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Genetic Disorders General:     more books (100)

Does It Run in the Family?: A Consumer's Guide to DNA Testing for Genetic Disorders by Doris Teichler Zallen, 1997-05-01 Genetic Disorders Sourcebook: Basic Consumer Health Information About Hereditary Diseases and Disorders, Including Cystic Fibrosis, Down Syndrome, Hemophilia, ... Disease (Health Reference Series) Genetic Disorders among the Jewish People by Professor Richard Merle Goodman, 1979-06-01 Genes in Medicine: Molecular biology and human genetic disorders by I. Rasko, C.S. Downes, 1994-09-30 Advances in Gene Technology: Human Genetic Disorders: Proceedings of the 16th Miami Winter Symposium (Icsu Short Reports, Vol 1) Population Structure and Genetic Disorders: Seventh Sigrid Juselius Foundation Symposium Genetic Disorders and Pregnancy Outcome The Student With a Genetic Disorder: Educational Implications for Special Education Teachers and for Physical Therapists, Occupational Therapists, A by Diane M. Plumridge, Robin Bennett, 1993-04 Genetic Disorders, Syndromology and Prenatal Diagnosis (Advances in the Study of Birth Defects) Laurie Blum's Free Money for Childhood Behavioral and Genetic Disorders (Blum, Laurie//Free Money for Child Care Series) by Laurie Blum, 1992-10 Genetic Disorders of the Skin Jewish Genetic Disorders: A Layman's Guide by Ernest L. Abel, 2008-08-27 Maternal Serum Screening for Fetal Genetic Disorders (Contemporary Management in Obstetrics) by Sherman Elias, 1992-07 The Human Genome: Features, Variations and Genetic Disorders (Genetics - Research and Issues)

lists with details

21. Mitoblog | Everything About Mitochondrial Disease
    Blog about mitochondrial disease.  
    http://www.mitoblog.org/
    
    Extractions: Information Media ... Everything about Mitochondrial Disease RSS Aug Dr. Fran Kendall, of Virtual Medical Practice, has put together a great document to start with when faced with the decisions surrounding a muscle biopsy -┬а┬а Muscle Biospy FAQs Jun Word has it that the 2011 Symposium will be in mid-June in CHICAGO in 2011! Stay tuned for more information as we get it! Apr Vamsi Mootha, MD, PhD at Harvard speaks on behalf of Mitoaction.org about the impact of the mitochondria on many common diseases and the aging process in this video. Definitely interesting! Apr Mar Hannah Poling case On the Autism Speaks blog, a recent article was posted that I feel would be very beneficial to the mito community and the autism community to read. It looks at the relationship between f ever and mitochondrial disease as a cause for autism and autistic regression . Clearly, this is a link that needs further study and serious research.

22. Chicago Center For Jewish Genetic Disorders Genetic Alliance
    The Center is dedicated to gathering and disseminating knowledge about Jewish genetic disorders and hereditary cancers. Its mission is to educate and serve health care  
    http://www.geneticalliance.org/organization/chicago-center-jewish-genetic-disord

23. Daunorubicin - Summary Of Product Characteristics (SPC) - Electronic Medicines C
    Congenital, familial and genetic disorders. General disorders and administration site conditions. Aplasia. Death, fulminant hyperpyrexia, perivenous extravasation (immediate local pain  
    http://www.medicines.org.uk/emc/medicine/4263
    
    Extractions: eMC Medicine Guides The electronic Medicines Compendium (eMC) contains information about UK licensed medicines. Search for: select select SPCs and PILs SPCs Only PILs Only Search Medicine or Company Name Search Full Document Advanced Search One Onslow Street, Guildford, Surrey, GU1 4YS, UK Telephone: +44 (0)1483 505 515 If you are going to contact a pharmaceutical company to either discuss a medicine, or report a suspected adverse event, to ensure that you receive complete and accurate information, please make sure that you contact the company that is the Marketing Authorisation (MA) holder (or the local/ country representative) of the medicine that you are actually using. Often several companies will hold MAs for the same medicine, and the Summary of Product Characteristics (SPC) may differ. The information in a company SPC relates specifically to that company's product and it cannot be assumed that it is applicable to a product from any other company. For example the medicines may have different excipients/ formulations or licensed indications/ contraindications for use. Accessing information inappropriately may have implications for patient safety and care should be taken to confirm that the correct source is used.

24. Chicago Center For Jewish Genetic Disorders | CCJGD
    A critical effort to provide public and professional education for many of the identified Jewish genetic disorders. Find info on screening and counseling, advocacy, events and community resources.  
    http://www.jewishgeneticscenter.org/

25. First Step Therapy Centre Case Studies
    Metabolic Genetic Disorders - General Physical Disabilities and also for - Stroke Brain Injury - Multiple Sclerosis (MS) - ParkinsonтАЩs Disease and other neurological  
    http://www.first-step-therapy.com/case_studies.html

26. AGENDA OF 211TH MEETING OF CENTRAL LICENSING
    Congenital and familial/genetic disorders; General disorders and administrative site conditions; Investigations; Injury and poisoning; Surgical and medical procedures  
    http://www.dcomoh.gov.pk/downloads/211 Meeting Misc (R-II South).doc
    
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    Keep this leaflet. You may need to read it again. If you have further questions, please ask your doctor or your pharmacist. This drug has been prescribed for you personally and you should not share your drug with other people. It may harm them, even if their symptoms are the same as yours.> [For medicinal products available without a prescription] 3. BEFORE YOU

27. Encyclopedia Of Genetic Disorders
    Has information on the underlying genetic mechanism.  
    http://health.enotes.com/genetic-disorders-encyclopedia/branchiootorenal-syndrom

28. Welcome | Cochrane Cystic Fibrosis And Genetic Disorders Group
    An international network of health care professionals, researchers and consumers preparing, maintaining, and disseminating systematic reviews of randomised control trials in the treatment of cystic fibrosis and other genetic disorders.  
    http://www.liv.ac.uk/CFGD/
    
    Extractions: Activities of the Group are co-ordinated by its Editorial Base, located within the Department of Child Health, University of Liverpool and based at Alder Hey Children's NHS Foundation Trust, Liverpool, United Kingdom. Published reviews and protocols On Issue 10, 2010 of The Cochrane Library we have published one new review 'Antibiotic adjuvant therapy for pulmonary infection in cystic fibrosis'. We have also updated the following reviews: In total the Group has 94 reviews and 18 protocols published on Issue 10, 2010 of The Cochrane Library. There are also 10 registered titles currently progressing to protocol status. The production of these reviews involves a network of almost 550 authors, consumers and referees throughout the world. We very much welcome interest from new consumers, referees and potential reviewers. Further information can be obtained by contacting the group. Regularly updated evidence-based healthcare databases User guides Access options Page last updated: Tue 26th Oct 2010 10:54:41 CEST Launch of the Safe Motherhood Initiative Evidence Aid for water safety and water related diseases Live broadcast from Keystone 21 October: "Can early stopped trials result in misleading results of systematic reviews?"

29. Pedigree Project
    R 576.50 Wor The World of Genetic Disorders. General Resources - start your Internet search with these sites Search terms the disease and use the words genetics or heredity  
    http://www.wtps.org/wths/imc/Pathfinders/heredity and diseasest.htm

30. Cohen Syndrome Encyclopedia Of Genetic Disorders
    Gives the state of knowledge of demographics, genetic cause, and symptoms.  
    http://health.enotes.com/genetic-disorders-encyclopedia/cohen-syndrome

31. ACDD - Links- Conditions- Genetic Disorders
    Links Conditions- Genetic Disorders. Genetic Disorders General. Dr. Greene's HouseCalls - A discussion of medical information on trisomy, trisomy 13, genetics, and his own  
    http://acdd.org/content.asp?id=228872

32. Hydrolethalus Syndrome Encyclopedia Of Genetic Disorders
    A patient s guide to Salonen-Herva-Norio Syndrome.  
    http://health.enotes.com/genetic-disorders-encyclopedia/hydrolethalus-syndrome

33. Division Of Medical Genetics ::
    The Division offers comprehensive Clinical Genetics Services for genetic and metabolic diseases including diagnosis, management, treatment, and genetic counseling.  
    http://pediatrics.duke.edu/modules/div_medgen_clinsvcs/index.php?id=1

34. Unique - The Rare Chromosome Disorder Support Group - Www.RareChromo.org
    Support and information for families of children with rare disorders.  
    http://www.rarechromo.org/
    
    Extractions: Home About Us Meet the Team Join Us ... Site Map We comply with the HONcode standard for trustworthy health information: verify here We were awarded the Charities Online Accounts Award 2006. Click here for more information. Click on the image above to download our free information leaflets on many chromosome disorders Click on the image above to purchase Unique Christmas cards Unique is a source of information and support to families and individuals affected by any rare chromosome disorder and to the professionals who work with them. Unique is a UK-based charity but welcomes members worldwide. Membership of Unique is free but the group receives no government funding and is heavily reliant on donations and fundraising to continue its work. Please help us in whatever way you can. You may have been given a diagnosis or indication of a chromosome disorder by a geneticist or other medical professional and they may have used a medical term which is unfamiliar to you. So to help you decide if Unique is the appropriate organisation for you, we thought it would be useful to describe the different categories of rare chromosome disorder. Rare chromosome disorders can be grouped as structural disorders, numerical disorders and other miscellaneous disorders. Structural disorders include:

35. Welcome To ArabianHorses.org
    Genetic Disorders General Information. AHA Code of Ethics Revision; Genetic Disorders and the Arabian Horse An Overview Genetic Disorders and the Arabian Horse - Genetic Diseases  
    http://www.arabianhorses.org/education/genetic/default.asp
    
    Extractions: Members Login To help support research efforts, the Arabian Horse Foundation was officially re-launched at the 2007 AHA Convention. This 501(c)(3) organization focuses on several areas of funding, including equine research specifically concerning disorders and illnesses that affect the Arabian breed. In May 2008, the Foundation named a Research Advisory Panel to assist the Foundation in prioritizing research projects for potential funding. Please participate in supporting the Foundation's efforts by sending your tax deductible contributions designated for research to: Arabian Horse Foundation, Treasurer - Jim Cada, 1024 K. St., Lincoln, NE 68508. For more information on the Foundation or to make a contribution online click here Click here to access the Question and Answer Forum found on the AHA Community Forum. If you are not yet a member of the Forums, sign-up today, registration is free. UC Davis Cerebellar Abiotrophy Information Cerebellar Abiotrophy: A Review Cerebellar-Abiotrophy.org

36. GendersInX.org
    Support and encouragement for people with congenital gender variations.  
    http://GendersInX.org

37. New Jersey Psychiatric Association
    Such disorders may have many sources, both physiological (such as genetic disorders, general medical illnesses, and local brain disease or dysfunction), and experiential (such as  
    http://www.psychnj.org/psych/index.htm

38. PCD Interest Group
    Information on a rare congenital disease.  
    http://www.p-c-d.org/en/
    
    Extractions: There also is an Online Brochure with more extensive information available on this site. It is the PCD Interest Group ( PCD Belangengroep ) that devotes for the interests of the patients. If you have any questions and/or remarks... Contact us by sending an E-mail to info@p-c-d.org Online Brochure FAQ's Articles ... Links Last change on this site: Friday December 21, 2007

39. Health/Medicine
    OMIM, Online Mendelian Inheritance in Man is a catalog of human genes and genetic disorders. General Science Full Text (OmniFile) Encyclopedia of Life Sciences  
    http://www.slc.edu/library/research_tools/databases/subjects/health.htm
    
    Extractions: N.B. If a database has an EXIT option please use it, as some databases restrict the number of simultaneous users. ScienceDirect MEDLINE (PubMed) The National Library of Medicine's gateway to MEDLINE, HealthStar, OLD MEDLINE, AIDSLINE, AIDSDRUGS, AIDSTRIALS, DIRLINE, HISTLINE and HSRPROJ. OMIM OMIM, Online Mendelian Inheritance in Man is a catalog of human genes and genetic disorders. General Science Full Text (OmniFile) Encyclopedia of Life Sciences This site is intended for scientists, students, librarians and other professionals who wish to search and use ELS material prior to official publication of the full work in 2001. The full-text of over 1800 articles can be searched on this site as well as author and contents details for a further 1150 articles currently in preparation. Cochrane Library MEDLINE plus Health information. Includes information on conditions, diseases and wellness, a medical encyclopedia and more.

40. MECP2 Duplication Syndrome
    Provides information and support for families affected by this genetic condition first discovered in 2005.  
    http://www.mecp2duplication.com/cms/
    
    Extractions: Home About MECP2 Families Community ... Join The Fight! Select Language English Arabic Bulgarian Chinese (Simplified) Chinese (Traditional) Croatian Czech Danish Dutch Finnish French German Greek Hindi Italian Japanese Korean Norwegian Polish Portuguese Romanian Russian Spanish Swedish Catalan Filipino Hebrew Indonesian Latvian Lithuanian Serbian Slovak Slovenian Ukrainian Vietnamese Albanian Estonian Galician Hungarian Maltese Thai Turkish Persian Afrikaans Malay Swahili Irish Welsh Belarusian Icelandic Macedonian Yiddish Main Menu Latest Updates My name is Pam Albert and I am the mother of 3 children тАУ Amber, Noah and Braden.┬а Noah passed away on March 24, 2006...a month away from his 6 th birthday. At the time of his passing, he had not been given a diagnosis, despite our efforts of having him seen by many doctors and put through numerous tests.┬а Doctors suspected that he had a mitochondrial disorder. On July 21, 2004, I was blessed with another son, Braden.┬а We knew that something was wrong when we noticed he wasnтАЩt tracking items with his eyes, was very floppy and not achieving milestones such as sitting and crawling.┬а When Braden was 2 years old, he was given the diagnosis of MECP2

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