Download Alport Syndrome - A Bibliography and Dictionary for by Philip M. Parker PDF

By Philip M. Parker

ISBN-10: 0497113236

ISBN-13: 9780497113230

ISBN-10: 1429496142

ISBN-13: 9781429496148

In March 2001, the nationwide Institutes of well-being issued the subsequent caution: "The variety of websites supplying health-related assets grows on a daily basis. Many websites supply necessary details, whereas others could have details that's unreliable or misleading." additionally, as a result of the speedy raise in Internet-based details, many hours will be wasted looking out, deciding upon, and printing. due to the fact in basic terms the smallest fraction of knowledge facing Alport syndrome is listed in se's, akin to or others, a non-systematic method of net study may be not just time eating, but in addition incomplete. This publication used to be created for doctors, scholars, and participants of most people who are looking to behavior clinical learn utilizing the main complicated 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

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Db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=11155669&query_hl=21&itool=pubmed_docsum 8 PubMed was developed by the National Center for Biotechnology Information (NCBI) at the National Library of Medicine (NLM) at the National Institutes of Health (NIH). The PubMed database was developed in conjunction with publishers of biomedical literature as a search tool for accessing literature citations and linking to full-text journal articles at Web sites of participating publishers. Publishers that participate in PubMed supply NLM with their citations electronically prior to or at the time of publication.

Source: Ophthalmic Genetics. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=11135492&query_hl=21&itool=pubmed_docsum • Absence of the alpha6(IV) chain of collagen type IV in Alport syndrome is related to a failure at the protein assembly level and does not result in diffuse leiomyomatosis. Author(s): Zheng K, Harvey S, Sado Y, Naito I, Ninomiya Y, Jacobs R, Thorner PS. Source: American Journal of Pathology. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=10362815&query_hl=21&itool=pubmed_docsum • Adenovirus-mediated gene transfer into kidney glomeruli using an ex vivo and in vivo kidney perfusion system - first steps towards gene therapy of Alport syndrome.

Author(s): Smeets HJ, Melenhorst JJ, Lemmink HH, Schroder CH, Nelen MR, Zhou J, Hostikka SL, Tryggvason K, Ropers HH, Jansweijer MC, et al. Source: Kidney International. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=1635357&query_hl=21&itool=pubmed_docsum • Differential diagnosis between X-linked Alport syndrome and thin basement membrane nephropathy. Author(s): Rizzoni G, Massella L. Source: Kidney International. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=15327434&query_hl=21&itool=pubmed_docsum • Diffuse esophageal leiomyomatosis in a patient with Alport syndrome: CT demonstration.

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Alport Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker

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