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         Phenylketonuria-pku Disorder:     more detail
  1. Treatment programs for PKU and selected other metabolic diseases in the United States: A survey (DHHS publication) by Virginia E Schuett, 1983
  2. University of Washington. School of Law. Student papers by David Ward, 1974
  3. A journey into the world of PKU by Kenneth W Wessel, 1991

41. PKU - The Disorder
Prevention is better than Treatment. Phenylketonuria (PKU). Phenylketonuria (PKU) is a disorder caused by an inborn error of metabolism.

42. Worldbook Medical Encyclopedia Pacemaker - Pyrosis PKU
Phenylketonuria ( PKU ) is a genetic disorder which prevents the normal use of protein food. http// 10.

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

44. Metabolic Disorders
Phenylketonuria (PKU) and HPA Phenylketonuria (PKU) is a hereditary disorder of metabolism of phenylalanine. A related condition

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

46. Health Info
Topic Overview Phenylketonuria (PKU) is a genetic disorder that causes the amino acid phenylalanine to build up in the blood. This

47. Disease Directory Rare Disorders Phenylketonuria
Phenylketonuria Phenylketonuria. Basic Information Phenylketonuria (PKU) is a rare, genetic disorder that affects the body s metabolic system.

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.

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

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

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

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

53. HighBeam Research: ELibrary Search: Results
Nutrition Today; February 1, 1991; Acosta, Phyllis B. Phenylketonuria (PKU) is an inherited disorder Collaborative Study of

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.

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.

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.

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.

58. Tetrahydrobiopterin Deficiency
Phenylketonuria (PKU) is a hereditary metabolic disorder characterized by the inability to metabolize the amino acid phenylalanine.

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.

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.

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