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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. Nursing
    PKU, or phenylketonuria, is an inherited (genetic) disorder that affectsabout one in every 15,000 infants born in the United States.  
    http://nursing.about.com/library/1999/bldyk040303.htm
    
    Extractions: zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a66' About Nursing Nursing Essentials ... Help w(' ');zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/7.htm','');w(xb+xb); Sign Up Now for the Nursing newsletter!

42. SurfWax -- Accumulating News And Reviews On 50,000 Topics
    to triple the number of newborn tests 7 Sep 2003 That s when the state began screeningnewborns for phenylketonuria (PKU) a faultygene disorder that makes  
    http://news.shopeasier.com/files/shopeasier_Phenylketonuria.html

43. 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

44. Phenylketonuria - PKU; Treatment, Prevention, Cure
    Phenylketonuria PKU Search here for information which may include treatment,diagnosis PKU (phenylketonuria) is an inherited disorder of body chemistry PKU  
    http://www.healthlinkusa.com/content/355.html

45. Information On Phenylalanine; Product Review Where To Buy
    It is important to note the disorder phenylketonuria (PKU), in which an individuallacks the enzyme necessary to metabolize phenylalanine.  
    http://www.allstarhealth.com/lj_c/Phenylalanine.htm
    
    Extractions: It is important to note the disorder phenylketonuria (PKU), in which an individual lacks the enzyme necessary to metabolize phenylalanine . Infants are tested for PKU within 48-72 hours of birth. If not treated before three weeks of age, PKU can lead to severe mental retardation. Symptoms of PKU begin to appear at about 3-6 months of age, and include eczema, delayed development, a small head and hyperactivity. Individuals with PKU must restrict phenylalanine from their diet and supplement with tyrosine L-phenylalanine may help fight symptoms of depression through the synthesis of L- tyrosine Tyrosine is an important precursor in the production of the neurotransmitters norepinephrine and dopamine, low levels of which are linked to depression.

46. Health Library -
    Phenylketonuria (PKU) is an inherited disorder in which the body cannot break downan amino acid called phenylalanine, which is a component of protein.  
    http://www.maimonidesmed.org/library/healthguide/en-us/support/topic.asp?hwid=st

47. Phenylketonuria (PKU)
    Phenylketonuria (PKU). Other Places To Get Help. Through a network system, CORD linkstogether individuals and families with the same rare disorder.  
    http://www.bchealthguide.org/kbase/topic/mini/hw44745/conres.htm
    
    Extractions: var hwPrint=1;var hwDocHWID="hw44745";var hwDocTitle="Phenylketonuria (PKU)";var hwRank="1";var hwSectionHWID="hw44745-ConRes";var hwSectionTitle="Other Places To Get Help";var hwSource="en-caQ2_05";var hwDocType="Mini"; Canadian Organization for Rare Disorders P.O. Box 814 Phone: 1-877-302-7273 toll-free

48. NewbornScreening3
    screening for a genetic disorder. A test developed in 1961 by Dr. Robert Guthrieof the University of Buffalo identified phenylketonuria (PKU), an inherited  
    http://www.pediatric-neurology-paris.org/asp/NewbornScreening3.asp
    
    Extractions: N ewborn screeningtesting infants for certain genetic anomalies, inborn errors of metabolism, and other disordershas been commonplace since the 1960s but has rarely been a topic for public discourse. Within the last year or two, though, newborn screening has become of interest not only to healthcare professionals and scientific researchers, but to a far broader audience. Articles in such publications as the Philadelphia Enquirer, US News and World Report, and The New York Times have explored the subject of screening. The Morbidity and Mortality Weekly Report , a publication of the Atlanta-based Centers for Disease Control and Prevention, reported on data from Georgia's screening program. The Maternal and Child Health Bureau (part of the federal Health Resources and Services Administration) and the American Academy of Pediatrics (AAP) have convened a task force on newborn screening to update the AAP's 1996 guidelines. The complete report is expected within the next few months. Many state legislatures are reexamining their current programs and debating expansion of testing requirements. The almost-complete Human Genome Project is expected to prompt still further discussion of issues surrounding testing for errors of metabolism and genetic disorders.

49. NORD - National Organization For Rare Disorders, Inc.
    devoted to providing news and information to all persons involved in the treatmentof phenylketonuria (PKU). This is a rare metabolic disorder caused by a  
    http://nord-rdb.com/search/orgdetail_full.html?org_name=National PKU News

50. NORD - National Organization For Rare Disorders, Inc.
    dedicated to providing support and services to children with phenylketonuria (PKU),their families, and all those involved in the treatment of this disorder.  
    http://nord-rdb.com/search/orgdetail_full.html?org_name=Children's PKU Network

51. OLS - Newborn Screening Disorders
    PHENYLKETONURIA (PKU). Classical PKU is a metabolic disorder resulting in the deficientproduction of the liver enzyme phenylalanine hydroxylase.  
    http://www.wvdhhr.org/labservices/labs/newborn/newborn_disorders.cfm?pfv=true

52. Medical Genetics - Overview Of Newborn Screening For Birth Defects
    Phenylketonuria (PKU) PKU is a recessive disorder which occurs in about one in 12,000live births and is caused by the absence of the enzyme phenylalanine  
    http://www.chkd.org/Genetics/overnew.asp?option=print

53. ForMyDiet E-Newsletter 4/28/04
    For example, researchers have been studying gene therapy for the treatment of metabolicdisorders such as Phenylketonuria (PKU), a disorder characterized by  
    http://www.formydiet.com/Information/eNewsletters.aspx?a=74

54. Inborn Errors Of Metabolism
    This requires close supervision by a registered dietitian or physician, and cooperationby parent(s). Phenylketonuria (PKU) A rare genetic disorder that can  
    http://www.formydiet.com/Information/Doc.aspx?a=23

55. DoctorGeorge.com - Your Family Doctor On The Web
    Phenylketonuria (PKU) Primarily affects newborns PKU is an inherited disorder causedby a build up of an amino acid called phenylalanine that, if left untreated  
    http://www.doctorgeorge.com/article.php?sid=945&mode=thread&order=0

56. NMAP The UK S Gateway To High Quality Internet Resources In
    for inborn errors of metabolism and detection of a range of metabolic disorderssuch as phenylketonuria (PKU) and MCAD deficiency, a disorder of fatty acid  
    http://nmap.ac.uk/browse/mesh/C0027617L0027617.html

57. Overview Of Newborn Screening For Birth Defects - Children S
    Phenylketonuria (PKU) PKU is a recessive disorder that occurs in about one in 12,000live births and is caused by the absence of the enzyme phenylalanine  
    http://www.chop.edu/consumer/your_child/wellness_index.jsp?id=-8584

58. Autistic Disorder - Children S Hospital Of Philadelphia
    which may cause autism, including FragileX, untreated phenylketonuria (PKU),neurofibromatosis, tuberous the autism is caused by a genetic disorder, or has no  
    http://www.chop.edu/consumer/your_child/wellness_index.jsp?id=-9360

59. Diabetes And Other Endocrine And Metabolic Disorders- Newborn Screening Tests
    phenylketonuria (PKU) PKU is an inherited disease in which the body cannot metabolizea galactosemia This is an inherited disorder in which the baby is unable  
    http://www.salemhospital.org/services/healthsource/content.php?pageid=P01967&asd

60. Growth And Development- Autistic Disorder
    which may cause autism, including FragileX, untreated phenylketonuria (PKU),neurofibromatosis, tuberous autism is caused due to a genetic disorder, or has no  
    http://www.salemhospital.org/services/healthsource/content.php?pageid=P02179&asd

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