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List of works by Valeria Vasta

A Korean Case of β-Ureidopropionase Deficiency Presenting with Intractable Seizure, Global Developmental Delay, and Microcephaly

scientific article published in February 2015

Altered redox status of coenzyme Q9 reflects mitochondrial electron transport chain deficiencies in Caenorhabditis elegans

scientific article published on 16 September 2010

Assay to measure oxidized and reduced forms of CoQ by LC-MS/MS.

scientific article published in January 2012

Molecular genetic testing of patients with monogenic diabetes and hyperinsulinism

scientific article published on 20 December 2014

Next generation sequence analysis for mitochondrial disorders

scientific article published on 23 October 2009

Next-generation sequencing for mitochondrial diseases: a wide diagnostic spectrum

scientific article published on 10 July 2012

Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly

scientific article

Targeted exome sequencing for mitochondrial disorders reveals high genetic heterogeneity

scientific article

The role of DMQ(9) in the long-lived mutant clk-1.

scientific article published on June 2011

Utility of next generation sequencing in genetic diagnosis of early onset neuromuscular disorders.

scientific article published on 29 January 2015

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