Graziela S. Ribas

Porto Alegre, RS, Brazil

Last Updated: 09/26/2026

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Found 21 publications

Treatment of maple syrup urine disease: Benefits, risks, and challenges of liver transplantation.

Treatment of maple syrup urine disease: Benefits, risks, and challenges of liver transplantation.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: October 17, 2022

Clinical findings of patients with hyperammonemia affected by urea cycle disorders with hepatic encephalopathy.

Clinical findings of patients with hyperammonemia affected by urea cycle disorders with hepatic encephalopathy.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: June 22, 2022

Hyperammonemia in Inherited Metabolic Diseases.

Hyperammonemia in Inherited Metabolic Diseases.

Journal: Cellular and molecular neurobiology
Published: June 28, 2021

Evidence that Oxidative Disbalance and Mitochondrial Dysfunction are Involved in the Pathophysiology of Fatty Acid Oxidation Disorders.

Evidence that Oxidative Disbalance and Mitochondrial Dysfunction are Involved in the Pathophysiology of Fatty Acid Oxidation Disorders.

Journal: Cellular and molecular neurobiology
Published: June 15, 2020

Selective Screening of Fatty Acids Oxidation Defects and Organic Acidemias by Liquid Chromatography/tandem Mass Spectrometry Acylcarnitine Analysis in Brazilian Patients.

Selective Screening of Fatty Acids Oxidation Defects and Organic Acidemias by Liquid Chromatography/tandem Mass Spectrometry Acylcarnitine Analysis in Brazilian Patients.

Journal: Archives of medical research
Published: June 14, 2018

Oxidative profile exhibited by Mucopolysaccharidosis type IVA patients at diagnosis: Increased keratan urinary levels.

Oxidative profile exhibited by Mucopolysaccharidosis type IVA patients at diagnosis: Increased keratan urinary levels.

Journal: Molecular genetics and metabolism reports
Published: March 05, 2017

Oxidative damage and redox in Lysosomal Storage Disorders: Biochemical markers.

Oxidative damage and redox in Lysosomal Storage Disorders: Biochemical markers.

Journal: Clinica chimica acta; international journal of clinical chemistry
Published: November 12, 2016

Selective screening of Niemann-Pick type C Brazilian patients by cholestane-3β,5α,6β-triol and chitotriosidase measurements followed by filipin staining and NPC1/NPC2 gene analysis.

Selective screening of Niemann-Pick type C Brazilian patients by cholestane-3β,5α,6β-triol and chitotriosidase measurements followed by filipin staining and NPC1/NPC2 gene analysis.

Journal: Clinica chimica acta; international journal of clinical chemistry
Published: April 08, 2016

Deleterious effects of interruption followed by reintroduction of enzyme replacement therapy on a lysosomal storage disorder.

Deleterious effects of interruption followed by reintroduction of enzyme replacement therapy on a lysosomal storage disorder.

Journal: Translational research : the journal of laboratory and clinical medicine
Published: October 29, 2015

Urinary biomarkers of oxidative stress and plasmatic inflammatory profile in phenylketonuric treated patients.

Urinary biomarkers of oxidative stress and plasmatic inflammatory profile in phenylketonuric treated patients.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: September 06, 2015

Investigation of inflammatory profile in MSUD patients: benefit of L-carnitine supplementation.

Investigation of inflammatory profile in MSUD patients: benefit of L-carnitine supplementation.

Journal: Metabolic brain disease
Published: March 02, 2015

Lipid, Oxidative and Inflammatory Profile and Alterations in the Enzymes Paraoxonase and Butyrylcholinesterase in Plasma of Patients with Homocystinuria Due CBS Deficiency: The Vitamin B12 and Folic Acid Importance.

Lipid, Oxidative and Inflammatory Profile and Alterations in the Enzymes Paraoxonase and Butyrylcholinesterase in Plasma of Patients with Homocystinuria Due CBS Deficiency: The Vitamin B12 and Folic Acid Importance.

Journal: Cellular and molecular neurobiology
Published: January 11, 2015
Showing 1-12 of 21

Last Updated: 09/26/2026