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Phenylketonuria-pku Disorder:     more detail

21st Century Ultimate Medical Guide to Phenylketonuria (PKU) - Authoritative Clinical Information for Physicians and Patients (Two CD-ROM Set) by PM Medical Health News, 2009-06-05 Phenylketonuria (PKU) Toolkit - Comprehensive Medical Encyclopedia with Treatment Options, Clinical Data, and Practical Information (Two CD-ROM Set) by U.S. Government, 2009-06-05 2009 Empowered Patient's Complete Reference to Phenylketonuria (PKU) - Diagnosis, Treatment Options, Prognosis (Two CD-ROM Set) by PM Medical Health News, 2009-06-05 Management of PKU Treatment programs for PKU and selected other metabolic diseases in the United States: A survey (DHHS publication) by Virginia E Schuett, 1983 A journey into the world of PKU by Kenneth W Wessel, 1991 S.B. 3018: Mandatory screening tests for PKU (University of Washington. School of Law. Student papers) by David Ward, 1974

lists with details

41. PKU - The Disorder
    Prevention is better than Treatment. Phenylketonuria (PKU). Phenylketonuria (PKU) is a disorder caused by an inborn error of metabolism.  
    http://www.rddiagnostics.com/pku_disorder.htm&e=747

42. Worldbook Medical Encyclopedia Pacemaker - Pyrosis PKU
    Phenylketonuria ( PKU ) is a genetic disorder which prevents the normal use of protein food. http//web.ukonline.co.uk/nspku/morepku.htm. 10.  
    http://www.s-books.com/wbmedical/32447/32633/1.htm&e=747

43. Gene Stories - Health
    This baby has been screened for Phenylketonuria (PKU). The test is positive. To develop this genetic disorder, the baby will have inherited a faulty gene from  
    http://www.bbc.co.uk/health/genes/road/childhood/newborn_pku.shtml&e=747

44. Metabolic Disorders
    Phenylketonuria (PKU) and HPA Phenylketonuria (PKU) is a hereditary disorder of metabolism of phenylalanine. A related condition  
    http://rarediseases.about.com/cs/metabolic/&e=747

45. BBlue Diaper Syndrome And Phenylketonuria Maisa Haddad
    amino acid metabolism. One of interest and that was not limited on information was the phenylketonuria (PKU) disorder. This was also  
    http://www-personal.umd.umich.edu/~jcthomas/JCTHOMAS/1997%20Case%20Studies/M%20H

46. Health Info
    Topic Overview Phenylketonuria (PKU) is a genetic disorder that causes the amino acid phenylalanine to build up in the blood. This  
    http://www.pamf.org/health/healthinfo/index.cfm?page=article&sgml_id=hw44745&e=7

47. Disease Directory Rare Disorders Phenylketonuria
    Phenylketonuria Phenylketonuria. Basic Information Phenylketonuria (PKU) is a rare, genetic disorder that affects the body s metabolic system.  
    http://www.diseasedirectory.net/Rare_Disorders/Phenylketonuria/default.aspx&e=74

48. AllRefer Health - Inborn Errors Of Metabolism (Branched Chain
    s). Phenylketonuria (PKU) A rare genetic disorder that can result in severe progressive mental retardation if untreated by diet.  
    http://health.allrefer.com/health/inborn-errors-of-metabolism-info.html&e=747

49. AllRefer Health - Epilepsy (Seizure Disorder)
    Epilepsy is a disorder involving repeated seizures of any type. phenylketonuria (PKU) can rarely cause seizures in infants; other metabolic diseases, such as  
    http://health.allrefer.com/health/epilepsy-info.html&e=747

50. TriButyrate® And Urea Cycle Disorder Research
    The most well known disorder in the larger group is phenylketonuria (PKU), characterized by an accumulation of the amino acid phenylalanine, which frequently  
    http://www.tributyrate.com/html/urea_cycle_disorder.html&e=747

51. Phenylketonuria
    Phenylketonuria (PKU) is a rare genetic disorder that results in excessive accumulation of the amino acid, phenylalanine, and reduced levels of the amino acid  
    http://www.mycustompak.com/healthNotes/Concern/Phenylketonuria.htm&e=747

52. EPEC - Educating Parents Of Extra-special Children
    Phenylketonuria (PKU). Phenylketonuria (PKU) is an inherited (genetic) disorder that is inherited from both parents. About one in  
    http://www.epeconline.com/PKU.html&e=747

53. HighBeam Research: ELibrary Search: Results
    Nutrition Today; February 1, 1991; Acosta, Phyllis B. Phenylketonuria (PKU) is an inherited disorder Collaborative Study of  
    http://www.highbeam.com/library/search.asp?FN=AO&refid=ency_refd&search_thesauru

54. HighBeam Research: ELibrary Search: Results
    .. Hawkins, 31, was born with phenylketonuria ( PKU), a grim disorder that can cause retardation and a variety of behavioral problems.  
    http://www.highbeam.com/library/search.asp?FN=AO&refid=ency_refd&search_thesauru

55. Pediatric Oncall - Phenylketonuria (PKU)
    PHENYLKETONURIA (PKU). UserName. Password. The specific type of mutation varies, resulting in variable severity in the clinical course of the disorder.  
    http://www.pediatriconcall.com/fordoctor/DiseasesandCondition/pku.asp&e=747

56. Phenylketonuria (PKU) General Overview
    Site Directory Phenylketonuria (PKU) General Overview Page. A. PKU is an enzymatic disorder that affects the way the body processes protein.  
    http://www.doh.wa.gov/EHSPHL/PHL/Newborn/pkugo.htm&e=747

57. Health Library -
    Phenylketonuria (PKU). Topic Overview. Phenylketonuria (PKU) is a genetic disorder that causes the amino acid phenylalanine to build up in the blood.  
    http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=

58. Tetrahydrobiopterin Deficiency
    Phenylketonuria (PKU) is a hereditary metabolic disorder characterized by the inability to metabolize the amino acid phenylalanine.  
    http://www.bchealthguide.org/kbase/nord/nord438.htm&e=747

59. Phenylketonuria - PKU; Treatment, Prevention, Cure
    PKU (phenylketonuria) is an inherited disorder of body chemistry PKU (phenylketonuria) is an inherited disorder of body Save on Phenylketonuria PKU books.  
    http://www.healthlinkusa.com/355a.asp&e=747

60. Phenylketonuria (PKU) - Preliminary Draft
    PKU is an autosomal/recessive inherited metabolic disorder. A person must receive 2 genes for PKU inorder to show symptoms of the disease.  
    http://srv2.lycoming.edu/~newman/courses/bio22298/disorderpapers/Pku/preliminary

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