List of works - Isabel Ibarra

An Amino Acid Signature Associated with Obesity Predicts 2-Year Risk of Hypertriglyceridemia in School-Age Children.

scientific article

An International Classification of Inherited Metabolic Disorders (ICIMD)

scientific article published on 19 December 2020

Biotin deprivation impairs mitochondrial structure and function and has implications for inherited metabolic disorders.

scientific article published in September 2015

Biotinidase knockout mice show cellular energy deficit and altered carbon metabolism gene expression similar to that of nutritional biotin deprivation: clues for the pathogenesis in the human inherited disorder.

scientific article

COMPARISON OF FREE CARNITINE LEVELS WITH NUTRITIONAL STATUS IN INFANTILE NEPHROPATHYC CISTINOSIS PATIENTS

scientific article published in December 2015

Causes of delay in referral of patients with phenylketonuria to a specialized reference centre in Mexico.

scientific article published in January 2011

Clinical and biochemical characteristics of patients with urea cycle disorders in a developing country.

scientific article published on 16 December 2009

Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: a worldwide collaborative project.

scientific article published in March 2011

Composition of gut microbiota in obese and normal-weight Mexican school-age children and its association with metabolic traits

scientific article published on 5 December 2017

Correspondence on ''experience with hyperphenylalaninemia in a developing country: unusual clinical manifestations and a novel gene mutation''

scientific article published on 01 February 2011

Diagnosis of inborn errors of metabolism.

scientific article published in March 2000

Effect of highly active antiretroviral therapy on homocysteine plasma concentrations in HIV-1-infected patients.

scientific article

Effect of supplementation during pregnancy with L-arginine and antioxidant vitamins in medical food on pre-eclampsia in high risk population: randomised controlled trial ⬇️

scientific article

Family history and obesity in youth, their effect on acylcarnitine/aminoacids metabolomics and non-alcoholic fatty liver disease (NAFLD). Structural equation modeling approach.

scientific article published on 21 February 2018

Genetic spectrum and clinical early natural history of glucose-6-phosphate dehydrogenase deficiency in Mexican children detected through newborn screening

scientific article published on 26 February 2021

Hepatorenal Tyrosinemia in Mexico: A Call to Action.

scientific article

Higher incidence of thyroid agenesis in Mexican newborns with congenital hypothyroidism associated with birth defects

scientific article published on 03 August 2011

Kernicterus in a boy with ornithine transcarbamylase deficiency: A case report.

scientific article

Metabolic screening and metabolomics analysis in the Intellectual Developmental Disorders Mexico Study

scientific article published in July 2017

Phenylalanine hydroxylase deficiency in Mexico: genotype-phenotype correlations, BH4 responsiveness and evidence of a founder effect

scientific article published on 26 July 2014

Temporal development of genetic and metabolic effects of biotin deprivation. A search for the optimum time to study a vitamin deficiency.

scientific article

The C677T polymorphism of the methylenetetrahydrofolate reductase gene is associated with idiopathic ischemic stroke in the young Mexican-Mestizo population.

scientific article published on 4 March 2010

[Characterization of inborn errors of intermediary metabolism in mexican patients].

scientific article

List of works by Isabel Ibarra

An Amino Acid Signature Associated with Obesity Predicts 2-Year Risk of Hypertriglyceridemia in School-Age Children.

An International Classification of Inherited Metabolic Disorders (ICIMD)

Biotin deprivation impairs mitochondrial structure and function and has implications for inherited metabolic disorders.

Biotinidase knockout mice show cellular energy deficit and altered carbon metabolism gene expression similar to that of nutritional biotin deprivation: clues for the pathogenesis in the human inherited disorder.

COMPARISON OF FREE CARNITINE LEVELS WITH NUTRITIONAL STATUS IN INFANTILE NEPHROPATHYC CISTINOSIS PATIENTS

Causes of delay in referral of patients with phenylketonuria to a specialized reference centre in Mexico.

Clinical and biochemical characteristics of patients with urea cycle disorders in a developing country.

Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: a worldwide collaborative project.

Composition of gut microbiota in obese and normal-weight Mexican school-age children and its association with metabolic traits

Correspondence on ''experience with hyperphenylalaninemia in a developing country: unusual clinical manifestations and a novel gene mutation''

Diagnosis of inborn errors of metabolism.

Effect of highly active antiretroviral therapy on homocysteine plasma concentrations in HIV-1-infected patients.

Effect of supplementation during pregnancy with L-arginine and antioxidant vitamins in medical food on pre-eclampsia in high risk population: randomised controlled trial ⬇️

Family history and obesity in youth, their effect on acylcarnitine/aminoacids metabolomics and non-alcoholic fatty liver disease (NAFLD). Structural equation modeling approach.

Genetic spectrum and clinical early natural history of glucose-6-phosphate dehydrogenase deficiency in Mexican children detected through newborn screening

Hepatorenal Tyrosinemia in Mexico: A Call to Action.

Higher incidence of thyroid agenesis in Mexican newborns with congenital hypothyroidism associated with birth defects

Kernicterus in a boy with ornithine transcarbamylase deficiency: A case report.

Metabolic screening and metabolomics analysis in the Intellectual Developmental Disorders Mexico Study

Phenylalanine hydroxylase deficiency in Mexico: genotype-phenotype correlations, BH4 responsiveness and evidence of a founder effect

Temporal development of genetic and metabolic effects of biotin deprivation. A search for the optimum time to study a vitamin deficiency.

The C677T polymorphism of the methylenetetrahydrofolate reductase gene is associated with idiopathic ischemic stroke in the young Mexican-Mestizo population.

[Characterization of inborn errors of intermediary metabolism in mexican patients].