Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
3 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Complex I deficiency, due to NDUFAF4 mutations, causes severe mitochondrial dysfunction and is associated to early death and dysmorphia.
Mitochondrion. 2020 Nov;55:78-84. doi: 10.1016/j.mito.2020.09.003. Epub 2020 Sep 17.
Mitochondrion. 2020.
PMID: 32949790
CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative.
Luque J, Mendes I, Gómez B, Morte B, López de Heredia M, Herreras E, Corrochano V, Bueren J, Gallano P, Artuch R, Fillat C, Pérez-Jurado LA, Montoliu L, Carracedo Á, Millán JM, Webb SM, Palau F; CIBERER Network; Lapunzina P.
Luque J, et al.
Clin Genet. 2022 May;101(5-6):481-493. doi: 10.1111/cge.14113. Epub 2022 Feb 4.
Clin Genet. 2022.
PMID: 35060122
Free PMC article.
Review.
Item in Clipboard
[Clinical outcomes of 2 pediatric patients with Gaucher's disease in enzyme replacement therapy for 9 years].
Quijada Fraile P, Martín Hernández E, Teresa García-Silva M.
Quijada Fraile P, et al. Among authors: teresa garcia silva m.
Med Clin (Barc). 2011 Sep;137 Suppl 1:43-5. doi: 10.1016/S0025-7753(11)70016-1.
Med Clin (Barc). 2011.
PMID: 22230125
Spanish.
Item in Clipboard
Cite
Cite