By Philip M. Parker
In March 2001, the nationwide Institutes of well-being issued the next caution: "The variety of sites delivering health-related assets grows on a daily basis. Many websites offer precious info, whereas others could have info that's unreliable or misleading." additionally, end result of the speedy bring up in Internet-based details, many hours could be wasted looking, deciding upon, and printing. seeing that merely the smallest fraction of knowledge facing Alport syndrome is listed in se's, akin to www.google.com or others, a non-systematic method of web study will be not just time eating, but additionally incomplete. This booklet was once created for doctors, scholars, and contributors of most people who are looking to behavior scientific examine utilizing the main complex instruments to be had and spending the smallest amount of time doing so.
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Extra info for Alport Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
Source: Nephron. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=8290008&query_hl=21&itool=pubmed_docsum • Alport syndrome, basement membranes and collagen. Author(s): Kashtan CE, Kleppel MM, Butkowski RJ, Michael AF, Fish AJ. Source: Pediatric Nephrology (Berlin, Germany). db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=2242324&query_hl=21&itool=pubmed_docsum 30 Alport Syndrome • Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?
Db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=9734596&query_hl=21&itool=pubmed_docsum • A monoclonal antibody marker for Alport syndrome identifies the Alport antigen as the alpha 5 chain of type IV collagen. Author(s): Ding J, Kashtan CE, Fan WW, Kleppel MM, Sun MJ, Kalluri R, Neilson EG, Michael AF. Source: Kidney International. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=8072264&query_hl=21&itool=pubmed_docsum • A mutation causing Alport syndrome with tardive hearing loss is common in the western United States.
2) detected by fluorescence in situ hybridization in a boy with Alport syndrome. Author(s): Balarin MA, da Silva Lopes VL, Varella-Garcia M. Source: American Journal of Medical Genetics. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=9934986&query_hl=21&itool=pubmed_docsum • A family with Alport syndrome and psychosis. Author(s): Shields GW, Pataki C, DeLisi LE. Source: Schizophrenia Research. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=2278984&query_hl=21&itool=pubmed_docsum • A family with X-linked Alport syndrome confirmed by skin biopsy.