V. Hamilton

发表

Identification of Four New Mutations in Chilean Patients with Various Forms of Maple Syrup Urine Disease and Genotype-Phenotype Correlations

W. A. Silva, I. Schwartz, G. Molfetta, 2019 .

Identification of Four Novel Mutations in Chilean Patients with Various Forms of Maple Syrup Urine Disease

W. A. Silva, I. Schwartz, G. Molfetta, 2020 .

Update on Dietary Compliance, Nutritional Status, and Neuropsychological Functioning in the Chilean Phenylketonuria cohort

M. F. Salazar, J. Cabello, C. Arias, 2021 .

Characterization of Phenyalanine Hydroxylase Gene Mutations in Chilean PKU Patients.

M. Ugarte, B. Pérez, L. Desviat, 2018, JIMD reports.

Myeloneuropathy from nitrous oxide abuse: unusually high methylmalonic acid and homocysteine levels.

C. Luzzio, A. Waclawik, Katalin Juhasz-Pocsine, 2003, WMJ : official publication of the State Medical Society of Wisconsin.

Molecular basis of various forms of maple syrup urine disease in Chilean patients

W. A. Silva, I. Schwartz, G. Molfetta, 2021, Molecular genetics & genomic medicine.

Chilean Nutrition Management Protocol for Patients With Phenylketonuria

G. Castro, V. Cornejo, V. Hamilton, 2017 .

Energy Expenditure in Chilean Children with Maple Syrup Urine Disease (MSUD).

J. Cabello, G. Castro, C. Arias, 2016, JIMD reports.

NTBC Treatment Monitoring in Chilean Patients with Tyrosinemia Type 1 and Its Association with Biochemical Parameters and Liver Biomarkers

K. Fuenzalida, C. Arias, M. J. Leal-Witt, 2021, Journal of clinical medicine.

First-year metabolic control guidelines and their impact on future metabolic control and neurocognitive functioning in children with PKU

J. Cabello, C. Arias, V. Cornejo, 2017, Molecular genetics and metabolism reports.

Diet therapy and metabolic control among Chilean adults with a neonatal diagnosis of Phenylketonuria

J. Cabello, C. Arias, M. J. Leal-Witt, 2024, Journal of Inborn Errors of Metabolism and Screening.