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Tyrosinemia: more detail | |||||
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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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