Detalhe da pesquisa
1.
A higher bacterial inward BCAA transport driven by Faecalibacterium prausnitzii is associated with lower serum levels of BCAA in early adolescents.
Mol Med
; 27(1): 108, 2021 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34525937
2.
Kernicterus in a boy with ornithine transcarbamylase deficiency: A case report.
Neuropathology
; 37(6): 586-590, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28815739
3.
Hepatorenal Tyrosinemia in Mexico: A Call to Action.
Adv Exp Med Biol
; 959: 147-156, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28755193
4.
Metabolic screening and metabolomics analysis in the Intellectual Developmental Disorders Mexico Study.
Salud Publica Mex
; 59(4): 423-428, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29211263
5.
Biotin deprivation impairs mitochondrial structure and function and has implications for inherited metabolic disorders.
Mol Genet Metab
; 116(3): 204-14, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26343941
6.
Tyrosinemia type I: clinical and biochemical analysis of patients in Mexico.
Ann Hepatol
; 13(2): 265-72, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24552869
7.
Hypogammaglobulinemia Class G Is Present in Compensated and Decompensated Patients with Propionate Defects, Independent of Their Nutritional Status.
Nutrients
; 16(11)2024 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38892708
8.
The BMI Z-Score and Protein Energy Ratio in Early- and Late-Diagnosed PKU Patients from a Single Reference Center in Mexico.
Nutrients
; 15(4)2023 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-36839315
9.
An early prediction model for gestational diabetes mellitus based on metabolomic biomarkers.
Diabetol Metab Syndr
; 15(1): 116, 2023 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37264408
10.
A Review of Disparities and Unmet Newborn Screening Needs over 33 Years in a Cohort of Mexican Patients with Inborn Errors of Intermediary Metabolism.
Int J Neonatal Screen
; 9(4)2023 Oct 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37873850
11.
In Silico Structural Protein Evaluation of the Phenylalanine Hydroxylase p.(Tyr77His) Variant Associated with Benign Hyperphenylalaninemia as Identified through Mexican Newborn Screening.
Children (Basel)
; 10(12)2023 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38136067
12.
Temporal development of genetic and metabolic effects of biotin deprivation. A search for the optimum time to study a vitamin deficiency.
Mol Genet Metab
; 107(3): 345-51, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23010431
13.
Functional characterization of the p.(Gln195His) or Tainan and novel p.(Ser184Cys) or Toluca glucose-6-phosphate dehydrogenase (G6PD) gene natural variants identified through Mexican newborn screening for glucose-6-phosphate dehydrogenase deficiency.
Clin Biochem
; 109-110: 64-73, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36089067
14.
A Longitudinal 1H NMR-Based Metabolic Profile Analysis of Urine from Hospitalized Premature Newborns Receiving Enteral and Parenteral Nutrition.
Metabolites
; 12(3)2022 Mar 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35323698
15.
Targeted Metabolomics Revealed a Sex-Dependent Signature for Metabolic Syndrome in the Mexican Population.
Nutrients
; 14(18)2022 Sep 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36145054
16.
Metabolic Reprogramming in SARS-CoV-2 Infection Impacts the Outcome of COVID-19 Patients.
Front Immunol
; 13: 936106, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36341434
17.
Genetic spectrum and clinical early natural history of glucose-6-phosphate dehydrogenase deficiency in Mexican children detected through newborn screening.
Orphanet J Rare Dis
; 16(1): 103, 2021 02 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33637102
18.
Brief Report: Delayed Diagnosis of Treatable Inborn Errors of Metabolism in Children with Autism and Other Neurodevelopmental Disorders.
J Autism Dev Disord
; 51(6): 2124-2131, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32880084
19.
Serum Metabolite Profile Associated with Sex-Dependent Visceral Adiposity Index and Low Bone Mineral Density in a Mexican Population.
Metabolites
; 11(9)2021 Sep 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34564420
20.
An Updated PAH Mutational Spectrum of Phenylketonuria in Mexican Patients Attending a Single Center: Biochemical, Clinical-Genotyping Correlations.
Genes (Basel)
; 12(11)2021 10 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34828281