41. Rare Disorders, Tyrosinemia More tyrosinemia Categories » Submit Your Site to the tyrosinemia category. Sponsored tyrosinemia Sites. Submit Your Site to the tyrosinemia category. http://www.iseekhealth.com/tyrosinemia-2211.php

Home About Us Contact Submit Your Site Search : Home Health Conditions and Diseases Rare Disorders ... Tyrosinemia More Tyrosinemia Categories: Submit Your Site to the Tyrosinemia category Sponsored Tyrosinemia Sites Promising Cancer Treatment The health benefits from cancer studies by doctors at the National Cancer Institute and John Hopkins School of Medicine are combined in a treatment called Controlled Amino Acid Therapy. CAAT has been proven to work with chemotherapy or alone. Promising Disease Treatment The health benefits from cancer studies by doctors at the National Cancer Institute and John Hopkins School of Medicine are combined in a treatment called Controlled Amino Acid Therapy. CAAT has been proven to work with chemotherapy or alone. WellnessBooks.com - Books For Getting Well Comprehensive resource to books on diseases, disorders and chronic illness. Includes community boards and chat and online ordering. MagnetTherapy.com Discover the healing power of magnets. Jewelry, mattresses, body wraps, insoles for shoes and much more. This ancient form of magnetic pain relief has proven to be effective for many users including many of todays professional atheletes. MagnetTherapy.com National Library of Medicine - The synonyms of Tyrosinemia 11, a summary and major features.

42. Health Professionals Guide To Newborn Screening: Tyrosinemia tyrosinemia. Treatment The treatment for tyrosinemia is the dietary restriction of phenylalanine, methionine, tyrosine and administration of the drug NTBC. http://www.slh.wisc.edu/newborn/guide/tyrosinemia.php

WSLH Newborn Guide Tyrosinemia ... Advisory Committee Health Professionals Guide to Newborn Screening: Newborn Screening Disorders Tyrosinemia Autosomal recessive amino acid disorder caused by a deficiency in the fumarylacetoacetate hydrolase enzyme activity causing the build up of the amino acid tyrosine in the blood. Early detection and treatment is successful in preventing poor growth, liver damage, swelling of the legs, and inappropriate bleeding. Prevalence (WI): Analyte Measured: Tyrosine Reporting Ranges: Feeding Effect: None Timing Effect: 24 hours of age: Results are valid Confirmation: Immediate consult with a metabolic specialist at one of the states two metabolic treatment centers. Treatment: The treatment for tyrosinemia is the dietary restriction of phenylalanine, methionine, tyrosine and administration of the drug NTBC. Although this treatment regime is successful in delaying the clinical symptoms of tyrosinemia, the only effective long-term treatment is liver transplantation. Information on treatment centers is also available on this site. For information about other screened disorders, click on the next page button, or follow one of these links:

43. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Rare_Disorders/Tyr News about tyrosinemia More news about tyrosinemia . Books about tyrosinemia More books about tyrosinemia . Links about tyrosinemia http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Rare_Disord

Match: sort by: relevance date Free Services Subscribe by email RSS newsfeeds PDA-friendly format loc="/images/" A A A Find Jobs In: Healthcare Engineering Accounting College Contract / Freelance Customer Service Diversity Engineering Executive Healthcare Hospitality Human Resources Information Tech International Manufacturing Nonprofit Retail All Jobs by Job Type All Jobs by Industry Relocating? Visit: Moving Resources Moving Companies Mortgage Information Mortgage Calculator Real Estate Lookup Front Page Today's Digest Week in Review Email Updates ... Rare Disorders Tyrosinemia (5 links) See Also: Health: Conditions and Diseases: Genetic Disorders Health: Conditions and Diseases: Nutrition and Metabolism Disorders News about Tyrosinemia [ More news about Tyrosinemia Books about Tyrosinemia [ More books about Tyrosinemia Links about Tyrosinemia Pediatric Database - Offers a definition of Tyrosinemia-1, the epidemiology, pathogenesis, clinical features, investigations and management. Tyrosinemia-11 - An in depth look at this disease from Pediatric Database including investigations and management. National Library of Medicine - The synonyms of Tyrosinemia 11, a summary and major features.

44. TYROSINEMIA - Meaning And Definition Of The Word tyrosinemia Encyclopædia Britannica tyrosinemia Encyclopædia Britannica Article. acid oxidase. This enzyme is not active in individuals with tyrosinemia. Clinical . http://www.hyperdictionary.com/dictionary/tyrosinemia

English Dictionary Computer Dictionary Thesaurus Dream Dictionary ... Medical Dictionary Search Dictionary: TYROSINEMIA: Dictionary Entry and Meaning WordNet Dictionary Definition: [n] autosomal recessive defect in ... retardation See Also: autosomal recessive defect autosomal recessive disease HOME ABOUT HYPERDICTIONARY

45. Tyrosinemia, Hereditary tyrosinemia, Hereditary. jaundice). tyrosinemia type I may progress to more serious complications such as severe liver disease. tyrosinemia http://www.meritcare.com/hwdb/showTopic.asp?pd_hwid=nord446

46. Conditions And Diseases - Tyrosinemia Top Links tyrosinemia Web Site Links. NORD tyrosinemia, Hereditary - Offers the synonyms, a general discussion and further resources. Pediatric http://www.disease-resources.com/Top_Health_Conditions_and_Diseases_Rare_Disorde

Sub Categories Related Healthcare Subjects Disabilities Environmental Health Fitness Health Insurance ... Men's Health Tyrosinemia Web Site Links NORD - Tyrosinemia, Hereditary Offers the synonyms, a general discussion and further resources. Pediatric Database Offers a definition of Tyrosinemia-1, the epidemiology, pathogenesis, clinical features, investigations and management. Tyrosinemia-11 An in depth look at this disease from Pediatric Database including investigations and management. National Library of Medicine The synonyms of Tyrosinemia 11, a summary and major features. Tyrosinemia For all people interested in connecting with others with this disease. Other Useful Health Web Links National Institutes of Health (NIH) US Government department in charge of medical research. AHRQ: Clinical Information Clinical information on evidence-based practice, clinical guidelines, medical effectiveness, pharmaceutical therapy, new technology, screening and preventive services, outcomes research, and the National Guideline Clearinghouse. The UK Health Technology Assessment Programme Site contains details of program's many projects and publications; an NHS national research and development initiative.

47. Congenital Tyrosinosis,Fumarylacetoacetase Deficiency,Hepatorenal Tyrosinemia,He Congenital tyrosinosis,Fumarylacetoacetase deficiency,Hepatorenal tyrosinemia,Hereditary tyrosinemia type 1,tyrosinemia type 1 acute form,tyrosinemia type 1 http://www.icomm.ca/geneinfo/tyrosin.htm

Congenital tyrosinosis,Fumarylacetoacetase deficiency,Hepatorenal tyrosinemia,Hereditary tyrosinemia type 1,Tyrosinemia type 1 acute form,Tyrosinemia type 1 chronic form,Congenital tyrosinosis,Fumarylacetoacetase deficiency,Hepatorenal tyrosinemia,Hereditary tyrosinemia type 1,Tyrosinemia type 1 acute form,Tyrosinemia type 1 chronic form For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX to Information on the Internet about Genetic Disorders and Birth Defects Genetic Information and Patient Services, Inc. (GAPS) HOME DISORDERS GLOSSARY Tyrosinemia, Hereditary also known as: Tyrosinemia I Tyrosinemia, Hereditary, Hepatorenal Type Tyrosyluria Hereditary tyrosinemia type 1 Fumarylacetoacetase deficiency Congenital tyrosinosis Hepatorenal tyrosinemia Disorder Subdivisions Tyrosinemia type 1, acute form Tyrosinemia type 1, chronic form (as defined by the National Organization for Rare Disorders PRELIMINARY DRAFT This preliminary draft has not been approved by our medical advisors; therefore, its accuracy cannot be guaranteed. Verification of medical accuracy is pending. This is the most current information that NORD has available at this time. Tyrosinemia type I is a rare genetic metabolic disorder characterized by lack of the enzyme fumarylacetoacetate hydrolase (FAH), which is needed to break down the amino acid tyrosine.

48. Information Center - Tyrosinemia (Condition Description) ForMyDiet is designed to make living with and managing a tyrosinemia diet a whole lot easier. Helping tyrosinemia, Go Back. Author http://www.formydiet.com/Information/Doc.aspx?a=65

49. Tyrosinemia ForMyDiet is designed to make living with and managing a tyrosinemia diet a whole lot easier. Helping tyrosinemia Home Page This http://www.formydiet.com/Information/disorder.aspx?a=5

50. Clinical Trial: Study Of NTBC For Tyrosinemia I Study of NTBC for tyrosinemia I. Purpose. OBJECTIVES I. Assess the safety and efficacy of NTBC in children with tyrosinemia I. II. http://www.clinicaltrials.gov/ct/gui/show/NCT00004443?order=6

51. Rare Disorders: Tyrosinemia Rare Disorders tyrosinemia. National Library of Medicine. The synonyms of tyrosinemia 11, a summary and major features. NORD tyrosinemia, Hereditary. http://www.puredirectory.com/Health/Conditions-and-Diseases/Rare-Disorders/Tyros

Rare Disorders: Tyrosinemia Home Health Conditions and Diseases Rare Disorders : Tyrosinemia google_ad_client = 'pub-3272565765518472';google_ad_width = 336;google_ad_height = 280;google_ad_format = '336x280_as';google_color_border = 'FFFFFF';google_color_bg = 'FFFFFF';google_ad_channel ='7485447737';google_alternate_color = 'FFFFFF';google_color_link = '0000FF';google_color_url = '008000';google_color_text = '000000'; Standard Listings National Library of Medicine The synonyms of Tyrosinemia 11, a summary and major features. NORD: Tyrosinemia, Hereditary Offers the synonyms, a general discussion and further resources. Pediatric Database Offers a definition of Tyrosinemia-1, the epidemiology, pathogenesis, clinical features, investigations and management. Tyrosinemia For all people interested in connecting with others with this disease. Tyrosinemia-11 An in depth look at this disease from Pediatric Database including investigations and management. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor PureDirectory.com uses a modified version of the Open Directory.

52. Tyrosinemia Liver. tyrosinemia. tyrosinemia is a genetic defect in metabolism, associated with severe liver disease. tyrosinemia. What is tyrosinemia? http://tjsamson.client.web-health.com/web-health/topics/GeneralHealth/generalhea

Liver Tyrosinemia Tyrosinemia is a genetic defect in metabolism, associated with severe liver disease. Tyrosinemia What is tyrosinemia? Tyrosinemia is a genetic disease, associated with the development of severe liver damage in affected infants. What causes tyrosinemia? Tyrosinemia occurs because of abnormalities (mutations) in an individual's DNA. DNA is the 'blueprint' for life, the set of instructions carried in the nucleus of every cell of the body (except red blood cells). A discrete unit of instruction contained in the DNA is called a gene. Most genes encode (carry information necessary for the synthesis of) proteins. Proteins, in turn, perform essential life functions. Each gene is present in 2 copies: one copy (or allele) inherited from the mother and one copy inherited from the father. Tyrosinemia occurs if a child has mutations in both copies (alleles) of a particular gene, the gene for fumarylacetoacetate hydrolase (FAH). A child can inherit 2 defective copies of the FAH gene if both parents are tyrosinemia carriers. (Each parent has one normal allele of the FAH gene and one defective allele.) Carriers do not have tyrosinemia because the normal copy of the FAH gene produces a normal FAH protein, compensating for the defective copy of the gene. In genetic terms, the normal allele of the gene is dominant and tyrosinemia is recessive.

53. Tyrosinemia tyrosinemia. tyrosinemia. What is tyrosinemia? tyrosinemia is a genetic disease, associated with the development of severe liver damage in affected infants. http://tjsamson.client.web-health.com/web-health/topics/GeneralHealth/generalhea

Liver Tyrosinemia Tyrosinemia is a genetic defect in metabolism, associated with liver disease Tyrosinemia What is tyrosinemia? Tyrosinemia is a genetic disease, associated with the development of severe liver damage in affected infants. What causes tyrosinemia? Tyrosinemia occurs because of abnormalities (mutations) in an individual's DNA. DNA is the "blueprint" for life, the set of instructions carried in the nucleus of every cell of the body (except red blood cells). A discrete unit of instruction contained in the DNA is called a gene. Most genes encode (carry information necessary for the synthesis of) proteins. Proteins, in turn, perform essential life functions. Each gene is present in two copies: one copy (or allele) inherited from the mother and one copy inherited from the father. Tyrosinemia occurs if a child has mutations in both copies (alleles) of a particular gene, the gene for fumarylacetoacetate hydrolase (FAH). A child can inherit two defective copies of the FAH gene if both parents are tyrosinemia carriers. (Each parent has one normal allele of the FAH gene and one defective allele.) Carriers do not have tyrosinemia because the normal copy of the FAH gene produces a normal FAH protein, compensating for the defective copy of the gene. In genetic terms, the normal allele of the gene is dominant and tyrosinemia is recessive.

54. Health Library - prevention. tyrosinemia, Hereditary. jaundice). tyrosinemia type I may progress to more serious complications such as severe liver disease. http://myhealth.barnesjewish.org/library/healthguide/illnessconditions/topic.asp

55. Health Library - tyrosinemia. Self Help Clearinghouse. Groupe Aide Aux Enfants Tyrosinemiques du Quebec. Model. One group in Quebec. Founded 1989. (Bilingual http://myhealth.barnesjewish.org/library/healthguide/selfhelp/topic.asp?hwid=shc

56. Health, Conditions And Diseases, Rare Disorders: Tyrosinemia NORD tyrosinemia, Hereditary Offers the synonyms, a general discussion and further resources. National Library of Medicine - The http://www.combose.com/Health/Conditions_and_Diseases/Rare_Disorders/Tyrosinemia

Top Health Conditions and Diseases Rare Disorders ... Tyrosinemia Related links of interest: Health:Conditions and Diseases:Genetic Disorders Health:Conditions and Diseases:Nutrition and Metabolism Disorders NORD: Tyrosinemia, Hereditary - Offers the synonyms, a general discussion and further resources. National Library of Medicine - The synonyms of Tyrosinemia 11, a summary and major features. Pediatric Database - Offers a definition of Tyrosinemia-1, the epidemiology, pathogenesis, clinical features, investigations and management. Tyrosinemia-11 - An in depth look at this disease from Pediatric Database including investigations and management. Tyrosinemia - For all people interested in connecting with others with this disease. A rare genetic metabolic disorder characterized by lack of the enzyme fumarylacetoacetate hydrolase (FAH), which is needed to break down the amino acid tyrosine. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor The combose.com directory is based on the Open Directory and has been modified and enhanced using our own technology.

57. :: Ez2Find :: Tyrosinemia Guide tyrosinemia, Guides, tyrosinemia. ez2Find Home Directory Health Conditions and Diseases Rare Disorders tyrosinemia (5) Related Categories http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas

Guide : Tyrosinemia Global Metasearch Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode All Words Any Word Phrase Results Timeout Depth Adult Filter Add to Favorites Other Search Web News Newsgroups Images Guides Tyrosinemia ez2Find Home Directory Health Conditions and Diseases ... Rare Disorders : Tyrosinemia Related Categories Health: Conditions and Diseases: Genetic Disorders Health: Conditions and Diseases: Nutrition and Metabolism Disorders Web Sites National Library of Medicine [Site Info] [Translate] [Open New Window] The synonyms of Tyrosinemia 11, a summary and major features. NORD: Tyrosinemia, Hereditary [Site Info] [Translate] [Open New Window] Offers the synonyms, a general discussion and further resources. URL: http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Tyrosinemia%2C%20Hereditary

58. Tyrosinemia: Liver Transplants Save A Child, Cincinnati Children's Hospital Medi Patient Stories. tyrosinemia Kyle Wimberg Thrives After Two Liver Transplants. At age 1, Kyle was diagnosed with a rare condition called tyrosinemia. http://www.cincinnatichildrens.org/about/patient/tyrosinemia-kyle-wimberg.htm

Home Contact Us Site Map Go to Advanced Search ... Stay Informed / Sign Up for Our eNewsletter Patient Stories Tyrosinemia: Kyle Wimberg Thrives After Two Liver Transplants "Things Could Be Worse" As printed in the February 2004 edition of Leaps and Bounds At age 1, Kyle was diagnosed with a rare condition called tyrosinemia . With his third birthday just around the corner, he has already endured two liver transplants , two bouts of viral mengitis, serum sickness, a form of cancer and two broken bones in his left leg. After all this little boy has been through, he's surprisingly happy and content. His contagious smile brightens your day, and his adorable wink makes you melt. Kyle Wimberg Thrives After Two Liver Transplants With his third birthday just around the corner, Kyle Wimberg already has endured two liver transplants, two bouts of viral meningitis, serum sickness, a form of cancer and two broken bones in his left leg. Yet his mother says, "Things could be worse." What she has learned is to appreciate what she and her family have. "When he was in so much pain, I prayed, 'Let him live.' But I also said to God, 'I'll be miserable for the rest of my life, but take him now if it will stop his suffering.' Today, I say 'thank you' for every day without pain," says Janet Wimberg. Like most healthy babies, Kyle was chubby, but his arms and legs were skinny. At his one-year checkup, scheduled on his first birthday, Kyle's pediatrician detected an enlarged

59. Tyrosinemia: Liver Transplants Save A Child, Cincinnati Children's Hospital Medi tyrosinemia Kyle Wimberg Thrives After Two Liver Transplants. Things Could Be Worse . At age 1, Kyle was diagnosed with a rare condition called tyrosinemia. http://www.cincinnatichildrens.org/about/patient/tyrosinemia-kyle-wimberg.htm?vi

60. Gimenei >> Health >> Conditions_and_Diseases >> Rare_Disorders >> Tyrosinemia Gimenei.com, Search for Scope All Words, Results per page 10. Request Timeout 2, http://www.gimenei.com/directory/top/Health/Conditions_and_Diseases/Rare_Disorde

Search for: Scope: All Words Any Word Phrase Results per page: Request Timeout: Search Depth: Gimenei Health Conditions and Diseases Rare Disorders Tyrosinemia

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