Author

Carla Cozzolino

Observed names: C. Cozzolino, Carla Cozzolino Phd, Cozzolino, Carla

Institution: CEINGE Biotecnologie Avanzate Franco Salvatore (Italy)

Observed institutions: Federico II University Hospital, CEINGE Biotecnologie Avanzate Franco Salvatore (Italy), University of Naples Federico II

OpenAlex ID: A5113841077

Targeted metabolomics in the expanded newborn screening for inborn errors of metabolism

2015 · Emanuela Scolamiero, Carla Cozzolino, et al. · Molecular BioSystems · 99

Mulibrey nanism: Two novel mutations in a child identified by Array CGH and DNA sequencing

2016 · Enza Mozzillo, Carla Cozzolino, et al. · American Journal of Medical Genetics Part A · 14

Biochemical and molecular characterization of 3-Methylcrotonylglycinuria in an Italian asymptomatic girl

2018 · Carla Cozzolino, Guglielmo RD Villani, et al. · Genetics and Molecular Biology · 13

Pearls & Oy-sters: Familial epileptic encephalopathy due to methylenetetrahydrofolate reductase deficiency

2014 · Gerarda Cappuccio, Carla Cozzolino, et al. · Neurology · 13

Novel deletion mutation in the cardiac sodium channel inactivation gate causes long QT syndrome

2012 · Nicola Detta, Giulia Frisso, et al. · International Journal of Cardiology · 10

Child Neurology: Recurrent rhabdomyolysis due to a fatty acid oxidation disorder

2013 · Gaetano Terrone, Margherita Ruoppolo, et al. · Neurology · 9

Biochemical and molecular characterization of 3-Methylcrotonylglycinuria in an Italian asymptomatic girl

2018 · Cozzolino, Carla, Villani, Guglielmo RD, et al. · Figshare

Deficit di 3-Metilcrotonil-CoA Carbossilasi: identificazione di due nuove mutazioni

2013 · Guglielmo Rosario Domeni Villani, C. Cozzolino, et al.

Works count: 9

Citation count: 158

H-index: 6

I10-index: 5