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         Pcc Deficiency:     more detail
  1. Optimization of cultural and nutritional conditions for accumulation of poly-@b-hydroxybutyrate in Synechocystis sp. PCC 6803 [An article from: Bioresource Technology] by B. Panda, P. Jain, et all 2006-07-01

21. Providence Health Services - Acidemia, Propionic
PCC Deficiency; Propionyl CoA Carboxylase Deficiency; Ketotic Glycinemia; Hyperglycinemia with Ketoacidosis and Lactic Acidosis, Propionic Type
http://www.providence.org/healthlibrary/contentViewer.aspx?hwid=nord500

22. Southeast NBS Genetics Collaborative HRSA Southeast NBS
PROP (PCC deficiency) S. SCAD (SCADD) SCHAD (SCHADD) T. TFP; TYR I; V. VLCAD (VLCADD) Clinical Trials; Medical Foods; Resources; Annual Meeting; Volunteer Opportunities
http://southeastgenetics.org/

23. What Is Acidemia, Propionic? - WrongDiagnosis.com
PropionylCoA carboxylase deficiency, propionicacidemia, hyperglycinemia with ketoacidosis and leukopenia, ketotic glycinemia, ketotic hyperglycinemia, PCC deficiency, Glycinemia
http://www.wrongdiagnosis.com/a/acidemia_propionic/basics.htm

24. List Of Genetic Disorders - Wikipedia, The Free Encyclopedia
The following is a list of genetic disorders and if known, causal type of mutation and the chromosome involved. The list of human genes includes genes not listed here, which also
http://en.wikipedia.org/wiki/List_of_genetic_disorders

25. Propionyl Coa Carboxylase Deficiency, Acidemia,Propionic
PCC Deficiency Propionyl CoA Carboxylase Acidemia,Isovaleric ( WebMD ) Important It is possible that
http://health-search.closerlooksearch.com/health-topics/P/propionyl-coa-carboxyl

26. GeneDx Tests Propionic Acidemia
PropionylCoA Carboxylase Deficiency, PCC Deficiency, glycinemia, ketotic, hyperglycinemia with ketoacidosis and leucopenia, ketotic hyperglycinemia, pccAC complementation group
http://www.genedx.com/services/dis_pcc.php

27. PROP HRSA Southeast NBS Genetics Collaborative
PROP (PCC deficiency) S. SCAD (SCADD) SCHAD (SCHADD) T. TFP; TYR I; V. VLCAD (VLCADD) Clinical Trials; Medical Foods; Resources; Annual Meeting; Volunteer Opportunities
http://southeastgenetics.org/disease.php/81/_/Propionic_acidemia

28. Scientific Commons Kinetic Analysis Of Genetic Complementation In
We studied genetic complementation of propionyl CoA carboxylase (PCC) deficiency in cultures of polyethylene glycol (PEG)induced heterokaryons, using mutant fibroblast lines
http://en.scientificcommons.org/19783704

29. Acidemia, Propionic
PCC Deficiency; Propionyl CoA Carboxylase Deficiency; Ketotic Glycinemia; Hyperglycinemia with Ketoacidosis and Lactic Acidosis, Propionic Type
http://www.stjohnsmercy.org/healthinfo/kb/default.asp?hwid=nord500

30. Amish, Mennonite, And Hutterite Genetic Disorder Database
Disorder; OMIM 606054 (Click to access OMIM database) Disorder Propionic acidemia Also known as PropionylCoA carboxylase deficiency PCC deficiency Glycinemia, ketotic
http://www.biochemgenetics.ca/plainpeople/singleview.php?id=2338

31. Acidemia, Propionic - Health.com
PCC Deficiency; Propionyl CoA Carboxylase Deficiency; Ketotic Glycinemia; Hyperglycinemia with Ketoacidosis and Lactic Acidosis, Propionic Type; Disorder Subdivisions
http://www.health.com/health/library/mdp/0,,nord500,00.html

32. Biotin - NuGOwiki
Propionic acidemia; Propionylcoa carboxylase deficiency; PCC deficiency; Glycinemia, ketotic; Hyperglycinemia with ketoacidosis and leukopenia; Ketotic hyperglycinemia OMIM 606054
http://wiki.nugo.org/index.php/Biotin

33. Propionic Acidemia - Genetics Home Reference
hyperglycinemia with ketoacidosis and leukopenia; ketotic glycinemia; ketotic hyperglycinemia; PCC deficiency; PROP; propionicacidemia; propionylCoA carboxylase deficiency
http://ghr.nlm.nih.gov/condition=propionicacidemia

34. Journal Of Clinical Investigation Heterozygote Expression In
measured propionyl coenzyme A carboxylase (PCC) activity in extracts of skin fibroblasts and peripheral blood leukocytes from controls and obligate heterozygotes for PCC deficiency
http://www.jci.org/articles/view/109221

35. Acidemia, Propionic
PCC Deficiency; Propionyl CoA Carboxylase Deficiency; Ketotic Glycinemia; Hyperglycinemia with Ketoacidosis and Lactic Acidosis, Propionic Type; Disorder Subdivisions
http://www.ghc.org/kbase/topic.jhtml?docId=nord500

36. The University Of Kansas Hospital - Acidemia, Propionic
PCC Deficiency; Propionyl CoA Carboxylase Deficiency; Ketotic Glycinemia; Hyperglycinemia with Ketoacidosis and Lactic Acidosis, Propionic Type
http://www.kumed.com/healthwise/healthwise.aspx?DOCHWID=nord500

37. Disease Information From NORD, National Organization For Rare
PCC Deficiency Propionyl CoA Carboxylase Deficiency Disorder Subdivisions. Propionic Acidemia, Type II (PCCB Deficiency) Propionic Acidemia, Type I (PCCA
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Acidemia, Pro

38. Acidemia, Propionic
PCC Deficiency; Propionyl CoA Carboxylase Deficiency; Ketotic Glycinemia; Hyperglycinemia with Ketoacidosis and Lactic Acidosis, Propionic Type; Disorder Subdivisions
http://children.webmd.com/acidemia-propionic

39. NEWBORN SCREENING
PCC deficiency; Ketotic glycinemia; Ketotic hyperglycinemia; Where can I find more information? Organic Acidemia Association http//www.oaanews.org
http://www.newbornscreening.info/Parents/organicaciddisorders/PA.html

40. CIGNA - Acidemia, Propionic
National Organization for Rare Disorders, Inc. Synonyms. PCC Deficiency; Propionyl CoA Carboxylase Deficiency; Ketotic Glycinemia; Hyperglycinemia with Ketoacidosis and Lactic
http://www.cigna.com/healthinfo/nord500.html

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