By Philip M. Parker
In March 2001, the nationwide Institutes of health and wellbeing issued the next caution: "The variety of sites providing health-related assets grows each day. Many websites supply priceless info, whereas others could have details that's unreliable or misleading." additionally, a result of swift elevate in Internet-based details, many hours could be wasted looking, determining, and printing. due to the fact simply the smallest fraction of knowledge facing 21-hydroxylase deficiency is listed in se's, corresponding to www.google.com or others, a non-systematic method of net examine might be not just time eating, but in addition incomplete. This ebook was once created for doctors, scholars, and participants 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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Extra resources for 21-Hydroxylase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
Author(s): Winkel CA, Casey ML, Worley RJ, Madden JD, MacDonald PC. Source: The Journal of Clinical Endocrinology and Metabolism. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=6600168&query_hl=4&itool=pubmed_docsum • Failure of angiotensin II to stimulate increases in concentrations of adrenal androgens, 17-hydroxyprogesterone, or adrenocorticotropin in congenital 21hydroxylase deficiency. Author(s): Wisgerhof M, Mellinger RC, Zafar MS. Source: The Journal of Clinical Endocrinology and Metabolism.
Source: Human Genetics. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=9580109&query_hl=4&itool=pubmed_docsum • Molecular genetic analysis of Tunisian patients with a classic form of 21-hydroxylase deficiency: identification of four novel mutations and high prevalence of Q318X mutation. Author(s): Kharrat M, Tardy V, M'Rad R, Maazoul F, Jemaa LB, Refai M, Morel Y, Chaabouni H. Source: The Journal of Clinical Endocrinology and Metabolism. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=14715874&query_hl=4&itool=pubmed_docsum • Molecular genetics of congenital adrenal hyperplasia (21-hydroxylase deficiency): implications for diagnosis, prognosis and treatment.
Source: Human Genetics. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=8707311&query_hl=4&itool=pubmed_docsum • Massive adrenocortical adenoma following long-term treatment of 21-hydroxylase deficiency. Author(s): Takahashi S, Minowada S, Tomita K, Katumata N, Tanaka T, Kitamura T. Source: The Journal of Urology. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=11832743&query_hl=4&itool=pubmed_docsum • Menstrual disturbance and hypersecretion of progesterone in women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.