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Pemphigus & Pemphigoid Patient Registry Launched

SACRAMENTO, California, USA (June 15, 2010) - The International Pemphigus & Pemphigoid Foundation (IPPF) has officially launched its Pemphigus-Pemphigoid Patient Registry. Pemphigus and pemphigoid (P-P) patients can now enter in specific illness and treatment/outcome information in an online registry tool that will provide researchers with valuable, hard to come by information about these rare diseases.

The registry was designed using SurveyGizmo.com, is HIPPA compliant, and the information is protected on their secure servers. The P-P Patient Registry has been approved by the United States Department of Health and Human ServicesOffice for Human Research Protection’s Institutional Review Board (IRB). The IPPF has a goal of adding 1,000 respondents to the registry by the end of 2010. This goal will provide a substantial amount of illness and treatment information needed to support research and discovery, increase P-P education among medical professionals, and support its patient advocacy campaigns.

On the foundation of the clinical information collected in patient databases and associated sample collections, we can systematically investigate disease mechanisms by relating clinical data to genetic, genomic, and proteomic disease factors,” said Dr. Animesh Sinha, Chief, N.V. Perricone Division of Dermatology and Cutaneous Sciences and Director, Center for Investigative Dermatology at Michigan State University. He believes that the P-P Registrycan be expected to yield relevant insights into general mechanisms of autoimmunity, and facilitate the development of novel therapies to help relieve the burden of human autoimmune disease.

The registry is only for pemphigus and pemphigoid patients and takes approximately 10 minutes to complete. Patients interested in participating are encouraged to visit the IPPF’s registry page at http://www.pemphigus.org/registry to learn more about the registry, download a guide to help them gather information on current and past medications, or participate.

The registry was designed using SurveyGizmo.com, is HIPPA compliant, and the information is protected on their secure servers. The P-P Patient Registry has been approved by the United States Department of Health and Human ServicesOffice for Human Research Protection’s Institutional Review Board (IRB). The IPPF has a goal of adding 1,000 respondents to the registry by the end of 2010. This goal will provide a substantial amount of illness and treatment information needed to support research and discovery, increase P-P education among medical professionals, and support its patient advocacy campaigns.

On the foundation of the clinical information collected in patient databases and associated sample collections, we can systematically investigate disease mechanisms by relating clinical data to genetic, genomic, and proteomic disease factors,” said Dr. Animesh Sinha, Chief, N.V. Perricone Division of Dermatology and Cutaneous Sciences and Director, Center for Investigative Dermatology at Michigan State University. He believes that the P-P Registrycan be expected to yield relevant insights into general mechanisms of autoimmunity, and facilitate the development of novel therapies to help relieve the burden of human autoimmune disease.

The registry is only for pemphigus and pemphigoid patients and takes approximately 10 minutes to complete. Patients interested in participating are encouraged to visit the IPPF’s registry page at http://www.pemphigus.org/registry to learn more about the registry, download a guide to help them gather information on current and past medications, or participate.

About the International Pemphigus & Pemphigoid Foundation (IPPF)
The International Pemphigus & Pemphigoid Foundation (IPPF) is an international patient organization that provides support, advocacy, awareness, and education to those affected by the rare, autoimmune blistering diseases (AIBD) pemphigus and pemphigoid. Since 1994, the IPPF has been a US-registered 501(c)(3) not-for-profit organization championing AIBD research, medical professional education, and public awareness. The IPPF offers support services to thousands of patients, cuidadores, and medical professional each year. For more information on the International Pemphigus & Pemphigoid Foundation, contact the IPPF at (855) 4-PEMPHIGUS, (916) 922-1298, or online at www.pemphigus.org.

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El registro de p y p ha sido aprobado por la Junta de revisión institucional de occidental (WIRB) y activamente es inscribir participantes.

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