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Title
Authors
Vol 5, No 4 (2015)
Cardiac involvement in children with neuro-muscular disorders
Arkhipova E.N.
PDF
(Rus)
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 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 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)
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 4 (2019)
Clinical examination of patients with late-onset Pompe disease: typical and not typical symptoms and signs
Nikitin S.S.
PDF
(Rus)
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 8, No 1 (2018)
Lack of vigilance is the main factor of late diagnosis of glycogen storage disease type II in the Republic of Kazakhstan
Kuzina L.A., Kaishibayeva G.S.
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 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)
1 - 10 of 10 Items

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