81. PillSupplier.com - Conditions And Diseases/Rare Disorders/Tyrosinemia Category tyrosinemia. HOME ABOUT US ORDER STATUS BMI CALCULATOR FAQ CONTACT US. Conditions and Diseases/Rare Disorders/tyrosinemia. Links http://www.pillsupplier.com/dir/975/

Category: Tyrosinemia HOME ABOUT US ORDER STATUS BMI CALCULATOR ... CONTACT US Prescription Drugs Diet Pills Adipex Bontril Didrex ... Login Conditions and Diseases/Rare Disorders/Tyrosinemia Links: National Library of Medicine [rate it] [review it] The synonyms of Tyrosinemia 11, a summary and major features. NORD - Tyrosinemia, Hereditary [rate it] [review it] Offers the synonyms, a general discussion and further resources. Pediatric Database [rate it] [review it] Offers a definition of Tyrosinemia-1, the epidemiology, pathogenesis, clinical features, investigations and management. Tyrosinemia [rate it] [review it] For all people interested in connecting with others with this disease. Tyrosinemia Group [rate it] [review it] Information about tyrosinemia, a rare metabolic disorder. Includes lists of links to other support groups, sources for low protein food, recipes, message board. Tyrosinemia-11 [rate it] [review it] An in depth look at this disease from Pediatric Database including investigations and management. Search Looking for something in particular? the entire directory only this category More search options Pages Updated On: Fri May 28 2004 - 04:41:17 About Us Frequently Asked Questions Contact Us Order Status ... Health Resources

82. TYROSINEMIA TYPE II: REPORT OF THE FIRST FOUR CASES IN SAUDI ARABIA tyrosinemia TYPE II REPORT OF THE FIRST. The clinical and biochemical data of four tyrosinemia type II patients were reviewed retrospectively. http://www.kfshrc.edu.sa/annals/185/97-329.html

TYROSINEMIA TYPE II: REPORT OF THE FIRST FOUR CASES IN SAUDI ARABIA M. Al-Essa, MD; M. Rashed, PhD; P.T. Ozand, MD, PhD Tyrosinemia type II (oculocutaneous tyrosinemia) is an autosomal recessive disorder due to deficiency of tyrosine aminotransferase, an enzyme involved in the metabolism of tyrosine. More than 50 cases have been reported to date. Most of the patients are Italian, German, French, Swedish, Spanish, Norwegian, American, Canadian, Australian, and Turkish Ashkenazi Jews. Almost half of the patients that have been reported are from Italy. Our files contain four patients under clinical follow-up with confirmed biochemical diagnosis for tyrosinemia type II. The aim of this study is to increase the awareness of the scientific and medical community, particularly in the kingdom of Saudi Arabia, of the clinical progression of this disease, the ability to make a diagnosis through tandem mass spectrometry (Ms/MS) and the rewarding clinical response and prevention of complications by use of dietary therapy. Patients and Methods From the Departments of Pediatrics and Biological and Medical Research, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

83. Tyrosinemia tyrosinemia. All those facts indicated an inherited condition of the type known as an autosomal recessive disease (1, 2). It was hereditary tyrosinemia. http://opbs.okstate.edu/~leach/Bioch5853/Minireviews/MR2.98 folder/KO.MR2.98/Min

Tyrosinemia Founding Fathers and Mothers Kenji Onodera Department of Biochemistry and Molecular biology, Oklahoma State University Here is an article from Natural History issued on June 1988 (1). Baby Pierre was born in Canada on March 7,1964, weighting a healthy six and three-quarter pounds. He fed very poorly from the start. So that he was hospitalized on September, but he gained only half a pound. He repeated vomiting, and his body are apparently weak, no muscle. Surprisingly, his urine always smelled of rotten cabbage. To keep him alive, the doctors decided to install a tube through his nose into his stomach. Once he gained weight by this treatment. On November 30, his condition suddenly changed, and he finally vomited blood and died. At the same time, Canadian physicians became increasingly aware of infants dying just like Baby Pierre. Most of patients of this disease were from the remote Chicoutimi area of Quebec Province, about 120 miles north from Quebec City. Their parents were all normal, but some of these parents lost three or four babies in this way. The patient was an equal number of boys and girls. All those facts indicated an inherited condition of the type known as an autosomal recessive disease (1, 2). It was hereditary tyrosinemia. Characteristics of tyrosinemia Statistics in Quebec, Canada

84. Tyrosinemia: The Quebec Experience tyrosinemia the Quebec experience. Khazal Paradis, MD. Table of contents. Introduction. Hepatorenal tyrosinemia is a disorder of aminoacid metabolism. http://collection.nlc-bnc.ca/100/201/300/cdn_medical_association/cim/vol-19/0311

Tyrosinemia: the Quebec experience Khazal Paradis, MD Division of Pediatric Gastroenterology­Nutrition, Department of Pediatrics, Hôpital Sainte-Justine, University of Montréal, Montréal, Que Clin Invest Med résumé Paper reprints may be obtained from: Dr. Khazal Paradis, Pediatric Gastroenterology­Nutrition, Hôpital Sainte-Justine, 3175 Côte Ste-Catherine, Montreal QC H3T 1C5; fax 514 345-4999 Contents Abstract Résumé Introduction Clinical presentation ... References Abstract was documented before transplantation in 54% of the cases. The rate normalized after liver transplantation in most patients, with rapid improvement in tubular function. However, patients with a severely low rate (less than 55 mL/min per 1.73 m ) before transplantation still had borderline renal function and poor growth after the transplantion, despite normal liver function. Therefore, for children with a consistently low GFR, careful consideration should be given to performing a combined liver­kidney transplantation, and a renal biopsy should form part of the pretransplantation evaluation. Résumé a été observé avant la transplantation chez 54 % des sujets. Le TFG était normal après la transplantation hépatique chez la plupart des sujets, avec une amélioration rapide de la fonction tubulaire. Par contre, les sujets avec un TFG gravement abaissé (moins de 55 mL/min par 1.73 m

85. Mioti: Diseases + Conditions Diseases + Conditions tyrosinemia. Search Mioti http://www.mioti.com/cat/condition/condition.asp?Cat=Tyrosinemia

86. ARUP Tyrosinemia (Hereditary) Metabolite tyrosinemia (Hereditary) Metabolite, , Allergens, A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P, Q, R, S, T, U, V, W, X, Y, Z, Search UG. 0080103 tyrosinemia (Hereditary) Metabolite. http://www.aruplab.com/guides/ug/tests/0080103tyrosinemia_20_28hereditary_29_20m

87. Molecular Analysis Of The Pathologies Associated With Hereditary Tyrosinemia Translate this page alérion Molecular analysis of the pathologies associated with hereditary tyrosinemia. http://www.ulaval.ca/vrr/bd/projet/fiche/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 Mot(s)-clé(s) apoptosis , catabolism , genetic disease , hepatocarcinoma , hereditary tyrosinemia , liver , mutation reversion , regeneration , tyrosine 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 début : Date de fin : Fiche numéro : Demande de correction

88. Entrez PubMed On the enzymic defects in hereditary tyrosinemia. Lindblad B, Lindstedt S, Steen G. The activity of the enzyme porphobilinogen synthase http://www.biomedcentral.com/pubmed/270706

Entrez PubMed Nucleotide Protein ... Books Search PubMed Protein Nucleotide Structure Genome Books CancerChromosomes 3D Domains Domains Gene GEO GEO DataSets HomoloGene Journals MeSH NCBI Web Site OMIM PMC PopSet SNP Taxonomy UniGene UniSTS for Limits Preview/Index History Clipboard ... Text Version Entrez PubMed Overview FAQ Tutorial New/Noteworthy ... E-Utilities PubMed Services Journals Database MeSH Database Single Citation Matcher Batch Citation Matcher ... Cubby Related Resources Order Documents NLM Gateway TOXNET Consumer Health ... PubMed Central Summary Brief Abstract Citation ASN.1 MEDLINE XML UI List LinkOut Related Articles Cited in Books CancerChrom Links Domain Links 3D Domain Links GEO DataSet Links Gene Links Genome Links GEO Links HomoloGene Links Nucleotide Links OMIM Links PMC Links Cited in PMC PopSet Links Protein Links SNP Links Structure Links UniSTS Links Show: Sort Author Journal Pub Date Text File Clipboard E-mail Order Proc Natl Acad Sci U S A. 1977 Oct;74(10):4641-5. Related Articles, Links On the enzymic defects in hereditary tyrosinemia. Lindblad B, Lindstedt S, Steen G. PMID: 270706 [PubMed - indexed for MEDLINE] Summary Brief Abstract Citation ASN.1

89. Tyrosinemia Home Up . Click Here! tyrosinemia. Click Here! Musice.net Just-recipes.net EnvyMag.com Scholarships-4u.com Shesearch.com Free http://www.health-server.com/tyrosinemia.htm

Home Up Tyrosinemia Music-e.net Just-recipes.net EnvyMag.com Scholarships-4u.com ... Sclerosing Cholangitis [ Tyrosinemia ] Wilson Disease Health By Category Health By Specialty Health Feedback ... Submit A Health Site

90. Tyrosinemia tyrosinemia Directory Guide to tyrosinemia sites on the internet. tyrosinemia. http://www.directory.net/Health/Conditions_and_Diseases/Rare_Disorders/Tyrosinem

Tyrosinemia Directory: Guide to Tyrosinemia sites on the internet. Search Engines: Google Yahoo MSN FindWhat ... City Guides Tyrosinemia Health Conditions and Diseases Rare Disorders Tyrosinemia Websites Pediatric Database http://www.icondata.com/health/pedbase/files/tyrosine.htm Offers a definition of Tyrosinemia-1, the epidemiology, pathogenesis, clinical features, investigations and management. Tyrosinemia-11 http://www.icondata.com/health/pedbase/files/tyrosin1.htm 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 http://groups.msn.com/tyrosinemia/ For all people interested in connecting with others with this disease. NORD: Tyrosinemia, Hereditary http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=tyrosinemia%2c%20hereditary Offers the synonyms, a general discussion and further resources. Got eight minutes? Join in and participate in Stanford's Web Credibility Project's latest study.

91. Tyrosinemia From Linkspider UK Health Directory tyrosinemia by Linkspider UK, tyrosinemia links and tyrosinemia topics from our Health directory. Directory Topic tyrosinemia assoicated to Health. http://linkspider.co.uk/Health/ConditionsandDiseases/RareDisorders/Tyrosinemia/

Match » -All words -Any word -Exact text Search » The Web Jobs / Vacancy Images / Photos FTP / Downloads United Kingdom United States of America Argentina Austria Australia Bangladesh Belgium Bolivia Brazil Bulgaria Canada Chile China Cuba Cyprus Czech Republic Czechoslovakia Denmark Dominican Republic Ecuador Egypt Estonia Finland France Germany Ghana Greece Hong Kong Hungary Iceland India Indonesia Ireland Israel Italy Japan Jordan Kenya Kuwait Latvia Lithuania Luxembourg Malaysia Malta Mexico Moldavia Monaco Morocco Mozambique Nepal Netherlands New Zealand Nicaragua Nigeria North Korea Norway Pakistan Panama Paraguay Peru Philippines Poland Portugal Qatar Romania Russian Federation Saudi Arabia Singapore South Africa South Korea Spain Sri Lanka Sweden Switzerland Taiwan Tanzania Thailand Tunisia Turkey Ukraine United Arab Emirates Uruguay Venezuela Yemen Yugoslavia Zambia Zimbabwe Ranking » On (no duplicate) Off (allow duplicate) Add my Site Toolbar Affiliates Directory Topic Tyrosinemia assoicated to Health Directory Tree: Top Health Conditions and Diseases Rare Disorders : Tyrosinemia ( See Also: Health: Conditions and Diseases: Genetic Disorders Health: Conditions and Diseases: Nutrition and Metabolism Disorders Pediatric Database - Offers a definition of Tyrosinemia-1, the epidemiology, pathogenesis, clinical features, investigations and management.

92. Health Library - tyrosinemia, Hereditary. Important It is possible that the main title of the report tyrosinemia, Hereditary is not the name you expected. http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/topic.asp?hw

93. NodeWorks - Conditions & Diseases: Rare Disorders: Tyrosinemia 1. National Library of Medicine The synonyms of tyrosinemia 11, a summary and major features. 2. NORD tyrosinemia, Hereditary http://dir.nodeworks.com/Health/Conditions_and_Diseases/Rare_Disorders/Tyrosinem

in entire NodeWorks Directory in Health in Rare Disorders in ++ Tyrosinemia Top Health Rare Disorders 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. 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. Tyrosinemia For all people interested in connecting with others with this disease. NodeWorks boosts web surfing! Page Returned in seconds - HTML Compressed Help build the largest human-edited directory on the web. Submit a Site Update a Site Open Directory Project Become an Editor

94. MedWebPlus Web Site ID 8664 http://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 Location: North America Canada Prince Edward Island Summerside Subjects: All Diseases Diseases and Conditions Metabolism, Inborn Errors Methylamines ... Privacy statement Powered by y-Base

95. MedWebPlus Web Site ID 11867 http://medwebplus.com/obj/11867

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-II http://www.icondata.com/health/pedbase/files/TYROSIN1.HTM Location: North America Canada Prince Edward Island Summerside Subjects: All Diseases Diseases and Conditions Metabolism, Inborn Errors Methylamines ... Privacy statement Powered by y-Base

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