L. Refosco

Nutritional Status and Body Composition in Patients With Hepatic Glycogen Storage Diseases Treated With Uncooked Cornstarch—A Controlled Study:

I. Perry, Bruna Santos, Tatiéle Nalin, 2017 .

Molecular characterization of phenylketonuria in South Brazil.

R. Desnick, R. Giugliani, R. Pires, 2003, Molecular genetics and metabolism.

[Management of a case of maple syrup urine disease--the use of gluco-insulinotherapy].

M. Sanseverino, R. Giugliani, E. A. Trotta, 1995, Jornal de Pediatria.

Glycogen storage disease type I: clinical and laboratory profile.

L. Schuler‐Faccini, Tatiéle Nalin, L. Refosco, 2014, Jornal de Pediatria.

Feeding Difficulties and Orofacial Myofunctional Disorder in Patients with Hepatic Glycogen Storage Diseases.

C. Martinez, Tatiéle Nalin, L. Refosco, 2019, JIMD reports.

Phenylketonuria and Gut Microbiota: A Controlled Study Based on Next-Generation Sequencing

V. Mai, L. Roesch, P. Dobbler, 2016, PloS one.

Description of a Nutrition Screening and Assessment Tool and Associations with Clinical Outcomes in Preterm Newborns.

J. Bernardi, L. Refosco, R. Sarmento, 2021, Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition.

Anthropometry, Nutritional Status, and Dietary Intake in Pediatric Patients with Osteogenesis Imperfecta

T. Félix, R. Giugliani, L. Refosco, 2014, Journal of the American College of Nutrition.

A Broad Characterization of Glycogen Storage Disease IV Patients: A Clinical, Genetic, and Histopathological Study

M. Shinawi, L. Refosco, I. Schwartz, 2023, Biomedicines.

A triple-blinded crossover study to evaluate the short-term safety of sweet manioc starch for the treatment of glycogen storage disease type Ia

T. Derks, Tatiéle Nalin, L. Refosco, 2021, Orphanet Journal of Rare Diseases.

Current Practices and Challenges in the Diagnosis and Management of PKU in Latin America: A Multicenter Survey

A. Mahfoud, A. Chiesa, Soraia Poloni, 2021, Nutrients.