Publications by authors named "Maria T Carbone"

Claim this Profile
D
DNAJC12 Disease: Clinical Spectrum and Long-Term Outcomes.
Filippo Manti, Giacomina Ricciardi, Francesca Nardecchia, Manuela Tolve, Cristiana Artiola, Maria Teresa Carbone

Neurol Genet· February 2026

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Transition in inherited metabolic diseases: the dietitians, pediatricians and adult physicians' point of view: the results of an Italian survey.
Alice Rossi, Chiara Pancaldi, Maria Giulia Regazzi, Giulio Agnelli, Valentina Assirelli, Maria Teresa Carbone

Orphanet J Rare Dis· May 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Are Phe-Free Protein Substitutes Available in Italy for Infants with PKU All the Same?
Elvira Verduci, Martina Tosi, Chiara Montanari, Mirko Gambino, Francesca Eletti, Maria Teresa Carbone

Nutrients· December 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Possible role of tryptophan metabolism along the microbiota-gut-brain axis on cognitive & behavioral aspects in Phenylketonuria.
Sara Parolisi, Chiara Montanari, Elisa Borghi, Chiara Cazzorla, Juri Zuvadelli, Maria T Carbone

Pharmacol Res· November 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
Q
Quality of life aspects of a low protein diet using GMP in patients with phenylketonuria.
Giulia Bensi, Maria Teresa Carbone, Maria Cristina Schiaffino, Sara Parolisi, Angela Pozzoli

J Int Med Res· September 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Expanded Newborn Screening in Italy Using Tandem Mass Spectrometry: Two Years of National Experience.
Margherita Ruoppolo, Sabrina Malvagia, Sara Boenzi, Carla Carducci, Carlo Dionisi-Vici, Maria Teresa Carbone

Int J Neonatal Screen· August 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Italian national consensus statement on management and pharmacological treatment of phenylketonuria.
Alberto Burlina, Giacomo Biasucci, Maria Teresa Carbone, Chiara Cazzorla, Sabrina Paci

Orphanet J Rare Dis· November 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Dysbiosis, Host Metabolism, and Non-communicable Diseases: Trialogue in the Inborn Errors of Metabolism.
Chiara Montanari, Sara Parolisi, Elisa Borghi, Lorenza Putignani, Giulia Bassanini, Maria Teresa Carbone

Front Physiol· September 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Creatine Levels in Patients with Phenylketonuria and Mild Hyperphenylalaninemia: A Pilot Study.
Elvira Verduci, Maria Teresa Carbone, Laura Fiori, Claudia Gualdi, Giuseppe Banderali

Life (Basel)· May 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The management of phenylketonuria in adult patients in Italy: a survey of six specialist metabolic centers.
Alberto Burlina, Vincenzo Leuzzi, Marco Spada, Maria Teresa Carbone, Sabrina Paci

Curr Med Res Opin· March 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Children with special health care needs attending emergency department in Italy: analysis of 3479 cases.
Paola Cianci, Valeria D'Apolito, Alex Moretti, Massimo Barbagallo, Sabrina Paci, Maria Teresa Carbone

Ital J Pediatr· November 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Nutrition, Microbiota and Role of Gut-Brain Axis in Subjects with Phenylketonuria (PKU): A Review.
Elvira Verduci, Maria Teresa Carbone, Elisa Borghi, Emerenziana Ottaviano, Alberto Burlina

Nutrients· October 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Neonatal malpractice claims in Italy: how big is the problem and which are the causes?
Vassilios Fanos, Paolo Tagliabue, Luigi Greco, Rino Agostiniani, Maria Teresa Carbone

J Matern Fetal Neonatal Med· May 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Five human phenylalanine hydroxylase proteins identified in mild hyperphenylalaninemia patients are disease-causing variants.
Aurora Daniele, Giuseppe Cardillo, Cinzia Pennino, Maria T Carbone, Domenico Scognamiglio

Biochim Biophys Acta· June 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis