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         Tyrosinemia:     more detail
  1. Tyrosinemia
  2. Palmoplantar Keratodermas: Papillon-lefèvre Syndrome, Palmoplantar Keratoderma, Meleda Disease, Tyrosinemia Type Ii, Howel-evans Syndrome
  3. Tyrosinemia - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-19
  4. Tyrosinemia: Webster's Timeline History, 1967 - 2007 by Icon Group International, 2010-06-11
  5. Dietary management of inherited metabolic disease: Phenylketonuria, galactosemia, tyrosinemia, homocystinuria, maple syrup urine disease by Phyllis B Acosta, 1976

1. Tyrosinemia - Wikipedia, The Free Encyclopedia
External links. GeneReview/NCBI/NIH/UW entry on tyrosinemia Type 1; University of Washington
http://en.wikipedia.org/wiki/Tyrosinemia

2. Tyrosinemia - What Does TYR Stand For? Acronyms And Abbreviations
Acronym Definition; TYR Tyrosine (Amino Acid) TYR Tyrosinase TYR tyrosinemia (types I, II and III) TYR The Young Riders (TV show) TYR Tyler, TX, USA Pounds Field
http://acronyms.thefreedictionary.com/tyrosinemia

3. NORD Tyrosinemia, Hereditary
Offers the synonyms, a general discussion and further resources.
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Tyrosinemia,

4. Tyrosinemia - Genetics Home Reference
tyrosinemia is a genetic disorder characterized by elevated blood levels of the amino acid tyrosine, a building block of most proteins. tyrosinemia is caused by the shortage
http://ghr.nlm.nih.gov/condition=tyrosinemia

5. Tyrosinemia Encyclopedia With 57,945 Entries From Biotech
This article needs additional citations for verification. Please help improve this article by adding reliable references. Unsourced material may be challenged and removed.
http://www.bionity.com/lexikon/e/Tyrosinemia/

6. Tyrosinemia EMedicine Pediatrics Genetics And Metabolic Disease
Overview Elevated blood tyrosine levels are associated with several clinical entities. The term tyrosinemia was first given to a clinical entity based on observations (eg
http://emedicine.medscape.com/article/949816-overview

7. (B) A Selective Advantage For Tyrosinemia In This Part Of Quebec.
Question 6 for The Death of Baby Pierre A Genetic Mystery, by Clyde Freeman Herreid, University at Buffalo. From the Case Study Collection of the National Center for Case Study
http://ublib.buffalo.edu/libraries/projects/cases/pier6.htm

8. Tyrosinemia Definition From Answers.com
An inborn metabolic disorder in which there is a deficiency of the enzyme p hydroxyphenylpyruvic acid oxidase with abnormally high blood levels of tyrosine and sometimes
http://www.answers.com/topic/tyrosinemia

9. Tyrosinemia Type I Definition - Medical Dictionary Definitions Of
Online Medical Dictionary and glossary with medical definitions
http://www.medterms.com/script/main/art.asp?articlekey=30897

10. Tyrosinemia Type I
Article describes tyrosinemia type I, its symptoms, diagnosis, and treatment.
http://rarediseases.about.com/od/rarediseasest/a/tyrosinemia.htm

11. TYROSINEMIA, TYPE II
Miscellaneous Information Diagnosis is confirmed by elevated tyrosine or its metabolites in urine and plasma. Assay of tyrosine aminotransferase is possible through a liver
http://www.oregon.gov/DHS/ph/nbs/docs/tyro-Type2.pdf

12. Tyrosinemia Symptoms, Diagnosis, Treatments And Causes
tyrosinemia information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
http://www.wrongdiagnosis.com/t/tyrosinemia/intro.htm

13. Biochemical Genetics Clinic - University Of Washington, Seattle
The University of Washington Biochemical Genetics Clinic web site provides resources to families of children with tyrosinemia and professionals who work with those children.
http://depts.washington.edu/tyros/

14. NEWBORN SCREENING
Disorder name tyrosinemia, type 1 Acronym FAH deficiency. What is tyrosinemia 1? What causes tyrosinemia 1? If tyrosinemia 1 is not treated, what problems occur?
http://www.newbornscreening.info/Parents/aminoaciddisorders/Tyrosinemia.html

15. Tyrosinemia A Rare Metabolic Disorder - Associated Content
Learn about the three forms of this rare metabolic disorder and how it prevents the body from being able to effectively break down the amino acid tyrosine. What can be done to
http://www.associatedcontent.com/article/2006938/tyrosinemia_a_rare_metabolic_di

16. Newborn Screening Program - Tyrosinemia
Followup After Confirmation of Diagnosis. These guidelines should be followed after a diagnosis of tyrosinemia has been confirmed Parents should understand that treatment is
http://www.idph.state.il.us/HealthWellness/fs/tyrosinemia.htm

17. Type I Tyrosinemia - Kosmix Reference, Videos, Images, News
Type I tyrosinemia is the most severe form of this disorder and is caused by a shortage of the enzyme fumarylacetoacetate hydrolase (), encoded by the gene FAH found on
http://health.kosmix.com/topic/Type_I_tyrosinemia

18. Symptoms Of Tyrosinemia - WrongDiagnosis.com
Symptoms of tyrosinemia including 26 medical symptoms and signs of tyrosinemia, alternative diagnoses, misdiagnosis, and correct diagnosis for tyrosinemia signs or tyrosinemia
http://www.wrongdiagnosis.com/t/tyrosinemia/symptoms.htm

19. SHS North America Tyrosinemia
XPhe, XTyr Analog Infants birth to 1 year Phenylalanine, Tyrosine-free......tyrosinemia Type I and Type II Products Recommended Age Groups
http://www.shsna.com/ca_english/pages/tyrosinemia.htm

20. Tyrosinemia Type 1 GeneReviews NCBI Bookshelf
Nitisinone treatment should begin as soon as the diagnosis of tyrosinemia type I is confirmed. Because nitisinone increases the blood concentration of tyrosine, dietary management
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tyrosinemia

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