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Title
Authors
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
Sharkova I.V., Dadali E.L.
PDF
(Rus)
Vol 5, No 4 (2015)
Cardiac involvement in children with neuro-muscular disorders
Arkhipova E.N.
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 5, No 3 (2015)
Comparative analysis of phenotypes features in two common genetic variants of limb-girdle muscular dystrophy
Sharkova I.V., Dadali E.L., Ugarov I.V., Ryzhkova O.P., Polyakov A.V.
PDF
(Rus) PDF
(Eng)
Vol 9, No 3 (2019)
The clinical case of limb-girdle muscle dystrophy 2Q associated with myasthenic syndrome and lung damage
Bardakov S.N., Deev R.V., Mavlikeev M.O., Umakhanova Z.R., Akhmedova P.G., Magomedova R.M., Zulfugarov K.Z., Tsargush V.A., Chekmareva I.A., Yakovlev I.A., Dalgatov G.D., Yakubovsky G.I., Isaev A.A.
PDF
(Rus)
Vol 6, No 1 (2016)
Laboratory studies and Pompe disease: from suspicion to therapy monitoring
Savost’yanov K.V., Nikitin S.S., Karpacheva K.E.
PDF
(Rus)
Vol 14, No 3 (2024)
Muscular dystrophy associated with the DMD gene in women
Vorontsova E.O., Zinina A.V., Shchagina O.A.
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 2 (2013)
Comparative analysis of features phenotype limb-girdle muscular dystrophy 2А and 2I types
Sharkova I.V., Dadali E.L., Ryzhkova O.P., Evdokimenkov V.N.
PDF
(Rus)
1 - 9 of 9 Items

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