i-cah.org
INTRODUCTION TO I-CAH | I-CAH RegistryThe International-CAH (I-CAH) network is an initiative to improve the clinical management of the rare disease Congenital Adrenal Hyperplasia.
http://www.i-cah.org/
The International-CAH (I-CAH) network is an initiative to improve the clinical management of the rare disease Congenital Adrenal Hyperplasia.
http://www.i-cah.org/
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INTRODUCTION TO I-CAH | I-CAH Registry | i-cah.org Reviews
https://i-cah.org
The International-CAH (I-CAH) network is an initiative to improve the clinical management of the rare disease Congenital Adrenal Hyperplasia.
i-cah.org
NEWS | I-CAH Registry
http://www.i-cah.org/news
Read about all the latest news and events happening at I-CAH here. If you have any questions or are looking for a particular event please contact us. Two new studies are underway that will be supported by the newly developed longitudinal module in the I-CAH registry: Management of Fludrocortisone and salt therapy in 0-3 year old children with congenital adrenal hyperplasia (CAH) (Claahsen, . I-CAH project group meets at ESPE. I-CAH longitudinal module launched. Launch of I-CAH Network Website. Sheffield...
TAIN Reports Successful Infacort® Trial | I-CAH Registry
http://www.i-cah.org/news/tain-reports-successful-infacort-trial
TAIN Reports Successful Infacort Trial. TAIN Reports Successful Infacort Trial. Posted on Wednesday, 04/Dec/2013. Cardiff, UK. The TAIN Consortium funded by the European Commission (FP7-HEALTH No: 281654) announced that a clinical trial of Infacort. Immediate release hydrocortisone granules for paediatric use) successfully achieved its primary outcome of demonstrating bioequivalence versus immediate release hydrocortisone tablets. Infacort.
FOR PATIENTS | I-CAH Registry
http://www.i-cah.org/for-patients
I-CAH seeks to support patients, children and parents by providing information, support and links, as well as developing research that will underpin improvements in the treatment of Congenital Adrenal Hyperplasia. I-CAH patient information sheet (child). I-CAH patient information sheets (adult). Congenital Adrenal Hyperplasia - Living with CAH Support Group (UK). Congenital Adrenal Hyperplasia adult information booklet - Dr G. Conway. CAH Support Group Links. CAH is Us - Parent and Patient support group.
FOR PHYSICIANS | I-CAH Registry
http://www.i-cah.org/for-physicians
I-CAH seeks to include physicians in research to optimise the care of patients with Congenital Adrenal Hyperplasia. I-CAH would encourage physicians to enrol their patients in the I-CAH Registry and participate in research. This website provides relevant links to the I-CAH Registry. And a list of recent publications. Merke DP, Bornstein SR. Congenital adrenal hyperplasia. Lancet. 2005;365(9477):2125-36. Auchus RJ, Witchel SF, Leight KR, Aisenberg J, Azziz R, Bachega TA, et al. Guidelines for the Deve...
Launch of I-CAH Network Website | I-CAH Registry
http://www.i-cah.org/news/launch-of-i-cah-network-website
Launch of I-CAH Network Website. Launch of I-CAH Network Website. Posted on Monday, 10/Nov/2014. Sheffield, UK. The I-CAH Network website has now been launched. The I-CAH Network is an initiative to improve the clinical management of Congenital Adrenal Hyperplasia (CA.
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INTRODUCTION TO I-CAH | I-CAH Registry
The International-CAH (I-CAH) network is an initiative to improve the clinical management of the rare disease Congenital Adrenal Hyperplasia. With a newly-created I-CAH Registry as its centrepiece, the initiative also focuses on providing information to patients and clinicians and developing research to optimise healthcare. The I-CAH Registry delivers a means of connecting clinical and research centres from around the world within a Virtual Research Environment (VRE) and will underpin research in...TAIN ...
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