21-Hydroxylase Deficiency - A Bibliography and Dictionary by Philip M. Parker PDF

By Philip M. Parker

ISBN-10: 0497112019

ISBN-13: 9780497112011

ISBN-10: 1429497335

ISBN-13: 9781429497336

In March 2001, the nationwide Institutes of health and wellbeing issued the subsequent caution: "The variety of websites delivering health-related assets grows each day. Many websites offer worthy info, whereas others can have info that's unreliable or misleading." additionally, as a result of swift raise in Internet-based info, many hours will be wasted looking, picking, and printing. because simply the smallest fraction of knowledge facing 21-hydroxylase deficiency is listed in se's, reminiscent of www.google.com or others, a non-systematic method of web study might be not just time eating, but in addition incomplete. This e-book used to be created for doctors, scholars, and individuals of most of the 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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In March 2001, the nationwide Institutes of wellbeing and fitness issued the next caution: "The variety of websites delivering health-related assets grows each day. Many websites supply precious info, whereas others can have info that's unreliable or deceptive. " moreover, as a result swift elevate in Internet-based info, many hours may be wasted looking, choosing, and printing.

Extra resources for 21-Hydroxylase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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Source: European Journal of Endocrinology / European Federation of Endocrine Societies. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=11022183&query_hl=4&itool=pubmed_docsum • Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency. Author(s): Nordenstrom A, Thilen A, Hagenfeldt L, Larsson A, Wedell A. Source: The Journal of Clinical Endocrinology and Metabolism. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=10323369&query_hl=4&itool=pubmed_docsum • Growth analysis in patients with 21-hydroxylase deficiency influence of glucocorticoid dosage, age at diagnosis, phenotype and genotype on growth and height outcome.

Author(s): Parlato F, Pisano G, Brillante M, Ferrone R, Cavalcanti MR, Cosentini E, Misiano G, Brai M, Bellastella A. Source: J Endocrinol Invest. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=7868802&query_hl=4&itool=pubmed_docsum • Impaired mineralocorticoid hormone responses to adrenocorticotropin stimulation: additional characterization of heterozygosity for the 21-hydroxylase deficiency type of congenital adrenal hyperplasia. Author(s): Pardini DP, Kater CE, Vieira JG, Biglieri EG. Source: The Journal of Clinical Endocrinology and Metabolism.

Author(s): Shinohara O, Ishiguro H, Shinagawa T, Kubota C. Source: Endocrine Journal. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=9790280&query_hl=4&itool=pubmed_docsum • Female pseudohermaphroditism due to classical 21-hydroxylase deficiency and insulin resistance in a girl with Turner syndrome. Author(s): Atabek ME, Kurtoglu S, Keskin M. Source: Turk J Pediatr. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=16052861&query_hl=4&itool=pubmed_docsum 26 21-Hydroxylase Deficiency • Female pseudohermaphroditism due to classical 21-hydroxylase deficiency in a girl with Turner syndrome.

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21-Hydroxylase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker


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