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Journal of Inherited Metabolic Disease|March 1, 1997
Progression of X-linked adrenoleukodystrophy under interferon-beta therapyG C Korenke, H J Christen, B Kruse, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
5 alpha-reductase deficiency in patients with micropenisY Z Gad, H Nasr, I Mazen, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Clinical approach to inherited peroxisomal disordersF Poggi-Travert, B Fournier, B T Poll-The, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Immunoblot analysis of peroxisomal proteins in liver and fibroblasts from patientsR J Wanders, C Dekker, R Ofman, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Neuropathology of peroxisomal diseasesJ J Martin
Journal of Inherited Metabolic Disease|January 1, 1996
Plasma total odd-chain fatty acids in the monitoring of disorders of propionate, methylmalonate and biotin metabolismM Coker, J B de Klerk, B T Poll-The, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Congenital nephrotic syndrome: a novel phenotype of type I carbohydrate-deficient glycoprotein syndromeM S van der Knaap, R A Wevers, L Monnens, et al.
Journal of Inherited Metabolic Disease|January 9, 2008
Amnionless (AMN) mutations in Imerslund-Gräsbeck syndrome may be associated with disturbed vitamin B12 transport into the CNSA S Luder, S M Tanner, A de la Chapelle, et al.
Journal of Inherited Metabolic Disease|November 11, 2016
Household financial burden of phenylketonuria and its impact on treatment in China: a cross-sectional studyLin Wang, Hui Zou, Fang Ye, et al.
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