ADRENOMYELONEUROPATHY-CLINICAL and BIOCHEMICAL DIAGNOSIS
Author:
Publisher
Wiley
Subject
Internal Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1445-5994.1983.tb02611.x/fullpdf
Reference33 articles.
1. Inborn errors of metabolism;Kolodny;Ann Neurol,1982
2. Biochemical genetics of neurologic disease;Rosenberg;N Engl J Med,1981
3. Adrenomyeloneuropathy: a probable variant of adrenoleukodystrophy. 1 Clinical and endocrinologic aspects;Griffin;Neurology (NY),1977
4. Adrenomyeloneuropathy: a probable variant of adrenoleukodystrophy. 2 General pathologic, neuropathology and biochemical aspects;Schaumburg;Neurology (NY),1977
5. Adrenoleukodystrophy: elevated C26 fatty acid in cultured skin fibroblasts;Moser;Ann Neurol,1980
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1. Accumulation and defective β-oxidation of very long chain fatty acids in Zellweger's syndrome, adrenoleukodystrophy and Refsum's disease variants;Clinical Genetics;2008-04-23
2. Prenatal diagnosis of X-linked adrenoleukodystrophy combining biochemical, immunocytochemical and DNA analyses;PRENATAL DIAG;1999
3. Prenatal diagnosis of X-linked adrenoleukodystrophy combining biochemical, immunocytochemical and DNA analyses;Prenatal Diagnosis;1999-04
4. X-linked adrenoleukodystrophy: The Australasian experience;AM J MED GENET;1998
5. X-linked adrenoleukodystrophy: The Australasian experience;American Journal of Medical Genetics;1998-04-13
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