W. G. Sherwood

发表

Cardiac manifestations in disorders of fat and carnitine metabolism in infancy.

R. Rowe, L. Benson, T. Ino, 1988, Journal of the American College of Cardiology.

The Genetic Heterogeneity of Lactic Acidosis: Occurrence of Recognizable Inborn Errors of Metabolism in a Pediatric Population with Lactic Acidosis

B. Robinson, Jennifer Taylor, J. Taylor, 1980, Pediatric Research.

Adult Onset Systemic Carnitine Deficiency: Favorable Response to L-Carnitine Supplementation

J. Deck, J. Murphy, G. Sawa, 1987, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Variable clinical presentation in patients with defective E1 component of pyruvate dehydrogenase complex.

B. Robinson, R. Petrova-Benedict, W. G. Sherwood, 1987, The Journal of pediatrics.

Lactic acidosis in biotin-responsive multiple carboxylase deficiency caused by holocarboxylase synthetase deficiency of early and late onset.

B. Robinson, M. Saunders, R. Gravel, 1982, The Journal of pediatrics.

A NEW SYNDROME OF FAMILIAL PANCREATIC AGENESIS: THE ROLE OF INSULIN AND GLUCAGON IN SOMATIC AND CELL GROWTH

D. Hill, G. Chance, D. Fraser, 1974, Pediatric Research.

Long-chain l-3-hydroxyacyl-coenzyme A dehydrogenase deficiency neuropathy: Response to cod liver oil

I. Tein, J. Vajsar, L. MacMillan, 1999, Neurology.

The molecular basis for the two different clinical presentations of classical pyruvate carboxylase deficiency.

B. Robinson, P. Goodyer, J. Oei, 1984, American journal of human genetics.

Pyruvate Dehydrogenase Phosphatase Deficiency: A Cause of Congenital Chronic Lactic Acidosis in Infancy

B. Robinson, W. G. Sherwood, 1975, Pediatric Research.

A Rotating Ring‐Disk Electrode Study of the Underpotential Deposition of Mercury on Gold

S. Bruckenstein, W. G. Sherwood, W. Sherwood, 1978 .

Hydroxymethylglutaryl CoA lyase deficiency: features resembling Reye syndrome.

O. Mamer, B. Robinson, A. Slyper, 1980, Neurology.

Multiple acyl-CoA dehydrogenase deficiency: A neonatal onset case responsive to treatment

Z. Verjee, W. G. Sherwood, 1985, Journal of Inherited Metabolic Disease.

Identification of urinary metabolites of (+/-)-2-(p-isobutylphenyl)propionic acid (Ibuprofen) by routine organic acid screening.

A. Bhala, M. Bennett, D. Hale, 1992, Clinica chimica acta; international journal of clinical chemistry.

Hyaline membrane disease. Effect of surfactant prophylaxis on lung morphology in premature primates.

E. Cutz, B. Robertson, G. Enhörning, 1978, The American journal of pathology.

Evidence for a defect of holocarboxylase synthetase activity in cultured lymphoblasts from a patient with biotin-responsive multiple carboxylase deficiency.

L. Surh, M. Saunders, R. Gravel, 1982, American journal of human genetics.

Fetal polycystic kidney disease associated with glutaric aciduria type II: an inborn error of energy metabolism.

R. Hogg, M. Bennett, W. G. Sherwood, 1996, American journal of perinatology.

Secondary 3-hydroxydicarboxylic aciduria mimicking long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

M. Bennett, A. Burlina, W. G. Sherwood, 1994, Journal of Inherited Metabolic Disease.

Deficiency of Dihydrolipoyl Dehydrogenase (a Component of the Pyruvate and α-Ketoglutarate Dehydrogenase Complexes): A Cause of Congenital Chronic Lactic Acidosis in Infancy

B. Robinson, Jennifer Taylor, J. Taylor, 1977, Pediatric Research.

Neonatal screening for biotinidase deficiency in north eastern italy

B. Bernardina, A. Burlina, D. Gaburro, 1988, European Journal of Pediatrics.

Fluid bed electrolysis of nickel

P. Queneau, W. G. Sherwood, D. Hodges, 1979 .

Current practices and improved recommendations for treating hereditary fructose intolerance.

W. G. Sherwood, L. Bell, W. Sherwood, 1987, Journal of the American Dietetic Association.

Secondary inhibition of multiple NAD-requiring dehydrogenases in respiratory chain complex I deficiency: Possible metabolic markers for the primary defect

K. Gibson, M. Bennett, A. Burlina, 1993, Journal of Inherited Metabolic Disease.

Pancreatitis in patients with organic acidemias.

J. T. Clarke, A. Zaritsky, S. Lawless, 1994, The Journal of pediatrics.

Lactic acidaemia

B. Robinson, W. G. Sherwood, W. Sherwood, 1984, Journal of Inherited Metabolic Disease.

Dilated cardiomyopathy with neutropenia, short stature, and abnormal carnitine metabolism.

L. Benson, T. Ino, R. Freedom, 1988, The Journal of pediatrics.

Lipoamide dehydrogenase deficiency.

B. Robinson, S. Kahler, M. O'Flynn, 1981, The New England journal of medicine.

DIHYDROLIPOYL DEHYDROGENASE DEFICIENCY - A CAUSE OF CONGENITAL LACTIC ACIDOSIS

B. Robinson, Jennifer Taylor, D. Fraser, 1977, Pediatric Research.

L-Carnitine and its role in medicine: from function to therapy

R. Ferrari, R. Ferrari, S. Mauro, 1992 .

An Analog Function Generator for Voltammetric Applications

W. G. Sherwood, D. F. Untereker, G. A. Martinchek, 1975 .

Digital function generator for electrochemical applications

D. Untereker, S. Bruckenstein, W. G. Sherwood, 1975 .

Phenotypic heterogeneity in the syndromes of 3-methylglutaconic aciduria.

I. Dianzani, R. Schutgens, K. Gibson, 1991, The Journal of pediatrics.

3-Oxothiolase Activities and [14C]-2-Methylbutanoic Acid Incorporation in Cultured Fibroblasts from 13 Cases of Suspected 3-Oxothiolase Deficiency

O. Søvik, K. Gibson, B. Robinson, 1990, Pediatric Research.

3-Hydroxydicarboxylic and 3-ketodicarboxylic aciduria in three patients: evidence for a new defect in fatty acid oxidation at the level of 3-ketoacyl-CoA thiolase.

W. G. Sherwood, M. J. Bennett, 1993, Clinical chemistry.

In utero central nervous system damage in pyruvate dehydrogenase deficiency.

B. Robinson, A. Kaplan, K. Aleck, 1988, Archives of neurology.

A Defect in Branched-Chain Amino Acid Metabolism in a Patient with Congenital Lactic Acidosis due to Dihydrolipoyl Dehydrogenase Deficiency

B. Robinson, Jennifer Taylor, W. G. Sherwood, 1978, Pediatric Research.

Acetoacetyl CoA thiolase deficiency: a cause of severe ketoacidosis in infancy simulating salicylism.

J. Balfe, O. Mamer, B. Robinson, 1979, The Journal of pediatrics.

Coffin-siris syndrome with normal plasma biotinidase activity

A. Munnich, D. Bonneau, A. Burlina, 1991, European Journal of Pediatrics.

Partial biotinidase deficiency associated with Coffin-Siris syndrome

F. Zacchello, A. Burlina, W. G. Sherwood, 1990, European Journal of Pediatrics.