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Homocystinuria:     more detail

Homocystinuria: Webster's Timeline History, 1966 - 2007 by Icon Group International, 2009-02-20 Homocystinuria: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Renee, MS Laux, 2005 Homocystinuria - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-20 Homocystinuria: A Risk Factor of Premature Vascular Disease by G.H.J. Boers, 1986-12 Homocystinuria: Clinical, biochemical and genetic aspects of cystathionine s-synthase and its deficiency in man (Acta paediatrica Scandinavica) by Flemming Skovby, 1985 Dietary management of inherited metabolic disease: Phenylketonuria, galactosemia, tyrosinemia, homocystinuria, maple syrup urine disease by Phyllis B Acosta, 1976 Homocysteine: An entry from Gale's <i>Gale Encyclopedia of Medicine, 3rd ed.</i> by Tish, A.M. Davidson, 2006

lists with details

21. Homocystinuria Symptoms, Diagnosis, Treatments And Causes
    homocystinuria information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.  
    http://www.wrongdiagnosis.com/h/homocystinuria/intro.htm

22. Homocystinuria
    Disorders of Amino Acid Metabolism Merck Manual, Home Edition; homocystinuria Illinois Department of Public Health; homocystinuria Genetics Home Reference  
    http://www.noah-health.org/en/genetic/conditions/homocyst.html

23. Newborn Screening Program - Homocystinuria
    All siblings of infants diagnosed with homocystinuria should be tested; and genetic counseling services should be offered to the family. Treatment. Early diagnosis and prompt  
    http://www.idph.state.il.us/HealthWellness/fs/homocystinuria.htm

24. Wilmington Health - Homocystinuria. Homocystinuria Is An
    homocystinuria. Christiana Care Hospitals, Wilmington/Newark area, DE, PA, NJ, MD homocystinuria is an inherited disorder that affects the metabolism of the amino acid methionine  
    http://www.christianacare.org/12349.cfm

25. Homocystinuria - Scripps Health - San Diego
    Causes, incidence, and risk factors. homocystinuria is inherited in families as an autosomal recessive trait. This means that the child must inherit the defective gene from  
    http://mobile.scripps.org/articles/3544-homocystinuria

26. Homocystinuria Caused By Cystathionine Beta-Synthase Deficiency
    GeneReviews designates a molecular genetic test as clinically available only if the test is listed in the GeneTests Laboratory Directory by either a US CLIAlicensed laboratory  
    http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=homocystinuria

27. Homocystinuria Overview - References, Advice, News, Videos, Coping
    Learn more about homocystinuria. Find the Web's best health guides, medical reports, news, videos and tools for homocystinuria. Share homocystinuria experiences and get advice  
    http://www.righthealth.com/topic/Homocystinuria

28. Homocystinuria Psychiatry At NYU Langone Medical Center
    homocystinuria is an inherited disorder involving the metabolism of an amino acid called methionine (MET). Amino acids are the building blocks of protein.  
    http://psych.med.nyu.edu/conditions-we-treat/conditions/homocystinuria

29. Homocystinuria Medical Information
    Article about homocystinuria. Includes illustrations and topical information provided by ADAM and Drugs.com.  
    http://www.drugs.com/enc/homocystinuria.html

30. Homocystinuria - Medpedia
    The information on this page is seed content provided by an organization. Please help improve this Article by adding to it. If you are a physician or PhD, learn how to edit. If  
    http://wiki.medpedia.com/Homocystinuria

31. Homocystinuria - Psychology Wiki
    homocystinuria, also known as Cystathionine beta synthase deficiency, is an inherited disorder of the metabolism of the amino acid methionine, often involving cystathionine  
    http://psychology.wikia.com/wiki/Homocystinuria

32. Kaiser Permanente Genetics Northern California
    homocystinuria is an inherited disorder that occurs when the body lacks an enzyme needed to break down protein. When the enzyme is missing, homocysteine builds up in the body  
    http://mydoctor.kaiserpermanente.org/ncal/specialty/genetics/resources/condition

33. Homocystinuria - Definition Of Homocystinuria In The Medical
    homocystinuria /ho mo cys tin uria/ (sis″tin-u re-ah) excessive homocystine in the urine, having various causes, some genetic; symptoms include developmental delay  
    http://medical-dictionary.thefreedictionary.com/homocystinuria

34. Homocystinuria Facts
    A fact sheet that briefly describes homocystinuria in infants and young children, its symptoms, treatments, and general outcomes.  
    http://www.doh.wa.gov/EHSPHL/PHL/Newborn/homocystinuria.htm

35. Homocystinuria - Overview
    homocystinuria Overview, homocystinuria is an inherited disorder that affec Causes, incidence, and risk factors homocystinuria is inherited in families as an  
    http://www.umm.edu/ency/article/001199.htm

36. Homocystinuria Definition - Medical Dictionary Definitions Of
    Online Medical Dictionary and glossary with medical definitions  
    http://www.medterms.com/script/main/art.asp?articlekey=3776

37. Homocystinuria (pathology) Britannica Online Encyclopedia
    homocystinuria (pathology), hereditary metabolic disorder involving methionine, a sulfurcontaining essential amino acid. The metabolic sequence of methionine normally begins  
    http://www.britannica.com/EBchecked/topic/270464/homocystinuria

38. Homocystinuria - NewbornScreening.Com
    Condition homocystinuria homocystinuria is caused when a baby is unable to use the amino acid methionine found in proteins of foods. This disorder can lead to mental  
    http://www.newbornscreening.com/cms/Homocystinuria.shtml

39. AllRefer Health - Homocystinuria Treatment Expectations
    homocystinuria Cystathionine beta synthase deficiency information center covers Definition, Disorders, Overview, Causes, Risk Factors, Symptoms Signs, Diagnosis Tests  
    http://health.allrefer.com/health/homocystinuria-treatment.html

40. Homocystinuria
    homocystinuria, also known as Cystathionine beta synthase deficiency or CBS deficiency, is an inherited disorder of the metabolism of the amino acid methionine, often involving  
    http://health.kosmix.com/topic/Homocystinuria

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