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Title
Authors
Vol 7, No 4 (2017)
Magnetic resonance imaging of the cauda equina in chronic inflammatory demyelinating polyneuropathy
Vasilenko A.F., Shestakova M.V., Kochetkov I.V., Karpova M.I.
PDF
(Rus)
Vol 4, No 2 (2014)
Muscle MRI / whole-body MRI in diagnosis and dynamic evaluation of neuro-muscular disorders
Carlier R.
PDF
(Rus)
Vol 9, No 3 (2019)
Infantile and early childhood onset of mitochondrial myopathy due to mutations in the TK2 gene with a phenotype of spinal muscular atrophy 5q: the first cases in Russia
Kurbatov S.A., Tsygankova P.G., Mollaeva K.Y., Bychkov I.O., Itkis Y.S., Zabnenkova V.V., Umakhanova Z.R., Geybatova L.G., Zakharova E.Y.
PDF
(Rus)
Vol 9, No 2 (2019)
Clinical and genetic characteristics of ponto-cerebellar hypoplasia caused by mutations in the TSEN54 gene (OMIM: 277470)
Dadali E.I., Akimova I.A., Semenova N.A., Guseva D.M., Shchagina O.A., Chukhrova A.I., Kanivets I.V., Korostelev S.A.
PDF
(Rus)
Vol 5, No 1 (2015)
The hereditary progressive muscular dystrophy type 2A (calpainopathy): a clinical case
Grishina D.A., Suponeva N.A., Shvedkov V.V., Belopasova A.V.
PDF
(Rus)
Vol 5, No 1 (2015)
Inherited progressive limb-girdle muscular dystrophy type 2A (calpainopathy): a review of literature
Grishina D.A., Suponeva N.A., Shvedkov V.V., Belopasova A.V.
PDF
(Rus)
Vol 3, No 1 (2013)
Autosomal dominant limb-girdle muscular dystrophy: Leyden–Möbius pelvifemoral form
Shnayder N.A., Nikolayeva T.Y., Boroeva E.N., Pshennikova G.M., Luginov N.V., Panina Y.S.
PDF
(Rus)
Vol 12, No 1 (2022)
Informative value of neurophysiological and neuroimaging research methods in the onset of spinal cord myelopathy: literature review and clinical observation
Kanshina D.S., Surma M.A., Badamshina E.V., Bronov O.Y.
PDF
(Rus)
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)
Guseva D.M., Dadali E.L.
PDF
(Rus)
1 - 9 of 9 Items

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