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Propionic Acidemia: more detail | |||||
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21. Neurologic Nonmetabolic Presentation Of Propionic Acidemia Archives of Neurology, a monthly professional medical journal published by the American Medical Association, publishes original, peerreviewed scientific research on the http://archneur.ama-assn.org/cgi/content/full/56/9/1143 |
22. Propionic Acidemia Research Network Facilitating communication between academic researchers, families and the medical community to advance studies on PA. http://www.paresearch.org/ |
23. Propionic Acidemia (Propionyl CoA Carboxylase Deficiency Overview In 1961, Childs et al published the earliest clinical report of a patient who was ultimately found to be affected by a deficiency of propionyl coenzyme A (CoA http://emedicine.medscape.com/article/948084-overview |
24. Propionic Acidemia In A Four-Month-Old Male A Case Study And H. Eugene Harker, MD, PhD *, John D. Emhardt, MD * and Bryan E. Hainline, MD, PhD † Departments of *Anesthesia and http://www.anesthesia-analgesia.org/content/91/2/309.full |
25. NORD Acidemia, Propionic Includes the synonyms, a general discussion and further resources. http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Acidemia, Pro |
26. Propionic Acidemia Foundation FAQ FAQ What is Propionic Acidemia (PA)? Propionic Acidemia is a rare disorder that is inherited from both parents. Neither parent shows symptoms, but both carry a defective gene http://pafoundation.com/faq.htm |
27. Propionic Acidemia Research Network Genetic Alliance The Propionic Acidemia Research Network facilitates communication between academic and clinical researchers, physicians and families to promote better treatments and a cure for http://www.geneticalliance.org/organization/propionic-acidemia-research-network |
28. PROPIONIC ACIDEMIA - OMIM Result OMIM, Online Mendelian Inheritance in Man, a database of human genes and genetic disorders developed by staff at Johns Hopkins and hosted on the Web by NCBI. http://www.ncbi.nlm.nih.gov/omim/606054 |
29. Nutricia North America Propionic Acidemia Sulfite Oxidase Deficiency Tyrosinemia Urea Cycle Disorders Neurology At A Glance http://www.shsna.com/pages/propianic_acidemia.htm onclick=sa_mpTC(event, this); |
30. NEWBORN SCREENING Disorder name Propionic Acidemia Acronym PA. What is PA? What causes PA? If PA is not treated, what problems occur? What is the treatment for PA? http://www.newbornscreening.info/Parents/organicaciddisorders/PA.html |
31. Propionic Acidemia A Neuropathology Case Report And Review Of Propionic acidemia is a disorder of branchchain amino acid and odd-chain fatty acid metabolism. http://www.medscape.com/medline/abstract/12873194 |
32. PROPIONIC ACIDEMIA Disease Name PROPIONIC ACIDEMIA (PROPIONYLCoA CARBOXYLASE DEFICIENCY; KETOTIC HYPERGLYCINEMIA) Classification Organic aciduria Inheritance Autosomal recessive Population Incidence http://www.oregon.gov/DHS/ph/nbs/docs/propionicacid.pdf |
33. Medical Home Portal - Propionic Acidemia Information, Tools, and Resources to aid Primary Care Physicians in caring for Children with Special Health Care Needs (CSHCN) and providing a Medical Home for all of their patients http://www.medicalhomeportal.org/newborn/propionic-acidemia |
34. Propionic Acidemia (pathology) Britannica Online Encyclopedia propionic acidemia (pathology), Email is the email address you used when you registered. Password is case sensitive. http://www.britannica.com/EBchecked/topic/664393/propionic-acidemia |
35. Metabolic Disease And Stroke - Propionic Acidemia EMedicine Neurology Overview Propionic acidemia is a metabolic disorder in which a defective enzyme, propionylcoenzyme A (CoA) carboxylase, results in an accumulation of propionic acid. http://emedicine.medscape.com/article/1161910-overview |
36. Home - Gwen For A Cure Finding a cure for Propionic Acidemia September 18, 2010 5th Annual Tailgate Party Corn Hole Tournament for PAF http://www.gwenforacure.com/ |
37. Anaplerotic Therapy In Propionic Acidemia - Full Text View The objective of this project is to define whether nutritional supplements (ornithine alphaketoglutarate, glutamine, or citrate) capable of filling-up the citric acid cycle http://clinicaltrials.gov/ct2/show/NCT00645879 |
38. Propionic Acidemia Information On Healthline Propionic acidemia is an inborn error of metabolism a rare inherited disorder in which the body is unable to break down and use certain proteins properly. As a result, massive http://www.healthline.com/galecontent/propionic-acidemia-1 |
39. Propionic Acidemia New England Consortium Of Metabolic Programs This acute illness protocol is a guideline for healthcare professionals treating the sick infant/child who has previously been diagnosed with propionic acidemia, an organic acid http://newenglandconsortium.org/for-professionals/acute-illness-protocols/organi |
40. Propionic Acidemia Propionic Acidemia Information for Parents Overview Propionic acidemia is a condition that affects infants from birth (congenital) and results from an inability of http://www.kdheks.gov/newborn_screening/download/parent_info/PROP_Info_for_Paren |
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