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  1. No Access

    Chapter

    Cholestatic Jaundice Associated with Carnitine Palmitoyltransferase IA Deficiency

    Liver dysfunction usually accompanies metabolic decompensation in fatty acid oxidation disorders, including carnitine palmitoyltransferase (CPT) Ia deficiency. Typically, the liver is enlarged with raised plas...

    A A M Morris, S E Olpin, M J Bennett… in JIMD Reports - Case and Research Reports, … (2013)

  2. No Access

    Article

    Pathophysiology of fatty acid oxidation disorders

    Mitochondrial fatty acid oxidation represents an important pathway for energy generation during periods of increased energy demand such as fasting, febrile illness and muscular exertion. In liver, the primary ...

    M. J. Bennett in Journal of Inherited Metabolic Disease (2010)

  3. No Access

    Article

    Longitudinal Assessment of Ovarian Perifollicular and Endometrial Vascularity by Power Doppler Ultrasound in Pregnant and Non-Pregnant Cycles in the IVF Setting

    Purpose: This longitudinal study aimed to compare ovarian perifollicular and endometrial blood flow (PFBF and EBF, respectively) during the follicular phase in pregnant and non-pregnant IVF cycles.

    S. M. Shrestha, M. F. Costello, P. Sjoblom… in Journal of Assisted Reproduction and Genet… (2004)

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    Article

    Enhanced systemic transgene expression after nonviral salivary gland transfection using a novel endonuclease inhibitor/DNA formulation

    Gene transfer to the major salivary glands is an attractive method for the systemic delivery of therapeutic proteins. To date, nonviral gene transfer to these glands has resulted in inadequate systemic protein...

    E J Niedzinski, Y-J Chen, D C Olson, E A Parker, H Park, J A Udove… in Gene Therapy (2003)

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    Article

    Quantitative measurement of total and free 3-hydroxy fatty acids in serum or plasma samples: short-chain 3-hydroxy fatty acids are not esterified

    Diagnostic protocols for disorders of mitochondrial fatty acid oxidation (FAO) generally include the measurement of plasma acylcarnitines. Many biochemical intermediates of FAO resulting from a metabolic block...

    P. M. Jones, A. B. Burlina, M. J. Bennett in Journal of Inherited Metabolic Disease (2000)

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    Article

    Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders

    Mitochondrial fatty acid oxidation disorders cause hypoglycaemia, hepatic dysfunction, myopathy, cardiomyopathy and encephalopathy. Despite their recognition for more than 15 years, diagnosis and treatment rem...

    J. J. Shen, D. Matern, D. S. Millington… in Journal of Inherited Metabolic Disease (2000)

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    Article

    The neuronal ceroid-lipofuscinoses (Batten disease): A new class of lysosomal storage diseases

    The neuronal ceroid-lipofuscinoses (Batten disease) are a group of severe neurodegenerative disorders characterized clinically by visual loss, seizures and psychomotor degeneration, and pathologically by loss ...

    M. J. Bennett, S. L. Hofmann in Journal of Inherited Metabolic Disease (1999)

  8. No Access

    Article

    Profound neurological phenotype in a patient presenting with disordered isoleucine and energy metabolism

    A. B. Burlina, K. M. Gibson, W. Ruitenbeek… in Journal of Inherited Metabolic Disease (1998)

  9. No Access

    Article

    Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease

    C. E. Mize, L. J. Waber, T. Anderson… in Journal of Inherited Metabolic Disease (1997)

  10. No Access

    Article

    Polyunsaturated fatty acids reverse the lysosomal storage and accumulation of subunit 9 of mitochondrial F1F0-ATP synthase in cultured lymphoblasts from patients with Batten disease

    M. J. Bennett, R. L. Boriack, R.-M. Boustany in Journal of Inherited Metabolic Disease (1997)

  11. No Access

    Article

    Late-onset holocarboxylase synthetase deficiency

    We report a 21-month-old female patient whose urine organic acid profile suggested a biotin utilization abnormality consistent with multiple carboxylase deficiency. For most previously reported patients, holoc...

    K. M. Gibson, M. J. Bennett, W. L. Nyhan… in Journal of Inherited Metabolic Disease (1996)

  12. No Access

    Article

    β-Ketothiolase (2-methylacetoacetyl-coenzyme a thiolase) deficiency: identification of two patients in israel

    K. M. Gibson, O. N. Elpeleg, M. J. Bennett in Journal of Inherited Metabolic Disease (1996)

  13. No Access

    Article

    Assignment of the human peroxisomal palmitoyl-CoA oxidase gene to chromosome 17q23-qter by PCR technique

    Human peroxisomal palmitoyl-CoA oxidase plays a pivotal role in the β-oxidation of fatty acids. Its importance is reflected by the severity of the disease associated with its deficiency in man. The gene was pr...

    N. N. Moghrabi, D. B. Dawson, M. J. Bennett in Journal of Inherited Metabolic Disease (1995)

  14. No Access

    Article

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

    M. J. Bennett, M. J. Weinberger, W. G. Sherwood… in Journal of Inherited Metabolic Disease (1994)

  15. No Access

    Article

    6-Methyluracil excretion in 2-methylacetoacetyl-CoA thiolase deficiency and in two children with an unexplained recurrent ketoacidaemia

    6-Methyluracil (6MU) has been identified in urine collected during acute illness in two children with β-ketothiolase deficiency (approximately 1 mmol/L) and in two children with recurrent infection-related ket...

    C. H. Cromby, N. J. Manning, R. J. Pollitt… in Journal of Inherited Metabolic Disease (1994)

  16. No Access

    Article

    Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chainl-3-hydroxyacyl-CoA dehydrogenase deficiency

    An infant with glycogen storage disease and prolonged malnourishment showed a urinary organic acid profile during an episode of fasting hypoglycaemia with inappropriate hypoketotic dicarboxylic aciduria that w...

    J. Bergoffen, P. Kaplan, D. E. Hale… in Journal of Inherited Metabolic Disease (1993)

  17. No Access

    Article

    Reliable prenatal diagnosis of Canavan disease (aspartoacylase deficiency): Comparison of enzymatic and metabolite analysis

    Prenatal diagnosis has been undertaken in 17 pregnancies in 15 families at risk for aspartoacylase deficiency. Amniocentesis was at 14–18 weeks gestation followed by measurement of amniotic fluidN-acetyl-l-aspart...

    M. J. Bennett, K. M. Gibson, W. G. Sherwood… in Journal of Inherited Metabolic Disease (1993)

  18. No Access

    Article

    Combined malonic, methylmalonic and ethylmalonic acid semialdehyde dehydrogenase deficiencies: An inborn error of β-alanine,l-valine andl-alloisoleucine metabolism?

    K. M. Gibson, C. F. Lee, M. J. Bennett, B. Holmes… in Journal of Inherited Metabolic Disease (1993)

  19. No Access

    Article

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

    M. J. Bennett, W. G. Sherwood, K. M. Gibson… in Journal of Inherited Metabolic Disease (1993)

  20. No Access

    Article

    Juvenile neuronal ceroid-lipofuscinosis: Characterization of the dyslipoproteinaemia and demonstration of membrane phospholipid and phospholipid-dependent signal transduction abnormalities in cultured skin fibroblasts

    M. J. Bennett, S. F. Poirier, L. Chern… in Journal of Inherited Metabolic Disease (1993)

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