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Genetic Disorders General:     more books (100)

The Gale Encyclopedia of Genetic Disorders (2 Volume Set) Genetic Disorders (Opposing Viewpoints) by Katherine Swarts, 2009-03-30 Genetic Skin Disorders (Oxford Monographs on Medical Genetics) by Virginia Sybert, 2010-06-09 Genetic Disorders of Human Sexual Development (Oxford Monographs on Medical Genetics) by Leonard Pinsky, Robert P. Erickson, et all 1999-06-17 Handbook of Genetic Communicative Disorders Handbook of Neurodevelopmental and Genetic Disorders in Children Genes, Brain and Development: The Neurocognition of Genetic Disorders (Series for the International Neuropsychological Society) The Encyclopedia of Genetic Disorders and Birth Defects (Facts on File Library of Health and Living) by James Wynbrandt, Mark D. Ludman, 2008-02-28 Outcomes in Neurodevelopmental and Genetic Disorders (Cambridge Child and Adolescent Psychiatry) Genetic Diagnosis of Endocrine Disorders Genetic Disorders Among Arab Populations The Gale Encyclopedia of Genetic Disorders Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects Life Span Development in Genetic Disorders: Behavioral and Neurobiological Aspects

lists with details

1. Inherited Genetic Disorders, General Policy
   BlueCross BlueShield of Tennessee Medical Policy Manual. General Policy for Inherited Genetic Disorders. PURPOSE. To establish a basis for determining the medical necessity of  
   http://www.bcbst.com/MPManual/General_Policy_for_Inherited_Genetic_Disorders.htm
   
   Extractions: BlueCross BlueShield of Tennessee Medical Policy Manual General Policy for Inherited Genetic Disorders PURPOSE To establish a basis for determining the medical necessity of genetic testing. DESCRIPTION Genetic testing involves the analysis of human DNA, RNA, chromosomes, proteins, and certain metabolites. These tests are used to detect certain hereditary diseases. When used in clinical settings, these tests can be used to predict risk of disease, identify carriers, and formulate prenatal diagnosis/prognosis. POLICY THE FOLLOWING POLICIES HAVE BEEN REVIEWED. PLEASE REFER TO THE POLICY TO DETERMINE MEDICAL APPROPRIATENESS. DIAGNOSTICS: Analysis of Human DNA in Stool Samples as a Technique for Colorectal Cancer Screening Cytochrome p450 Genotyping Gene Expression Profiling Assays as a Technique to Determine Prognosis for Managing Breast Cancer Treatment Gene-based Tests for Screening, Detection, and/or Management of Prostate Cancer Genetic Testing: Alzheimer's Disease Genetic Testing: BRCA1 or BRCA2 for Breast or Ovarian Cancer Genetic Testing: Congenital Cardiac Channelopathies Genetic Testing: Cutaneous Malignant Melanoma Genetic Testing: Cystic Fibrosis Genetic Testing:

2. INSTITUTE OF MOLECULAR BIOLOGY BIOTECHNOLOGY
   Molecular Aspect of Biodiversity General Genomics Immunology Semester 1 Semester 2 Year 2 Semester 3 Semester 4 Microbial Genetics Cell Signaling Transduction Genetic Disorders General  
   http://uol.edu.pk/wp-content/uploads/2010/06/Institute-of-Molecular-Biology-Biot

3. 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
   
   Extractions: The Role of Diet in Genetic Disorders Many researchers and support groups state that birth defects and genetic disorders, especially connective tissue disorders such as Marfan syndrome osteogenesis imperfecta and Ehlers-Danlos syndrome , can't possibly be cured through diet because they are inherited genetic disorders. This conclusion is invalid simply because many birth defects and inherited genetic disorders have been found to be improved, or even cured, through diet. The old school of thinking that a birth defect or inherited disorder had to be caused by a single gene is no longer widely held in medical circles. The breakthrough concept in research is that many birth defects and inherited disorders are influenced by both genes and environmental factors, especially nutrition. Genes may make people susceptible to certain defects and disorders, but they are often only a part of the picture. "Genes are not necessarily destiny. They are influenced by the chemistry of what we consume." - article on

4. Genetic Screening Directory
   Information and Resources for all Jewish Genetic Diseases.  
   http://www.mazornet.com/genetics/geneticscreeningdirectory.htm
   
   Extractions: A Layman's Guide Today is: jewish genetic diseases,tay-sachs,blooms disease,neimann-pick,chron's disease supervision,kosher directory GENERAL INFO Home Page Genetic Screening Labs A Brief Key to Genetics JEWISH GENETIC DISEASES Beta Thalassemia Bloom's Syndrome Canavan Disease Crohn's Disease ... Bookstore JEWISH GUIDES Jewish Living Guide Bar Mitzvah Guide Jewish Wedding Guide Jewish Holidays ... Infertility and Judaism INFORMATION Advertise With Us About Us Genetic Screening - A Partial Directory

5. Department Of Molecular Biology And Genetics
   Other publications (cancer, genetic disorders, general) BuyukderimOzcelik I, z elik T. Science flourishes in a secular democracy. Nature 433355 (2005).  
   http://www.fen.bilkent.edu.tr/~bilmbg/Research/groups/TayfOzc Publications.htm
   
   Extractions: Tayfun Ozcelik Lab Specialty in Medical Genetics Dissertation SYP1 ve SYP2 genlerinin kromozomal lokalizasyonları, 8/1990, Uta Francke, Stanford University. Chapters in books Özçelik T., "Moleküler Genetikte Temel Kavramlar" in OBSTETRİK: Maternal·Fetal Tıp ve Perinatoloji (Edited by MS Beksaç, N. Demir, A. Koç). pp. 641-51, Ankara: Medical Network, (2001). Hüner, M. Demirkol, N. Çine, T. Baykal, G. Çarbat, M. Çalışkan, N. Aydınlı, M. Özmen,Y. Seçkin, Özçelik T,. "The PAH Splicing Mutation IVS10nt546 in Late Diagnosed PKU Patients is Associated with Hypsarrytmia", "Diagnosis and Treatment of Inborn Errors of Metabolism: Contributions to an Equal Opportunity for Children in Asia and Europe" M. Demirkol and Y.S. Shin .eds., 79-84, Published by the Turkish Society for PKU. Istanbul Branch, (1996). Özçelik T, N. Çine, G. Hüner, T. Baykal, G. Şarbat, M. Demirkol. "Molecular Genetic Approaches to the Diagnosis of Phenylketonuria in Istanbul", "Diagnosis and Treatment of Inborn Errors of Metabolism: Contributions to an Equal Opportunity for Children in Asia and Europe" M. Demirkol and Y.S. Shin .eds., 73-78, Published by the Turkish Society for PKU. Istanbul Branch, (1996). Reviews Özçelik T., "Farmakogenetik" Dokuz Eylül Tıp Fak Der, (2001).

6. Your Genes, Your Health
   The DNA Learning Center s multimedia guide to genetic disorders. Complete in depth articles about each disease listed.  
   http://www.ygyh.org/
   
   Extractions: DNA Learning Center Home MORE DNALC SITES: DNA Interactive Eugenics Archive DNA from the Beginning Inside Cancer ... NEW! Your Genes, Your Health Blog! Olive Oil and Nutrigenomics The effect of foods on gene expression is a fairly new area of science termed nutrigenomics. Many people are highly interested in how they may protect or prevent disease or conditions by applying diets appropriate to ones genetic make-up. Although early in its stages nutrigenomics has identified some very interesting findings. [...] GO TO BLOG Explore Inside Cancer : A Multimedia Guide to Cancer Biology . The site features interviews with researchers and stunning animations on the biology of cancer. The information within this web site is for educational purposes only, and should not be used as medical advice. A physician should be consulted for any diagnosis and treatment options.

7. PTC Therapeutics — Genetic Disorders: Ataluren
   Ataluren for Genetic Disorders Ataluren (PTC124 ) is an investigational drug designed to enable the formation of a functioning protein in patients with genetic disorders due to a  
   http://www.ptcbio.com/3.1.1_genetic_disorders.aspx

8. Introduction To MedDRA And Its Use
   18 Other (Cause/Association) Congenital, familial and genetic disorders General disorders and administration site conditions Infections and infestations Injury, poisoning and procedural  
   http://www.hptn.org/web documents/AnnualMeeting2006/TuesPresentations/MedDRAtrai

9. Alkaptonuria - Wikipedia, The Free Encyclopedia
   Encyclopedia article on this rare inherited genetic disorder.  
   http://en.wikipedia.org/wiki/Alkaptonuria
   
   Extractions: Homogentisic acid ICD E ILDS ... Alkaptonuria Alkaptonuria black urine disease or alcaptonuria ) is a rare inherited genetic disorder of phenylalanine and tyrosine metabolism. This is an autosomal recessive condition that is due to a defect in the enzyme homogentisate 1,2-dioxygenase EC ), which participates in the degradation of tyrosine. As a result, a toxic tyrosine byproduct called homogentisic acid (or alkapton) accumulates in the blood and is excreted in urine in large amounts(hence -uria ). Excessive homogentisic acid causes damage to cartilage ochronosis , leading to osteoarthritis ) and heart valves as well as precipitating as kidney stones . Treatment with nitisinone , which suppresses homogentisic acid production, is being studied. Alkaptonuria is more common in Slovakia and the Dominican Republic than in other countries. Alkaptonuria is often asymptomatic , but the sclera of the eyes may be pigmented (often only at a later age) , and the skin may be darkened in sun-exposed areas and around sweat glands ; sweat may be coloured brown. Urine may turn brown if collected and left exposed to open air, especially when left standing for a period of time.

10. Health > Conditions And Diseases > Genetic Disorders
    The inherited disorder, or even genetic disease is a disease caused by abnormal expression of one or even additional cistron within the individual stimulating the clinical phenotype.  
    http://genetic-disorders.generalanswers.org/
    
    Extractions: The inherited disorder , or even genetic disease is a disease caused by abnormal expression of one or even additional cistron within the individual stimulating the clinical phenotype. There are the total of imaginable drives for hereditary disease: It can be from either the mutation in a factor, effecting its work. Triplet expansion repetition mutations could induced Fragile X syndrome or Huntington's disease, by modification of gene expression or even benefit of work, severally. Defective cistron come typically inherited from either a parents. In that pack, the congenital disease is referred to as a congenital disease . This could typically happen unexpectedly after 2 hardy carriers of the defective recessive gene reproduce, but can likewise happen whilst a defective factor is dominant. Single gene disorders The total of congenital disease come due to the vary of one gene , resulting within an enzyme or other protein thalassemia appearing to have enhanced trend lines to malaria . Many inherited disorder come sex-linked, meaning that they afflict a single sex good deal extra commons than a more because a mutation is placed on the X (or even, seldom, on the Y) chromosome.

11. Master Index
    A Abatacept Abdominal Aortic Aneurysm, Endovascular Stent Grafting Abdominoplasty / Panniculectomy / Lipectomy Ablation Treatments for Barrett’s Esophagus  
    http://www.bcbst.com/MPManual/!SSL!/WebHelp/Welcome.htm
    
    Extractions: Medical Policy Manual Master Index A B C D ... Z A Abatacept Abdominal Aortic Aneurysm, Endovascular Stent Grafting Abdominoplasty / Panniculectomy / Lipectomy Ablation Treatments for Barrett’s Esophagus ... Alimta® Allergy Immunotherapy, Allergy Testing, Capecitabine ... CardioVAD™ Cardioverters, Carimune® NF Carotid Intimal-Medial Thickness (IMT), Ultrasonographic Measurements as an Assessment of Subclinical Atherosclerosis

12. Jeans For Genes - Changing The World For Children With Genetic Disorders
    Australian member of parliament, Maria Vamvakinou, announces a day to promote awareness of genetic disorders.  
    http://www.jeansforgenes.com/

13. General Resources - Sciences, Life Sciences, Medicine, Genetic Disorders, Genera
    (General Resources)StudySphere Educational Resource for language school, study abroad, education online, education, school, high school, career education, business school, driver  
    http://www.studysphere.com/Site/Sphere_3561.html

14. Has Anyone Here Donated (or Considered) Eggs? - Bodybuilding.com Forums
    I understand that they want someone to be of good genetic health ie no family history of genetic disorders, general good health, and even someone with a certain look to them (tall  
    http://forum.bodybuilding.com/showthread.php?t=120423671

15. DEBRA Canada 1-800-313-3012
    Includes articles, news, and information about this genetic disorder.  
    http://www.debracanada.org/
    
    Extractions: Email DEBRA Canada FOLLOW US ON A small group of relatives and friends of EB patients founded DEBRA Canada in 1998. That informal group has evolved into a Board of 10 people who meet monthly to fulfill the association’s goals. DEBRA Canada’s goals are: * Be a source of authoritative information for EB families. * Support EB families and give them a sense of community. * Provide funding for the unique medical care needs of EB families. * Heighten awareness of EB in Canada. * Make available funding for research in the hope that there will one day be a cure for all forms of EB While the largest group of DEBRA Canada’s members and volunteers are located in Southern Ontario, our membership crosses Canada from coast to coast. If you have EB or know someone who does, please subscribe – or encourage them to subscribe – to our mailing list. You will receive the association’s newsletter, which is full of current, practical information, and events announcements. We need to know you are out there. We want to help.

16. Genetic Disorders - General Practice Notebook
    In general, genetic disorders can either be problems with whole or part of a chromosome, or problems at the level of the gene. The latter group divides into the autosomal and  
    http://www.gpnotebook.co.uk/simplepage.cfm?ID=-1925906425

17. GENERAL CLINICAL MANAGEMENT OF PREGNANT SUBSTANCE USING WOMEN
    British Columbia Reproductive Care Program November, 1999 Page 1 of 8 Substance Use Guideline 3 GENERAL CLINICAL MANAGEMENT OF PREGNANT SUBSTANCE USING WOMEN INTRODUCTION This guideline is  
    http://www.perinatalservicesbc.ca/sites/bcrcp/files/Guidelines/SubstanceUse/Guid

18. MCAD Deficiency (MCADD) - Supplemental Screening Could Save Your Childs Life.
    Dedicated to raising awareness of the genetic disorder known as MCAD deficiency and the importance of early detection.  
    http://www.mcadangel.com
    
    Extractions: Alexis' MCADD Story A lexis had just turned 8 years old when a silent and deadly killer called MCADD swiftly took her life. Her "Birthday Girl" ribbon still hung on her bedroom door. She had a 5 month-old baby sister that she had been wishing for ever since she learned what a baby sister was. Alexis had no previous symptoms or serious illnesses, and there was no reason for her family to think she was anything but perfectly healthy. She led a normal, active life as a second grader at Southeast Elementary in Parkville, MO. She took gymnastics and played soccer and softball. She loved her family, and she loved her life. Alexis stayed home from school on March 6 with the stomach flu. The next morning she was found in her bed, unconscious and unresponsive.

19. General Resources - Education Resource - StudySphere
    Congenital, Hereditary, and Neonatal Diseases and Abnormalities Votes0 Start ki.se Education Research Library About Karolinska Institutet Search ki.se Search staff About  
    http://www.studysphere.com/education/Genetic-Disorders-General-Resources-3561.ht

20. MEDICINES CONTROL COUNCIL
    Congenital and familial/genetic disorders; General disorders and administrative site conditions; Investigations; Injury and poisoning; Surgical and medical procedures  
    http://www.mccza.com/genericDocuments/2.16_PI_for_human_medicines_Aug09_v3.doc

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