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Human Genetics|October 1, 1991
X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetusL Van Maldergem, M Espeel, F Roels, et al.Virchows Archiv : an International Journal of Pathology|July 6, 2000
Hepatic peroxisomes in isolated hyperpipecolic acidaemia: evidence supporting its classification as a single peroxisomal enzyme deficiencyI Kerckaert, B T Poll-The, M Espeel, et al.European Journal of Pediatrics|December 1, 1996
Isolated dihydroxyacetonephosphate-acyl-transferase deficiency in rhizomelic chondrodysplasia punctata: clinical presentation, metabolic and histological findingsH Hebestreit, R J Wanders, R B Schutgens, et al.Pediatric Radiology|November 3, 1998
Chondrodysplasia punctata with multiple congenital anomalies: a new syndrome?G R Mortier, L M Messiaen, M Espeel, et al.Neurology|November 18, 1998
Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann diseaseM R Baumgartner, N M Verhoeven, C Jakobs, et al.Neuromuscular Disorders : NMD|January 1, 1992
Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal beta-oxidationL Van Maldergem, M Espeel, R J Wanders, et al.The Journal of Pediatrics|October 1, 1994
A new type of peroxisomal disorder with variable expression in liver and fibroblastsH Mandel, M Espeel, F Roels, et al.European Journal of Cell Biology|August 1, 1995
Immunolocalization of a 43 kDa peroxisomal membrane protein in the liver of patients with generalized peroxisomal disordersM Espeel, F Roels, M Giros, et al.Hepatology (Baltimore, Md.)|August 1, 1995
Peroxisome mosaicism in the livers of peroxisomal deficiency patientsM Espeel, H Mandel, F Poggi, et al.Annals of Neurology|January 13, 2000
Atypical refsum disease with pipecolic acidemia and abnormal catalase distributionM R Baumgartner, G A Jansen, N M Verhoeven, et al.Pageof 4