Search Results - "Tarksh, M A"

Polymorphism of exon 4 in the CANP-3 gene in patients with primary myopathies by Lipatova, N A, Krakhmaleva, I N, Shishkin, S S, Shakhovskaia, N I, Podnikova, N I, Lunga, I N, Tarksh, M A, Gerasimova, N L

“…The structures of the gene for calpain (CANP-3) and of the DMD gene were analyzed in patients with primary myopathies [limb-girdle muscular distrophy (LGMD)…”
Get more information

Dystrophin gene expression in patients with Duchenne muscular dystrophy after myoblast transplantation by Shishkin, S S, Terekhov, S M, Krokhina, T B, Shakhovskaia, N I, Podobedova, A N, Linnaia, G F, Tarasov, V I, Ovchinnikov, V I, Krakhmaleva, I N, Zakharov, S F, Ershova, E S, Limborskaia, S A, Pogoda, T V, Zotikov, E A, Kut'ina, R M, Tarksh, M A, Sukhorukov, V S, Gerasimova, N L

“…Based on originally designed technique of myoblast cultivation and in accordance with the approved by the Russian Ministry of Health "one muscle treatment"…”
Get more information

A databank on Russian families with hereditary neuromuscular diseases by Lunga, I N, Shishkin, S S, Shakhovskaia, N I, Gerasimova, N L, Zelinskaia, D I, Khodunova, A A, Shakhovskiĭ, V A, Tarksh, M A, Krakhmaleva, I N

“…The information about 5 thousands Russian families with hereditary neuromuscular disorders (HNMD) was collected by means of both different genetic…”
Get more information

The use of low doses of prednisolone for the treatment of patients with Duchenne-Becker myodystrophy by Shakhovskaia, N I, Shishkin, S S, Skozobtseva, L F, Shakhovskiĭ, V A, Rodnikova, N I, Lunga, I N, Tarksh, M A, Gerasimova, N L, Krakhmaleva, I N

“…A special program for long-term application of low-dose prednisolone treatment in Duchenne-Becker muscular dystrophy with complex control of the patients'…”
Get more information