kozlovskaya L.I.
|
| Vol 15, No 2 (2025) |
Clinical and epidemiological features of amyotrophic lateral sclerosis in the Republic of Bashkortostan (Russia) |
(Rus)
|
|
Pervushina E.V., Kutlubaev M.A., Bakhtiyarova K.Z.
|
| Vol 13, No 1 (2023) |
Clinical and genetic characteristics and an algorithm for the differential diagnosis of progressive muscular dystrophies that manifest after a period of normal motor development |
(Rus)
|
|
Sharkova I.V., Dadali E.L.
|
| Vol 7, No 3 (2017) |
Clinical and genetic characteristics and diagnosis of hereditary variants of neonatal epilepsy |
(Rus)
|
|
Semenova N.A., Dadali E.L., Sharkov A.A., Akimova I.A.
|
| Vol 10, No 3 (2020) |
Clinical and genetic characteristics of 2 patients from Russia with autosomal-recessive microcephaly type 2, due to mutations of the WDR62 gene (OMIM: 604317) |
(Rus)
|
|
Guseva D.M., Dadali E.L.
|
| Vol 7, No 3 (2017) |
Clinical and genetic characteristics of autosomal recessive axonal neuropathy with neuromyotonia in Russian patients |
(Rus)
|
|
Dadali E.L., Nikitin S.S., Kurbatov S.A., Murtazina A.F., Sharkova I.V., Shchagina O.A., Konovalov F.A.
|
| Vol 10, No 2 (2020) |
Clinical and genetic characteristics of Charcot–Marie–Tooth disease type 4D (type Lom) in Russia |
(Rus)
|
|
Murtazina A.F., Shchagina O.A., Milovidova T.B., Dadali E.L., Rudenskaya G.E., Kurbatov S.A., Fedotova T.V., Nikitin S.S., Sparber P.A., Orlova M.D., Polyakov A.V.
|
| Vol 10, No 1 (2020) |
Clinical and genetic characteristics of congenital muscular dystrophies (Part 1) |
(Rus)
|
|
Chausova P.A., Ryzhkova O.P., Polyakov A.V.
|
| Vol 10, No 2 (2020) |
Clinical and genetic characteristics of congenital muscular dystrophies (part 2) |
(Rus)
|
|
Chausova P.A., Ryzhkova O.P., Polyakov A.V.
|
| Vol 11, No 2 (2021) |
Clinical and genetic characteristics of distal arthrogryposis caused by mutations in the PIEZO2 gene |
(Rus)
|
|
Markova T.V., Dadali E.L., Nikitin S.S., Murtazina A. ., Mironovich O.L., Kanivets I. .
|
| Vol 8, No 3 (2018) |
Clinical and genetic characteristics of new allele variants of the Mowat–Wilson syndrome caused by ZEB2 gene mutations |
(Rus)
|
|
Akimova I.A., Markova T.V., Konovalov F.A., Antonets A.V., Dadali E.L.
|
| Vol 9, No 3 (2019) |
Clinical and genetic characteristics of Nonaka myopathy (GNE-myopathy) in russian patients |
(Rus)
|
|
Dadali E.L., Sharkova I.V., Rudenskaya G.E., Nikitin S.S., Murtazina A.F., Ryzhkova O.P., Chukhrova A.L.
|
| Vol 9, No 2 (2019) |
Clinical and genetic characteristics of ponto-cerebellar hypoplasia caused by mutations in the TSEN54 gene (OMIM: 277470) |
(Rus)
|
|
Dadali E.I., Akimova I.A., Semenova N.A., Guseva D.M., Shchagina O.A., Chukhrova A.I., Kanivets I.V., Korostelev S.A.
|
| Vol 13, No 2 (2023) |
Clinical and genetic characteristics of primary hypertrophic osteoarthropathy |
(Rus)
|
|
Dadali E.L., Markova T.V., Kenis V.M., Nagornova T.S., Nikitin S.S.
|
| Vol 10, No 1 (2020) |
Clinical and genetic characteristics of the early 66th type epileptic encephalopathy (literature review and own observation) |
(Rus)
|
|
Markova T.V., Borovikov A.O., Lozier E.R., Isaev A.A., Kaimonov V.S., Pomerantseva E.A., Konovalov F.A., Schagina O.A., Dadali E.L.
|
| Vol 13, No 3 (2023) |
Clinical and genetic characteristics of the first Russian patient with a syndrome of craniofacial dysmorphia-deafness-anomalies of the upper limbs, caused by a mutation in the PAX3 gene |
(Rus)
|
|
Markova T.V., Mavlyukeeva V.V., Ginzburg B.G., Shchagina O.A., Nikitin S.S., Dadali E.L.
|
| Vol 9, No 1 (2019) |
Clinical and genetic characteristics of the syndrome of contractures of the limbs and face, hypothony and psychomotor retardation (OMIM: 616 266), caused by mutations in the NALCN gene |
(Rus)
|
|
Borovikov A.O., Sharkova I.V., Ryzhkova O.P., Chukhrova A.L., Schagina O.A., Markova T.V., Dadali E.L.
|
| Vol 11, No 1 (2021) |
Clinical and genetic characteristics of type 3 lissencephaly caused by a mutation in the TUBA1A gene (OMIM: 611603) |
(Rus)
|
|
Guseva D.M., Markova T.V., Bessonova L.A., Nikitin S.S., Dadali E.L., Shchagina O.A.
|
| Vol 13, No 3 (2023) |
Clinical and genetic characteristics of type 7 distal arthrogryposis caused by a pathogenic variant in the MYH8 gene |
(Rus)
|
|
Sharkova I.V., Nikitin S.S., Markova T.V., Voskanyan A.E., Melnik E.A., Shchagina O.A., Dadali E.L.
|
| Vol 10, No 1 (2020) |
Clinical and genetic characteristics of X-linked mental retardation 102 type caused by novel mutations in the DDX3X gene (OMIM:300958) |
(Rus)
|
|
Dadali E.L., Markova T.V., Levchenko O.A., Chukhrova A.L., Shchagina O.A.
|
| Vol 10, No 4 (2020) |
Clinical and genetic charsteristics of the Bosch–Boonstra–Schaaf syndrome due to novel mutations in the NR2F1 gene |
(Rus)
|
|
Dadali E.L., Borovikov A.O., Shchagina O.A., Mironovich O.L.
|
| Vol 6, No 3 (2016) |
Clinical and immunological features and treatment of myasthenia gravis in the elderly (review) |
(Rus)
|
|
Alekseeva T.M., Kosachev V.D., Khalmurzina A.N.
|
| Vol 9, No 1 (2019) |
Clinical case of Parry–Romberg syndrome |
(Rus)
|
|
Voitenkov V.B., Komantsev V.N., Ekusheva E.V., Skripchenko N.V., Marchenko N.V.
|
| Vol 3, No 2 (2013) |
Clinical case of the late diagnosis of neurolipomatosis (Dercum’s disease) |
(Rus)
|
|
Shnayder N.A., Kiselev I.A., Dmitrenko D.V.
|
| Vol 8, No 3 (2018) |
Clinical case study of Kearns–Sayre syndrome: diagnosis, methods of treatment |
(Rus)
|
|
Vlasenko S.V., Ponomarenko E.N., Kushnir G.M., Korsunskaya L.L., Larina N.V., Shalanin V.V., Usulceva N.I.
|
| Vol 9, No 4 (2019) |
Clinical examination of patients with late-onset Pompe disease: typical and not typical symptoms and signs |
(Rus)
|
|
Nikitin S.S.
|
| Vol 6, No 2 (2016) |
Clinical experience of myasthenic crisis management in Amur region |
(Rus)
|
|
Kon’kova D.Y., Karnaukh V.N., Duleba A.P.
|
| Vol 15, No 1 (2025) |
Clinical features of fatigue in amyotrophic lateral sclerosis |
(Rus)
|
|
Pervushina E.V., Kutlubaev M.A.
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| Vol 5, No 4 (2015) |
Clinical heterogeneity in Fabry disease |
(Rus)
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Salogub G.N.
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| Vol 6, No 1 (2016) |
Clinical Practice Guidelines for delivery of healthcare to patients with Pompe disease |
(Rus)
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Nikitin S.S., Kutsev S.I., Basargina E.N., Mikhaylova S.V., Zakharova E.Y., Larionova V.I., Polyakova S.I., Kotlukova N.P., Arkhipova E.N., Kovalchuk M.O., Buchinskaya N.V.
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| Vol 2, No 2 (2012) |
Clinico‑genetic heterogeneity of chondrodysthrophic myotonia |
(Rus)
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Shnayder N.A.
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| Vol 11, No 1 (2021) |
Co-contraction in patients with obstetric palsy (literature review) |
(Rus)
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Agranovich O.E.
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| Vol 14, No 2 (2024) |
Cognitive and emotional disturbances in adult patients with myotonic dystrophy type 1 |
(Rus)
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Erokhina E.K., Shamtieva K.V., Melnik E.A., Kazakov D.O., Kurbatov S.A., Pavlikova E.P., Tikhonova O.A., Mershina E.A., Sinitsyn V.E., Vlodavets D.V.
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| Vol 7, No 2 (2017) |
Comparative analysis of excitability of radicular and intramuscular axonal systems in healthy volunteers during peripheral magnetic stimulation |
(Rus)
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Blokhina V.N., Kuznetsov A.N., Vinogradov O.I., Voytenkov V.B., Melikyan E.G., Nikolaev S.G.
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| Vol 3, No 2 (2013) |
Comparative analysis of features phenotype limb-girdle muscular dystrophy 2А and 2I types |
(Rus)
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Sharkova I.V., Dadali E.L., Ryzhkova O.P., Evdokimenkov V.N.
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