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

1. Homocystinuria MedlinePlus Medical Encyclopedia
homocystinuria is an inherited disorder that affects the metabolism metabolism of the amino acid amino acid methionine. Causes
http://www.nlm.nih.gov/medlineplus/ency/article/001199.htm

2. OMIM Homocystinuria Due To Cystathionine Beta-Synthase Deficiency
Technical article from Online Mendelian Inheritance in Man.
http://www.ncbi.nlm.nih.gov/omim/236200

3. Patient UK Homocystinuria
Factsheet on this metabolic disorder, its description, pathophysiology, epidemiology, clinical findings, presentation, investigations, complications, management, prognosis and differential diagnosis.
http://www.patient.co.uk/doctor/Homocystinuria.htm

4. Homocystinuria - Wikipedia, The Free Encyclopedia
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://en.wikipedia.org/wiki/Homocystinuria

5. Homocystinuria - WrongDiagnosis.com
homocystinuria symptoms, causes, diagnosis, and treatment information for homocystinuria (homocystinuria) with alternative diagnoses, fulltext book chapters, misdiagnosis
http://www.wrongdiagnosis.com/medical/homocystinuria.htm

6. NORD Homocystinuria
Offers alternative names, a general discussion and further resources.
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Homocystinuri

7. Homocystinuria - Genetics Home Reference
homocystinuria is an inherited disorder in which the body is unable to process certain building blocks of proteins (amino acids) properly. The most common form of the condition
http://ghr.nlm.nih.gov/condition=homocystinuria

8. Homocystinuria
ekonsil is an online health community providing a large database of health articles, news, post from users and and a fulltext search.
http://www.ekonsil.com/Homocystinuria

9. HOMOCYSTINURIA
Disease Name homocystinuria CYSTATHIONINE BETASYNTHASE DEFICIENCY, CBS DEFICIENCY, homocystinuria, PYRIDOXINE-RESPONSIVE Classification Sulfur amino acid disorder Inheritance
http://oregon.gov/DHS/ph/nbs/docs/homocys.pdf

10. Homocystinuria EMedicine Dermatology
Overview homocystinuria is an inherited autosomal recessive defect in methionine metabolism that is caused by a deficiency in cystathionine synthase. This defect leads to a
http://emedicine.medscape.com/article/1115062-overview

11. Homocystinuria - Definition
homocystinuria, also known as Cystathionine beta synthase deficiency, is inherited disorder of the metabolism of the amino acid methionine. It is inherited an autosomal recessive
http://www.wordiq.com/definition/Homocystinuria

12. Homocystinuria Definition From Answers.com
A hereditary disease characterized by a deficiency of the enzyme serine dehydratase causing incompletely dislocated lenses after the age of 10, thromboembolisms, and usually
http://www.answers.com/topic/homocystinuria

13. Homocystinuria - Wikidoc
You don't need to be EditorIn-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this
http://www.wikidoc.org/index.php/Homocystinuria

14. Genetic Disorders The Links To Diet
Explores the role of diet in birth defects and genetic disorders. Includes nutritional links to disorders such as Down syndrome, cerebral palsy, homocystinuria, and cystic fibrosis.
http://www.ctds.info/genetic_disorders.html

15. Homocystinuria - Symptoms, Diagnosis, Treatment Of Homocystinuria
Free articles and multimedia from The NY Times, including information on symptoms, diagnosis, treatments, tests, and surgical procedures, as well as current news and interviews
http://health.nytimes.com/health/guides/disease/homocystinuria/overview.html

16. Homocystinuria
This page includes the following topics and synonyms homocystinuria.
http://www.fpnotebook.com/Endo/Metabolism/Hmcystnr.htm

17. Homocystinuria - Treatment
homocystinuria Treatment, homocystinuria is an inherited disorder that affec Treatment There is no cure for homocystinuria. However, many people respond to high doses of
http://www.umm.edu/ency/article/001199trt.htm

18. Homocystinuria - Content Viewer
Definition. homocystinuria is an inherited disorder involving the metabolism of an amino acid called methionine (MET). Amino acids are the building blocks of protein.
http://www.svmh.com/health/content.aspx?chunkiid=11776

19. Homocystinuria Treatment Medication - EMedicine Dermatology
Treatment homocystinuria is an inherited autosomal recessive defect in methionine metabolism that is caused by a deficiency in cystathionine synthase. This defect leads to a
http://emedicine.medscape.com/article/1115062-treatment

20. Surgical Hospital Of Oklahoma - Homocystinuria
Definition. homocystinuria is an inherited disorder involving the metabolism of an amino acid called methionine (MET). Amino acids are the building blocks of protein.
http://www.sh-ok.com/apps/HealthGate/Article.aspx?chunkiid=11776

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