Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Igor O. Bychkov"'
Autor:
Tatyana V. Markova, Vladimir M. Kenis, Evgeniy V. Melchenko, Peter A. Sparber, Marina S. Petukhova, Igor O. Bychkov, Tatyana S. Nagornova, Olga L. Shatokhina, Elena L. Dadali
Publikováno v:
Travmatologiâ i Ortopediâ Rossii, Vol 27, Iss 3, Pp 71-83 (2021)
Introduction. Desbuquois dysplasia is a rare skeletal dysplasia with an autosomal recessive inheritance, resembling to the group of multiple joint dislocations. The disease is caused by mutations in the CANT1 and XYLT1 genes, the protein products of
Externí odkaz:
https://doaj.org/article/bf1dfd3e1b1e4ddd8249e3cf94d73f95
Autor:
Olga S. Chumakova, Natalia V. Milovanova, Igor O. Bychkov, Ekaterina Y. Zakharova, Elena A. Mershina, Valentin E. Sinitsin, Dmitry A. Zateyshchikov
Publikováno v:
Cardiology Research. 13:398-404
Autor:
Vladimir M. Kenis, Leonid V. Gorobets, Alena Yu. Dimitrieva, Alisa A. Zhmurova-Kriventsova, Igor O. Bychkov, Galina V. Baydakova, Tatiana V. Markova, Ekaterina Yu. Zakharova
Publikováno v:
Pediatric Traumatology, Orthopaedics and Reconstructive Surgery. 10:285-294
BACKROUND: Mucopolysaccharidoses are a group of lysosomal storage diseases belonging to orphan diseases. Certain types of mucopolysaccharides have a typical musculoskeletal findings and radiological changes. The mucopolysaccharidosis IVB is a rare ty