Cerebro-hepato-renal (Zellweger) syndrom... [Johns Hopkins Med J. 1982] - PubMed

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Very long chain fatty acids in genetic peroxisomal disease fibroblasts: differences between the cerebro-hepato-renal (Zellweger) syndrome and adrenoleukodystrophy variants. [Clin Chim Acta. 1986]
Very long chain fatty acids in genetic peroxisomal disease fibroblasts: differences between the cerebro-hepato-renal (Zellweger) syndrome and adrenoleukodystrophy variants.
Molzer B, Korschinsky M, Bernheimer H, Schmid R, Wolf C, Roscher A. Clin Chim Acta. 1986 Nov 30; 161(1):81-90.
Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy. [Proc Natl Acad Sci U S A. 1984]
Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy.
Singh I, Moser AE, Goldfischer S, Moser HW. Proc Natl Acad Sci U S A. 1984 Jul; 81(13):4203-7.
Neonatal adrenoleukodystrophy. Impaired plasmalogen biosynthesis and peroxisomal beta-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fibroblasts. [J Neurol Sci. 1987]
Neonatal adrenoleukodystrophy. Impaired plasmalogen biosynthesis and peroxisomal beta-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fibroblasts.
Wanders RJ, Schutgens RB, Schrakamp G, Tager JM, Van den Bosch H, Moser AB, Moser HW. J Neurol Sci. 1987 Feb; 77(2-3):331-40.
Review The peroxisome: nervous system role of a previously underrated organelle. The 1987 Robert Wartenberg lecture. [Neurology. 1988]
Review The peroxisome: nervous system role of a previously underrated organelle. The 1987 Robert Wartenberg lecture.
Moser HW. Neurology. 1988 Oct; 38(10):1617-27.
Review Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes. [Am J Med Genet. 1986]
Review Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes.
Kelley RI, Datta NS, Dobyns WB, Hajra AK, Moser AB, Noetzel MJ, Zackai EH, Moser HW. Am J Med Genet. 1986 Apr; 23(4):869-901.

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Cited by 19 PubMed Central articles

The Δ4-desaturation pathway for DHA biosynthesis is operative in the human species: differences between normal controls and children with the Zellweger syndrome. [Lipids Health Dis. 2010]
The Δ4-desaturation pathway for DHA biosynthesis is operative in the human species: differences between normal controls and children with the Zellweger syndrome.
Martinez M, Ichaso N, Setien F, Durany N, Qiu X, Roesler W. Lipids Health Dis. 2010 Sep 9; 9:98. Epub 2010 Sep 9.
The peroxisome: still a mysterious organelle. [Histochem Cell Biol. 2008]
The peroxisome: still a mysterious organelle.
Schrader M, Fahimi HD. Histochem Cell Biol. 2008 Apr; 129(4):421-40. Epub 2008 Feb 15.
Leopard spot retinal pigmentation in infancy indicating a peroxisomal disorder. [Br J Ophthalmol. 2004]
Leopard spot retinal pigmentation in infancy indicating a peroxisomal disorder.
Lyons CJ, Castano G, McCormick AQ, Applegarth D. Br J Ophthalmol. 2004 Feb; 88(2):191-2.

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Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: sim...
Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acids.
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Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acids.

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