Concetta Meli

Clinical Practice Guidelines for Clostridium difficile Infection in Adults and Children: 2017 Update by the Infectious Diseases Society of America (IDSA) and Society for Healthcare Epidemiology of America (SHEA)

ASL mRNA-LNP Therapeutic for the Treatment of Argininosuccinic Aciduria Enables Survival Benefit in a Mouse Model

Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision

How Good is Endoscopic Ultrasound in Differentiating Various T Stages of Rectal Cancer? Meta-Analysis and Systematic Review

Identification and Evaluation of Children With Autism Spectrum Disorders

Colorectal cancer

Clinical Practice Guidelines for Clostridium difficile Infection in Adults: 2010 Update by the Society for Healthcare Epidemiology of America (SHEA) and the Infectious Diseases Society of America (IDSA)

Suggested guidelines for the diagnosis and management of urea cycle disorders

Tetrahydrobiopterin as an Alternative Treatment for Mild Phenylketonuria

How were new medicines discovered?

Autism

Prenatal Valproate Exposure and Risk of Autism Spectrum Disorders and Childhood Autism

Occurrence, genotoxicity, and carcinogenicity of regulated and emerging disinfection by-products in drinking water: A review and roadmap for research

Pseudomembranous colitis associated with chemotherapy with 5-fluorouracil

22q11.2 deletion syndrome

The Genetics of Autism

Geometric and Electronic Structure/Function Correlations in Non-Heme Iron Enzymes

Robots for Use in Autism Research

Missense mutations in the phenylalanine hydroxylase gene (PAH) can cause accelerated proteolytic turnover of PAH enzyme: A mechanism underlying phenylketonuria

Defective folding and rapid degradation of mutant proteins is a common disease mechanism in genetic disorders

Randomized, Controlled Trial of an Intervention for Toddlers With Autism: The Early Start Denver Model

Autism spectrum disorders—A genetics review

Evaluation of the rat micronucleus test with bone marrow and peripheral blood: Summary of the 9th collaborative study by CSGMT/JEMS·MMS

Symmetry-free cryo-EM structures of the chaperonin TRiC along its ATPase-driven conformational cycle

Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management

A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype

Comparision between transrectal ultrasonography and computed tomography with rectal inflation of gas in preoperative staging of lower rectal cancer

Autism and Phenylketonuria

Activity of 1,2-dimethylhydrazine in the mouse bone marrow micronucleus assay using a triple- and a single-dosing protocol

Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

Dihydropyrimidine dehydrogenase deficiency and acute neurological presentation