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Valentina Lodato

Observed names: Lodato, Valentina, V. Lodato
Observed institutions: Azienda Ospedaliera San Camillo-Forlanini, Bambino Gesù Children's Hospital, ERN GUARD-Heart, Carlo Forlanini Hospital, Istituti di Ricovero e Cura a Carattere Scientifico, Sapienza University of Rome
ORCID: 0000-0001-9476-3575
Observed ORCID: 0000-0001-9476-3575
OpenAlex ID: A5040785515
Cardiomyopathies in Children and Systemic Disorders When Is It Useful to Look beyond the Heart?
2022 · Valentina Lodato, Giovanni Parlapiano, et al. · Journal of Cardiovascular Development and Disease · 22
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Genetics in Congenital Heart Diseases
2021 · Anwar Baban, Valentina Lodato, et al. · Heart Failure Clinics · 16
Scoliosis secondary to ganglioneuroma: a case report and up to date literature review
2014 · Patrizia D’Eufemia, Enrico Properzi, et al. · Journal of Pediatric Orthopaedics B · 15
Myocardial and Arrhythmic Spectrum of Neuromuscular Disorders in Children
2021 · Anwar Baban, Valentina Lodato, et al. · Biomolecules · 13
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Child abuse and osteogenesis imperfecta: how can they be still misdiagnosed? A case report.
2012 · Patrizia D'Eufemia, Marta Palombaro, et al. · Europe PMC (PubMed Central) · 13
Specifications and validation of the ACMG/AMP criteria for clinical interpretation of sequence variants in collagen genes associated with joint hypermobility
2023 · Maria Pia Leone, Silvia Morlino, et al. · Human Genetics · 12
The Language of Pain in the Hypermobile Ehlers–Danlos Syndrome: Metaphors as a Key to Understanding the Experience of Pain and as a Rehabilitation Tool
2023 · Filippo Camerota, Rachele Mariani, et al. · Brain Sciences · 9
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Congenital Defects in a Patient Carrying a Novel Homozygous AEBP1 Variant: Further Expansion of the Phenotypic Spectrum of Ehlers–Danlos Syndrome Classical-like Type 2?
2022 · Niccolò Di Giosaffatte, Alessandro Ferraris, et al. · Genes · 9
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Cardiovascular Involvement in Pediatric FLNC Variants: A Case Series of Fourteen Patients
2022 · Anwar Baban, Viola Alesi, et al. · Journal of Cardiovascular Development and Disease · 9
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Serum creatine kinase isoenzymes in children with osteogenesis imperfecta
2016 · P. D’Eufemia, R. Finocchiaro, et al. · Osteoporosis International · 9
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Serum brain-type creatine kinase increases in children with osteogenesis imperfecta during neridronate treatment
2014 · Patrizia D’Eufemia, Roberto Finocchiaro, et al. · Pediatric Research · 9
1p36 Deletion Syndrome and the Aorta: A Report of Three New Patients and a Literature Review
2021 · Valentina Lodato, Valeria Orlando, et al. · Journal of Cardiovascular Development and Disease · 7
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Ebstein's anomaly in a child with osteogenesis imperfecta type I.
2011 · Patrizia D'Eufemia, Mauro Celli, et al. · PubMed · 4
Padlock Assay in Transthyretin Amyloidosis: A Feasibility Study
2026 · Maria Grazia Di certo, Francesca Gabanella, et al. · Current Gene Therapy
Novel Pathogenic Variant Confirms the Association of REST and Jones Syndrome
2025 · Valentina Lodato, Massimo Galli, et al. · Clinical Genetics
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Fetal Rhabdomyoma of the Larynx in an Adult
2024 · Massimo Fusconi, Fabiana Zaccarelli, et al. · Ear Nose & Throat Journal
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Erratum to: Serum creatine kinase isoenzymes in children with osteogenesis imperfecta
2016 · P. D’Eufemia, R. Finocchiaro, et al. · Osteoporosis International
Works count: 19
Citation count: 147
H-index: 9
I10-index: 6
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