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21. AllRefer Health - Phenylketonuria (PKU, Neonatal Phenylketonuria) phenylketonuria PKU, Neonatal phenylketonuria information center covers Definition, Disorders, Overview, Causes, Risk Factors, Symptoms Signs, Diagnosis Tests, Treatment http://health.allrefer.com/health/phenylketonuria-info.html |
22. BioMarin Pharmaceutical Inc. Researches and develops therapies for debilitating, fatal, chronic genetic disorders causing enzyme deficiency of carbohydrate metabolism, such as phenylketonuria. Headquarters in Novato, California. (Nasdaq BMRN). http://www.biomarinpharm.com/ |
23. Phenylketonuria Tests And Diagnosis - MayoClinic.com phenylketonuria — Comprehensive overview covers symptoms, treatment (including diet information) of this rare birth defect. http://www.mayoclinic.com/health/phenylketonuria/DS00514/DSECTION=tests-and-diag |
24. Phenylketonuria Summary And Analysis Summary BookRags.com phenylketonuria summary with 18 pages of lesson plans, quotes, chapter summaries, analysis, encyclopedia entries, essays, research information, and more. http://www.bookrags.com/Phenylketonuria |
25. Phenylketonuria Symptoms, Diagnosis, Treatments And Causes phenylketonuria information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis. http://www.wrongdiagnosis.com/p/phenylketonuria/intro.htm |
26. Phenylketonuria A US Department of Health and Human Service project providing information on genetic and rare diseases. A comprehensive body of resources on phenylketonuria http://rarediseases.info.nih.gov/GARD/Disease.aspx?PageID=4&DiseaseID=7383 |
27. Phenylketonuria EMedicine Pediatrics Genetics And Metabolic Disease Overview phenylketonuria (PKU) is an inborn error of protein metabolism that results from an impaired ability to metabolize the essential amino acid phenylalanine. Classic http://emedicine.medscape.com/article/947781-overview |
28. Phenylketonuria - PKU - Inherited Metabolic Disorder Information about phenylketonuria (PKU), an inherited metabolic disorder, including symptoms, testing, diagnosis, and treatment. http://rarediseases.about.com/od/metabolicdisorders/a/phenylketonuria.htm |
29. PKU – Phenylketonuria – Join The PKU.com Community Welcome to PKU.com, your PKU (phenylketonuria) web portal. PKU.com has created an online resource for the PKU (phenylketonuria) community. Education, support, and community http://www.pku.com/ |
30. Phenylketonuria Genes And Disease NCBI Bookshelf phenylketonuria (PKU) is an inherited error of metabolism caused by a deficiency in the enzyme phenylalanine hydroxylase. Loss of this enzyme results in mental retardation http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gnd&part=phenylketonuria |
31. Phenylketonuria - Simple English Wikipedia, The Free Encyclopedia phenylketonuria (sometimes called PKU) is a genetic disorder (a disease a person is born with) where a person's body cannot break down an amino acid called phenylalanine. http://simple.wikipedia.org/wiki/Phenylketonuria |
32. Phenylketonuria LIVESTRONG.COM phenylketonuria PKU is a rare condition in which a baby is born without the ability to properly break down an amino acid called phenylalanine. PKU Neonatal phenylketonuria http://www.livestrong.com/phenylketonuria/ |
33. Phenylketonuria - Psychology Wiki phenylketonuria (PKU) is an autosomal recessive genetic disorder characterized by a deficiency in the enzyme phenylalanine hydroxylase (PAH). This enzyme is necessary to http://psychology.wikia.com/wiki/Phenylketonuria |
34. Phenylketonuria Information! phenylketonuria (PKU) is a rare, inherited metabolic disease that results in mental retardation and other neurological problems when treatment is not started within the first http://www.sweetpoison.com/phenylketonuria.html |
35. National PKU News The National PKU News web site provides news and information about phenylketonuria, a rare, inherited metabolic disease. Web site sections include About PKU, PKU Support http://www.pkunews.org/ |
36. Phenylketonuria - Definition Of Phenylketonuria By The Free Online phen yl ke to nu ri a (f n lk t n-r-, -y r-, f n l-) n. Abbr. PKU. A genetic disorder in which the body lacks the enzyme necessary to metabolize phenylalanine to tyrosine. http://www.thefreedictionary.com/phenylketonuria |
37. Phenylketonuria phenylketonuria Definition phenylketonuria (PKU) is a rare condition in which a baby is born without the ability to properly break down an amino acid called phenylalanine. http://adam.about.com/encyclopedia/infectiousdiseases/Phenylketonuria.htm |
38. Phenylketonuria - Vitacost phenylketonuria (PKU) is a rare genetic disorder that results in excessive accumulation of the amino acid, phenylalanine, and reduced levels of the amino acid, Ltyrosine, in http://www.vitacost.com/Healthnotes/Concern/Phenylketonuria.aspx |
39. Phenylketonuria Definition - Medical Dictionary Definitions Of Online Medical Dictionary and glossary with medical definitions http://www.medterms.com/script/main/art.asp?articlekey=4869 |
40. Phenylketonuria - Definition And More From The Free Merriam Definition of word from the MerriamWebster Online Dictionary with audio pronunciations, thesaurus, Word of the Day, and word games. http://www.merriam-webster.com/dictionary/phenylketonuria |
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