CVO facebook page is a support community for caregivers, friends, and patients living with Cryoglobulinemia. The organization will be opening a global website in the very near future which can be found at www.cryogroup.com
Networks
CFRI seeks to inform, engage and empower the CF community to reach the highest possible quality of life. Founded in 1975, Cystic Fibrosis Research, Incorporated (CFRI) is a 501(c)(3) charitable organization. EIN #51-0169988 1731 Embarcadero Road, Suite 210 Palo Alto, CA 94303 Toll-free: 855-237-4669 Telephone: 650-404-9975 Fax: 650-404-9981 E-mail: [email protected]: http://www.cfri.org
Mission Statement CRF’s mission is to support bench, clinical and translational cystinosis research to find better treatments and a cure for cystinosis. Research The Cystinosis Research Foundation is dedicated to finding better treatments to improve the quality of life for those with cystinosis and to ultimately find a cure for...
Human cytomegalovirus is a species of virus that belongs to the viral family known as Herpesviridae or herpesviruses. It is typically abbreviated as HCMV and is alternatively known as human herpesvirus-5 (HHV-5). Within Herpesviridae, HCMV belongs to the Betaherpesvirinae subfamily, which also includes cytomegaloviruses from other mammals.
ytomegalovirus (CMV) is a virus related to the herpes virus. It is so common that almost all adults in developing countries and 50% to 85% of adults in the United States have been infected.
The Dystrophic Epidermolysis Bullosa Research Association of America (debra of America) is the only U.S. nonprofit providing all-inclusive support to the EB Community, through funding research for a cure and by providing free programs and services for those with: Epidermolysis Bullosa (EB) — “The Worst Disease You’ve Never Heard Of.” EB is...
Dermatology Online Journal 13 (1): 17 Glomuvenous malformations by Henning et al., 2007.