Inmaculada Rueda
Overview
Explore the profile of Inmaculada Rueda including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
7
Citations
200
Followers
0
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Related Specialties
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Top 10 Co-Authors
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Recent Articles
1.
Sandoval-Talamantes A, Mori M, Santos-Simarro F, Garcia-Minaur S, Mansilla E, Tenorio J, et al.
Genes (Basel)
. 2023 Apr;
14(4).
PMID: 37107578
Autism spectrum disorders (ASD) comprise a group of neurodevelopmental disorders (NDD) characterized by deficits in communication and social interaction, as well as repetitive and restrictive behaviors, etc. The genetic implications...
2.
Pacio Miguez M, Santos-Simarro F, Garcia-Minaur S, Velazquez Fragua R, Del Pozo A, Solis M, et al.
Am J Med Genet A
. 2020 Aug;
182(10):2222-2225.
PMID: 32808430
No abstract available.
3.
Dayaldasani A, Ruiz-Escalera J, Rodriguez-Espinosa M, Rueda I, Perez-Valero V, Yahyaoui R
Int J Vitam Nutr Res
. 2015 Apr;
84(1-2):92-7.
PMID: 25835239
Introduction: Low maternal vitamin B12 status is a risk factor for various adverse pregnancy outcomes. Although vitamin B12 deficiency is not a primary target of newborn screening (NBS) programs, measurements...
4.
Rocha H, Castineiras D, Delgado C, Egea J, Yahyaoui R, Gonzalez Y, et al.
JIMD Rep
. 2014 Jul;
16:89-94.
PMID: 25012579
Mitochondrial fatty acid β-oxidation disorders (FAOD) are main targets for newborn screening (NBS) programs, which are excellent data sources for accurate estimations of disease birth prevalence. Epidemiological data is of...
5.
Yahyaoui R, Rueda I, Dayaldasani A, Boemer F
Med Clin (Barc)
. 2014 Jun;
144(4):181-2.
PMID: 24889749
No abstract available.
6.
Yahyaoui R, Espinosa M, Gomez C, Dayaldasani A, Rueda I, Roldan A, et al.
Mol Genet Metab
. 2011 Jun;
104(3):414-6.
PMID: 21641254
Neonatal onset of carnitine palmitoyltransferase II (CPT II) deficiency is an autosomal recessive, often lethal disorder of the mitochondrial beta-oxidation of long-chain fatty acids. It is a rare multiorgan disease...
7.
McHugh D, Cameron C, Abdenur J, Abdulrahman M, Adair O, Al Nuaimi S, et al.
Genet Med
. 2011 Feb;
13(3):230-54.
PMID: 21325949
Purpose: To achieve clinical validation of cutoff values for newborn screening by tandem mass spectrometry through a worldwide collaborative effort. Methods: Cumulative percentiles of amino acids and acylcarnitines in dried...