WELCOME Welcome to the Acoustic Neuroma Association website. We are a patient member organization, providing information and support to persons diagnosed with or treated for acoustic neuroma and other benign tumors of the cranial nerves. The Acoustic Neuroma Association creates and publishes a quarterly newsletter, distributes patient information booklets, presents a biennial national symposium, provides access to a network of local support groups, and maintains this website for pa ...

go to Shufflebrain main menu AGENESIS OF THE CORPUS CALLOSUM -- index and preliminary remarks What's in the Literature? web contact: pietsch@indiana.edu ACC -- AGENESIS OF THE CORPUS CALLOSUM-- refers to the congential absence of the brain's corpus callosum -- the massive formation of nerve fibers bridging the two cerebral hemispheres. (When partial or incomplete, the term dysgenesis is sometimes used.) Once thought to be a rare condition, ACC has been turning up with increasing frequency ev ...

AISSG Home Page About this Site Contact Us What is AIS? Complete AIS Partial AIS Related Conditions Group Literature Group Meetings Raising Awareness Announcements AIS in Articles/Books Debates/Discussions Personal Stories Obtaining/Facing Diagnosis Orchidectomy (Gonadectomy) HRT/Osteoporosis Vaginal Hypoplasia Genital Plastic Surgery Patients' Charter Recommended Clinicians Research Studies Fertility Advances Informationen in Deutsch Información en Español Inform ...

Alpha-1 Association's mission is to identify those affected by Alpha-1 Antitrypsin Deficiency and to improve the quality of their lives through support, education and advocacy. AlphaNet's mission is to improve the lives of those affected with Alpha-1 Antitrypsin Deficiency by creating and disseminating a wide range of expert disease management services, while providing significant contributions toward research for a cure. The Alpha-1 Foundation is dedicated to providing the leadership and resources that will result in increased research, improved health, worldwide detection and a cure for Alpha-1 Antitrypsin Deficiency.

Welcome to: - New NASS website For Patients NASS SYMPOSIUM - 22ND APRIL 2006 University Of The West Of England, Frenchay Campus, Bristol Places Still Available only £5 per person Click here for more info & to reserve your place Ankylosing Spondylitis & You If you are suffering from ankylosing spondylitis, which we'll call AS for short, you may well have various questions about the disease. At the National Ankylosing Spondylitis Society (NASS) ...

CASE.EDU: HOME | DIRECTORIES | SEARCH Center for Inherited Disorders of Energy Metabolism Home Faculty/Staff Testing CPT Codes & Price List Laboratory Requisition Mycoplasma Testing Shipping Instructions CLIA Certificates Contact Us SEARCH SITE NAME: RELATED SITES: Center for Human Genetics >> University Hospitals Health System >> Case School of Medicine >> Our Mission Is to provide comprehensive diagnostic laboratory services to facilitate diagnosis and trea ...

Information for genetic professionals, University of Kansas Medical Center, with clinical, research, and educational resources for genetic counselors, clinical geneticists, and medical geneticists Societies • Support Groups • Clinics • Clinical Resources • OMIM • GeneReviews • GeneTests • PubMed • Labs • Genome Resources • ELSI • Careers • Professional Education • Genetic Computer Resources • Genetic Education Center • Cytogenetics • Other Medical / Health • Internet Information • Other ...

CGSC: The Coli Genetic Stock Collection at the E.coli Genetic Resource Center, MCD Biology Department, Yale University CGSC: To retrieve information on strains, mutations, genes, and gene products, please use this webserver access to the CGSC Database: CGSC DB-WebServer: Strains, Mutations, Genes and Gene Products The CGSC Database of E.coli genetic information includes genotypes and reference information for the strains in the CGSC collection, gene names, properties, and linkage map, gene ...

Metabolic Disorders Bernardo Haddock Lobo Goulart & Samanta Teixeira Basto Medstudents' Homepage Ehler Danlos Syndrome Definition Ehler Danlos syndrome is one of the inheritable connective tissues disorders along with: Marfan syndrome, pseudoxantoma elasticum, osteogenese imperfecta, chondrodysplasias, epidermolysis bullosa and Alport syndrome. It comprises a group of ten different subtypes. The main clinical manifestations are skin fragility, abnormal scar formation, exces ...

Funded by the National Institutes of Health 06/10/06 344 GeneReviews 1,120Clinics 602Laboratories testing for 1,269Diseases 973 Clinical 296 Research only More usage statistics (For Laboratory/Clinic Contacts, User Groups) Welcome to the GeneTests Web site, a publicly funded medical genetics information resource developed for physicians, other healthcare providers, and researchers, available at no cost to all interested persons. Us ...

Funded by the National Institutes of Health 06/10/06 344 GeneReviews 1,120Clinics 602Laboratories testing for 1,269Diseases 973 Clinical 296 Research only More usage statistics (For Laboratory/Clinic Contacts, User Groups) Welcome to the GeneTests Web site, a publicly funded medical genetics information resource developed for physicians, other healthcare providers, and researchers, available at no cost to all interested persons. Us ...

International organizations on Autosomal Recessive Inclusion Body Myopathy Autosomal Recessive Inclusion Body Myopathies are also known as IBM2, r-HIBM, IBM type AR1a, Quadriceps Sparing h-IBM, Nonaka's Myopathy, or DMRV (Distal Myopathy with Rimmed Vacuoles). For more information about this disorder you may visit the OMIM database Welcome to www.hibm.org Please visit A.R.M website by clicking on the above logo on the map Web Services Provided by HIBM Research Group ©2002-2006 Hosted by Colocation America

ican (International Children's Anophthalmia Network) is a parent support group for families with a child with anophthalmia or microphthalmia. The original objectives of the group are to: Support parents and children Connect parents Share information Provide education Gather medical/legal/governmental information Support and encourage research about microphthalmia and anophthalmia Support scholarships and grants Bulletin Board-the latest information about ican. Issues of , ican's family newsletter, are now available. ican Brochure To contact ican please call 1-800-580-ican ican Homepage Movements On-Line Homepage To ican Comments

HALIFAX, NOVA SCOTIA | CANADA B3H 4R2 | +1 (902) 494-2211 PEOPLE SUBJECT Search Text: IS Web Server Retired The web server on is.dal.ca has been retired. All web sites formerly accessible here should have been moved to new locations. If you are seeing this page instead of the site you expected, the following things may help you to find its new location. If you are using a URL of the form http://is.dal.ca/~user or http://www.dal.ca/~user, try http://myweb.dal.ca/user. Use the search box above to find the new location of site according to some characteristic such as its subject area. Send email to ucis-netsys@dal.ca with a subject such as "Trying to find web site".Copyright 2003-2005 Dalhousie University. All rights reserved. Disclaimer Last Updated: Oct 5, 2005

Home | Medical Dictionary | Contact Us About Us Patients and Visitors Health Conditions Healthcare Professionals Programs and Services Programs and Services Medical Genetics Institute Contact Us Graduate Medical Education In the News Our Expert Team Treatments/Programs Applying the Latest in Medical Genetics to Patient Care and Research Cedars-Sinai has become one of the leading medical centers in the world in applying the di ...

• Database Subscriptions Many libraries, schools, universities, and hospitals subscribe to NORD's Rare Disease Database for unlimited access to reports on more than 1,150 diseases. • Index of Rare Diseases This is the list of diseases currently covered in the Rare Disease Database. • Rare Disease Database Search this database for reports on more than 1,150 diseases. View sample report • Index of Organizations This is the list of organizations in NORD's Organizational Databas ...

NTD Laboratories is a specialty laboratory that focuses on prenatal screening for birth defects. We are proud to have pioneered first trimester screening for Down Syndrome and Trisomy 18 utilizing our free Beta assay in 1995. We provide our services to universities, medical centers, hospitals, other laboratories, and obstetricians throughout the United States and internationally. We also support an extensive research division and our findings are published in many peer-reviewed medical journals. Upcoming NT Training Courses IRAsm The new Instant Risk Assessment Program Click here for the "Finger-Stick" Instructional Video THE FASTER STUDY HAS ARRIVED Click here for more information.

Section Home Books, Brochures & Materials Become a Member of SAA Featured article on Ankylosing Spondylitis SAA Update: Learn What's New! STAND TALL Silicone Bracelets Support Our Mission To Cure Ankylosing Spondylitis Site Map SAA Members can download this entire issue by clicking here From a Humble Beginning: Ankylosing Spondylitis Genetic Research Paves the Way As SAA's exe ...

Return to Archive Syndromes Which Often Result in Combined Vision and Hearing Loss by Kate Moss, Family Training Specialist, TSBVI Outreach Usher Syndrome is one disorder that comes to mind readily for professionals in both the field of vision and hearing when they think of syndromes which result in dual sensory impairment or deaf-blindness. However, there are many syndromes that have both vision and hearing impairment as part of the conditions that define the syndrome. It is important to ...

Welcome to the World Arnold Chiari Malformation Association Committed to the most accurate and current understanding of Chiari Malformations and treatments. Our Mission Statement Staffed by volunteers, the World Arnold Chiari Malformation Association is committed to providing support, current information, and understanding to those affected by the Arnold Chiari malformation and syringomyelia. It is also our goal to raise the awareness of, and educate the medical community as ...

Home Mito Info About UMDF Chapters & Groups Resources Library Fundraising Symposium Research "To promote research and education for the diagnosis, treatment and cure of mitochondrial disorders and to provide support to affected individuals and families."Join Make a Donation Merchandise Member Log-In Mito Doc Contact Us Welcome to UMDF! Purchase UMDF apparel and gift items here. Since 1996, the United Mitochondrial Disease Foundation has funded just under $3,000,000 i ...

Welcome to UPSIDE! - an informal society of individuals, parents, and friends involved with the world of Down Syndrome. Quick Jump Menu Child of the Month | All our Kids | Ramblings Newsletters | Upcoming Events | Links to More Information Please sign our GuestBook UPSIDE! Child of the Month Kelsay Kelsay is a fun 3-year old who dances and sings; she loves dogs and horses, even riding our pony (with a little help). Newsletters Kitsap County's UPSIDE! Society Newsle ...

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Usher Syndrome Who to Contact Where to Go to Chat with Others Learn More About It Web Sites Who to Contact Usher Family Support 4918 42nd Avenue, S Minneapolis, MN 55417 (612) 724-6982 kadbmn@aol.com Where to Go to Chat with Others Usher-Friends A Friendly Chat Group for People with Usher Syndrome The Deaf-Blind List Learn More About It Usher syndrome From the National Institute on Deafness and Other Communication Disorders The Unique ...

The Genesis Fund a new beginning in the TREATMENT and PREVENTION of birth defects about usdonation centerspecial eventsnewsletterour sponsorscontact us National Birth Defects CenterThe Pregnancy Exposure InfoLineTherapy and the Performing Arts Click Below For Latest News Craig Stadler Smith & Wollensky Dinner - June 7th, 2006 - 2006 Marks the 25th Anniversary of The John Havlicek Fishing Tournament - Ken Hodge Joins The Genesis Fund as their inaugural Executi ...

Who helps families cope with genetic disorders? Genetic counselors are health professionals who work as members of a health care team providing information and support to families who have members with birth defects or genetic disorders, to individuals who themselves are affected with a genetic condition and to families who may be at risk for a variety of inherited problems. Genetic counselors identify families at risk, obtain the family medical history, obtain and interpret medical records and ...