Showing results (231-240 of 295) with videos related to
Sort By:
Pageof 30
Clinical Neurology and Neurosurgery|June 1, 1993
Delay in diagnosis of X-linked adrenoleukodystrophyB M van Geel, J Assies, E B Haverkort, et al.Journal of Inherited Metabolic Disease|January 1, 1996
ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophyS Kemp, P A Mooyer, P A Bolhuis, et al.Neurology|February 1, 1995
The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2): compiled data from 10 pedigreesP G Barth, G Blennow, H G Lenard, et al.Journal of Inherited Metabolic Disease|January 1, 1990
The inborn errors of peroxisomal beta-oxidation: a reviewR J Wanders, C W van Roermund, R B Schutgens, et al.AJNR. American Journal of Neuroradiology|June 19, 2004
Peroxisomal biogenesis disorder: comparison of conventional MR imaging with diffusion-weighted and diffusion-tensor imaging findingsBirgitta S M ter Rahe, Charles B L M Majoie, Erik M Akkerman, et al.Molecular Genetics and Metabolism|April 3, 2004
Spastic diplegia and periventricular white matter abnormalities in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, a defect of isoleucine metabolism: differential diagnosis with hypoxic-ischemic brain diseasesBwee Tien Poll-The, Ronald J A Wanders, Jos P N Ruiter, et al.Heart (British Cardiac Society)|March 20, 1998
The heart in limb girdle muscular dystrophyA J van der Kooi, W G de Voogt, P G Barth, et al.Infection Control and Hospital Epidemiology|November 8, 2016
Association Between Storage Interval and Contamination of Reprocessed Flexible Endoscopes in a Pediatric Gastrointestinal Procedural UnitPatricia Scanlon, Kathleen Flaherty, Erik A Reilly, et al.Biochemical and Biophysical Research Communications|August 27, 1999
Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patientsN Shimozawa, Z Zhang, Y Suzuki, et al.Journal of Inherited Metabolic Disease|January 1, 1993
L-2-hydroxyglutaric acidaemia: clinical and biochemical findings in 12 patients and preliminary report on L-2-hydroxyacid dehydrogenaseP G Barth, G F Hoffmann, J Jaeken, et al.Pageof 30