Similar articles for PMID: 6709009

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1984	7
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1

The cerebrohepatorenal (Zellweger) syndrome. Increased levels and impaired degradation of very-long-chain fatty acids and their use in prenatal diagnosis.

Moser AE, Singh I, Brown FR 3rd, Solish GI, Kelley RI, Benke PJ, Moser HW. Moser AE, et al. N Engl J Med. 1984 May 3;310(18):1141-6. doi: 10.1056/NEJM198405033101802. N Engl J Med. 1984. PMID: 6709009

2

Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders.

Wanders RJ, van Roermund CW, van Wijland MJ, Schutgens RB, Heikoop J, van den Bosch H, Schram AW, Tager JM. Wanders RJ, et al. J Clin Invest. 1987 Dec;80(6):1778-83. doi: 10.1172/JCI113271. J Clin Invest. 1987. PMID: 3680527 Free PMC article.

3

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

Brown FR 3rd, McAdams AJ, Cummins JW, Konkol R, Singh I, Moser AB, Moser HW. Brown FR 3rd, et al. Johns Hopkins Med J. 1982 Dec;151(6):344-51. Johns Hopkins Med J. 1982. PMID: 7176294 No abstract available.

4

Phytanic acid and very long chain fatty acids in genetic peroxisomal disorders.

Molzer B, Kainz-Korschinsky M, Sundt-Heller R, Bernheimer H. Molzer B, et al. J Clin Chem Clin Biochem. 1989 May;27(5):309-14. J Clin Chem Clin Biochem. 1989. PMID: 2474624

5

Adrenoleukodystrophy: survey of 303 cases: biochemistry, diagnosis, and therapy.

Moser HW, Moser AE, Singh I, O'Neill BP. Moser HW, et al. Ann Neurol. 1984 Dec;16(6):628-41. doi: 10.1002/ana.410160603. Ann Neurol. 1984. PMID: 6524872

6

[Diagnosis of Zellweger's cerebrohepatorenal syndrome].

Schutgens RB, Heymans HS, Purvis R, Wanders RJ, Schrakamp G, van den Bosch H. Schutgens RB, et al. Tijdschr Kindergeneeskd. 1984 Dec;52(6):231-8. Tijdschr Kindergeneeskd. 1984. PMID: 6528320 Dutch.

7

Prenatal diagnosis of Zellweger syndrome by measurement of very long chain fatty acid (C26:0) beta-oxidation in cultured chorionic villous fibroblasts: implications for early diagnosis of other peroxisomal disorders.

Wanders RJ, van Wijland MJ, van Roermund CW, Schutgens RB, van den Bosch H, Tager JM, Nijenhuis A, Tromp A. Wanders RJ, et al. Clin Chim Acta. 1987 Jun 15;165(2-3):303-10. doi: 10.1016/0009-8981(87)90175-6. Clin Chim Acta. 1987. PMID: 3652452

8

The cerebrohepatorenal (Zellweger) syndrome: an improved method for the biochemical diagnosis and its potential value for prenatal detection.

Roscher A, Molzer B, Bernheimer H, Stöckler S, Mutz I, Paltauf F. Roscher A, et al. Pediatr Res. 1985 Sep;19(9):930-3. doi: 10.1203/00006450-198509000-00013. Pediatr Res. 1985. PMID: 4047762

9

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. Kelley RI, et al. Am J Med Genet. 1986 Apr;23(4):869-901. doi: 10.1002/ajmg.1320230404. Am J Med Genet. 1986. PMID: 3515938 Review.

10

Analysis of very long-chain fatty acids and plasmalogen in the erythrocyte membrane: a simple method for the detection of peroxisomal disorders and discrimination between adrenoleukodystrophy and Zellweger syndrome.

Tanaka K, Nishizawa K, Yamamoto H, Naruto T, Izeki E, Taga T, Shimada M, Saeki Y. Tanaka K, et al. Neuropediatrics. 1990 Aug;21(3):119-23. doi: 10.1055/s-2008-1071476. Neuropediatrics. 1990. PMID: 2234315

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