Download X-Linked Adrenoleukodystrophy - A Bibliography and by Philip M. Parker PDF

By Philip M. Parker

In March 2001, the nationwide Institutes of healthiness issued the subsequent caution: "The variety of sites supplying health-related assets grows on a daily basis. Many websites supply useful details, whereas others can have info that's unreliable or misleading." moreover, as a result quick raise in Internet-based details, many hours may be wasted looking, determining, and printing. considering that merely the smallest fraction of data facing X-linked adrenoleukodystrophy is listed in se's, reminiscent of www.google.com or others, a non-systematic method of web study should be not just time eating, but additionally incomplete. This ebook used to be created for doctors, scholars, and individuals of most people who are looking to behavior clinical examine utilizing the main complex instruments to be had and spending the smallest amount of time doing so.

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Author(s): Yasutake T, Yamada T, Furuya H, Shinnoh N, Goto I, Kobayashi T. Source: Journal of the Neurological Sciences. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=7561948&query_hl=11&itool=pubmed_docsum • Molecular species of phosphatidylcholine containing very long chain fatty acids in human brain: enrichment in X-linked adrenoleukodystrophy brain and diseases of peroxisome biogenesis brain. Author(s): Sharp P, Johnson D, Poulos A. Source: Journal of Neurochemistry. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=1702833&query_hl=11&itool=pubmed_docsum • Monozygotic twins with X-linked adrenoleukodystrophy and different phenotypes.

Author(s): Chiu HC, Liang JS, Wang JS, Lu JF. Source: Pediatric Neurology. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=16996397&query_hl=11&itool=pubmed_docsum • Mutational analysis and genotype-phenotype correlation of 29 unrelated Japanese patients with X-linked adrenoleukodystrophy. Author(s): Takano H, Koike R, Onodera O, Sasaki R, Tsuji S. Source: Archives of Neurology. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=10190819&query_hl=11&itool=pubmed_docsum • Mutational analysis and the pathogenesis of variant X-linked adrenoleukodystrophy phenotypes.

Author(s): Moser HW. Source: Current Opinion in Neurology. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=7551122&query_hl=1&itool=pubmed_docsum • Adrenoleukodystrophy. The chain shortening of erucic acid (22:1(n-9)) and adrenic acid (22:4(n-6)) is deficient in neonatal adrenoleukodystrophy and normal in X-linked adrenoleukodistrophy skin fibroblasts. Author(s): Christensen E, Gronn M, Hagve TA, Kase BF, Christophersen BO. Source: Biochimica Et Biophysica Acta. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=2538146&query_hl=1&itool=pubmed_docsum • Adrenoleukodystrophy: a link between adrenal insufficiency and school performance.

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