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Homocystinuria: more detail | ||||
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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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