81. 3-Hydroxypropionate: Significance Of β-Oxidation Of Propionate In Patien Two patients with propionic acidemia due to a defect in propionylCoA carboxylase propionic acidemia in patients with ketotic hyperglycinemia. http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=389649

82. Inhibition By Propionyl-coenzyme A Of N-acetylglutamate Synthetase In Rat Liver propionic acidemia in patients with ketotic hyperglycinemia. A case of methylmalonic and propionic acidemia due to methulmalonylCoA carbonylmutase http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=371306

83. 3-Hydroxypropionate: Significance Of {beta} -Oxidation Of Propionate In Patients Two patients with propionic acidemia due to a defect in propionylCoA carboxylase metabolized 1-14Cpropionate to urinary methylcitrate and http://www.pnas.org/cgi/content/abstract/69/10/2807

This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Add to My File Cabinet ... Cited by other online articles PubMed PubMed Citation Articles by Ando, T. Articles by Hull, D. October 1, 1972 Toshiyuki Ando, Karsten Rasmussen, William L. Nyhan, and David Hull C]Propionate administered intravenously was metabolized to methylmalonate, to 3-hydroxypropionate, and to methylcitrate in the urine of a patient with methylmalonic acidemia. L-[U- C]Isoleucine and L-[U- C]valine were also converted to urinary methylmalonate and to 3-hydroxypropionate in the patient. Two patients with propionic acidemia due to a defect in propionyl-CoA carboxylase metabolized [1- This article has been cited by other articles in HighWire Press -hosted journals: W. Z. Martini, W. C. Stanley, H. Huang, C. D. Rosiers, C. L. Hoppel, and H. Brunengraber Quantitative assessment of anaplerosis from propionate in pig heart in vivo Am J Physiol Endocrinol Metab, February 1, 2003; 284(2): E351 - 356.

84. NORD - National Organization For Rare Disorders, Inc. Includes the synonyms, a general discussion and further resources. http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Acidemia, Pro

85. Acidemia, Propionic - St. Joseph Mercy, Ann Arbor Michigan acidemia, propionic St. Joseph Mercy Health System Hospitals serving Ann Arbor, SE Michigan, Washtenaw County, Livingston County, Wayne County, http://www.sjmercyhealth.org/12316.cfm

@import url(default.css); Online Health Information Health Information - Rare Diseases and Disorders Back to Health Library Print This Page Email to a Friend National Organization for Rare Disorders, Inc. Acidemia, Propionic Synonyms Disorder Subdivisions General Discussion Resources ... For a Complete Report Important It is possible that the main title of the report Acidemia, Propionic 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 PCC Deficiency Propionyl CoA Carboxylase Deficiency Ketotic Glycinemia Hyperglycinemia with Ketoacidosis and Lactic Acidosis, Propionic Type Disorder Subdivisions Propionic Acidemia, Type I (PCCA Deficiency) Propionic Acidemia, Type II (PCCB Deficiency) General Discussion Propionic Acidemia is a rare metabolic disorder characterized by deficiency of propionyl CoA carboxylase, an enzyme involved in the breakdown (catabolism) of the chemical "building blocks" (amino acids) of certain proteins. Symptoms most commonly become apparent during the first weeks of life and may include abnormally diminished muscle tone (hypotonia), poor feeding, vomiting, listlessness (lethargy), excessive loss of fluids from bodily tissues (dehydration), and episodes of uncontrolled electrical activity in the brain (seizures). Without appropriate treatment, coma and potentially life-threatening complications may result. In rare cases, the condition may become apparent later during infancy and may be associated with less severe symptoms and findings. Propionic Acidemia is inherited as an autosomal recessive trait.

86. Acidemia, Propionic - Synonyms Of Augusta, Georgia acidemia, propionic Synonyms - University Health Care System of Augusta, Georgia. http://www.universityhealth.org/12860.cfm

About University About Augusta Business and Industry Contact UHCS ... Nutrition Search Information on diseases and health concerns, including symptoms, treatment options, and prevention. Acidemia, Propionic Synonyms Disorder Subdivisions General Discussion Resources ... For a Complete Report Important It is possible that the main title of the report Acidemia, Propionic 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 PCC Deficiency Propionyl CoA Carboxylase Deficiency Ketotic Glycinemia Hyperglycinemia with Ketoacidosis and Lactic Acidosis, Propionic Type Disorder Subdivisions Propionic Acidemia, Type I (PCCA Deficiency) Propionic Acidemia, Type II (PCCB Deficiency) General Discussion Propionic Acidemia is a rare metabolic disorder characterized by deficiency of propionyl CoA carboxylase, an enzyme involved in the breakdown (catabolism) of the chemical "building blocks" (amino acids) of certain proteins. Symptoms most commonly become apparent during the first weeks of life and may include abnormally diminished muscle tone (hypotonia), poor feeding, vomiting, listlessness (lethargy), excessive loss of fluids from bodily tissues (dehydration), and episodes of uncontrolled electrical activity in the brain (seizures). Without appropriate treatment, coma and potentially life-threatening complications may result. In rare cases, the condition may become apparent later during infancy and may be associated with less severe symptoms and findings. Propionic Acidemia is inherited as an autosomal recessive trait.

87. Arch Neurol -- Abstract: Cerebellar Hemorrhage Complicating Methylmalonic And Pr Methylmalonic (MMA) and propionic (PPA) acidemias are inherited disorders characterized by a wide spectrum of clinical and biochemical findings. http://archneur.ama-assn.org/cgi/content/abstract/41/12/1293

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA (1998-2004) JAMA CareerNet For The Media Meetings Peer Review Congress Vol. 41 No. 12, December 1984 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Dave P Steinman L Contact me when this article is cited Cerebellar hemorrhage complicating methylmalonic and propionic acidemia P. Dave, R. G. Curless and L. Steinman Methylmalonic (MMA) and propionic (PPA) acidemias are inherited disorders characterized by a wide spectrum of clinical and biochemical findings. We report the neuropathologic findings in two young infants with MMA and PPA in which death probably resulted from cerebellar hemorrhage. When combined with a previous report of isovaleric acidemia complicated by diffuse subarachnoid and parenchymal cerebellar hemorrhage, it is apparent that

88. Health/Conditions And Diseases/Genetic Disorders/Propionic Acidemia -- The Docto Ask the doctor. Get free medical consultation and advice. Choose a medical specialist and post your question! Doctors in all medical fields are available. http://www.thedoctorslounge.net/dir/Health/Conditions_and_Diseases/Genetic_Disor

Advertisement Powered by Careerbuilder Search for: Home Humor Advertising Contact ... Links Specialties Cardiology Chest diseases Dermatology Endocrinology ... Urology Other Sections Membership Research Tools Medical Tutorials Medical Software ... Specialized Centers Headlines: The Medical Website Directory Popular Categories Popular Links Web Sites report abuse/spam url: report-abuse.dmoz.org/?cat=Health/Conditions_and_D... Dr. Greene: Breastfeeding with a Metabolic Disorder and Propionic Acidemia Breastfeeding a child with propionic acidemia is discussed in this question and answer format. url: www.drgreene.com/21_692.html eMedicine An in depth look at Propionic acidemia. url: www.emedicine.com/NEURO/topic577.htm NORD: Acidemia, Propionic Includes the synonyms, a general discussion and further resources. url: www.rarediseases.org/search/rdbdetail_abstract.htm... Propionic Acidemia Foundation The PAF is an organization that funds academic and medical research leading to better treatments and a cure of propionic acidemia, an inborn error of metabolism. url: pafoundation.com

89. مرض ارتفاع ال& The summary for this Esperanto page contains characters that cannot be correctly displayed in this language/character set. http://www.werathah.com/meta/ppa.htm

( Propionic Acidemia PPA) Aminoacids Propionic acid ) PPA ( Propionic acidemia ) ( PA ) Enzyme Am m onia ( Valine )

90. ¡i¨u¨£¿ò¶Ç¯e¯f¤@ÂI³q¡j - ¥Í¤Æ¿ò¶ÇÀËÅç«Ç The summary for this Chinese (Traditional) page contains characters that cannot be correctly displayed in this language/character set. http://ntuh.mc.ntu.edu.tw/gene/genehelp/database/disease/Propionic_acidemia_9404

¤þ»Ä¦å¯g Propionic acidemia ·J¾ã¡G³¢´f¬ ¼¶¤åº[½s¼f¡G¦¶³ÍÅïÂå®v ¯f¦]¾Ç¡G ¬°¤@¥NÁ©ʯe¯f¡A­ì¦]¬°¤þñQ°ò»²»¯ÀAßn¤Æ»¯À (propionyl-coenzyme A carboxylase) ¯Ê³´¡A¦¹»¯Àªº§@¥Î¬°¨ÏÓi°ò»Ä¥NÁ¤ÏÀ³¤¤ªº¤¤¶¡²£ª«¡G¤þ»Ä (propionic acid )Âà¤Æ¦¨¥Ò°ò¤þ¤G»Ä (methylmalonic acid)¡C µo¥Í²v¡G ¦b¬ü°ê 1/35,000~1/75,000¡A ¨Æ¹ê¤Wµo¥Í²v¥i¯à§ó°ª¡C ²±¦æ²v¤´µL§¹¾ã¤§²Î­p¦Ó¤£±o¤§ ¥i¯à¦³®a±Ú¯f¥v¡A¤×¨ä¬OµLªk¸ÑÄÀªº·s¥Í¨à¦º¤`©Î¤â¨¬¤§¶¡´¿¦³à¬»Ä¤¤¬rªºµo§@¡C¤Ö³¡¥÷ªº±wªÌ¨¨S¦³³o»ò¿E¯Pªº¯gª¬¡A¦Ó¬O¦]º¥¶i¦¡ªº¤ß´¼µo®i¿ð½w¤~±a¨Ó¨DÂå¡C ¥NÁ¤Wªºªí¼x ¯«¸g¾Ç¤Wªºªí¼x ¦å²G¾Ç¤Wªºªí¼x ¨ä¥Lªí¼x apneas §C¦åÁÞ hypoglycemia Áý­¹±¡ªp®t poor feeding ¹¦R vomiting À¦¨à´Áªº¦Ù¦×±i¤O§C¤Uinfantile hypotonia ·s¥Í¨à´ÁÅöíw neonatal seizures (¬ù30%±wªÌ) ´¼¯à¿ð½w mental retardation ©À¯]µß¯fªº­«Âеo¥Í¾É­P¸g±`©Êªº·P¬V ¼È®É©Êªºµµ½I¯f purpura ¯f²z©Ê°©§é³y¦¨°©½è²¨P ¿ò¶Ç¼Ò¦¡¡G ²£¥Í¯Ê³´¬°²Ä¤Q¤T¹ï¬V¦âÅé¤W¦ì¸m ªvÀø¡G neomycin ¡C­Y¦å¤¤®ò­È¤´µLªk±±¨î¡A»Ý­n¥H¸¡½¤³zªR§ïµ½¦å¤¤à¬»Ä»PÓi°ò»Äªº­È¡C¦]¦³¾÷»Ä°ï¿n³y¦¨ carnitine¯Ê ¥F¡A¥²¶·¸É¥R L-carnitine ¡C ªø´ÁªvÀø¤W¡A¦¹¯g±wªÌÀ³µ¹¤©¯S®í°t¤è¥¤¯» Milupa OS-1 ¡A¦¹¥¤¯»¤£§t²§¥ÕÓi»Ä (iosleucine) ¡Aõé¯óÓi»Ä (valine)¡A ¥Ò²¸Ói»Ä (methionine) ¤ÎĬÓi»Ä (threonine) ¹w«á¡G ºô¯¸Ápµ¸¤H¡G³¢´f¬ ±M¥ô§U²z «Øij¨Ï¥ÎMicrosoft IE 5.0 ¥H¤Wªºª©¥»¡A¸ÑªR«×³]©w¦b 800 x 600 ¥H¹F¨ì³Ì¨ÎÂsÄý®ÄªG

91. ¿ò¶Ç¯e¯f¿Ô¸ßªA°Èµ¡¤f The summary for this Chinese (Traditional) page contains characters that cannot be correctly displayed in this language/character set. http://www.bhp.doh.gov.tw/genetic-counseling/datebase/disease/Propionic_acidemia

¥»¯¸¦¨¥ß©v¦® ¯e¯f¶µ¥Ø¤ÎÀËÅç ¦@¥Î©Ê¿ò¶Ç¯e¯fÀËÅ綵¥Ø ¿ò¶Ç¯e¯f¶EÂ_Âà¶EªA°È ... ½u¤W¿Ô¸ß ªù¶E¿Ô¸ß¬ö¿ý ¬Ûö·s»D ºô¯¸ºûÅ@¡G ³¢´f¬ ³Ì«á§ó·s¤é´Á ¤þ»Ä¦å¯g Propionic acidemia ·J¾ã¡G³¢´f¬ ¤é´Á¡G ¼¶¤åº[½s¼f¡G¦¶³ÍÅïÂå®v ¤é´Á¡G Åý§Ú³]·Q ¦bÁc¬P¤¤ ¦³¤@Áû¬P¤Þ»â§Úªº¤H¥Í ¬ï¹L¥¼ª¾ªº¶Â·t ¯f¦]¡G ¬°¤@¥NÁ©ʯe¯f¡A­ì¦]¬°¤þñQ°ò»² Aßn¤Æ µo¥Í²v¡G ¦b¬ü°ê1/35,000~1/75,000¡A¨Æ¹ê¤Wµo¥Í²v¥i¯à§ó°ª¡C ¿ò¶Ç¼Ò¦¡¡G ¥i¯à¦³®a±Ú¯f¥v¡A¤×¨ä¬OµLªk¸ÑÄÀªº·s¥Í¨à¦º¤`©Î¤â¨¬¤§¶¡´¿¦³à¬»Ä¤¤¬rªºµo§@¡C¤Ö³¡¥÷ªº±wªÌ¨¨S¦³³o»ò¿E¯Pªº¯gª¬¡A¦Ó¬O¦]¤ß´¼µo®i¿ð½w¤~±a¨Ó¨DÂå¡C ¥NÁ¤Wªºªí¼x ¯«¸g¾Ç¤Wªºªí¼x ¦å²G¾Ç¤Wªºªí¼x ¨ä¥Lªí¼x apneas §C¦åÁÞhypoglycemia Áý­¹±¡ªp®t poor feeding ¹¦R vomiting À¦¨à´Áªº¦Ù¦×±i¤O§C¤Uinfantile hypotonia ·s¥Í¨à´ÁÅöíw neonatal seizures (¬ù30%±wªÌ) ´¼¯à¿ð½w mental retardation ©À¯]µß¯fªº­«Âеo¥Í¾É­P¸g±`©Êªº·P¬V ¼È®É©Êªºµµ½I¯fpurpura ¯f²z©Ê°©§é³y¦¨°©½è²¨P ªvÀø¡G ¹w«á¡G ¬Ûö¹ÎÅé¡G http://www.pku.org.tw

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 5     81-91 of 91    Back | 1  | 2  | 3  | 4  | 5