Experienced in Carbamoyl Phosphate Synthetase 1 Deficiency

Jessica L. Faverzani

Porto Alegre, RS, BR 
Experienced in Carbamoyl Phosphate Synthetase 1 Deficiency
Porto Alegre, RS, BR 
OverviewLocationsClinical Research

Overview

Jessica Faverzani practices in Porto Alegre, Brazil. Ms. Faverzani is rated as an Experienced expert by MediFind in the treatment of Carbamoyl Phosphate Synthetase 1 Deficiency. Her top areas of expertise are Phenylketonuria (PKU), Glutaric Acidemia Type 1, Orotic Aciduria Type 1, and Primary Carnitine Deficiency.

Her clinical research consists of co-authoring 18 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Carbamoyl Phosphate Synthetase 1 Deficiency.

Gender
Female

Locations

Porto Alegre, RS 90035003, Brazil

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.

18 Total Publications

Nitisinone treatment protect hereditary tyrosinemia type I patients against inflammation, DNA and protein oxidative damage by decreasing succinylacetone levels.
Nitisinone treatment protect hereditary tyrosinemia type I patients against inflammation, DNA and protein oxidative damage by decreasing succinylacetone levels.
Journal: Metabolic brain disease
Published: February 06, 2025

Areas of Expertise

MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.

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