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         Fabrys Disease:     more books (19)
  1. Fabry Disease
  2. Joe Learns About Fabry Disease by Dawn Laney, 2009-09-06
  3. Fabry Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-16
  4. The Official Parent's Sourcebook on Fabry's Disease: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-09
  5. Fabry's disease database will facilitate diagnosis.(Clinical Rounds): An article from: Family Practice News by Nancy Walsh, 2004-10-15
  6. First-degree atrioventricular block and restrictive physiology as cardiac manifestations of Fabry's disease. (Case Report).: An article from: Southern Medical Journal by Arnon Blum, Haim Ashkenazi, et all 2003-02-01
  7. Fabry disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Holly, MS, CGC Ishmael, 2005
  8. Enzyme Replacement Resolves Fabry Disease.(Brief Article): An article from: Family Practice News by Mitchel L. Zoler, 2001-03-01
  9. Fabry disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Holly, MS, CGC Ishmael, Rosalyn, MD Carson-Dewitt, 2005
  10. Dainippon Sumitomo Pharma Announces Launch of "Replagal(R) 3.5 mg" for Anderson-Fabry Disease.: An article from: JCN Newswires by Gale Reference Team, 2007-02-15
  11. Genzyme receives broad patent covering gene therapy for Fabry disease.(Brief Article)(Statistical Data Included): An article from: BIOTECH Patent News
  12. European database providing information on fabry's disease.(Clinical Rounds): An article from: Skin & Allergy News by Nancy Walsh, 2005-01-01
  13. The Official Parent's Sourcebook on Fabry's Disease: A Revised and Updated Direc by Icon Health Publications,
  14. Six diagnostic possibilities for painful, red feet. (Different Treatment Options).: An article from: Pediatric News by Betsy Bates, 2003-02-01

1. Fabry Disease Causes, Symptoms, Diagnosis, And Treatment On
Read about Fabry disease, a genetic condition with symptoms such as decreased sweating, fever, small, raised reddishpurple blemishes, bruning sensations in the hands, and
http://www.medicinenet.com/fabrys_disease/article.htm

2. Fabrys Disease
For Patients. Securely connects you to portions of your medical record My Chart; Online second opinions from top specialists My Consult; Schedule and pay your medical bills at your
http://my.clevelandclinic.org/disorders/Fabrys_Disease/hic_Fabrys_Disease.aspx

3. Fabry Disease Symptoms, Causes, Treatment - Is There Any Treatment
Read about Fabry disease, a genetic condition with symptoms such as decreased sweating, fever, small, raised reddishpurple blemishes, bruning sensations in the hands, and
http://www.medicinenet.com/fabrys_disease/page2.htm

4. Fabry's Disease Symptoms, Diagnosis, Treatments And Causes
Replagal Enzyme Replacement Therapy for Children With Fabry Disease This study is no longer recruiting patients (Current 23 Nov 2006) - Replagal (Galactosidase Alfa)
http://www.wrongdiagnosis.com/f/fabrys_disease/intro.htm

5. Fabry
alternative titles fabry disease. angiokeratoma, diffuse andersonfabry disease hereditary dystopic lipidosis alpha-galactosidase a deficiency gla deficiency
http://www.lymphedemapeople.com/thesite/fabrys_disease.htm

6. Fabry Disease Information Page National Institute Of Neurological
Fabry's Disease information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS).
http://www.ninds.nih.gov/disorders/fabrys/fabrys.htm

7. Fabry Community
Provides information and support for people with Fabry disease, their caregivers and families, and their health care providers.
http://www.fabrycommunity.com/

8. Fabry Disease - Wikipedia, The Free Encyclopedia
Fabry disease (also known as Fabry's disease, AndersonFabry disease, angiokeratoma corporis diffusum and alpha-galactosidase A deficiency) is a rare X-linked recessive
http://en.wikipedia.org/wiki/Fabry's_disease

9. Fabry Disease
Deficiency of the lysosomal enzyme αgalactosidase A leads to progressive accumulation of glycosphingolipids, predominantly globotriaosylceramide (GL-3), in many body tissues
http://www.lysosomallearning.com/healthcare/about/lsd_hc_abt_fabry.asp

10. Fabry Disease Facts For Patients And Their Families
The Mount Sinai School of Medicine provides information about symptoms, diagnosis, management, and enzyme replacement therapy. Register for the International Center for Fabry Disease mailing list.
http://www.mssm.edu/genetics/fabry/

11. Fabry Disease - Definition Of Fabry Disease In The Medical
disease /dis ease/ (dĭzēz ) any deviation from or interruption of the normal structure or function of any body part, organ, or system that is manifested by a characteristic set
http://medical-dictionary.thefreedictionary.com/Fabry disease

12. Fabrazyme - A Treatment For Fabry Disease
This web site is intended for use by European physicians only. You must log-in to use this site.
http://www.fabrazyme.com/

13. Fabry Disease Background - Contact A Family Directory
Contact a Family is a UK charity for families with disabled children. We offer information on specific conditions and rare disorders.
http://www.cafamily.org.uk/Direct/f09.html

14. Fabry Disease Registry
Information about an ongoing observational database that tracks the natural history and clinical outcomes of patients with this disease.
http://www.fabryregistry.com

15. Your Health - Fabry Disease
Ask the Librarian! Our librarians will help you research a specific health topic Conditions InDepth A reference guide to more than 100 health and medical conditions
http://www.aurorahealthcare.org/yourhealth/healthgate/getcontent.asp?URLhealthga

16. EMedicine Fabry Disease
University of Texas MD describes symptoms, treatment, and prognosis for patients suffering with this rare but severe lysosomal disorder.
http://www.emedicine.com/neuro/topic579.htm

17. Fabry Support And Information Group
Fabry Support Information Group What is Fabry Disease
http://www.fabry.org/

18. Fabry Disease
Fabry disease (also known as Fabry's disease, AndersonFabry disease, angiokeratoma corporis diffusum and alpha-galactosidase A deficiency) is a rare X-linked recessive (inherited
http://health.kosmix.com/topic/Fabry_disease

19. Fabry Disease EMedicine Pediatrics Genetics And Metabolic Disease
Overview Fabry disease is an Xlinked lysosomal storage disease that is caused by deficient activity of lysosomal enzyme α-galactosidase A (α-Gal A). Most
http://emedicine.medscape.com/article/951451-overview

20. Fabry Disease Definition From Answers.com
n. A sexlinked disorder of glycolipid metabolism characterized by a variety of progressive symptoms including fevers, hypertension , and purple skin lesions , with death
http://www.answers.com/topic/fabry-s-disease

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