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Neglected patellar tendon rupture in tibial tubercle avulsion fracture in an adolescent: A case report

La Pediatria medica e chirurgica, 2022-10, Vol.44 (s1)

2022

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Avascular necrosis of the first metatarsal head in adolescence: A case report

La Pediatria medica e chirurgica, 2022-10, Vol.44 (s1)

2022

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Acquired genu recurvatum in a skeletally immature patient treated by physeal distraction: A case report

La Pediatria medica e chirurgica, 2022-10, Vol.44 (s1)

2022

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Simultaneous subtalar arthroeresis, midfoot soft tissue release, and talo-navicular arthrodesis in children with planovalgus neurologic foot

European journal of orthopaedic surgery & traumatology, 2024-05, Vol.34 (4), p.2163-2170

2024

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Le fratture diafisarie del femore

Lo scalpello, 2018-12, Vol.32 (3), p.303-308

2018

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Pianificazione preoperatoria: parametri biomeccanici e nuove tecnologie

Lo scalpello, 2017-12, Vol.31 (3), p.208-212

2017

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Septic physeal separation of proximal femur in a newborn

Journal of orthopaedics and traumatology, 2009-06, Vol.10 (2), p.105-110

2009

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Role of sialidase Neu3 and ganglioside GM3 in cardiac fibroblasts activation

Biochemical journal, 2020-09, Vol.477 (17), p.3401-3415

2020

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Challenges in Brugada Syndrome Stratification: Investigating SCN5A Mutation Localization and Clinical Phenotypes

International journal of molecular sciences, 2023-12, Vol.24 (23), p.16658

2023

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Brugada syndrome genetics is associated with phenotype severity

European heart journal, 2021-03, Vol.42 (11), p.1082-1090

2021

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Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights

International journal of molecular sciences, 2023-10, Vol.24 (20), p.15089

2023

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Clinical Considerations for a Family with Dilated Cardiomyopathy, Sudden Cardiac Death, and a Novel TTN Frameshift Mutation

International journal of molecular sciences, 2021-01, Vol.22 (2), p.670

2021

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Calcium in Brugada Syndrome: Questions for Future Research

Frontiers in physiology, 2018-08, Vol.9, p.1088-1088

2018

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Alterations of the Sialylation Machinery in Brugada Syndrome

International journal of molecular sciences, 2022-11, Vol.23 (21), p.13154

2022

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Novel SCN5A p.V1429M Variant Segregation in a Family with Brugada Syndrome

International journal of molecular sciences, 2020-08, Vol.21 (16), p.5902

2020

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Novel SCN5A p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths

International journal of molecular sciences, 2021-04, Vol.22 (9), p.4700

2021

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Abstract P1099: Evidence Of Sialylation Pathway Alterations In Peripheral Blood Of Brugada Syndrome Patients

Circulation research, 2022-08, Vol.131 (Suppl_1)

2022

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Genotype-Phenotype Correlation in a Family with Brugada Syndrome Harboring the Novel p.Gln371 Nonsense Variant in the SCN5A Gene

International journal of molecular sciences, 2019-11, Vol.20 (22), p.5522

2019

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Challenges in Brugada Syndrome Stratification: Investigating ISCN5A/I Mutation Localization and Clinical Phenotypes

International journal of molecular sciences, 2023-11, Vol.24 (23)

2023

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PO-01-216 ALTERATIONS OF SIALYLATION MACHINERY IN PERIPHERAL BLOOD OF BRUGADA SYNDROME PATIENTS

Heart rhythm, 2023-05, Vol.20 (5), p.S165-S165

2023

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Novel SCN5A p.W697X Nonsense Mutation Segregation in a Family with Brugada Syndrome

International journal of molecular sciences, 2019-10, Vol.20 (19), p.4920

2019

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Genotype/Phenotype Relationship in a Consanguineal Family With Brugada Syndrome Harboring the R1632C Missense Variant in the SCN5A Gene

Frontiers in physiology, 2019-05, Vol.10, p.666

2019

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PO-02-146 MULTI-OMICS ANALYSIS REVEALS THE METABOLIC AND POLYGENIC BASIS OF BRUGADA SYNDROME

Heart rhythm, 2023-05, Vol.20 (5), p.S264-S264

2023

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Unravelling Novel ISCN5A/I Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights

International journal of molecular sciences, 2023-10, Vol.24 (20)

2023

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SCN5A Nonsense Mutation and NF1 Frameshift Mutation in a Family With Brugada Syndrome and Neurofibromatosis

Frontiers in genetics, 2019-02, Vol.10, p.50

2019

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Neglected patellar tendon rupture in tibial tubercle avulsion fracture in an adolescent: A case report

Avascular necrosis of the first metatarsal head in adolescence: A case report

Acquired genu recurvatum in a skeletally immature patient treated by physeal distraction: A case report

Simultaneous subtalar arthroeresis, midfoot soft tissue release, and talo-navicular arthrodesis in children with planovalgus neurologic foot

Le fratture diafisarie del femore

Pianificazione preoperatoria: parametri biomeccanici e nuove tecnologie

Septic physeal separation of proximal femur in a newborn

Role of sialidase Neu3 and ganglioside GM3 in cardiac fibroblasts activation

Challenges in Brugada Syndrome Stratification: Investigating SCN5A Mutation Localization and Clinical Phenotypes

Brugada syndrome genetics is associated with phenotype severity

Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights

Clinical Considerations for a Family with Dilated Cardiomyopathy, Sudden Cardiac Death, and a Novel TTN Frameshift Mutation

Calcium in Brugada Syndrome: Questions for Future Research

Alterations of the Sialylation Machinery in Brugada Syndrome

Novel SCN5A p.V1429M Variant Segregation in a Family with Brugada Syndrome

Novel SCN5A p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths

Abstract P1099: Evidence Of Sialylation Pathway Alterations In Peripheral Blood Of Brugada Syndrome Patients

Genotype-Phenotype Correlation in a Family with Brugada Syndrome Harboring the Novel p.Gln371 Nonsense Variant in the SCN5A Gene

Challenges in Brugada Syndrome Stratification: Investigating ISCN5A/I Mutation Localization and Clinical Phenotypes

PO-01-216 ALTERATIONS OF SIALYLATION MACHINERY IN PERIPHERAL BLOOD OF BRUGADA SYNDROME PATIENTS

Novel SCN5A p.W697X Nonsense Mutation Segregation in a Family with Brugada Syndrome

Genotype/Phenotype Relationship in a Consanguineal Family With Brugada Syndrome Harboring the R1632C Missense Variant in the SCN5A Gene

PO-02-146 MULTI-OMICS ANALYSIS REVEALS THE METABOLIC AND POLYGENIC BASIS OF BRUGADA SYNDROME

Unravelling Novel ISCN5A/I Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights

SCN5A Nonsense Mutation and NF1 Frameshift Mutation in a Family With Brugada Syndrome and Neurofibromatosis

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