Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Schwartz, Ida VD"'
Autor:
Loret, Amaury, Jacob, Claire, Mammou, Saloua, Bigot, Adrien, Blasco, Hélène, Audemard-Verger, Alexandra, Schwartz, Ida VD, Mulleman, Denis, Maillot, François
Publikováno v:
Orphanet Journal of Rare Diseases; 8/10/2023, Vol. 18 Issue 1, p1-11, 11p
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 5, Iss 1, p 14 (2010)
Abstract Most lysosomal diseases (LD) are inherited as autosomal recessive traits, but two important conditions have X-linked inheritance: Fabry disease and Mucopolysaccharidosis II (MPS II). These two diseases show a very different pattern regarding
Externí odkaz:
https://doaj.org/article/a00de65997eb401c845a1d7580d90e66
Autor:
Schwartz, Ida VD, Ribeiro, Márcia G., Mota, João G., Toralles, Maria Betânia P., Correia, Patrícia, Horovitz, Dafne, Santos, Emerson S., Monlleo, Isabella L., Fett-Conte, Agnes C., Sobrinho, Ruy P. Oliveira, Norato, Denise Y. J., Paula, Anna Carolina, Kim, Chong A., Duarte, Andréa R., Boy, Raquel, Valadares, Eugênia, De Michelena, Maria, Mabe, Paulina, Martinhago, Cyro D., Pina-Neto, João M.
Publikováno v:
Acta Paediatrica; 04022007, p63-70, 8p, 2 Charts, 2 Graphs