21. Archive Of Advisor Updates course work), or will have earned 24 hours by the end of the Spring 2004 term willstill be permitted to remediate the science pcc deficiency in the Fall 2004 http://www.advising.eku.edu/archiveupdate.php

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22. Transitions Placement Testing - Deficiencies You are NOT eligible to take a placement test for a pcc deficiency. Youradvisor will assist you in scheduling the appropriate course work. http://www.nku.edu/~admitnku/Transitions/placement/deficiencies.htm

23. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/P Click Here. Top Health Conditions and Diseases P (0 links). pcc deficiency@(4); POEMS Syndrome@ (2); Pain@ (39); Pallister Killian Mosaic Syndrome@ (3); http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/P

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24. P From Linkspider UK Health Directory Directory Tree Top Health Conditions and Diseases P (). pcc deficiency; POEMSSyndrome; Pain; Pallister Killian Mosaic Syndrome; PallisterHall Syndrome; http://linkspider.co.uk/Health/ConditionsandDiseases/P/

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25. J Med Genet -- Muro Et Al. 36 (5): 412 movement disorder. 14 15 Therefore, prenatal diagnosis plays an importantrole in genetic counselling in families with pcc deficiency. http://jmg.bmjjournals.com/cgi/content/full/36/5/412

HOME HELP FEEDBACK SUBSCRIPTIONS ... Email this link to a friend eLetters: Submit a response to this article Similar articles found in: J Med Genet PubMed PubMed Citation Search PubMed for articles by: Muro, S Ugarte, M Alert me when: new articles cite this article Download to Citation Manager Collections under which this article appears: Genetics J Med Genet 412-414 ( May ) Short report Feasibility of DNA based methods for prenatal diagnosis and carrier detection of propionic acidaemia S Muro a a a a P Briones b A Ribes b M Ugarte a a b Correspondence to: Dr Ugarte. Received 27 April 1998 Revised version accepted for publication 8 September 1998 Abstract Top Abstract Introduction Patients and methods Results and discussion References Propionic acidaemia (PA) is an autosomal recessive disease caused by a genetic deficiency of propionyl-CoA carboxylase (PCC). Defects in the PCCA and PCCB genes that code for the and subunits of PCC, respectively, are responsible for PA. A proband with PA was previously shown to carry the c1170insT mutation and the private L519P mutation in the PCCB gene. Here we report the prenatal diagnosis

26. Heterozygote Expression In Propionyl Coenzyme A Carboxylase Deficiency DIFFERENC A carboxylase (PCC) activity in extracts of skin fibroblasts and peripheral bloodleukocytes from controls and obligate heterozygotes for pcc deficiency. http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=371850

27. Cathy Read 090 College Reading Read 090L Additional Lab Hour Recommended TS 098 Introductionto Social Science (pcc deficiency in History) Special sections paired http://www.louisville.edu/~cwleis01/

Cathy Leist, Coordinator (502-852-8105) E-mail: cwleis01@athena.louisville.edu Courses Offered TS 101 Read 095 * College Study Strategies Read 090 College Reading Read 090L Additional Lab Hour Recommended TS 098 Introduction to Social Science PCC Deficiency in History) permission for registration. Student Success Workshops: Miller Hall First-Year Resource Center Workshop Schedule Strategic Learning Lab: Strickler Hall 329 Drop assistance for students interested in learning styles, critical reading, lecture note-taking, and test-taking. Wednesday 12:00-2:00 Thursday 12:30-2:30

28. :: Ez2Find :: P 4) PassiveAggressive Personality Disorder (5) Patellofemoral Disorder (7) PathologicNystagmus (6) Pathological Gambling (77) pcc deficiency (4) Pectus http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas

Guide : P Global Metasearch Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode All Words Any Word Phrase Results Timeout Depth Adult Filter Add to Favorites Other Search Web News Newsgroups Images Guides P ez2Find Home Directory Health Conditions and Diseases : P A B C D ... Pyromania Last update: 19:24 PT, Monday, March 8, 2004 Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Portions powered by ez2find.com

29. RedNova News: Propionic Acidemia February 01, 2003. RedNova Health Link. Propionic Acidemia. Synonymspcc deficiency. Propionyl CoA Carboxylase Deficiency. Ketotic Glycinemia. http://www.rednova.com/news/stories/2/2003/02/01/story049.html

Forum Check E-mail My RedNova Join Us ... Tell a Friend - Win $500 Search February 01, 2003 RedNova Health Link Propionic Acidemia Synonyms: PCC Deficiency Propionyl CoA Carboxylase Deficiency Ketotic Glycinemia Hyperglycinemia with Ketoacidosis and Lactic Acidosis, Propionic Type More from the world's of science, space, and technology from RedNova Email this story to a friend Post your thoughts on this story

30. SearchBug Directory: Health: Conditions_and_Diseases: P 4) PassiveAggressive Personality Disorder (5) Patellofemoral Disorder (7) PathologicNystagmus (6) Pathological Gambling (78) pcc deficiency (4) Pectus http://www.searchbug.com/directory.aspx/Health/Conditions_and_Diseases/P/

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31. SLCentral Directory - Health - Conditions And Diseases - P Gambling@ (74); pcc deficiency@ (4); Pectus Excavatum@ (9); Pediculosis@(28); Pellagra@ (3); Pelvic Inflammatory Disease PID@ (11); Pelvic http://www.slcentral.com/directory/index.php/Health/Conditions_and_Diseases/P/

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32. Propionic Acidemia - Genetics Home Reference pcc deficiency; propionylCoA carboxylase deficiency; propionicacidemia. SeeHow are genetic conditions and genes named? in Help Me Understand Genetics. http://ghr.nlm.nih.gov/condition=propionicacidemia

A service of the U.S. National Library of Medicine Home Search Conditions Genes ... Help Propionic acidemia Related Gene(s) Quick links to this topic MedlinePlus Health Information Educational resources Information pages Patient support For patients and families Gene Reviews Clinical summary Gene Tests DNA test labs PubMed Recent literature OMIM Genetic disorder catalog Propionic acidemia What is propionic acidemia? Propionic acidemia is an inherited disorder in which the body is unable to process certain proteins and lipids (fats) properly. The condition, which usually appears in early infancy, is characterized by poor feeding, vomiting, weak muscle tone (hypotonia), and lethargy. The effects of propionic acidemia can be life-threatening. How common is propionic acidemia? Propionic acidemia occurs in about 1 in 100,000 live births in the United States. The condition appears to be more common in Saudi Arabia, with a frequency of 1 in 2,000 to 5,000 people. What genes are related to propionic acidemia? Mutations in the PCCA and PCCB genes cause propionic acidemia.

33. Nature Publishing Group Finally, the homology model allows structural interpretation of pcc deficiency diseasemutations, reinforcing the value of TC as a model for biotindependent http://www.nature.com/cgi-taf/DynaPage.taf?file=/emboj/journal/v22/n10/full/7590

34. P In Health > Conditions And Diseases Gambling@ (76); pcc deficiency@ (4); Pectus Excavatum@ (9); Pediculosis@(28); Pellagra@ (3); Pelvic Inflammatory Disease PID@ (11); Pelvic http://ilectric.com/glance/Health/Conditions_and_Diseases/P/

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35. Carnitine Deficiency Syndromes that occurs in infancy. It is caused by a deficiency of the enzyme propionylCoAcarboxylase (pcc). The initial symptoms of Propionic http://www.bchealthguide.org/kbase/nord/nord60.htm

document.write(''); var hwPrint=1; var hwDocHWID="nord60"; var hwDocTitle="Carnitine Deficiency Syndromes"; var hwRank="1"; var hwSectionHWID="nord60"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; National Organization for Rare Disorders, Inc. Carnitine Deficiency Syndromes Important It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms Carnitine Deficiency, Myopathic Carnitine Deficiency, Primary Carnitine Deficiency, Secondary Muscle Carnitine Deficiency Renal Reabsorption of Carnitine, Defect Disorder Subdivisions Myopathic Carnitine Deficiency Systemic Carnitine Deficiency Related Disorders List Information on the following diseases can be found in the Related Disorders section of this report: Isovaleric Acidemia Propionic Acidemia Methylmalonic Acidemia Mitochondrial Cytopathies General Discussion Carnitine Deficiency Syndrome is a rare metabolic disorder that may be inherited in some cases, or occur as a result of other metabolic disorders. Carnitine functions in the body as a carrier of fatty acids to the energy centers in muscles (mitochondria). A deficiency of carnitine, normally produced by the liver and kidneys, can result in extreme muscle weakness and other related symptoms.

36. Descriptions For Disorders Detectable Via MS/MS Using Newborn Disorder Betaketothiolase deficiencyAKA 3-Oxothiolase deficiency; BKDDiagnostic Metabolites on AKA PA, Propionyl CoA carboxylase (pcc) deficiencyDiagnostic Metabolites on MS/MS http://www.dhs.cahwnet.gov/org/pcfh/GDB/html/NBS/Disorders Detectable.pdf

37. EMedicine - Protein C Deficiency : Article By Eleanor S Pollak, MD C concentrate have been documented in several cases of homozygous deficiency. DrugName, Prothrombin complex concentrate pcc contains plasmaderived vitamin K http://www.emedicine.com/med/topic1923.htm

(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Patient Education Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Medicine, Ob/Gyn, Psychiatry, and Surgery Hematology Protein C Deficiency Last Updated: May 21, 2004 Rate this Article Email to a Colleague Synonyms and related keywords: thrombophilia, hypercoagulability AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Eleanor S Pollak, MD , Associate Director of Special Coagulation, Assistant Professor, Department of Pathology and Laboratory Medicine, Section of Hematology and Coagulation, University of Pennsylvania Eleanor S Pollak, MD, is a member of the following medical societies: American Society of Hematology College of American Pathologists , and National Multiple Sclerosis Society Editor(s): David Aboulafia, MD , Medical Director, Bailey-Boushay House; Clinical Professor, Department of Medicine, Division of Hematology, University of Washington; Francisco Talavera, PharmD, PhD

38. Hemophilia: Factor VII Deficiency It has been shown to be effective in controlling bleeding in FactorVII deficiency. Like pcc, it is treated to kill known viruses. http://www.hemophilia.ca/en/2.3.5.php

Other Factor Deficiencies Factor VII Deficiency Other Factor Deficiencies Factor VII Deficiency What is Factor VII Deficiency? Are there different types of Factor VII Deficiency? Is Factor VII Deficiency common? How is Factor VII Deficiency passed on? ... When are Factor VII concentrates infused? What is Factor VII Deficiency? Factor VII (pronounced Factor 7) Deficiency is a very rare bleeding disorder. It also goes by the name Alexander's Disease. Factor VII is a trace protein in the blood. It plays a role in the coagulation cascade, the chain reaction that is set in motion when there is an injury to a blood vessel. Factor VII is activated, or "turned on", by tissue thromboplastin. It is turned into Factor VIIa (the "a" stands for "activated"). Factor VIIa in turn activates Factor X (pronounced Factor 10) and Factor IX (pronounced Factor 9), allowing the clotting process to continue. For more information on blood clotting, see "The clotting problem in Hemophilia" In Factor VII Deficiency, this protein is present at lower levels than normal. Sometimes, there is no Factor VII at all. Are there different types of Factor VII Deficiency?

39. Hemophilia: Factor II (Prothrombin) Deficiency to control bleeding Fresh frozen plasma; Prothrombin complex concentrates (pcc)containing prothrombin and If vitamin K deficiency is the cause of the disorder http://www.hemophilia.ca/en/2.3.2.php

Other Factor Deficiencies Factor II Deficiency (Prothrombin Deficiency) Other Factor Deficiencies Factor II Deficiency (Prothrombin Deficiency) What is Factor II Deficiency? Are there different types of Factor II Deficiency? Is Factor II Deficiency common? How is Congenital Factor II Deficiency passed on? ... What treatments are available to control bleeding? What is Factor II Deficiency? Factor II (pronounced Factor 2) Deficiency is a bleeding disorder. It is due to one of two causes: a lower than normal amount of prothrombin in the blood or prothrombin which does not work properly. Prothrombin is a protein in the bloodstream, which is important in the clotting process. Factor Xa, another blood protein, changes prothrombin (Factor II) into thrombin. Thrombin, in turn, continues the coagulation chain reaction. Without prothrombin, the process breaks down. For more information on blood clotting, see "The clotting problem in Hemophilia" Are there different types of Factor II Deficiency? Yes, there are two different types. Congenital Factor II Deficiency - This is an hereditary condition. People are born with it.

40. What Is The PCC who complete the pcc but have one low ACTE/SAT/COMPASS score.Students who are stipulatedare required to enroll in a course that fulfills their deficiency each http://www.nku.edu/~aarc/restdefpcc.htm

What does it mean to be restricted or stipulated? When a student applies to NKU, the Office of Admissions will review the student's high school record and ACTE/SAT/COMPASS scores. The University has specific score cutoffs in the areas of English, Math and Reading which determine a student's admission status - Regular, Restricted or Stipulated. Students are identified as having a low ACTE score if any of the English, Math, and/or Reading subscores are less than an 18. Students with SAT scores rather than ACT scores for admission purposes must meet the following criteria: "low SAT score" in Verbal section is less than 480; "low SAT score" in Math section is less than 440. Equivalent COMPASS scores are used for students who take that test. In addition, students' records are examined to determine if they have met the Pre-College Curriculum, which is a set of specified courses completed in a high school program, as follows: English - 4 units (English I, II, III, IV) Mathematics - 3 units (Algebra I, Algebra II, and Geometry) Science - 2 units (Biology I; Chemistry I or Physics I)

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