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Galactosemia:     more books (24)

Galactosemia - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-09-28 Galactosemia - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-16 Galactosemia: Webster's Timeline History, 1917 - 2007 by Icon Group International, 2009-07-08 Is galactosemia variant Tx overkill? Or necessary? Clinically benign, long-term risks unknown.(Clinical Rounds): An article from: Pediatric News by Sherry Boschert, 2004-01-01 Gale Encyclopedia of Medicine: Galactosemia by CGC Amy Vance MS, 2002-01-01 Galactosemia: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Deanna, RN Swartout-Corbeil, 2006 Galactosemia: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Amy, MS, CGC Vance, 2005 Galactosemia by david hsia, 1969-01-01 Galactosemia in infancy: diagnosis, management, and prognosis.: An article from: Pediatric Nursing by Maureen A. Chung, 1997-11-01 Galactosemia: An entry from Gale's <i>Gale Encyclopedia of Medicine, 3rd ed.</i> by Amy, MS, CGC Vance, Teresa Odle, 2006 Genetics & Inherited Conditions: Aarskog Syndrome-galactosemia (Salem Health) Galactosemia; annotated bibliography (United States. Dept. of Health, Education, and Welfare. [DHEW publication) by Donough O'Brien, 1971 Congenital Galactosemia, a Single Enzymatic Block in Galactose Metabolism. Extract from: Science, vol. 123, 1956. by Kurt J., et al. ISSELBACHER, 1956-01-01 Dietary management of inherited metabolic disease: Phenylketonuria, galactosemia, tyrosinemia, homocystinuria, maple syrup urine disease by Phyllis B Acosta, 1976

lists with details

61. Galactosemia
    Classic galactosemia is an inherited disease. Due to a defective gene, A less severe form of this disease is Duarte galactosemia (also called  
    http://healthgate.partners.org/browsing/browseContent.asp?fileName=22824.xml&tit

62. GeneReviews: Galactosemia
    Your browser does not support HTML frames so you must view galactosemia in a slightly less readable form. Please follow this link to do so.  
    http://www.geneclinics.org/query?dz=galactosemia

63. Galactosemics.org
    This area is for general discussions related to galactosemia. This section is for discussions about galactosemia conferences, and for posting notes from  
    http://www.galactosemics.org/forums/

64. Galactosemia From PerkinElmer - USA
    The incidence of galactosemia is 114000 – 160000. The untreated disorder will cause poor development, and in the worst case fatality.  
    http://las.perkinelmer.com/Catalog/default.htm?CategoryID=Galactosemia

65. Galactosemia - Children's Hospital Boston
    Home galactosemia. Flower galactosemia. Programs that treat this condition or perform this procedure. Metabolism Program. Unfortunately, at this time,  
    http://www.childrenshospital.org/az/Site934/mainpageS934P0.html
    
    Extractions: or find by letter: A-F G-L M-R S-Z My Child Has... Home Galactosemia Galactosemia Programs that treat this condition or perform this procedure Metabolism Program Unfortunately, at this time, we are not able to provide information about this condition or procedure. However, we will be frequently adding and updating information in Child Health A to Z. So please bookmark this site and visit us again soon. Children's Hospital Boston is the primary pediatric teaching hospital of Harvard Medical School Contact Us Privacy Accessibility Give Now Children's Hospital Boston 300 Longwood Avenue Boston MA 02115

66. Galactosemia | Free Term Papers
    galactosemia galactosemia is an inborn error of metabolism. Because of energy barriers, essentially none of the chemical reactions that take place in living  
    http://www.oppapers.com/term-papers/38045.html
    
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67. Galactosemia | Free Term Papers
    galactosemia galactosemia is a genetically inherited metabolic disorder. This disorder leaves the disabled with a partial or complete lack of the enzyme  
    http://www.oppapers.com/term-papers/42272.html
    
    Extractions: Ads_kid=0;Ads_bid=0;Ads_xl=0;Ads_yl=0;Ads_xp='';Ads_yp='';Ads_xp1='';Ads_yp1='';Ads_opt=0;Ads_wrd='[KeyWord]';Ads_prf='';Ads_par='';Ads_cnturl='';Ads_sec=0;Ads_channels='ROI_Casino,ROI_Dating,ROI_Over 18,_GNM_18+,_GNM_Casino,_GNM_CollegeWeb,_GNM_Dating,_GNM_NewsInformation,_GNM_QLook,_GNM_QPlus,_GNM_RON_J,_GNM_RON_Q'; SEARCH BROWSE JOIN FOR FREE TOP LISTS ... CHUCKIII RSS Feed Custom Essays Term Papers Internships Frat ... Files Search Over 50,000 Term Papers at FratFiles.com Go Directly to FratFiles.com Silver soul's elation, for my mind is their creation. - towlieforever

68. -- Altered Metabolism Of Galactose Due To Deficient Enzyme Activity Or Impaired
    galactosemia results from the deficiency of one of three different enzymes, Classic galactosemia refers to the complete deficiency of the GALT enzyme.  
    http://pedclerk.bsd.uchicago.edu/galactosemia.html
    
    Extractions: GALACTOSEMIA Definition: Milk and dairy products contain lactose (glucose + galactose), the major dietary source of galactose. The metabolism of galactose produces fuel for cellular metabolism through its conversion to glucose-1-phosphate. Galactose also plays an important role in the formation of glycoproteins, glycolipids, and glycosaminoglycans. Galatactosemia is the altered metabolism of galactose due to deficient enzyme activity or impaired liver function resulting in elevated blood galactose concentration. Galactosemia results from the deficiency of one of three different enzymes, each with a distinct phenotype. Disorder Enzyme Deficiency Symptoms Description Classic Galactosemia Galactose-1-phospate uridyl transferase (GALT) Liver and renal dysfunction, cataracts, abnormal neurodevelopment, premature ovarian failure Most common and most severe form. Galactokinase Deficiency Galactokinase Bilateral cataracts, will resolve with dietary therapy Benign Generalized UDPgalactose-4-epimerase Deficiency Uridine diphosphate galactose 4-epimerase Similar to classic galactosemia with additional findings of hypotonia and nerve deafness Benign variant is common, when the defect is localized to red blood cells- no treatment required

69. Galactosemia
    galactosemia is a hereditary disease that is caused by the lack of a liver Final galactosemia results are faxed to the physician/health care provider  
    http://www.dhss.mo.gov/Lab/Newborn/Galactosemia.html
    
    Extractions: DHSS Home State Home Ask Us Home ... Contact Us breadCrumbs("main",">>","index.htm","crumb","crumb","crumb","0"); Galactosemia is a hereditary disease that is caused by the lack of a liver enzyme required to digest galactose. The genetic disorder is transmitted as an autosomal recessive disease. Galactose is a breakdown product of lactose, which is most commonly found in milk products. When galactose cannot be broken down, it builds up in the cells and becomes toxic. If not diagnosed and treated it can lead to diarrhea, dehydration, jaundice, hepatic failure, hypoglycemia, cataracts, developmental retardation and death. Sepsis due to E. coli seems to be particularly frequent among galactosemic neonates and is usually the cause of death. Treatment of the disease consists of withdrawal of all foods containing lactose and galactose from the diet. Prevalence in Missouri: Analyte Measured: Galactose-1-Phosphate Uridyl Transferase Reporting Results: Normal:

70. Galactosemia - YourDictionary.com - American Heritage Dictionary
    Search Mamma.com for galactosemia . TYPE IN YOUR WORD CLICK GO! Search. Normal, Definitions, Short defs. (Pronunciation Key). ga·lac·to·se·mi·a Listen  
    http://www.yourdictionary.com/ahd/g/g0012000.html

71. Galactosemia
    Health care centre, teaching and research hospital Vancouver Hospital and Health Sciences Centre in British Columbia Canada.  
    http://www.vanhosp.bc.ca/html/wellness_amdc_findout_galactosemia.html

72. BioMed Central | Full Text | The Clinical And Molecular Spectrum Of Galactosemia
    A positive diagnosis of galactosemia was made in 17 patients between the years 1980 to galactosemia is an autosomally inherited disorder of galactose  
    http://www.biomedcentral.com/1471-2431/2/7

73. Caremark.com
    galactosemia is an inherited disease in which the transformation of galactose to If galactosemia is untreated, high levels of galactose cause vomiting,  
    http://www.caremark.com/wps/portal/_s.155/5522/.cmd/ad/.pm/-/.c/1703/.ce/5535/.p

74. Icon Health Publications Galactosemia A Medical Dictionary
    Icon Health Publications galactosemia A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References,Conservative,Book Club  
    http://www.forbesbookclub.com/bookpage.asp?prod_cd=IR060

75. Disorders Associated With Carbohydrate Metabolism
    See episode 210, March 9, 1981, The Red/White Blues. Family Village on galactosemia Links to OMIM References G6PD and Favism Lactose Intolerance  
    http://www.people.virginia.edu/~rjh9u/lactase.html

76. The Columbia Encyclopedia, Sixth Edition: Galactosemia@ HighBeam Research
    The Columbia Encyclopedia, Sixth Edition galactosemia@ HighBeam Research.  
    http://www.highbeam.com/ref/doc0.asp?docid=1E1:galactsem

77. SimulConsult Cases Blog: Galactosemia
    His neonatal screening test, which showed galactosemia, was not received at the testing lab until 3 days after his death. Click hyperlinked findings in the  
    http://simulconsult.com/neurologicalsyndromes/reports/galactosemia.html
    
    Extractions: Cases Blog: Galactosemia A September 1999 account on the Save Babies Through Screening Foundation web site told the tragic story of T . He went home at 24 hours of age with plans to get his neonatal screening at 5 days of age: When we took him in for the test, the doctor realized T had jaundice and performed a test for that as well. His jaundice level was 29.8 which is critically high. T was admitted back to the hospital for four days under bili lights to bring his jaundice level down. While at the hospital, he became increasingly more lethargic , non-responsive to pain, and continuously vomited feedings. All these complaints were dismissed because they seem to be such "common" symptoms for newborns. He went home but returned within hours due to extreme lethargy and he died several days later of septicemia. His neonatal screening test, which showed Galactosemia, was not received at the testing lab until 3 days after his death. Click hyperlinked findings in the description above to see differential diagnoses for the individual finding using SimulConsult Neurological Syndromes.

78. OMIM - GALACTOSEMIA
    http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=230400

79. Entrez PubMed
    CONCLUSION The development of POF in females with galactosemia is more likely if the patient s genotype is Q188R/Q188R, if the mean erythrocyte Gal1-P is  
    http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1

80. POF Support Group: Galactosemia And Turners Syndrome
    This site provides support and information for women with Premature Ovarian Failure (POF). Endocrine disorder affecting women under 40, causes profound  
    http://www.pofsupport.org/information/resources/linkgts.htm

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