Lista de obras - Morteza Pourfarzam - Dominio Público Uruguay

"So doctor, what exactly is wrong with my muscles? Glutaric aciduria type II presenting in a teenager"

scientific article published on 21 August 2006

26 Synthesis, purification, and characterization of dicarboxylylmono-coenzyme A esters

artículo científico publicado el 1 de enero de 1997

A review of strategies for untargeted urinary metabolomic analysis using gas chromatography-mass spectrometry

scientific article published on 18 May 2020

A splice junction mutation in muscle carnitine palmitoyltransferase II deficiency

artículo científico publicado en 2003

Analysis of mitochondrial fatty acid oxidation intermediates by tandem mass spectrometry from intact mitochondria prepared from homogenates of cultured fibroblasts, skeletal muscle cells, and fresh muscle.

artículo científico publicado en 2002

Association of the total cholesterol content of erythrocyte membranes with the severity of disease in stable coronary artery disease.

artículo científico publicado en 2014

Biochemical changes in blood of type 2 diabetes with and without metabolic syndrome and their association with metabolic syndrome components

artículo científico publicado en 2015

Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency.

artículo científico publicado en 1999

Combined enzyme defect of mitochondrial fatty acid oxidation

artículo científico publicado en 1992

ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency

artículo científico publicado en 2007

Elevated plasma myeloperoxidase levels in relation to circulating inflammatory markers in coronary artery disease

artículo científico publicado en 2011

Expression and clinicopathological significance of lipin-1 in human breast cancer and its association with p53 tumor suppressor gene

artículo científico publicado en 2020

Fatty acid oxidation in peripheral blood cells: characterization and use for the diagnosis of defects of fatty acid oxidation.

artículo científico publicado en 1995

Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen.

artículo científico publicado en 2003

Impaired ketogenesis in fructose-1,6-bisphosphatase deficiency: a pitfall in the investigation of hypoglycaemia.

artículo científico publicado en 1995

Increased membrane lipid peroxidation and decreased Na+/K+-ATPase activity in erythrocytes of patients with stable coronary artery disease.

artículo científico publicado en 2015

Intermediates of myocardial mitochondrial beta-oxidation: possible channelling of NADH and of CoA esters

artículo científico publicado en 1999

Intermediates of peroxisomal beta-oxidation of [U-14C]hexadecanedionoate. A study of the acyl-CoA esters which accumulate during peroxisomal beta-oxidation of [U-14C]hexadecanedionate and [U-14C]hexadecanedionoyl-mono-CoA

artículo científico publicado en 1992

Investigation of membrane fatty acid profiles in erythrocytes of patients with stable coronary artery disease.

artículo científico publicado en 2016

Lipid-storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late-onset multiple acyl-CoA dehydrogenation deficiency.

artículo científico publicado en 2004

Measurement of acyl-CoA dehydrogenase activity in cultured skin fibroblasts and blood platelets

artículo científico publicado en 1992

Methylmalonic acidaemia: examination of genotype and biochemical data in 32 patients belonging to mut, cblA or cblB complementation group.

artículo científico publicado en 2007

Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency.

artículo científico publicado en 2003

N-acetylglutamate synthetase deficiency: favourable experience with carbamylglutamate.

artículo científico publicado en 1998

Neonatal hyperammonemia caused by a defect of carnitine-acylcarnitine translocase

scientific article published on 01 November 1995

Normal acylcarnitines in maternal urine during a pregnancy affected by glutaric aciduria type II

artículo científico publicado en 1999

Plasma coenzyme Q(10) in children and adolescents undergoing doxorubicin therapy

scientific article published on 01 December 2000

Serum paraoxonase 1 activity is associated with fatty acid composition of high density lipoprotein

artículo científico publicado en 2013

Skeletal muscle mitochondrial beta-oxidation of dicarboxylates

scientific article published on 01 February 1993

So doctor, what exactly is wrong with my muscles? Glutaric aciduria type II presenting in a teenager

artículo científico publicado en 2006

Synthesis, characterisation and high-performance liquid chromatography of C6C16 dicarboxylyl-mono-coenzyme A and -mono-carnitine esters ⬇️

artículo científico publicado el 4 de octubre de 1991

Lista de obras de Morteza Pourfarzam

"So doctor, what exactly is wrong with my muscles? Glutaric aciduria type II presenting in a teenager"

26 Synthesis, purification, and characterization of dicarboxylylmono-coenzyme A esters

A review of strategies for untargeted urinary metabolomic analysis using gas chromatography-mass spectrometry

A splice junction mutation in muscle carnitine palmitoyltransferase II deficiency

Analysis of mitochondrial fatty acid oxidation intermediates by tandem mass spectrometry from intact mitochondria prepared from homogenates of cultured fibroblasts, skeletal muscle cells, and fresh muscle.

Association of the total cholesterol content of erythrocyte membranes with the severity of disease in stable coronary artery disease.

Biochemical changes in blood of type 2 diabetes with and without metabolic syndrome and their association with metabolic syndrome components

Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency.

Combined enzyme defect of mitochondrial fatty acid oxidation

ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency

Elevated plasma myeloperoxidase levels in relation to circulating inflammatory markers in coronary artery disease

Expression and clinicopathological significance of lipin-1 in human breast cancer and its association with p53 tumor suppressor gene

Fatty acid oxidation in peripheral blood cells: characterization and use for the diagnosis of defects of fatty acid oxidation.

Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen.

Impaired ketogenesis in fructose-1,6-bisphosphatase deficiency: a pitfall in the investigation of hypoglycaemia.

Increased membrane lipid peroxidation and decreased Na+/K+-ATPase activity in erythrocytes of patients with stable coronary artery disease.

Intermediates of myocardial mitochondrial beta-oxidation: possible channelling of NADH and of CoA esters

Intermediates of peroxisomal beta-oxidation of [U-14C]hexadecanedionoate. A study of the acyl-CoA esters which accumulate during peroxisomal beta-oxidation of [U-14C]hexadecanedionate and [U-14C]hexadecanedionoyl-mono-CoA

Investigation of membrane fatty acid profiles in erythrocytes of patients with stable coronary artery disease.

Lipid-storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late-onset multiple acyl-CoA dehydrogenation deficiency.

Measurement of acyl-CoA dehydrogenase activity in cultured skin fibroblasts and blood platelets

Methylmalonic acidaemia: examination of genotype and biochemical data in 32 patients belonging to mut, cblA or cblB complementation group.

Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency.

N-acetylglutamate synthetase deficiency: favourable experience with carbamylglutamate.

Neonatal hyperammonemia caused by a defect of carnitine-acylcarnitine translocase

Normal acylcarnitines in maternal urine during a pregnancy affected by glutaric aciduria type II

Plasma coenzyme Q(10) in children and adolescents undergoing doxorubicin therapy

Serum paraoxonase 1 activity is associated with fatty acid composition of high density lipoprotein

Skeletal muscle mitochondrial beta-oxidation of dicarboxylates

So doctor, what exactly is wrong with my muscles? Glutaric aciduria type II presenting in a teenager

Synthesis, characterisation and high-performance liquid chromatography of C6C16 dicarboxylyl-mono-coenzyme A and -mono-carnitine esters ⬇️