A quantitative assessment of the evolution of cerebellar syndrome in children with phosphomannomutase-deficiency (PMM2-CDG).

Autor: Serrano, Natalia Lourdes1,2,3, De Diego, Victor1,2, Cuadras, Daniel4, Monseny, Antonio F. Martinez5, Velázquez-Fragua, Ramón6, López, Laura7, Felipe, Ana8, Gutiérrez-Solana, Luis G.7, Macaya, Alfons8, Pérez-Dueñas, Belén1,2, Serrano, Mercedes1,2,5,9 mserrano@hsjdbcn.org, Martinez Monseny, Antonio F5 (AUTHOR), CDG Spanish-Consortium (CORPORATE AUTHOR)
Zdroj: Orphanet Journal of Rare Diseases. 9/15/2017, Vol. 12, p1-6. 6p.
Databáze: Academic Search Ultimate