By Philip M. Parker
In March 2001, the nationwide Institutes of overall healthiness issued the next caution: "The variety of sites providing health-related assets grows each day. Many websites offer worthy details, whereas others can have details that's unreliable or misleading." moreover, due to the swift elevate in Internet-based details, many hours will be wasted looking out, settling on, and printing. on account that merely the smallest fraction of data facing Fabry disorder is listed in se's, equivalent to www.google.com or others, a non-systematic method of web study could be not just time eating, but in addition incomplete. This ebook was once created for doctors, scholars, and individuals of most people who are looking to behavior scientific study utilizing the main complex instruments on hand and spending the smallest amount of time doing so.
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In March 2001, the nationwide Institutes of well-being issued the next caution: "The variety of websites providing health-related assets grows on a daily basis. Many websites offer worthy details, whereas others can have info that's unreliable or deceptive. " additionally, a result of fast bring up in Internet-based details, many hours should be wasted looking out, determining, and printing.
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Additional info for Fabry Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
Source: Bulletin of Experimental Biology and Medicine. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=12802435&query_hl=14&itool=pubmed_docsum • Pathologic quiz case: an unsuspected cause of nephrotic syndrome. Heterozygous Fabry disease. Author(s): Thamboo TP, Sivaraman P, Chan NH. Source: Archives of Pathology & Laboratory Medicine. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=15086291&query_hl=14&itool=pubmed_docsum • Pathophysiology and assessment of neuropathic pain in Fabry disease.
Source: American Journal of Human Genetics. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=16773563&query_hl=14&itool=pubmed_docsum 30 Fabry Disease • High overexpression of the human alpha-galactosidase A gene driven by its promoter in transgenic mice: implications for the treatment of Fabry disease. Author(s): Ashley GA, Desnick RJ, Gordon RE, Gordon JW. Source: Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=12033283&query_hl=14&itool=pubmed_docsum • High prevalence of subclinical hypothyroidism in patients with Anderson-Fabry disease.
Author(s): Ries M, Moore DF, Robinson CJ, Tifft CJ, Rosenbaum KN, Brady RO, Schiffmann R, Krasnewich D. Source: Genetics in Medicine : Official Journal of the American College of Medical Genetics. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=16481892&query_hl=14&itool=pubmed_docsum • Quantitative evaluation of sphingolipids using delayed extraction matrix-assisted laser desorption ionization time-of-flight mass spectrometry with sphingosylphosphorylcholine as an internal standard. Practical application to cardiac valves from a patient with Fabry disease.
Fabry Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker