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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 basis
E G Van Grunsven, E van Berkel, H Lemonde, et al.
Lancet (London, England)
|
March 20, 2004
"African medicine" and Reye's syndrome
Birgit Wittenstein, Valerie Rogers, Vas Novelli, et al.
Archives of Disease in Childhood
|
April 20, 1999
Outcome of medium chain acyl-CoA dehydrogenase deficiency after diagnosis
C 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 Constraint
John K Young, Benjamin T Clayton, Alexandra Kikonyogo, et al.
Archives of Disease in Childhood
|
October 26, 2005
The significance of elevated CSF lactate
S 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 dioxygenase
T C Gibbs, J Payan, E M Brett, et al.
Gastroenterology
|
February 1, 1993
Nodular transformation of the liver associated with portal and pulmonary arterial hypertension
B Portmann, S Stewart, T W Higenbottam, et al.
American Journal of Medical Genetics
|
April 10, 1995
Prenatal diagnosis of Smith-Lemli-Opitz syndrome
J 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 deficiency
Bernhard 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 trainees
Sean D Raj, Joshua T Clayton, Karuna M Raj, et al.
Page
of 25
Search research articles
Search
Showing results (101-110 of 248) with videos related to
Sort By:
Page
of 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 basis
E G Van Grunsven, E van Berkel, H Lemonde, et al.
Lancet (London, England)
|
March 20, 2004
"African medicine" and Reye's syndrome
Birgit Wittenstein, Valerie Rogers, Vas Novelli, et al.
Archives of Disease in Childhood
|
April 20, 1999
Outcome of medium chain acyl-CoA dehydrogenase deficiency after diagnosis
C 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 Constraint
John K Young, Benjamin T Clayton, Alexandra Kikonyogo, et al.
Archives of Disease in Childhood
|
October 26, 2005
The significance of elevated CSF lactate
S 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 dioxygenase
T C Gibbs, J Payan, E M Brett, et al.
Gastroenterology
|
February 1, 1993
Nodular transformation of the liver associated with portal and pulmonary arterial hypertension
B Portmann, S Stewart, T W Higenbottam, et al.
American Journal of Medical Genetics
|
April 10, 1995
Prenatal diagnosis of Smith-Lemli-Opitz syndrome
J 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 deficiency
Bernhard 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 trainees
Sean D Raj, Joshua T Clayton, Karuna M Raj, et al.
Page
of 25