41. Health Library: All Topics: T: Tyrosinemia - Healthfinder® healthfinder® home page, healthfinder® — your guide to reliable healthinformation. health library. just for you. health care. organizations. http://www.healthfinder.gov/Scripts/SearchContext.asp?topic=881

42. Health Library: All Topics: T: Tyrosinemia - Healthfinder® home health library all topics T tyrosinemia. categories and relatedtopics. find a specific kind of information on tyrosinemia http://www.healthfinder.gov/Scripts/SearchContext.asp?topic=881&refine=1

43. Tyrosinemia tyrosinemia. tyrosinemia Reaching out and connecting tyrosinemia familiesthroughout the world .. Purpose tyrosinemia. tyrosinemia-11 - http://www.health-nexus.org/tyrosinemia.htm

Health-Nexus.Com Health-Nexus.Net The #1 Health information site Home ... Up Search Health-Nexus for: Match ALL words Match ANY word Email this page to a friend ! Post a question or comment on our Message Board Home Page Health Specialties Health News ... Alternative Health Options Substance Abuse Animal Health Search: Books Magazines Video Keywords: Find it Here Tyrosinemia tyrosinemia Reaching out and connecting Tyrosinemia families throughout the world..... Purpose: To allow a forum for families to share experiences and tips for management of tyrosinemia. tyrosinemia-11 ... liver and renal functions are not affected. in Tyrosinemia-I, the damage is not done by the build-up of tyrosine but by ... Tyrosinemia Management Tyrosinemia: Background C. Ronald ... of Medicine Seattle, WA Tyrosinemia-I is a rare but devastating ... six months of age. If tyrosinemia-I is unrecognized and ... before 10 years of age. Tyrosinemia is inherited as an autosomal ... CLA - Tyrosinemia cd3. This site is hosted by Netfirms Web Hosting. Alagille's Syndrome. Neonatal Hepatitis. Biliary Atresia. Nutrition and the Liver. Galactosemia. Type I Glycogen Storage Disease. Gilbert's...

44. TYROSINEMIA tyrosinemia, Welcome! For more information on tyrosinemia check outthe tyrosinemia Community at .. http//communities.msn http://www.geocities.com/tyriii/tyrosinemia_page.html

TYROSINEMIA Welcome! For more information on tyrosinemia check out the Tyrosinemia Community at ....... http://communities.msn.com/tyrosinemia/home.htm thanks!! My Favorite Links: Tyrosinemia chat page http://communities.msn.com/tyrosinemiacommunitychat Tyrosinemia community http://communities.msn.com/tyrosinemia/home.htm My Info: Name: tyriii Email: tyriii@yahoo.com

45. TIROSINEMIA Translate this page Bibliografía. Bergeron P, Laberge C, Grenier A. Hereditary tyrosinemia in the provinceof Quebec prevalence at birth and geographic distribution. Clin Genet. http://www.geocities.com/rodriguezlanza/marl2.htm

TIROSINEMIA Dr. Manuel A. Rodriguez Lanza Residente del postgrado de Pediatría, Hospital Militar "Dr. Carlos Arvelo", Departamento de Pediatría e-mail: marl1@hotmail.com Palabras claves: tirosinemia, errores innatos del metabolismo. Key Words: tyrosinemia, inborn errors of metabolism La tirosinemia es un error innato del metabolismo que muestra niveles elevados de tirosina. Existen tres tipos: tirosinemia neonatal tirosinemia tipo I (tirosinosis) tirosinemia tipo II (sindrome de Richner-Hanhart) Incidencia Tirosinemia tipo I: En USA: en 1991: 1/47000 nacidos vivos. En Canada: en Quebec:1/12500 en Lac-St Jean de Quebec: 1/685 En Suecia: En Noruega: En Bélgica: Tirosinemia tipo II No ha sido bien establecida. Genética Localización cromosómica: Fumarilacetoacetasa hidrolasa (FAH): 15q23-q25 (tirosinemia tipo I) Tirosina aminotransferasa (TAT): 16q22-q24 (tirosinemia tipo II) Herencia: Autosómico recesivo. Varones=Hembras. Variabilidad étnica y racial: Mayormente en raza blanca.

46. Child Development And Rehabilitation Center At OHSU CDRC Home Clinical Programs at CDRC - Metabolic Clinic - Available Materials- tyrosinemia Urea Cycle Disorders. tyrosinemia. Acquiring Samples. http://cdrc.ohsu.edu/home/Clinical_Programs_at_CDRC/Metabolic_Clinic/Available_M

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47. MedWebPlus Web Site ID 8664 A free service to help you find health sciences information quickly and easily. PEDBASEtyrosinemiaI. http//www.icondata.com/health/pedbase/files/TYROSINE.HTM http://www.medwebplus.com/obj/8664

Main About MWP Contribute to MWP Contact Us A service of Flexis, Inc. Welcome to MedWebPlus 2.3! A free service to help you find health sciences information quickly and easily. PEDBASE Tyrosinemia-I http://www.icondata.com/health/pedbase/files/TYROSINE.HTM Uptime grade: A Usage grade: Popularity: N/A Location: North America Canada Prince Edward Island Summerside Subjects: All Diseases Diseases and Conditions Metabolism, Inborn Errors Methylamines ... Privacy statement Powered by y-Base

48. Mouse Models For The Human Disease Of Chronic Hereditary Tyrosinemia Mouse models for the human disease of chronic hereditary tyrosinemia.ORNL researchers found that a nearby gene that is also knocked http://www.eurekalert.org/features/doe/2001-06/drnl-mmf061802.php

Text-Only Privacy Policy Site Map Mouse models for the human disease of chronic hereditary tyrosinemia ORNL researchers found that a nearby gene that is also knocked out by irradiation causes chronic hereditary tyrosinemia in mice, a disease that also afflicts humans. Patients with this disease can develop a wide range of liver and kidney problems, as well as problems affecting the eye, the skin of the feet and hands, and the central nervous system. Using the powerful mutagen ENU to alter a single DNA base pair in this gene, ORNL biologists recently produced two mouse models that more closely mimic the gene mutation that causes chronic hereditary tyrosinemia in humans. Normal mice and people metabolize tyrosine, an amino acid available in food, to make melanin, a type of pigment produced in large amounts by dark-skinned people. But people and mice with the disease lack a normally functioning protein (enzyme) to carry out one step of the tyrosine metabolism process, which involves a series of enzymes. So, unless people with this disease are put on a special tyrosine-free diet, a substance that is not broken down because of the absence of a normally functioning enzyme will build up to toxic levels in the liver and kidneys, a fatal condition in mice. By sequencing the same chromosomal region from both normal and abnormal mice and comparing the sequences, ORNL biologists identified new mouse models that carry mutations in this enzyme in the tyrosine breakdown pathway. "Mice with this disease die of poisoned livers," says ORNL biologist Dabney Johnson. "A by-product of the botched metabolism process is succinyl acetone, which accumulates in the liver and is excreted in urine where it serves as a diagnostic indicator of the disease.

49. 1Up Health > Health Links Directory > Conditions And Diseases: Rare Disorders: T Conditions and Diseases Rare Disorders tyrosinemia . Sites. National Libraryof Medicine The synonyms of tyrosinemia 11, a summary and major features. http://www.1uphealth.com/links/rare-disorders-tyrosinemia.html

Home Contact Us Privacy Caring For Your Well Being Alternative Medicine Clinical Trials Health News Poisons ... Health Topics A-Z Search 1Up Health Health Directory Addictions Alternative Animal ... Weight Loss By Demography Child Health Teen Health Men's Health Women's Health ... Rare Disorders : Tyrosinemia Description See Related Categories Health: Conditions and Diseases: Genetic Disorders Health: Conditions and Diseases: Nutrition and Metabolism Disorders Sites 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. Tyrosinemia Group Information about tyrosinemia, a rare metabolic disorder. Includes lists of links to other support groups, sources for low protein food, recipes, message board. Help build the largest human-edited directory on the web.

50. 1Up Health > Health Links Directory >Conditions And Diseases:Rare Disorders:Tyro 1UpHealth Health Directory Conditions_and_Diseases Rare_Disorderstyrosinemia A rare genetic metabolic disorder characterized http://www.1uphealth.com/links/desc-560.html

Home Contact Us Privacy Caring For Your Well Being Alternative Medicine Clinical Trials Health News Poisons ... Health Topics A-Z Search 1Up Health Health Directory Addictions Alternative Animal ... Weight Loss By Demography Child Health Teen Health Men's Health Women's Health ... Tyrosinemia 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 Parts of the directory made available on 1UpHealth have been modified. External Web site links provided on this site are meant for convenience and for informational purposes only; they do not constitute an endorsement. Search: The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only they do not constitute endorsements of those other sites. Home Contact Us Privacy Links Directory

51. FDA Approves Orfadin (Nitisinone) For Hereditary Tyrosinemia Type 1 Title FDA Approves Orfadin (Nitisinone) For Hereditary tyrosinemia Type 1 URLhttp//www.pslgroup.com/dg/21301E.htm Doctor's Guide January 23, 2002. http://www.docguide.com/dg.nsf/PrintPrint/3808C5836588C3C085256B4A005135F2

To print: Select File and then Print from your browser's menu Title: FDA Approves Orfadin (Nitisinone) For Hereditary Tyrosinemia Type 1 URL: http://www.pslgroup.com/dg/21301E.htm Doctor's Guide January 23, 2002 BETHESDA, MD January 23, 2002 The U.S. Food and Drug Administration (FDA) approved a new drug yesterday, nitisinone capsules, to treat hereditary tyrosinemia type 1 (HT-1), a rare pediatric disease causing progressive liver failure and liver cancer in young children. Fewer than 100 children in the United States are affected by HT-1. Nitisinone, which will be marketed under the name Orfadin, is an orphan drug. Orphan products are developed to treat rare diseases, or conditions that affect fewer than 200,000 people in the U.S. The Orphan Drug Act provides a seven-year period of exclusive marketing to the first sponsor who obtains marketing approval for a designated orphan drug. Because of liver failure or liver cancer, children with hereditary tyrosinemia type I rarely survive into their twenties without a liver transplant. However, for children treated early enough with nitisinone, liver failure and liver cancer occur at much-reduced rates. Nitisinone was studied in more than 180 patients with a median age of nine months when therapy started. When the drug was combined with a restricted diet, the four-year survival rate of children under two months of age at the time of diagnosis was 88 percent. Historical data for children treated with dietary restrictions alone shows a survival rate of 29 percent for the same time period.

52. Allestra - Tyrosinemia Search through websites about tyrosinemia on Allestra or if you have a website about tyrosinemia, submit it and have it live within 24 hours. http://www.allestra.com/health_and_fitness/diseases_and_conditions/alphabetic_li

Submit a Site New Sites Added Make Allestra Your Homepage Search through websites about Tyrosinemia on Allestra or if you have a web site about Tyrosinemia, submit it and have it live within 24 hours. Allestra Home Submit a Site Add a quality content site to the Allestra search directory. Earn Extra Revenue Join the Allestra Partner Network today! Free Search Boxes Add Allestra's quality content search to your site. Tyrosinemia Home Alphabetic List of Conditions Related Searches Metabolic Disorders Rare Disorders Websites Submit a Site to the Tyrosinemia Category Tyrosinemia Community Comprehensive source of information on tyrosinemia that includes low protein food sources, recipes, journal articles, support group, chat, message board, pediatricians guides, pictures and more. Add to Favorites Submit a Site to the Tyrosinemia Category Allestra Home Submit a Site ... Link to Us

53. Health Library - Tyrosinemia, Hereditary FREE. tyrosinemia, Hereditary. jaundice). tyrosinemia type I may progressto more serious complications such as severe liver disease. http://hvlib.integris-health.com/Library/HealthGuide/IllnessConditions/topic.asp

54. Health Library - Tyrosinemia tyrosinemia. Self Help Clearinghouse. Groupe Aide Aux Enfants Tyrosinemiquesdu Quebec. Model. One group in Quebec. Founded 1989.Provides http://www.billingsclinic.com/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29t

55. Short Description Of Cell Lines. Pathology Tyrosinemia, Type I * Version 4.200103, Short description of cell lines. Pathology tyrosinemia,type I * 276700 OMIM record. By selecting the cell line http://www.biotech.ist.unige.it/cldb/pat139.html

56. FDA Approves Orfadin For Hereditary Tyrosinemia Type 1 Vol 11, No 3 (March 2002). FDA Approves Orfadin for Hereditary tyrosinemiaType 1. ROCKVILLE, Maryland—The US Food and Drug Administration http://www.intouchlive.com/journals/oncnews/n0203ff.htm

Vol 11, No 3 (March 2002) FDA Approves Orfadin for Hereditary Tyrosinemia Type 1 ROCKVILLE, Maryland—The US Food and Drug Administration (FDA) has approved the orphan drug Orfadin (nitisinone capsules, Swedish Orphan International) for treating hereditary tyrosinemia type 1 (HT-1), a rare pediatric disease that causes progressive liver failure and liver cancer. In announcing its approval decision, the agency warned that only physicians experienced in treating the disease should prescribe Orfadin. Rare Diseases Therapeutics, Inc., of Nashville, Tennessee, is the drug’s US distributor. HT-1 results from the inhibition of an enzyme involved in an early step in the tyrosine catabolic pathway. The disorder is present at birth and manifests itself within weeks or months in the failure of the infant to thrive and by symptoms of hepatomegaly, edema, ascites, melena, and hemorrhagic diathesis. HT-1 is fatal in the first year of life without therapy, and treated patients rarely live into their 20s without a liver transplant. Fewer than 100 children in the United States have the disease. The agency acted after reviewing a study of more than 180 patients (median age, 9 months) treated with Orfadin and a diet that restricted intake of the amino acids tyrosine and phenylalanine. In that trial, children less than 2 months old at the time of diagnosis had a 4-year survival rate of 88%. Historical data on children treated with dietary restrictions alone puts the 4-year survival rate at 29%.

57. Neuropathy: Childhood Nonprogressive; Death at 3 months in 1 patient. tyrosinemia l Fumarylacetoacetase; Chromosome 15q23-q25; Recessive Onset Neonatal Infantile; http://www.neuro.wustl.edu/neuromuscular/time/child.html

Front Search Index Links ... Patient Info CHILDHOOD ONSET POLYNEUROPATHIES See storage inclusions Hereditary Axonal or Neuronal Myelin disorders A-beta-lipoproteinemia Adrenomyeloneuropathy An- ... Glycogenosis, Type 3 HMSN: II Infantile axonal + Respiratory failure Infantile Onset Spinocerebellar Ataxia (IOSCA) LCHADD ... Lethal neonatal Methylenetetrahydrofolate Reductase Mitochondrial MNGIE NARP Leigh ... Sensory Neuropathies Spinal muscular atrophy: Proximal Distal Tyrosinemia Carbohydrate-deficient glycoprotein ... Farber's lipogranulomatosis HMSN Dominant: CMT: IA IB III HNPP ... Thermosensitive Recessive: CMT: III 4D (LOM) HMSN-R CNS X-linked: IX Krabbe Metachromatic Leukodystrophy Niemann-Pick ... Thermosensitive Acquired Immune Toxic CIDP Acute motor axonal neuropathy (AMAN) Diphtheria ... Drugs Metabolic Other Diabetes Mellitus Vitamin B deficiency Carpal tunnel syndrome STORAGE INCLUSIONS Type Disease Cellular localization Osmophilic with periodicity Bilbao Metachromatic Leukodystrophy Schwann cell Macrophage Axon Fabry's Vascular Perineurial Schwann cell, non-myelinating Niemann-Pick, Type 1 All except axon Batten-Kufs Schwann cell Vascular Fibroblast Toxic (Lysosomal) Amiodarone Chloroquine Perhexiline Similar inclusions: Cockayne Nerve: Perineurial;

58. WebGuest - Open Directory Health Conditions And Diseases the entire directory. Sites National Library of Medicine The synonyms of tyrosinemia11, a summary and major features. http://directory.webguest.com/index.cgi/Health/Conditions_and_Diseases/Rare_Diso

59. Molecular Analysis Of The Pathologies Associated With Hereditary Tyrosinemia Translate this page Alérion Molecular analysis of the pathologiesassociated with hereditary tyrosinemia. http://www.ulaval.ca/vrr/rech/Proj/72121.html

Molecular analysis of the pathologies associated with hereditary Tyrosinemia Subvention Instituts de recherche en santé du Canada Subventions de fonctionnement Description Domaine(s) de recherche Maladies de l'appareil digestif Maladies du foie Chercheur(s) Robert M. Tanguay , Médecine, Département de médecine, responsable du projet Tranche(s) de financement Instituts de recherche en santé du Canada Date de fin: Demande de correction

60. Health Library - Tyrosinemia Your Health. Search. tyrosinemia. Self Help Clearinghouse. Groupe Aide AuxEnfants Tyrosinemiques du Quebec. Model. One group in Quebec. Founded 1989. http://yourhealth.stlukesonline.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=

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