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5. A magnetic resonance approach to metabolic disorders in childhood. Barkovich AJ Rev Neurol; 2006 Oct; 43 Suppl 1():S5-16. PubMed ID: 17061196 [TBL] [Abstract][Full Text] [Related]
6. New concepts in the diagnosis and treatment of lysosomal and peroxisomal disorders. Moser HW Curr Opin Neurol Neurosurg; 1992 Jun; 5(3):355-8. PubMed ID: 1623264 [TBL] [Abstract][Full Text] [Related]
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9. [Peroxisomal disorders--is diagnosis possible in Czechoslovakia?]. Hyánek J; Kozich V; Pehal F Cesk Pediatr; 1990 Jan; 45(1):51-2. PubMed ID: 2393931 [No Abstract] [Full Text] [Related]
10. [Clinical aspects of hereditary peroxisomal disorders]. Billette de Villemeur T; Poll The BT; Saudubray JM Minerva Pediatr; 1991 Mar; 43(3):115-23. PubMed ID: 1870505 [No Abstract] [Full Text] [Related]
11. Diagnosis of peroxisomal disorders with neurological involvement. Molzer B Padiatr Padol; 1993; 28(1):43-8. PubMed ID: 8446428 [TBL] [Abstract][Full Text] [Related]
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14. Organelle pathology in metabolic neuromuscular disease: an overview. Becker LE Can J Vet Res; 1990 Jan; 54(1):1-14. PubMed ID: 2407327 [TBL] [Abstract][Full Text] [Related]
15. Peroxisomal disorders: clinical commentary and future prospects. Wilson GN; Holmes RD; Hajra AK Am J Med Genet; 1988 Jul; 30(3):771-92. PubMed ID: 2461077 [TBL] [Abstract][Full Text] [Related]
16. Inborn errors of metabolism (IEM) -- an Indian perspective. Kumta NB Indian J Pediatr; 2005 Apr; 72(4):325-32. PubMed ID: 15876762 [TBL] [Abstract][Full Text] [Related]
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