Laura Bruni
Biographic Data
| ID | 8251260 |
|---|---|
| NAME | Laura Bruni |
| GIVEN NAMES | Laura |
| FAMILY NAME | Bruni |
| SIGNATURE | BRUNI L |
| AFFILIATIONS | University of Bologna |
| VERIFIED | No |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 2 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2021 |
| LATEST PUBLICATION YEAR | 2023 |
| H-INDEX | 0 |
A Case of Acrodermatitis Dysmetabolica in a Child Affected by Citrullinemia Type I
An infant with a prenatal diagnosis of citrullinemia, who started standard treatment at birth (L-arginine; sodium benzoate and a personalized diet characterized by a low protein intake and supplementation of essential nutrients and amino acids), presented at 4 months of age with extended, progressive, and severe skin lesions consistent with acrodermatitis dysmetabolica. Guidelines for the diagnosis and management of urea cycle disorders underline…
Pyelonephritis in Pediatric Uropathic Patients
Pyelonephritis (PN) represents an important cause of morbidity in the pediatric population, especially in uropathic patients. The aim of the study is to demonstrate differences between PNs of uropathic patients and PNs acquired in community in terms of uropathogens involved and antibiotic sensitivity; moreover, to identify a proper empiric therapeutic strategy. A retrospective study was conducted on antibiograms on urine cultures from PNs in vesi…
No prominent works on this page.
Pyelonephritis in Pediatric Uropathic Patients
Pyelonephritis (PN) represents an important cause of morbidity in the pediatric population, especially in uropathic patients. The aim of the study is to demonstrate differences between PNs of uropathic patients and PNs acquired in community in terms of uropathogens involved and antibiotic sensitivity; moreover, to identify a proper empiric therapeutic strategy. A retrospective study was conducted on antibiograms on urine cultures from PNs in vesi…
A Case of Acrodermatitis Dysmetabolica in a Child Affected by Citrullinemia Type I
An infant with a prenatal diagnosis of citrullinemia, who started standard treatment at birth (L-arginine; sodium benzoate and a personalized diet characterized by a low protein intake and supplementation of essential nutrients and amino acids), presented at 4 months of age with extended, progressive, and severe skin lesions consistent with acrodermatitis dysmetabolica. Guidelines for the diagnosis and management of urea cycle disorders underline…
Biology (2 works) · Internal Medicine (2 works) · Medicine (2 works) · Pediatrics (2 works) · Acrodermatitis (1 work) · Amino acid (1 work) · Antibiotics (1 work) · Arginine (1 work) · Bacteria (1 work) · Biochemistry (1 work)