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European Psychiatry : the Journal of the Association of European Psychiatrists|February 18, 2017
Dimensional and discrete variations on the psychosis continuum in a Dutch crowd-sourcing population sampleJ T W Wigman, K J Wardenaar, R B K Wanders, et al.
Orphanet Journal of Rare Diseases|November 17, 2023
Abnormal activation of MAPKs pathways and inhibition of autophagy in a group of patients with Zellweger spectrum disorders and X-linked adrenoleukodystrophyVincenza Gragnaniello, Daniela Gueraldi, Andrea Puma, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 26, 2023
Autosomal dominant Zellweger spectrum disorder caused by de novo variants in PEX14 geneHans R Waterham, Janet Koster, Merel S Ebberink, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
Hypothalamus amyloid levels are associated with early sex-dependent alterations in energy homeostasis in TgF344-AD ratsCaleb M Levine, Cameron Caggiano, Thea Anderson, et al.
Biochemical and Biophysical Research Communications|February 15, 1985
Peroxisomal beta-oxidation enzyme proteins in the Zellweger syndromeJ M Tager, W A Van der Beek, R J Wanders, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 27, 1999
Quantitative acylcarnitine profiling in fibroblasts using [U-13C] palmitic acid: an improved tool for the diagnosis of fatty acid oxidation defectsF V Ventura, C G Costa, E A Struys, et al.
European Journal of Biochemistry|July 8, 1998
Carnitine palmitoyltransferase II specificity towards beta-oxidation intermediates--evidence for a reverse carnitine cycle in mitochondriaF V Ventura, L Ijlst, J Ruiter, et al.
The European Respiratory Journal|August 2, 2006
Very long-chain acyl-CoA dehydrogenase deficiency presenting as acute hypercapnic respiratory failureM K H Tong, C-S Lam, T W L Mak, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1991
Very large peroxisomes in distinct peroxisomal disorders (rhizomelic chondrodysplasia punctata and acyl-CoA oxidase deficiency): novel dataD De Craemer, M J Zweens, S Lyonnet, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 7, 2009
Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiencyLap-Kay Law, Nelson L S Tang, Joannie Hui, et al.
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