V. Lodato

Cardiomyopathies in Children and Systemic Disorders When Is It Useful to Look beyond the Heart?

M. Digilio, A. Novelli, M. Raponi, 2022, Journal of cardiovascular development and disease.

Ebstein's anomaly in a child with osteogenesis imperfecta type I.

L. Sangiorgi, P. D'eufemia, M. Celli, 2011, Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases.

Genetics in Congenital Heart Diseases: Unraveling the Link Between Cardiac Morphogenesis, Heart Muscle Disease, and Electrical Disorders.

F. Drago, G. Parlapiano, A. Baban, 2021, Heart failure clinics.

Myocardial and Arrhythmic Spectrum of Neuromuscular Disorders in Children

E. Bertini, F. Drago, D. Martinelli, 2021, Biomolecules.

Cardiovascular Involvement in Pediatric FLNC Variants: A Case Series of Fourteen Patients

A. D’Amico, A. Amodeo, A. Novelli, 2022, Journal of cardiovascular development and disease.

1p36 Deletion Syndrome and the Aorta: A Report of Three New Patients and a Literature Review

M. Digilio, A. Novelli, M. Bengala, 2021, Journal of cardiovascular development and disease.

Child abuse and osteogenesis imperfecta: how can they be still misdiagnosed? A case report.

L. Sangiorgi, P. D'eufemia, M. Celli, 2012, Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases.

Serum creatine kinase isoenzymes in children with osteogenesis imperfecta

P. D'eufemia, M. Celli, R. Finocchiaro, 2016, Osteoporosis International.

Serum brain-type creatine kinase increases in children with osteogenesis imperfecta during neridronate treatment

P. D'eufemia, M. Celli, R. Finocchiaro, 2014, Pediatric Research.

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?

I. Bottillo, P. Grammatico, L. Laino, 2022, Genes.

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

M. Pasquini, F. Camerota, C. Celletti, 2023, Brain Sciences.

Specifications and validation of the ACMG/AMP criteria for clinical interpretation of sequence variants in collagen genes associated with joint hypermobility

L. Micale, B. Pasini, C. Fusco, 2023, Human Genetics.

Scoliosis secondary to ganglioneuroma: a case report and up to date literature review

M. Tetti, P. D'eufemia, P. Persiani, 2014, Journal of pediatric orthopedics. Part B.