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P T Clayton

Showing results (51-60 of 101) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1989
Peroxisomal enzyme deficiency in X-linked dominant Conradi-Hünermann syndromeP T Clayton, D C Kalter, D J Atherton, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1986
Subacute combined degeneration of the cord, dementia and parkinsonism due to an inborn error of folate metabolismP T Clayton, I Smith, B Harding, et al.
Bioorganic & Medicinal Chemistry|May 30, 2001
New synthesis of (+/-)-alpha-CMBHC and its confirmation as a metabolite of alpha-tocopherol (vitamin E)S A Pope, G E Burtin, P T Clayton, et al.
Lancet (London, England)|May 16, 2003
Neonatal epileptic encephalopathyP T Clayton, R A H Surtees, C DeVile, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Bifunctional protein deficiency: complementation within the same group suggesting differential enzyme defects and clues to the underlying basisE G Van Grunsven, E van Berkel, H Lemonde, et al.
Archives of Disease in Childhood|April 20, 1999
Outcome of medium chain acyl-CoA dehydrogenase deficiency after diagnosisC J Wilson, M P Champion, J E Collins, et al.
Archives of Disease in Childhood|October 26, 2005
The significance of elevated CSF lactateS L Chow, Z J Rooney, M A Cleary, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1993
Peripheral neuropathy as the presenting feature of tyrosinaemia type I and effectively treated with an inhibitor of 4-hydroxyphenylpyruvate dioxygenaseT C Gibbs, J Payan, E M Brett, et al.
Gastroenterology|February 1, 1993
Nodular transformation of the liver associated with portal and pulmonary arterial hypertensionB Portmann, S Stewart, T W Higenbottam, et al.
American Journal of Medical Genetics|April 10, 1995
Prenatal diagnosis of Smith-Lemli-Opitz syndromeJ M McGaughran, P T Clayton, K A Mills, et al.
Pageof 11

Showing results (51-60 of 101) with videos related to

Sort By:
Pageof 11
Journal of Inherited Metabolic Disease|January 1, 1989
Peroxisomal enzyme deficiency in X-linked dominant Conradi-Hünermann syndromeP T Clayton, D C Kalter, D J Atherton, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1986
Subacute combined degeneration of the cord, dementia and parkinsonism due to an inborn error of folate metabolismP T Clayton, I Smith, B Harding, et al.
Bioorganic & Medicinal Chemistry|May 30, 2001
New synthesis of (+/-)-alpha-CMBHC and its confirmation as a metabolite of alpha-tocopherol (vitamin E)S A Pope, G E Burtin, P T Clayton, et al.
Lancet (London, England)|May 16, 2003
Neonatal epileptic encephalopathyP T Clayton, R A H Surtees, C DeVile, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Bifunctional protein deficiency: complementation within the same group suggesting differential enzyme defects and clues to the underlying basisE G Van Grunsven, E van Berkel, H Lemonde, et al.
Archives of Disease in Childhood|April 20, 1999
Outcome of medium chain acyl-CoA dehydrogenase deficiency after diagnosisC J Wilson, M P Champion, J E Collins, et al.
Archives of Disease in Childhood|October 26, 2005
The significance of elevated CSF lactateS L Chow, Z J Rooney, M A Cleary, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1993
Peripheral neuropathy as the presenting feature of tyrosinaemia type I and effectively treated with an inhibitor of 4-hydroxyphenylpyruvate dioxygenaseT C Gibbs, J Payan, E M Brett, et al.
Gastroenterology|February 1, 1993
Nodular transformation of the liver associated with portal and pulmonary arterial hypertensionB Portmann, S Stewart, T W Higenbottam, et al.
American Journal of Medical Genetics|April 10, 1995
Prenatal diagnosis of Smith-Lemli-Opitz syndromeJ M McGaughran, P T Clayton, K A Mills, et al.
Pageof 11