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         Urea Cycle Disorders:     more detail
  1. Urea cycle disorders: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Julianne Remington, 2005
  2. Congenital disorders of the urea cycle and ammonia detoxication (Monographs in paediatrics) by Jean Pierre Colombo, 1971
  3. The Pediatrician's Guide to Ornithine Transcarbamylase Deficiency . . . and other Urea Cycle Disorders (The National Organization for Rare Disorders, NORD Guides for Physicians #2) by The National Organization for Rare Disorders, 1999
  4. Inherited disorders of the urea cycle by George K Summer, 1973
  5. CONGENIAL DISORDERS OF THE UREA CYCLE AND AMMONIA DETOXICATION( Monographs in Pediatrics) by J.P. Colombo, 1971
  6. Congenital Disorders of the Urea Cycle and Ammonia Detoxication Volume I
  7. Congenital Disorders of the Urea Cycle and Ammonia Detoxication Volume I by Jean-Pierre Colombo, 1971-01-01
  8. Urea Cycle Diseases (Advances in Experimental Medicine & Biology)

81. Searchalot Directory For Urea Cycle
Related Web Sites. urea cycle disorders Information, medical links and a messageboard. The true story of a one family's struggle with this illness.
http://www.searchalot.com/Top/Health/ConditionsandDiseases/GeneticDisorders/Urea
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  • Urea Cycle Disorders - Information, medical links and a message board. The true story of a one family's struggle with this illness.
  • National Urea Cycle Disorders Foundation - Information about the organization as well as the disease. Family support, membership, newborn screening project and medical information.
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82. The Health Library — Nutritional & Metabolic
urea cycle disorders. Understanding the BasicsNational urea cycle disordersFoundation. urea cycle disordersMead Johnson. Werner Syndrome (Progeria).
http://healthlibrary.stanford.edu/resources/internet/bodysystems/nutrition5.html
Diseases and Disorders Use these links to jump directly to your topic of interest: Caffeine Carbohydrates Fats Fiber ... Page 4 Page 5 Page 6 Page 7 Metabolic Diseases (G - L)
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Gaucher's Disease:MEDLINEplus Gaucher's Disease:NINDS Gaucher Disease Treatment Program:Mt. Sinai School of Medicine Gaucher Disease: Diagnosis and Treatment:University of Pittsburgh [PDF] Gaucher Disease: A Clinical Trial of Gene Therapy:University of Pittsburgh [PDF] National Gaucher Foundation Genes and Disease: Gaucher Disease:National Center for Biotechnology Information Gaucher Disease:GeneReviews, University of Washington
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FAQs About GA (Glutaric Acidemia):International Organization of Glutaric Acidemia Glutaric Acidemia Type I:Mead Johnson Glutaric Acidemia II (GA2/ MADD):FOD Communication Network GA2 Guide for Parents:FOD Communication Network [PDF]
Glycogen Storage Diseases
What Is Glycogen Storage Disease (GSD)?:Association for Glycogen Storage Disease

83. WebGuest - Open Directory : Health : Conditions And Diseases : Genetic Disorders
Sites National urea cycle disorders Foundation Information about theorganization as well as the disease. Family support, membership
http://directory.webguest.com/index.cgi/Health/Conditions_and_Diseases/Genetic_D
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the entire directory only in Top Health Conditions and Diseases Genetic Disorders : Urea Cycle

Sites:
  • National Urea Cycle Disorders Foundation - Information about the organization as well as the disease. Family support, membership, newborn screening project and medical information.
  • Urea Cycle Disorders - Information, medical links and a message board. The true story of a one family's struggle with this illness.
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84. Health Library Find Information On Hereditary Urea Cycle
NATIONAL urea cycle disorders FOUNDATION 4841 Hill Street; La Canada, CA 91011Phone 818790-2460 Toll-Free 1-800-38-NUCDF Website http//www.nucdf.
http://www.mercksource.com/pp/us/cns/cns_hl_adam.jspzQzpgzEzzSzppdocszSzuszSzcns

85. Home From The Director Members Associates Faculty Organization
JA, LeMons C, Rosen M, Ahrens M, Vonachen S and Cederbaum SD (2001) Psychosocialissues and coping strategies in families affected by urea cycle disorders.
http://www.mrrc.npi.ucla.edu/mrrc/faculty.asp?faculty=432

86. Current Strategied For The Management Of Neonatal Urea Cycle Disorders
2001/6/18 Current strategies for the management of neonatal urea cycle disorders.This page uses frames, but your browser doesn't support them.
http://kid.gsnu.ac.kr/JOURNAL/2001/010512/J010512UCD.htm
This page uses frames, but your browser doesn't support them.

87. My Book Marks
treatment and cure. urea cycle disorders. 2endure; UMN; Ucyclyd; HereditaryUrea cycle abnormality; Kreb Henseleit Urea cycle; Krebs
http://wwwiti.cs.uni-magdeburg.de/~chen/bookmark/ureacycle.html

88. WebMD -
UR urea Breath Test medicaltest-topic urea cycle Disorder Discussion Board - ureacycle disorders shc urea cycle Disorder, Arginase Type nord urea cycle
http://my.webmd.com/content/healthwise/106/26297.htm
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89. Urea Cycle And Related Disorders
Browse forwards .. Index .. Substances .. Menu Thispage last modified 21 Feb 1996. Pathway Webmaster, Oxford, UK.
http://oxmedinfo.jr2.ox.ac.uk/Pathway/Miscell/17160.htm
Browse forwards ........ Index Substances Menu This page last modified 21 Feb 1996.
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90. TriButyrate® And Urea Cycle Disorder Research
to treat urea cycle Disorder in the United States of America. Inborn errors ofurea Synthesis are rare and belong to the larger group of disorders of amino
http://www.tributyrate.com/html/urea_cycle_disorder.html
INBORN ERRORS OF UREA SYNTHESIS
(UREA CYCLE DISORDER) tri Butyrate triple crown america, inc
., at the request of Johns Hopkins Hospital as a treatment for inborn errors of Urea Synthesis/Urea Cycle Disorder. For this indication tri Butyrate
Inborn errors of Urea Synthesis are rare and belong to the larger group of disorders of amino acid metabolism, which are genetically determined and caused by enzyme defects. The most well known disorder in the larger group is phenylketonuria (PKU), characterized by an accumulation of the amino acid phenylalanine, which frequently results in mental and psychomotor retardation, if not treated.
The disorders of inborn errors of Urea Synthesis are less known, but are life threatening conditions associated with hyperammonemia or high plasma glutamine levels, often resulting in coma and death in infants, if not treated immediately. Non-Toxic
Since 1987 this compound, with generic name (Sodium) Phenylbutyrate, has been the treatment of choice for these diseases, recommended at a dosage of 450 to 500 mg/kg bodyweight per day. Approximately 1500 children worldwide are alive today and well because of

91. Congenital Disorders Of The Urea Cycle And Ammonia Detoxication J P Colombo
Congenital disorders of the urea cycle and Ammonia Detoxication JP Colombo. SubjectTitle Congenital disorders of the urea cycle and Ammonia Detoxication
http://www.book-planet.co.uk/J-P-Colombo-Congenital-Disorders-of-t-3805511620.ht
Congenital Disorders of the Urea Cycle and Ammonia Detoxication J P Colombo
Subject:
Title: Congenital Disorders of the Urea Cycle and Ammonia Detoxication
Author: J P Colombo
H J Kaufmann Progress in Paedi...
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Miloslav Rechcigl World Review...

L D L Osa Aspects and Treatmen...
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92. WND 2 For Consumers
For use in the nutritional management of children and adults with urea cycledisorders under the direct and continuing supervision of a doctor.
http://www.meadjohnson.com/metabolics/2wnd2.html
For use in the nutritional management of children and adults with urea cycle disorders under the direct and continuing supervision of a doctor. WND stands for Waste Nitrogen Disorder. WND 2 is a dietary powder for children and adults with urea cycle disorders. Persons with urea cycle disorders are not able to convert a by-product of the nitrogen in protein, ammonia, into urea which can be harmlessly passed through the urine. Too much ammonia in the blood and body tissues can lead to serious health problems. WND 2 is designed to meet the protein needs of children and adults with urea cycle disorders by providing all essential amino acids but no non-essential amino acids. Humans must consume the essential amino acids to grow, develop, and maintain body tissues normally. The protein in regular foods contains both essential and non-essential amino acids, all of which carry nitrogen. WND 2 provides essential protein components without extra nitrogen; 100 g of powder provides 8.2 g of protein equivalents (8% of Calories). The fat content of WND 2 — 23% of Calories — supplies generous amounts of omega-3 and omega-6 essential fatty acids. Carbohydrate contributes 69% of Calories. The vitamin and mineral levels are appropriate for children or adults.

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