Daniela Verrigni

Disease-Causing SDHAF1 Mutations Impair Transfer of Fe-S Clusters to SDHB

Nunziata Maio, Daniele Ghezzi, Daniela Verrigni et al. · Cell Metabolism · 2015 · 116 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

COQ4 Mutations Cause a Broad Spectrum of Mitochondrial Disorders Associated with CoQ10 Deficiency

Gloria Brea‐Calvo, Tobias B. Haack, Daniela Karall et al. · The American Journal of Human Genetics · 2015 · 109 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Succinate‐CoA ligase deficiency due to mutations in <i>SUCLA2</i> and <i>SUCLG1</i>: phenotype and genotype correlations in 71 patients

Rosalba Carrozzo, Daniela Verrigni, Magnhild Rasmussen et al. · Journal of Inherited Metabolic Disease · 2015 · 88 citations

Life Sciences, Genetics, Molecular Genetics +11

A new simple and rapid LC–ESI-MS/MS method for quantification of plasma oxysterols as dimethylaminobutyrate esters. Its successful use for the diagnosis of Niemann–Pick type C disease

Sara Boenzi, Federica Deodato, Roberta Taurisano et al. · Clinica Chimica Acta · 2014 · 71 citations

Life Sciences, Biochemistry, Analytical Chemistry +10

A novel AIFM1 mutation expands the phenotype to an infantile motor neuron disease

Daria Diodato, Giorgio Tasca, Daniela Verrigni et al. · European Journal of Human Genetics · 2015 · 69 citations

Medicine, Genetics, Molecular Genetics +14