Consensus concept of modern effective therapy for Duchenne muscular dystrophy
Duchenne muscular dystrophy is a genetic orphan neuromuscular disease caused by a mutation in the DMD gene encoding the protein dystrophin. As a result of developing and progressive muscle damage and atrophy, children lose the ability to walk, develop respiratory and cardiac disorders. The core elem...
Saved in:
| Main Authors: | T. A. Gremyakova, S. B. Artemyeva, E. N. Baybarina, N. D. Vashakmadze, V. I. Guzeva, E. V. Gusakova, L. M. Kuzenkova, A. E. Lavrova, O. A. Lvova, S. V. Mikhaylova, L. P. Nazarenko, S. S. Nikitin, A. V. Polyakov, E. L. Dadali, A. G. Rumyantsev, G. E. Sakbaeva, V. M. Suslov, O. I. Gremyakova, A. A. Stepanov, N. I. Shakhovskaya |
|---|---|
| Format: | Article |
| Language: | Russian |
| Published: |
ABV-press
2023-06-01
|
| Series: | Нервно-мышечные болезни |
| Subjects: | |
| Online Access: | https://nmb.abvpress.ru/jour/article/view/539 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
The concept of “ambulatory” and “non-ambulatory” in patients with Duchenne muscular dystrophy: definitions and criteria
by: T. A. Gremyakova, et al.
Published: (2022-06-01) -
CLIPPERS. Three clinical cases and review
by: L. N. Prakhova, et al.
Published: (2020-01-01) -
Experience of observing patients with Duchenne myopathy
by: L. I. Minaycheva, et al.
Published: (2023-12-01) -
Positive experience in treating patients with Duchenne muscular dystrophy caused by a nonsense mutation: family clinical case
by: L. S. Kraeva, et al.
Published: (2024-09-01) -
Intra‐arterial transplantation of HLA‐matched donor mesoangioblasts in Duchenne muscular dystrophy
by: Giulio Cossu, et al.
Published: (2015-11-01)