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10.1210/jc.2014-4357 http://scihub22266oqcxt.onion/10.1210/jc.2014-4357 C4333044!4333044!25575015     free     free     free Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Clin+Endocrinol+Metab 2015 ; 100 (3): 803-11 Nephropedia Template TP {{tp|p=25575015|t=2015. Endocrine Disorders in Fanconi Anemia: Recommendations for Screening and Treatment |pdf=|usr=}}{{25575015}} gab.com Text Endocrine Disorders in Fanconi Anemia: Recommendations for Screening and Treatment JO: J Clin Endocrinol Metab http://www.kidney.de/pget.php?&tw=1&pmid=25575015 #FOAvip Context:: Endocrine problems are common in patients with Fanconi anemia (FA). About 80% of children and adults with FA have at least one endocrine abnormality, including short stature, GH deficiency, abnormal glucose or insulin metabolism, dyslipidemia, hypothyroidism, pubertal delay, hypogonadism, or impaired fertility. The goal of this report is to provide an overview of endocrine abnormalities and guidelines for routine screening and treatment to allow early diagnosis and timely intervention. Evidence Acquisition:: This work is based on a comprehensive literature review, including relevant articles published between 1971 and 2014, and proceedings of a Consensus Conference held by the Fanconi Anemia Research Fund in 2013. Evidence Synthesis:: The panel of experts collected published evidence and discussed its relevance to reflect current information about the endocrine care of children and adults with FA before the Consensus Conference and through subsequent deliberations that led to the consensus. Conclusions:: Individuals with FA should be routinely screened for endocrine abnormalities, including evaluation of growth; glucose, insulin, and lipid metabolism; thyroid function; puberty; gonadal function; and bone mineral metabolism. Inclusion of an endocrinologist as part of the multidisciplinary patient care team is key to providing comprehensive care for patients with FA. Twit Text FOAVip Endocrine Disorders in Fanconi Anemia: Recommendations for Screening and Treatment ????J Clin Endocrinol Metab http://www.kidney.de/pget.php?&tw=1&pmid=25575015 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25575015 #FOAvip English Wikipedia <ref>{{Cite pmid|25575015}}</ref> Endocrine Disorders in Fanconi Anemia: Recommendations for Screening and Treatment #MMPMID25575015 Petryk A; Kanakatti Shankar R; Giri N; Hollenberg AN; Rutter MM; Nathan B; Lodish M; Alter BP; Stratakis CA; Rose SR J Clin Endocrinol Metab 2015[Mar]; 100 (3): 803-11 PMID25575015show ga Context:: Endocrine problems are common in patients with Fanconi anemia (FA). About 80% of children and adults with FA have at least one endocrine abnormality, including short stature, GH deficiency, abnormal glucose or insulin metabolism, dyslipidemia, hypothyroidism, pubertal delay, hypogonadism, or impaired fertility. The goal of this report is to provide an overview of endocrine abnormalities and guidelines for routine screening and treatment to allow early diagnosis and timely intervention. Evidence Acquisition:: This work is based on a comprehensive literature review, including relevant articles published between 1971 and 2014, and proceedings of a Consensus Conference held by the Fanconi Anemia Research Fund in 2013. Evidence Synthesis:: The panel of experts collected published evidence and discussed its relevance to reflect current information about the endocrine care of children and adults with FA before the Consensus Conference and through subsequent deliberations that led to the consensus. Conclusions:: Individuals with FA should be routinely screened for endocrine abnormalities, including evaluation of growth; glucose, insulin, and lipid metabolism; thyroid function; puberty; gonadal function; and bone mineral metabolism. Inclusion of an endocrinologist as part of the multidisciplinary patient care team is key to providing comprehensive care for patients with FA. äEndocrine Disorders in Fanconi Anemia: Recommendations for Screening a(epmc).pdf DeepDyve Pubget Overpricing