Primary Coenzyme Q10 Deficiency (COQ10D)
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-66816-1_1868-3
Reference20 articles.
1. Cretoiu D, Pavelescu L, Duica F, Radu M, Suciu N, Cretoiu SM (2018) Myofibers. Adv Exp Med Biol 1088:23–46. https://doi.org/10.1007/978-981-13-1435-3_2
2. Desbats MA, Lunardi G, Doimo M, Trevisson E, Salviati L (2015a) Genetic bases and clinical manifestations of Coenzyme Q10 (CoQ 10) deficiency. J Inherit Metab Dis 38:145–156. https://doi.org/10.1007/s10545-014-9749-9
3. Desbats MA et al (2015b) Primary Coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure. Eur J Hum Genet 23:1254–1258. https://doi.org/10.1038/ejhg.2014.277
4. Drovandi S et al (2022a) Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency. Kidney Int 102:604–612. https://doi.org/10.1016/j.kint.2022.04.029
5. Drovandi S et al (2022b) Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy. Kidney Int 102:592–603. https://doi.org/10.1016/j.kint.2022.02.040
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