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T Clayton

Showing results (101-110 of 248) with videos related to

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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.
Lancet (London, England)|March 20, 2004
"African medicine" and Reye's syndromeBirgit Wittenstein, Valerie Rogers, Vas Novelli, 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.
International Journal of Molecular Sciences|February 26, 2013
Structural Characterization of an LPA1 Second Extracellular Loop Mimetic with a Self-Assembling Coiled-Coil Folding ConstraintJohn K Young, Benjamin T Clayton, Alexandra Kikonyogo, 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.
Developmental Medicine and Child Neurology|April 8, 2010
Seizures and paroxysmal events: symptoms pointing to the diagnosis of pyridoxine-dependent epilepsy and pyridoxine phosphate oxidase deficiencyBernhard Schmitt, Matthias Baumgartner, Philippa B Mills, et al.
Clinical Imaging|February 12, 2021
Motivation: how to create a cohort of engaged, energized, and happy radiology traineesSean D Raj, Joshua T Clayton, Karuna M Raj, et al.
Pageof 25

Showing results (101-110 of 248) with videos related to

Sort By:
Pageof 25
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.
Lancet (London, England)|March 20, 2004
"African medicine" and Reye's syndromeBirgit Wittenstein, Valerie Rogers, Vas Novelli, 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.
International Journal of Molecular Sciences|February 26, 2013
Structural Characterization of an LPA1 Second Extracellular Loop Mimetic with a Self-Assembling Coiled-Coil Folding ConstraintJohn K Young, Benjamin T Clayton, Alexandra Kikonyogo, 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.
Developmental Medicine and Child Neurology|April 8, 2010
Seizures and paroxysmal events: symptoms pointing to the diagnosis of pyridoxine-dependent epilepsy and pyridoxine phosphate oxidase deficiencyBernhard Schmitt, Matthias Baumgartner, Philippa B Mills, et al.
Clinical Imaging|February 12, 2021
Motivation: how to create a cohort of engaged, energized, and happy radiology traineesSean D Raj, Joshua T Clayton, Karuna M Raj, et al.
Pageof 25