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Zellweger-like phenotype in two siblings: a defect in peroxisomal beta-oxidation with elevated very long-chain fatty acids but normal bile acids.
J Inherit Metab Dis. 1992;15(3):381-4. doi: 10.1007/BF02435982.
J Inherit Metab Dis. 1992.
PMID: 1405475
No abstract available.
Plasma lipoproteins and monocyte-macrophages in a peroxisome-deficient system: study of a patient with infantile refsum disease.
Mandel H, Berant M, Meiron D, Aizin A, Oiknine J, Brook JG, Aviram M.
Mandel H, et al. Among authors: aizin a.
J Inherit Metab Dis. 1992;15(5):774-84. doi: 10.1007/BF01800020.
J Inherit Metab Dis. 1992.
PMID: 1279267
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A new type of peroxisomal disorder with variable expression in liver and fibroblasts.
Mandel H, Espeel M, Roels F, Sofer N, Luder A, Iancu TC, Aizin A, Berant M, Wanders RJ, Schutgens RB.
Mandel H, et al. Among authors: aizin a.
J Pediatr. 1994 Oct;125(4):549-55. doi: 10.1016/s0022-3476(94)70006-0.
J Pediatr. 1994.
PMID: 7931872
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Haemophagocytosis in hereditary fructose intolerance: a diagnostic dilemma.
Mandel H, Gozal D, Aizin A, Tavori S, Jaffe M.
Mandel H, et al. Among authors: aizin a.
J Inherit Metab Dis. 1990;13(3):267-9. doi: 10.1007/BF01799369.
J Inherit Metab Dis. 1990.
PMID: 2122082
No abstract available.
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Mucolipidosis III presenting as a rheumatological disorder.
Brik R, Mandel H, Aizin A, Goldscher D, Ziegler M, Bialik V, Berant M.
Brik R, et al. Among authors: aizin a.
J Rheumatol. 1993 Jan;20(1):133-6.
J Rheumatol. 1993.
PMID: 8441145
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[Inborn errors of metabolism: lessons from a clinical case].
Mandel H, Mendelsohn H, Aizin A, Dar H, el-Peleg O.
Mandel H, et al. Among authors: aizin a.
Harefuah. 1989 Aug;117(3-4):51-6.
Harefuah. 1989.
PMID: 2572520
Hebrew.
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