Veronica Bindi

Research Protocol at Hospital De Pediatría Prof. Dr. Juan P. Garrahan

Based in Buenos, Argentina

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Seniority

Staff

Department

Healthcare & Human Services

Location

Buenos

Industry

Hospitals and Health Care

Company size

3K

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Email

1 credit

v•••••••@garrahan.gov.ar

Phone

5 credits

+54 ••• •••• ••••

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Background

About Veronica Bindi

I am a pediatrician with a strong background in molecular biology and Inborn Errors of Metabolism (IEM). I have over 10 years of experience at Hospital Juan P. Garrahan, where I have led research projects and collaborated with multidisciplinary teams in the care of pediatric patients with complex metabolic disorders. I am committed to innovation in precision medicine and eager to explore opportunities that contribute to advancing research and treatment for rare metabolic diseases. My passion for molecular biology and genetics led me to specialize in the diagnosis and treatment of rare metabolic disorders. Throughout my career, I have gained expertise in clinical research, inborn errors of metabolism, and molecular biology. Additionally, I enjoy teaching and training new professionals in the field. In 2024, I completed a Master’s degree in Medical Molecular Biology at the University of Buenos Aires, where I developed a pioneering study on hepatic glycogenosis and its correlation with phenotype in Argentine patients, which was approved by the hospital's Ethics Committee. My work includes advanced tools such as protein modeling and bioinformatics analysis, aiming to improve the diagnosis and treatment of rare metabolic diseases. I am also conducting a doctoral research project focusing on missense variants and their functional impact on hepatic glycogenosis. This project aims to translate scientific findings into practical improvements that benefit pediatric patients and their families. Throughout my career, I have contributed to advancing knowledge in inborn errors of metabolism, genetics, and molecular biology through various scientific publications. My work has focused on the diagnosis and treatment of rare metabolic diseases, with a special emphasis on cobalamin deficiency, urea cycle disorders, and mitochondrial diseases in pediatric populations. I am open to new opportunities in the field of molecular biology and inborn errors of metabolism. If you would like to learn more about my background or explore potential collaborations, I would be happy to connect. verogbindi@gmail.com

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