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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

81. Tyrosinemia
SUBCATEGORIES. Up. tyrosinemia tyrosinemia http//communities.msn.comFor all people interested in connecting with others with this disease.
http://www.medlina.com/tyrosinemia.htm
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Tyrosinemia Tyrosinemia - http://communities.msn.com
For all people interested in connecting with others with this disease. Pediatric Database - http://www.icondata.com
Offers a definition of Tyrosinemia-1, the epidemiology, pathogenesis, clinical features, investigations and management. Tyrosinemia-11 - http://www.icondata.com
An in depth look at this disease from Pediatric Database including investigations and management. National Library of Medicine - http://www.nlm.nih.gov The synonyms of Tyrosinemia 11, a summary and major features. SUBCATEGORIES Up powered by A merica M edica, I nc. info@medlina.com New York City

82. Tyrosinemia There Are Several Known Disorders Of Tyrosine
tyrosinemia Type I affects approximately 150,000 to 1100,000 livebirths in the US. Due to an enzyme defect, blood and tissue
http://www.shsna.com/html/tyrosinemia.htm
Tyrosinemia There are several known disorders of tyrosine metabolism which are due to defects in enzymes metabolizing this particular amino acid.
Tyrosinemia Type I affects approximately 1:50,000 to 1:100,000 live births in the U.S.. Due to an enzyme defect, blood and tissue levels of the amino acids tyrosine and phenylalanine as well as related toxic metabolites are elevated. The disease is characterized by severe impairment of liver and renal tubular function, failure to thrive, rickets, cataracts, hypertension, and peripheral nerve deficiencies. Mental retardation may occur. If untreated, tyrosinemia may lead to progressive liver, renal, and brain damage and often fatal pathogenesis. Tyrosinemia Type II is a rare metabolic disorder caused by a defect of another enzyme responsible for the tyrosine metabolism. Blood and tissue levels of tyrosine are elevated and the excretion of phenolic acids is increased. Untreated children suffer from skin lesions on the fingers, palms of the hands, and soles of the feet; corneal erosions have been reported. Mental retardation often occurs. If diagnosed and treated during infancy, these symptoms may be prevented and the disorder may be managed by diet. Dietary treatment for both types consists of a diet restricted in tyrosine and phenylalanine. Type I also requires monitoring of methionine. Such a diet restricts all foods high in protein (meat, dairy, fish, poultry, etc.) and includes prescribed amounts of low protein medical foods, low protein cereals, fruits, and vegetables. Without additional calories, nutrients, and essential and non-essential amino acids (excluding tyrosine, phenylalanine and where necessary methionine), the patient would experience malnutrition. Therefore, an important part of the patient's daily intake must come from a medical food lacking the mentioned amino acids, but containing all other nutrients and essential and non-essential amino acids.

83. UK.SearchEngine.com - Finds It Fast!
tyrosinemia. additional tyrosinemia Categories for tyrosinemia see also/TOP/Health Rare_Disorders/tyrosinemia other tyrosinemia Sites
http://uk.searchengine.com/Top/Health/Conditions_and_Diseases/Rare_Disorders/Tyr
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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.
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.
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84. Tyrosinemia Website Results :: Linkspider UK
tyrosinemia Websites from the Linkspider UK. tyrosinemia Directory. Complete Resultsfor tyrosinemia Related Topics. tyrosinemia Websites from Linkspider UK.
http://www.linkspider.co.uk/Health/ConditionsandDiseases/RareDisorders/Tyrosinem
Tyrosinemia Websites from Linkspider UK Keyword: Tyrosinemia Linkspider UK Directory
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85. Listings Of The World Health Conditions And Diseases Rare
Search, Complete Directory. National Library of Medicine Post Review The synonymsof tyrosinemia 11, a summary and major features.
http://listingsworld.com/Health/Conditions_and_Diseases/Rare_Disorders/Tyrosinem

86. TenderCare4Kids: Links
tyrosinemia, Back to Index. Go, MSN Support Group, Go, PEDBASE Pagediscussing tyrosinemia. Go, eMedicine tyrosinemia medical paper.
http://www.tendercare4kids.com/Merchant2/linksmain.mv?showcat tyro

87. ORNL Review Vol. 34, No. 1, 2001
Mouse Models for the Human Disease of Chronic Hereditary tyrosinemia.See Related Articles Searching for Mouse Models of Human Disorders
http://www.ornl.gov/ORNLReview/v34_1_01/tyrosinemia.htm
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Mouse Models for the Human Disease of Chronic Hereditary Tyrosinemia
See Related Articles: Searching for Mouse Models of Human Disorders
Obesity-related Gene in Mouse Discovered at ORNL
When a section of mouse chromosome 7 containing the coat color c gene is deleted by exposing mice to radiation, "albino" mice are born with a white, hairless coat. 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.

88. Titre Publication Tyrosinemia Nom De La Source Liver Disease
Translate this page Titre publication tyrosinemia. Nom de la source Liver Disease in Children- 2ème édition. Nom de l'auteur. Ponderation. Cote. Chercheur Principal? 1-.
http://biochempharma.com/publications/publications/detail/1602

89. Titre Presentation Hereditary Tyrosinemia Multisystemic
Titre presentation Hereditary tyrosinemia multisystemic imaging with pathologicalcorrelations. Nom du congrès International Pediatric Radiology.
http://biochempharma.com/publications/presentations/detail/7

90. Membres Du Labo Tanguay
Translate this page étudiante / student Ph.D. Tyrosinémie / tyrosinemia. Jean-François Boisclaire-Lachance.stagiaire/trainee. Tyrosinémie / tyrosinemia. Natacha Dreumont.
http://www.rsvs.ulaval.ca/~labrt/membres.html
membres.html TEXTBlWd  ±a#±”P“ ²g Membres courants du laboratoire - Current lab members
Anciens membres du labo - Past lab members
Membres courants du laboratoire - Current lab members Nom / Name Position Projet / Project Courrier / Web
Email / Web
Anne Bergeron
stagiaire/trainee Natacha Dreumont Rossana Jorquera Assistante de rech. / Research assistant Francine Lettre Assistante de rech. / Research assistant Antonella Maresca stagiaire/trainee Heat shock Heat shock Jacques Poudrier Heat shock Heat shock Tangchun Wu Heat shock Anciens membres du labo - Past lab members Nom / Name Position Projet / Project Courrier / Web
Email / Web
Assistante de rech. / Research assistant Mireille D'Astous Marie Duval Assistante de rech. / Research assistant Tout / All Yutaka Inaguma Post-doc Heat shock Denis R. Joanisse Post-doc Heat shock Julie Marchand Heat shock Heat shock Alexia Tolis Page d'accueil Home page

91. Health Library - Tyrosinemia
Search. tyrosinemia. Self Help Clearinghouse. Groupe Aide Aux EnfantsTyrosinemiques du Quebec. Model. One group in Quebec. Founded 1989.
http://www.uvmc.com/library/healthguide/SelfHelp/topic.asp?hwid=shc29tyr

92. Jhhs.client.web-health.com/web-health/topics/GeneralHealth/generalhealthsub/gene
Missing DocumentGeneralHealth/generalhealthsub/generalhealth/gastrohealth/tyr.htmltoppath/home/sites/webhealth/common/topics joined/home/sites/web-health
http://jhhs.client.web-health.com/web-health/topics/GeneralHealth/generalhealths

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