C. Roe

发表

Parenteral and enteral metabolism of anaplerotic triheptanoin in normal rats . II . Effects on lipolysis , glucose production , and liver acyl-CoA profile

Guo-Fang Zhang, L. Gu, R. Kombu, 2010 .

Pyruvate carboxylase deficiency: clinical and biochemical response to anaplerotic diet therapy.

F. Mochel, D. Rabier, C. Roe, 2005, Molecular genetics and metabolism.

Pyruvate carboxylase deficiency: mechanisms, mimics and anaplerosis.

C. Roe, I. Marín-Valencia, J. Pascual, 2010, Molecular genetics and metabolism.

Urinary Excretion of l-Carnitine and Acylcarnitines by Patients with Disorders of Organic Acid Metabolism: Evidence for Secondary Insufficiency of l-Carnitine

R. Chalmers, C. Hoppel, C. Roe, 1984, Pediatric Research.

Rapid diagnosis of phenylketonuria by quantitative analysis for phenylalanine and tyrosine in neonatal blood spots by tandem mass spectrometry.

D. Millington, C. Roe, D. Chace, 1993, Clinical chemistry.

Identification of 3-methylglutarylcarnitine. A new diagnostic metabolite of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency.

D. Maltby, D. Millington, C. Roe, 1986, The Journal of clinical investigation.

Medium-chain acyl-coenzyme A dehydrogenase deficiency and sudden infant death.

Y. T. Chen, C. Roe, A. K. Iafolla, 1991, The New England journal of medicine.

Octanoic Acid Produces Accumulation of Monoamine Acidic Metabolites in the Brain: Interaction with Organic Anion Transport at the Choroid Plexus

G. Breese, C. Roe, TC. S. Kim, 1992, Journal of neurochemistry.

The role of tandem mass spectrometry in the diagnosis of fatty acid oxidation disorders.

Y. T. Chen, D. Millington, C. Roe, 1992, Progress in clinical and biological research.

A sensitivity analysis of enzymatic estimation of infarct size.

C. Starmer, C. Roe, 1975, Circulation.

The Relationship between Enzymatic and Histologic Estimates of the Extent of Myocardial Infarction in Conscious Dogs with Permanent Coronary Occlusion

C. Starmer, F. Cobb, C. Roe, 1977, Circulation.

Nonlinear Relationship Between Creatine Kinase Estimates and Histologic Extent of Infarction in Conscious Dogs: Effects of Regional Myocardial Blood Flow

P. McHale, F. Cobb, C. Roe, 1980, Circulation.

Diagnosis of Acute Myocardial Infarction in a Community Hospital: Significance of CPK‐MB Determination

G. Wagner, S. Roark, C. Roe, 1976, Circulation.

The importance of identification of the myocardial-specific isoenzyme of creatine phosphokinase (MB form) in the diagnosis of acute myocardial infarction.

R. Rosati, G. Wagner, A. Wallace, 1973, Circulation.

Combined isoenzyme analysis in the diagnosis of myocardial injury: application of electrophoretic methods for the detection and quantitation of the creatine phosphokinase MB isoenzyme.

G. Wagner, C. Roe, L. Limbird, 1972, The Journal of laboratory and clinical medicine.

Differentiation of long-chain fatty acid oxidation disorders using alternative precursors and acylcarnitine profiling in fibroblasts.

C. Roe, E. Struys, C. Vianey‐Saban, 2006, Molecular genetics and metabolism.

Recent developments in the investigation of inherited metabolic disorders using cultured human cells.

C. Roe, D. Roe, 1999, Molecular genetics and metabolism.

REMOVED: Short-chain acyl-CoA dehydrogenase gene mutation (319 C>T) presents with clinical heterogeneity and is candidate founder mutation in Ashkenazi Jewish population.

D. Lev, S. Korman, N. Gregersen, 2007, Molecular genetics and metabolism.

Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes.

D. Maltby, D. Millington, C. Roe, 1986, The Journal of pediatrics.

Validity of estimating myocardial infarct size from serial measurements of enzyme activity in the serum.

C. Roe, 1977, Clinical chemistry.

The Importance of Identification of the Myocardial‐Specific Isoenzyme of Creatine Phosphokinase (MB Form) in the Diagnosis of Acute Myocardial Infarction

R. Rosati, G. Wagner, A. Wallace, 1973 .

Table 1 . Relation between CK-MB Area and EKG Diagnostic Category in 77 Patients Undergoing Coronary Artery Surgery

Steven, G. Wagner, C. Roe, 2004 .

L-carnitine enhances excretion of propionyl coenzyme A as propionylcarnitine in propionic acidemia.

T. Bohan, C. Hoppel, D. Maltby, 1984, The Journal of clinical investigation.

Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groups.

C. Hoppel, D. Millington, C. Roe, 1983, Archives of disease in childhood.

The mutational spectrum in very long-chain acyl-CoA dehydrogenase deficiency

P. Bross, B. Andresen, P. Divry, 1996, Journal of Inherited Metabolic Disease.

Quantitative assay of free and total carnitine using tandem mass spectrometry.

D. Millington, C. Roe, D. Norwood, 1990, Clinica chimica acta; international journal of clinical chemistry.

Endogenous catabolism is the major source of toxic metabolites in isovaleric acidemia.

D. Maltby, D. Millington, C. Roe, 1987, The Journal of pediatrics.

Hepatic Carnitine Palmitoyltransferase I Deficiency Presenting as Maternal Illness in Pregnancy

R. Wanders, C. Roe, C. Greenberg, 2000, Pediatric Research.

Myocardial Infarct Extension: Incidence and Relationship to Survival

D. Harrison, F. Cobb, C. Roe, 1982, Circulation.

Acute myocardial infarction and MB creatine phosphokinase. Relationship between onset of symptoms of infarction and appearance and disappearance of enzyme.

F. Cobb, C. Roe, R. G. Irvin, 1980, Archives of internal medicine.

Pedigree testing in duchenne muscular dystrophy

C. Roe, A. Roses, G. Nicholson, 1977, Annals of neurology.

Late appearance of skin rash and abnormal serum enzymes in Rocky Mountain spotted fever. A case report.

P. Banks, C. Roe, D. Sexton, 1975, The Journal of pediatrics.

Recognition of Postoperative Acute Myocardial Infarction: Application of Isoenzyme Techniques

G. Wagner, H. Oldham, S. H. Dixon, 1973, Circulation.

Parenteral and enteral metabolism of anaplerotic triheptanoin in normal rats.

G. Kutz, Wolf-Ulrich Brewer, C. Roe, 2006, American journal of physiology. Endocrinology and metabolism.

on gluconeogenesis and lipolysis in rats Effects of a high-fat diet and voluntary wheel running

Christopher J. Davidson, R. Bergman, T. Zderic, 2015 .

2,4-Dienoyl-coenzyme A reductase deficiency: a possible new disorder of fatty acid oxidation.

D. Millington, C. Roe, H. Sprecher, 1990, The Journal of clinical investigation.

Anaplerotic diet therapy in inherited metabolic disease: Therapeutic potential

F. Mochel, C. Roe, 2006, Journal of Inherited Metabolic Disease.

Role of Common Gene Variations in the Molecular Pathogenesis of Short-Chain Acyl-CoA Dehydrogenase Deficiency

J. Vockley, D. Babovic‐Vuksanovic, A. Sewell, 2001, Pediatric Research.

Very long chain acyl-CoA dehydrogenase deficiency: successful treatment of acute cardiomyopathy.

C. Roe, H. Sprecher, C. Vianey‐Saban, 1996, Biochemical and molecular medicine.

Lactate dehydrogenase isoenzyme 5 in detecting carriers of Duchenne muscular dystrophy

A. Roses, C. Roe, G. Nicholson, 1977, Neurology.

The Genes for the α and β Subunits of the Mitochondrial Trifunctional Protein Are Both Located in the Same Region of Human Chromosome 2p23

H. Heng, C. Roe, Bing-zhi Yang, 1996 .

Relation of creatine kinase isoenzyme MB to postoperative electrocardiographic diagnosis in patients undergoing coronary-artery bypass surgery.

G. Wagner, F. Cobb, C. Roe, 1979, Clinical chemistry.

Anaplerotic Triheptanoin Diet Enhances Mitochondrial Substrate Use to Remodel the Metabolome and Improve Lifespan, Motor Function, and Sociability in MeCP2-Null Mice

Min Jung Park, G. Ronnett, C. Roe, 2014, PloS one.

Adult Polyglucosan Body Disease (APBD): Anaplerotic diet therapy (Triheptanoin) and demonstration of defective methylation pathways.

T. Bottiglieri, C. Roe, E. Arning, 2009, Molecular genetics and metabolism.

Diagnostic and prognostic significance of electrocardiographic and CPK isoenzyme changes following coronary bypass surgery: correlation with findings at one year.

G. Wagner, H. Oldham, C. Roe, 1977, American heart journal.

Persistence of MB isoenzyme of creatine phosphokinase in the serum after minor iatrogenic cardiac trauma. Absence of postmortem evidence of myocardial infarction.

A. Tonkin, G. Wagner, C. Roe, 1975, Circulation.

Assay of the concentration and (13)C isotopic enrichment of propionyl-CoA, methylmalonyl-CoA, and succinyl-CoA by gas chromatography-mass spectrometry.

C. Roe, H. Brunengraber, F. David, 2002, Analytical biochemistry.

Inherited disorders of mitochondrial fatty acid oxidation: a new responsibility for the neonatologist.

C. Roe, 2002, Seminars in neonatology : SN.

Biochemical analysis of bacterial macromutations.

C. Roe, K. You, 1971, Zeitschrift fur allgemeine Mikrobiologie.

Interrelations between C4 Ketogenesis, C5 Ketogenesis, and Anaplerosis in the Perfused Rat Liver*

Guo-Fang Zhang, C. Roe, H. Brunengraber, 2009, The Journal of Biological Chemistry.

Mathematical modifications fail to improve CPK estimates of extent of infarct.

C. Starmer, F. Cobb, C. Roe, 1977, Circulation.

The Effect of an Amino Acid-lowering Diet on the Rate of Melphalan Entry into Brain and Xenotransplanted Glioma1

D. Bigner, D. Groothuis, B. Lippitz, 2006 .

The Effect of an Amino Acid-lowering Diet on the Rate of Melphalan Entry into Brain and Xenotransplanted Glioma 1

D. Bigner, D. Groothuis, B. Lippitz, 2006 .

The effect of an amino acid-lowering diet on the rate of melphalan entry into brain and xenotransplanted glioma.

D. Groothuis, B. Lippitz, H. Friedman, 1992, Cancer research.

Carnitine palmitoyltransferase II deficiency

C. Roe, H. Brunengraber, D. Roe, 2008, Neurology.

Persistence of MB Isoenzyme of Creatine Phosphokinase in the Serum after Minor latrogenic Cardiac Trauma

G. Wagner, C. Roe, D. Hackel, 2005 .

Evaluation of Myocardial Damage in Patients Undergoing Coronary‐Artery Bypass Procedures with Halothane‐N2O Anesthesia and Adjuvants

N. Kouchoukos, E. Blackstone, C. Roe, 1977, Anesthesia and analgesia.

Tandem mass spectrometry: A new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolism

D. L. Norwood, D. Millington, C. Roe, 1990, Journal of Inherited Metabolic Disease.

Retrospective diagnosis of carnitine-acylcarnitine translocase deficiency by acylcarnitine analysis in the proband Guthrie card and enzymatic studies in the parents

D. Millington, C. Roe, A. Legrand, 1996, Journal of Inherited Metabolic Disease.

Application of fast atom bombardment with tandem mass spectrometry and liquid chromatography/mass spectrometry to the analysis of acylcarnitines in human urine, blood, and tissue.

D. Millington, C. Roe, D. Norwood, 1989, Analytical biochemistry.

Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients.

P. Divry, C. Roe, C. Vianey‐Saban, 1998, Clinica chimica acta; international journal of clinical chemistry.

Familial infantile apnea and immature beta oxidation

C. Roe, I. Browning, A. K. Iafolla, 1995, Pediatric pulmonology.

Intravenous L-Carnitine and Acetyl-L-Carnitine in Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency and Isovaleric Acidemia

S. Heales, D. Millington, C. Roe, 1994, Pediatric Research.

Amelioration of proximal renal tubular dysfunction in type I glycogen storage disease with dietary therapy.

R. Coleman, Yuan-Tsong Chen, C. Roe, 1990, The New England journal of medicine.

Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolism.

S. Cederbaum, C. Roe, L. Sweetman, 1998, Molecular genetics and metabolism.

Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype.

C. Roe, C. Vianey‐Saban, D. Roe, 2001, Clinica chimica acta; international journal of clinical chemistry.

The effect of reestablishing coronary blood flow on the release of Creatine Phosphokinase — MB isoenzyme in experimental myocardial infarction

G. Wagner, C. Roe, J. Jarmakani, 1973 .

Electron transfer flavoprotein

A. Engel, C. Roe, F. Frerman, 1990, Neurology.

Rapid Publication 2 , 4-Dienoyl-Coenzyme A Reductase Deficiency : A Possible New Disorder of Fatty Acid Oxidation

D. Millington, C. Roe, H. Sprecher, 2013 .

l-Carnitine prevents mitochondrial damage induced by octanoic acid in the rat choroid plexus

C. Roe, W. Ambrose, C. Kim, 1990, Brain Research.

Clinical effects of L-carnitine supplementation on apnea and growth in very low birth weight infants.

C. Roe, L. Sweetman, J. Whitfield, 2003, Pediatrics.

Effect of triheptanoin on muscle metabolism during submaximal exercise in horses.

M. McCue, C. Roe, B. Essén-Gustavsson, 2009, American journal of veterinary research.

Carnitine/acylcarnitine translocase deficiency (neonatal phenotype): successful prenatal and postmortem diagnosis associated with a novel mutation in a single family.

C. Roe, M. Brivet, B. Z. Yang, 2001, Molecular genetics and metabolism.

Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuria.

C. Roe, C. Francomano, D. Rosenblatt, 1988, The Journal of pediatrics.

Familial neonatal SIDS revealing carnitine-acylcarnitine translocase deficiency

C. Roe, J. Saudubray, P. de Lonlay, 2000, European Journal of Pediatrics.

Medium-chain acyl-coenzyme A dehydrogenase deficiency: clinical course in 120 affected children.

C. Roe, R. Thompson, A. K. Iafolla, 1994, The Journal of pediatrics.

The L-3-hydroxyacyl-CoA dehydrogenase deficiency.

T. Hashimoto, J. H. Wright, D. Hale, 1990, Progress in clinical and biological research.

Diagnostic and Therapeutic Implications of Medium-Chain Acylcarnitines in the Medium-Chain Acyl-CoA Dehydrogenase Deficiency

T. Bohan, D. Maltby, D. Millington, 1985, Pediatric Research.

Rapid diagnosis of maple syrup urine disease in blood spots from newborns by tandem mass spectrometry.

D. Millington, C. Roe, D. Chace, 1995, Clinical chemistry.

Death caused by perioperative fasting and sedation in a child with unrecognized very long chain acyl-coenzyme A dehydrogenase deficiency.

C. Roe, L. Sweetman, H. Wiltse, 2000, The Journal of pediatrics.

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood.

Y. T. Chen, Yuan-Tsong Chen, D. Millington, 1993, American journal of human genetics.

Identification of a novel mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency.

C. Zhou, C. Roe, M. Dasouki, 2000, Molecular genetics and metabolism.

Electron transfer flavoprotein

A. Engel, C. Roe, F. Frerman, 1990, Neurology.

Evidence for Intermediate Channeling in Mitochondrial -Oxidation (*)

C. Roe, H. Sprecher, H. Schulz, 1995, The Journal of Biological Chemistry.

Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency

K. Tanaka, D. Hale, D. Millington, 1990, Journal of Inherited Metabolic Disease.

Kinetic analysis ofl-carnitine uptake by the choroid plexus

C. Roe, C. Kim, 1991, Brain Research.

Medium-chain acyl-CoA dehydrogenase deficiency.

D. Millington, C. Roe, 1989, The New England journal of medicine.

POST-MORTEM RECOGNITION OF INHERITED METABOLIC DISORDERS FROM SPECIFIC ACYLCARNITINES IN TISSUE IN CASES OF SUDDEN INFANT DEATH

D. Maltby, D. Millington, C. Roe, 1987, The Lancet.

Differentiation of isomeric acylcarnitines using tandem mass spectrometry.

S. Gaskell, D. Maltby, D. Millington, 1986, Analytical chemistry.

L-carnitine therapy in isovaleric acidemia.

T. Bohan, D. Maltby, D. Millington, 1984, The Journal of clinical investigation.

l-Carnitine: therapeutic strategy for metabolic encephalopathy

C. Roe, C. S. Kim, D. Dorgan, 1984, Brain Research.

Application of high resolution fast atom bombardment and constant B/E ratio linked scanning to the identification and analysis of acylcarnitines in metabolic disease.

D. Maltby, D. Millington, C. Roe, 1984, Biomedical mass spectrometry.

L-Carnitine insufficiency in disorders of organic acid metabolism: response to L-carnitine by patients with methylmalonic aciduria and 3-hydroxy-3-methylglutaric aciduria.

C. Hoppel, D. Millington, C. Roe, 1984, Journal of inherited metabolic disease.

PRENATAL DIAGNOSIS OF MITOCHONDRIAL FATTY ACID OXIDATION DEFECTS

M. Bialer, C. Roe, R. Wappner, 1996, Prenatal diagnosis.

Secondary carnitine insufficiency in disorders of organic acid metabolism: modulation of acyl-CoA/CoA ratios by l-carnitine in vivo

C. Hoppel, D. Millington, C. Roe, 1983 .

Parenteral nutrition in propionic and methylmalonic acidemia.

S. Cederbaum, D. Maltby, D. Millington, 1989, The Journal of pediatrics.

Evidence for a short-chain carnitine-acylcarnitine translocase in mitochondria specifically related to the metabolism of branched-chain amino acids.

C. Roe, M. Brivet, L. Sweetman, 2000, Molecular genetics and metabolism.

Methylmalonic aciduria in pregnancy: a case report.

C. Roe, D. Roe, J. Iams, 1995, American journal of obstetrics and gynecology.

Purification and substrate specificities of bacterial hydroxysteroid dehydrogenases.

N. Kaplan, C. Roe, 1969, Biochemistry.

Affinity chromatography of Pseudomonas salicylate hydroxylase.

C. Roe, K. You, 1981, Analytical biochemistry.

Urine and serum lactic dehydrogenase, lactic dehydrogenase isoenzymes, and alkaline phosphatase in the nephrotic syndrome.

P. Baker, C. Roe, E. DeLong, 1981, Kidney international.

Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride.

C. Roe, H. Brunengraber, F. David, 2002, The Journal of clinical investigation.

Long‐chain 3‐hydroxyacylCoA dehydrogenase deficiency: a new case presenting with liver dysfunction, cholestasis and fibrosis

R. Wanders, D. Rabier, C. Roe, 2002, Acta paediatrica.

A case of glutaric acidemia type I: effect of riboflavin and carnitine.

C. Roe, P. Lipkin, M. Batshaw, 1988, The Journal of pediatrics.

Characterization of new diagnostic acylcarnitines in patients with beta-ketothiolase deficiency and glutaric aciduria type I using mass spectrometry.

D. Maltby, D. Millington, C. Roe, 1987, Biomedical & environmental mass spectrometry.

Neuropsychiatric manifestations of defect in mitochondrial beta oxidation response to riboflavin.

W. Triggs, C. Roe, W. Rhead, 1992, Journal of neurology, neurosurgery, and psychiatry.

Effect of dietary fats with odd or even numbers of carbon atoms on metabolic response and muscle damage with exercise in Quarter Horse-type horses with type 1 polysaccharide storage myopathy.

M. McCue, C. Roe, S. Valberg, 2010, American journal of veterinary research.

Maternal and fetal tissue distribution of L-carnitine in pregnant mice: low accumulation in the brain.

C. Roe, C. S. Kim, Charles R. Roe, 1992, Fundamental and applied toxicology : official journal of the Society of Toxicology.

Phytanic acid and pristanic acid are oxidized by sequential peroxisomal and mitochondrial reactions in cultured fibroblasts.

R. Wanders, R. Wanders, C. Roe, 1998, Journal of lipid research.

Valproylcarnitine: a novel drug metabolite identified by fast atom bombardment and thermospray liquid chromatography-mass spectrometry.

T. Bohan, A. Yergey, D. Millington, 1985, Clinica chimica acta; international journal of clinical chemistry.

Coronary Perfusion Versus Cold Ischemic Arrest During Aortic Valve Surgery: A Randomized Study

N. Kouchoukos, E. Blackstone, R. Karp, 1974, Circulation.

Importance of blood-collection tubes in plasma lidocaine determinations.

C. Roe, P. Routledge, D. Shand, 1979, Clinical chemistry.

Short-chain acyl-CoA dehydrogenase deficiency in a 16-year-old girl with severe muscle wasting and scoliosis

A. Aguzzi, S. Krähenbühl, C. Roe, 1997, Journal of Inherited Metabolic Disease.

Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene.

K. Kristiansen, P. Bross, B. Andresen, 1996, Human molecular genetics.

Enzymatic alterations in Reye's syndrome: prognostic implications.

L. Schonberger, C. Roe, J. Sidbury, 1975, Pediatrics.

Methylmalonic semialdehyde dehydrogenase deficiency: psychomotor delay and methylmalonic aciduria without metabolic decompensation.

Robert A. Harris, R. Harris, C. Roe, 1998, Molecular genetics and metabolism.

2-Methylbutyryl-Coenzyme A Dehydrogenase Deficiency: A New Inborn Error of L-Isoleucine Metabolism

J. Vockley, R. Steiner, R. Schutgens, 2000, Pediatric Research.

Fatty Acid Metabolism and Reye's Syndrome

D. Millington, C. Roe, D. Roe, 1993 .

Choice of oils for essential fat supplements can enhance production of abnormal metabolites in fat oxidation disorders.

C. Roe, D. Roe, M. Wallace, 2007, Molecular genetics and metabolism.

Identification of a new mutation in medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.

Y. T. Chen, C. Roe, Y. Bao, 1992, American journal of human genetics.

The safety of induced ventricular fibrillation during cardiopulmonary bypass in nonhypertrophied hearts.

H. Pass, R. Anderson, J. Cox, 1977, The Journal of thoracic and cardiovascular surgery.

Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin.

E. Leshinsky‐Silver, D. Lev, J. Vockley, 2008, Molecular genetics and metabolism.

Characterization of the bidirectional promoter region between the human genes encoding VLCAD and PSD-95.

C. Roe, Li-Feng Zhang, Bing-zhi Yang, 2003, Genomics.

Identification of four novel mutations in patients with carnitine palmitoyltransferase II (CPT II) deficiency.

D. Rabier, C. Roe, M. Brivet, 1998, Molecular genetics and metabolism.

Acute profound dystonia in infants with glutaric acidemia.

C. Stanley, C. Stanley, D. Finegold, 1989, Pediatrics.

Citrate therapy in argininosuccinate lyase deficiency.

C. Roe, A. K. Iafolla, D. Gale, 1990, The Journal of pediatrics.

Carnitine homeostasis in the organic acidurias.

D. Millington, C. Roe, D. Norwood, 1990, Progress in clinical and biological research.

Treatment of inborn errors of urea synthesis.

T. Bohan, C. Roe, 1982, The New England journal of medicine.

Intraoperative detection of myocardial damage during coronary artery surgery by plasma creatine phosphokinase isoenzyme analysis.

H. Oldham, S. H. Dixon, C. Roe, 1973, Surgery.

Diagnosis of myocardial infarction by serum isoenzyme analysis.

C. Roe, 1977, Annals of clinical and laboratory science.

Enzymatic Estimation: Confounding Effects of Blood Flow to Infarcted Myocardium

F. Cobb, C. Roe, 1982 .

Anaplerotic treatment of long-chain fat oxidation disorders with triheptanoin: Review of 15 years Experience.

C. Roe, H. Brunengraber, 2015, Molecular genetics and metabolism.

Studies on the oxidation of phytanic acid and pristanic acid in human fibroblasts by acylcarnitine analysis

R. Wanders, C. Roe, N. Verhoeven, 1998, Journal of Inherited Metabolic Disease.

Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidation

J. Gargus, C. Roe, M. Bocian, 2003, Journal of Inherited Metabolic Disease.

Anaplerotic molecules: Current and future

C. Roe, H. Brunengraber, 2006, Journal of Inherited Metabolic Disease.

Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans.

S. Cederbaum, B. Andresen, J. Vockley, 2002, Molecular genetics and metabolism.

Triheptanoin for glucose transporter type I deficiency (G1D): modulation of human ictogenesis, cerebral metabolic rate, and cognitive indices by a food supplement.

Jason Y. Park, Hanzhang Lu, L. Good, 2014, JAMA neurology.

Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency.

C. Roe, Y. Matsubara, K. Narisawa, 1990, Biochemical and biophysical research communications.

Improved detection of the G1528C mutation in LCHAD deficiency.

C. Roe, M. Nada, B. Z. Yang, 1996, Biochemical and Molecular Medicine.

A novel mutation identified in carnitine palmitoyltransferase II deficiency.

C. Roe, B. Z. Yang, J. Ding, 1998, Molecular genetics and metabolism.

Maximum dose, safety, tolerability and ketonemia after triheptanoin in glucose transporter type 1 deficiency (G1D)

Jason Y. Park, S. Shinnar, C. Roe, 2023, Scientific Reports.

Saturable accumulation of the anionic herbicide, 2,4-dichlorophenoxyacetic acid (2,4-D), by rabbit choroid plexus: early developmental origin and interaction with salicylates.

C. Roe, L. O'Tuama, J. Mann, 1983, The Journal of pharmacology and experimental therapeutics.

Pristanic acid beta-oxidation in peroxisomal disorders: studies in cultured human fibroblasts.

R. Wanders, C. Roe, N. Verhoeven, 1997, Biochimica et biophysica acta.

Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch families

M. Durán, C. Roe, P. Barth, 1998, Neuromuscular Disorders.

Hepatic enzymes of tyrosine metabolism in tyrosinemia II.

L. Goldsmith, C. Roe, J. Thorpe, 1979, The Journal of investigative dermatology.

The genes for the alpha and beta subunits of the mitochondrial trifunctional protein are both located in the same region of human chromosome 2p23.

H. Heng, C. Roe, B. Z. Yang, 1996, Genomics.

Systemic metabolic abnormalities in adult-onset acid maltase deficiency: beyond muscle glycogen accumulation.

C. Roe, J. Pascual, 2013, JAMA neurology.

Variations in IBD (ACAD8) in Children with Elevated C4-Carnitine Detected by Tandem Mass Spectrometry Newborn Screening

R. Wanders, B. Andresen, N. Gregersen, 2006, Pediatric Research.

Prenatal diagnosis of multiple acyl‐CoA dehydrogenase deficiency: association with elevated α‐fetoprotein and cystic renal changes

M. Lovell, C. Roe, F. Frerman, 2001, Prenatal diagnosis.

Rapid Publication

T. Bohan, D. Maltby, D. Millington, 2003 .

Screening for Duchenne muscular dystrophy.

A. Roses, C. Roe, G. Nicholson, 1977, Pediatrics.

Detection of gene defects in branched-chain amino acid metabolism by tandem mass spectrometry of carnitine esters produced by cultured fibroblasts.

C. Roe, D. Roe, 2000, Methods in Enzymology.

The role of raw starches in the treatment of type I glycogenosis.

Y. T. Chen, C. Roe, J. Sidbury, 1986, Archives of internal medicine.

Synthesis and human applications of stable isotope labelled L-carnitine

D. Maltby, D. Millington, C. Roe, 1988 .

Glutaryl-coenzyme A dehydrogenase deficiency: a distinct encephalopathy.

F. Hanefeld, H. Bremer, C. Roe, 1991, Pediatrics.

Triheptanoin for glucose transporter type I deficiency (G1D): modulation of human ictogenesis, cerebral metabolic rate, and cognitive indices by a food supplement.

Jason Y. Park, Hanzhang Lu, L. Good, 2014, JAMA neurology.

Investigation of beta-oxidation intermediates in normal and MCAD-deficient human fibroblasts using tandem mass spectrometry.

C. Roe, D. Chace, H. Sprecher, 1995, Biochemical and molecular medicine.

Hypoketotic hypoglycemic coma in a 21-month-old child.

C. Roe, M. Bennett, P. Rinaldo, 1999, Annals of emergency medicine.

Hypoketotic Hypoglycemic Coma in a

C. Roe, P. Rinaldo, M. Bennett, 1999 .

Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groups.

C. Hoppel, D. Millington, C. Roe, 1983, Archives of disease in childhood.

Diagnosis of Acute Myocardial Infarction in a Community Hospital Significance of CPK-MB Determination

G. Wagner, S. Roark, C. Roe, 2005 .

Parenteral and enteral metabolism of anaplerotic triheptanoin in normal rats. II. Effects on lipolysis, glucose production, and liver acyl-CoA profile.

Frederick Allen, G. Kutz, Wolf-Ulrich Brewer, 2010, American journal of physiology. Endocrinology and metabolism.

Rapid Publication L-Carfitine Therapy in Isovaleric Acidemia

T. Bohan, D. Maltby, D. Millington, 2013 .

Rapid 2,4-Dienoyl-Coenzyme A Reductase Deficiency: A Possible New Disorder of Fatty Acid Oxidation

B. S. Mohammed, D. Millington, C. Roe, 2022 .