Geometry.Net - the online learning center
Home  - Health_Conditions - Phenylketonuria
e99.com Bookstore
  
Images 
Newsgroups
Page 2     21-40 of 52    Back | 1  | 2  | 3  | Next 20
A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z  

         Phenylketonuria:     more books (92)
  1. Phenylketonuria - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-18
  2. Report of the NIH Consensus Development Conference on Phenylketonuria (PKU) (SuDoc HE 20.3352:P 52) by U.S. Dept of Health and Human Services, 2001
  3. Phenylketonuria: An entry from Gale's <i>Gale Encyclopedia of Medicine, 3rd ed.</i> by Marshall, MA Letcher, 2006
  4. Phenylketonuria: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Marshall, MA Letcher, 2005
  5. Mental and neuromuscular symptoms in tryptophan deficiency: Pellagra, carcinoidosis, phenylketonuria, Hartnup disease and disturbances of tryptophan metabolism ... psychiatrica Scandinavica.Supplementum) by Jörgen Lehmann, 1972
  6. Gale Encyclopedia of Medicine: Phenylketonuria by Marshall G. Letcher MA, 2002-01-01
  7. Inborn Errors of Metabolism: Phenylketonuria, Sly Syndrome, Myoadenylate Deaminase Deficiency, Glycogen Storage Disease Type V
  8. Low Protein Cookery for Phenylketonuria
  9. 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
  10. Autosomal recessive disorders: Tay-Sachs disease, Phenylketonuria, Cystic fibrosis, Canavan disease, Wilson's disease, Lafora disease
  11. International Symposium on Phenylketonuria and Allied Disorders Tel-Aviv 1969
  12. Genetic, Epidemiological and Clinical Studies of Phenylketonuria (Oligophrenia Phenylpyrouvica Folling) in Norway by Letten Fegersten Saugstad, 1975
  13. Phenylketonuria: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Marshall, MA Letcher, Rosalyn, MD Carson-DeWitt, 2006
  14. Low Protein Cookery for Phenylketonuria 3rd Edition. by Virginia E. Schuett, 1997-01-01

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

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z  

Page 2     21-40 of 52    Back | 1  | 2  | 3  | Next 20

free hit counter