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Genetic Disorders General:     more books (100)

FAMOUS PEOPLE AND GENETIC DISORDERS: FROM MONARCHS TO GENIUSES- A PORTRAIT OF THEIR GENETIC ILLNESSES by Nicola C Ho, 2007-02-07 Living with Genetic Disorder: The Impact of Neurofibromatosis 1 by Joan Ablon, 1999-08-30 Genetic Disorders and the Fetus: Diagnosis, Prevention, and Treatment Genetics of Mental Disorders: What Practitioners and Students Need to Know by Stephen V. Faraone Phd, Ming T. Tsuang, et all 2001-12-15 Genetics of Movement Disorders by Stefan M. Pulst, 2002-10-17 Medical Genetics: Its Application to Speech, Hearing, and Craniofacial Disorders (Genetics and Communication Disorders) by Nathaniel H. Robin, 2008-02-01 Arab Genetic Disorders: A Layman's Guide by Ernest L. Abel, 2003-02-10 Genetics and Psychiatric Disorders Inherited Disorders of the Skeleton (Genetics in Medicine and Surgery) by Peter Beighton, 1988-10 The Genetics of Mood Disorders (Johns Hopkins Series in Contemporary Medicine and Public Health) by Dr. Ming T. Tsuang MD PhD DSc, Dr. Stephen V. Faraone PhD, 1990-05-01 Handbook of Genetic Skin Disorders by Fred M. Novice MD, Daniel W. Collison MD, et all 1994-01-15 The Genetics of Neurological Disorders by Michael Baraitser, 1997-12-15 The Genetics of Locomotor Disorders (Monographs on Medical Genetics) by Cedric Oswald Carter, T.J. Fairbank, 1974-09-26 Genetics of Hematological Disorders by Christos S. Bartsocas, 1991-12-01

lists with details

41. HON Mother & Child Glossary, G
    Genetic disorders . General anaesthesia, during Birth . Generalised Anxiety Disorder . Genital herpes  
    http://www.hon.ch/Dossier/MotherChild/glossary/g.html

42. Genetic Diseases
    Provides information on a number of genetic and rare diseases.  
    http://www.genetic-diseases.net
    
    Extractions: @import url( http://www.genetic-diseases.net/wp-content/themes/classic/style.css ); The four types of (human) Genetic diseases are: 1) Single-gene/monogenic Genetic Diseases: In this category the starting point is a mutation/change in one gene. The next question is how a change in the sequence of a single gene can cause severe disorders. Genes code for proteins which are some of the most important tools for the living beings, and also take place in the structures of the cells. The results of a mutation that happens in a part of gene that codes for a functional part of a protein are unwelcome. 2) Multifactorial/Polygonic Genetic Diseases: The second type of human genetic diseases is caused by mutations in more than one genes. The environment combines with these mutations in order these diseases to appear. We can easily conclude that polygenic disorders are more complicated than the previous type (single gene diseases). These abnormalities are also difficult to analyze, because there are many factors that researchers should take into consideration in order to reach to some useful conclusions. Many well known chronic diseases are Multifactorial Genetic Diseases. Everybody knows Alzheimer, diabetes, obesity and arthritis. Besides many cancer types are caused by multi mutations. 3) Chromosomal Genetic Diseases: Chromosomes are big DNA molecules composed from genes. The chromosomes are located in the cell nucleus. Abnormalities in the structure, number (and not only) of the chromosomes can cause some of the most dangerous genetic disorders. This type of disorders seem to be much easier to observe because they are, sometimes, detected by examination with microscope. Down Syndrome is the most well known disease caused by chromosomal abnormalities.

43. Reference Section Finder
    Genetic disorders; General health and medical guides Merck, Mayo Clinic; University medical letters; Sample questions for this type of resource. I need advice on how to find the best  
    http://www.ohsu.edu/xd/education/library/research-assistance/reference-finder.cf
    
    Extractions: Suggest Purchase This resource is intended to help you understand why the OHSU Library Reference Collection is divided into sections and how to find what you need. To locate a specific title in the Reference Collection you will need the section number and the call number , which are both found in the catalog The dictionary section contains a wide range of medical, scientific, and general-interest dictionaries. See Section 6 for foreign language dictionaries. What is a prone board? What do you call it when you are afraid of ghosts? Where is a picture of an ingrown toenail?

44. Noonan's Syndrome [GUCH]
    Account of her life with the disorder.  
    http://www.guch.org.uk/experiences/stories/subject/noonans
    
    Extractions: You are here: Home Living with a Heart Defect Members Stories Sorted by Subject By Michelle Ellis I am almost 21 years old and was born in Brussels. I was a prem. baby.. born by caesarean at 33 weeks. I was born with a hole in my heart, mild PS (which I still have), ptosis, strabismus. They didn't operate on my heart till I was 4 years old when they closed the ASD I had. I also had a series of operations for my squint and ptosis. The early years were very difficult naturally. I apparently was a very stubborn baby that would not eat and would be sick! I was bad with lumpy food as well (?!) Those first few years I was sick quite a lot with ear infections and tonsillitis, bronchitis etc. etc. I was also very short, and low weight was a problem for a short while. I find it hard to concentrate also and was bullied quite a lot. It was 2 years ago now that NS started to become a familiar term to me. I quickly found The Noonan Syndrome Support Group. I receive a great amount of support from this group and am a member of the ListServer. In October last year I attended the conference organised by this group. It was amazing! I met people like me, people who understood me. I shared laughs, tears of compassion and understanding and our hopes and fears for the future. The doctors really wanted to learn what WE had gone through as kids living with this little known disorder to help our kids now and the future. Dr Noonan was there and I talked to her! I never thought I'd be able to meet her, and here I was in the USA talking to THE Dr Noonan, who has tirelessly researched this disorder.

45. Lending Library
    genetic disorders general health hemophilia hospital juvenile arthritis learning disabilities mental health parents and professionals mental health - children  
    http://www.nhfv.org/LendingLibrary.html

46. Frankiepants.com
    Personal site about a child with this disorder. Provides details about the condition.  
    http://www.frankiepants.com
    
    Extractions: Thursday, May 20, 2010 Hi, everyone! Tomorrow, May 21st, Frankie will be turning 7 YEARS OLD! WOW!! He has grown out of "baby"... out of "toddler"... into my little man. We're hoping for nice weather this weekend so we can take him to his most favorite place... the beach. I know tomorrow will be beautiful, but Frank & I may end up taking one for the team if the temperature drops on Saturday! Frankie absolutely LOVES the beach and the pool. He does not care AT ALL how cold the water is. He truly missed his calling as a Navy Seal! We have started to wean Frankie off of his steroids (again). This time, we are hoping that he won't have to go right back on it again. If we are successful, we can wean him off of the Pepcid, and then maybe the Reglan and Creon. I'm not going to get my hopes up just yet... but we are getting there. On a much more somber note, I have to take the time to pay respect to two wonderful people in my life who passed suddenly last week. My cousin Hazel (Father's side) and my aunt Paddy (mom's sister). Hazel was too young to leave this world. She had just had a baby girl, Arianna, four weeks ago. Her birthday was Mother's Day. She deserved to be here much longer than this. Her daughter deserved to have her more than four weeks as her mother on this earth. Her husband deserved to spend the rest of their lives together, growing old, raising children, spoiling grandchildren... I am still grieving. I am going to miss her funeral tomorrow. I am going to miss her forever.

47. PhD Program In Molecular And Regenerative Medicine
    PhD program in Molecular and Regenerative medicine Welcome to the web site of the PhD program in Molecular and Regenerative Medicine, offered by University of Modena and Reggio  
    http://www.sdmmr.unimore.it/
    
    Extractions: PhD course in Molecular and Regenerative Medicine You are using an unsupported browser : the site will not function properly. To get a supported browser, click here click here The PhD school in Molecular and Regenerative Medicine, PhD program in Molecular and Regenerative Medicine includes two main thematic areas:

48. Ectodermal Dysplasia Society
    Information about the organization as well as the ED condition. Includes links, news articles and contact details.  
    http://www.ectodermaldysplasia.org/
    
    Extractions: Ectodermal Dysplasia Society Welcome to the ED Society website Welcome About ED Society What is ED Genetics ... Incontinentia Pigmenti Membership Members Login User name Password Forgotten Password? The Ectodermal Dysplasia Society is a charity dedicated to improving the health and wellbeing of people whose lives are affected by Ectodermal Dysplasia (ED). We work together with people who have ED, their families, researchers, health and other professionals to develop and share expertise, increase awareness and understanding, and assist with the day-to-day management of ED. Although the ED Society is based in the UK we support individuals, families and professionals worldwide. If you are international and there is not a support organisation in your country please contact us at diana@ectodermaldysplasia.org To get the most from this site, we recommend you login to our membership area . Signing up takes just a few minutes but enables you to access more information, read articles and stories or visit our photo gallery. The Ectodermal Dysplasia Society is a UK registered charity.

49. Basically FX - Living With Fragile X Syndrome
    Personal story of a family living with Fragile X Syndrome.  
    http://basicallyfx.com
    
    Extractions: var path="http://www.basicallyfx.com/wp-content/plugins/flexible-lightbox/images/"; Living with Fragile X Syndrome In April of 2006 our family received the life changing news that our son had a genetic mutation called Fragile X Syndrome. Like most people in this country, we had never heard of this condition even though it had been affecting Umma and her family for many years. The goal of this website is to share our story and connect with other parents of children with Fragile X and, just maybe, spread the word about this disorder so we are no longer greeted with "fragile what?" anytime we discuss our son's challenges and special needs. 25 Things about life with Fragile X A guaranteed motivator. I smell like maple syrup. Fragile X Webring Prev. Random Next Home ... Join Select Category Adventures in medication Autism News Fragile X Conference Fragile X Memories Fragile X News Life with Fragile X Syndrome Non Sequitur Potty Talk School Select Month November 2010 October 2010 September 2010 August 2010 July 2010 June 2010 May 2010 April 2010 March 2010 February 2010 January 2010 December 2009 November 2009 October 2009 September 2009 August 2009 July 2009 June 2009 May 2009 April 2009 March 2009 February 2009 January 2009 December 2008

50. Genzyme Genetics - - Company News & Executive Profiles | BNET
    Genzyme Genetics Latest company news analysis, recent events, stock quotes, earning call transcripts, with profiles and descriptions of top business executives  
    http://www.bnet.com/company/genzyme genetics

51. Growth Charts For Children With Down Syndrome
    Charts included are for height, weight, and head circumferences. Printable.  
    http://www.growthcharts.com
    
    Extractions: About the author About Down Syndrome Down syndrome is a genetic condition in which there are three 21st chromosomes instead of the usual two. Most people have 46 chromosomes per cell originating from the 23 chromosomes in the mother's egg and 23 in the father's sperm. Not all people with Down syndrome have the same chromosomal arrangement, however. Ninety-five percent of people with Down syndrome (trisomy 21) have 47 chromosomes per cell (they have an extra #21 chromosome). This common type of trisomy 21 is called non-disjunction Three to four percent of people with Down syndrome have Robertsonian Translocation , where the number of chromosomes is normal, but the extra chromosome 21 material is attached with chromosome 14. The remainder have a rare type of Down syndrome in which some of their cells have 46 chromosomes and some have 47 chromosomes. This is called

52. CGD Research Trust - Details On RDFunding - The Research And Development Informa
    The CGD Research Trust is funding vital state of the art research at a time when Britain is a world leader in the treatment of genetic disorders. General Information  
    http://www.rdfunding.org.uk/queries/ListCharityDetails.asp?CharityID=627

53. Down Syndrome
    A listing of organizations worldwide, support groups, and toy catalogs for children of special needs.  
    http://www.nas.com/downsyn/

54. Department Of Pediatrics
    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/print.php?id=1

55. Down Syndrome For New Parents
    Dedicated to providing parents with information about Down syndrome.  
    http://www.downsyn.com

56. Neurological Conditions Treated By The First Step Therapy Centre, Newry
    Metabolic Genetic Disorders - General Physical Disabilities The programme is tailored to the child’s needs following a detailed assessment of their potential for improvement  
    http://www.first-step-therapy.com/conditions.html
    
    Extractions: - General Physical Disabilities The programme is tailored to the child’s needs following a detailed assessment of their potential for improvement and recovery. We always take a positive approach to care and with the dedication of the patient and the family, improvements usually can be made. Please contact us to arrange an initial consultation and a FREE detailed assessment of the patient (adult or child). Why not contact us today to see how we can help you on Free Call 0800 56 77 560 (UK only). If calling from Republic of Ireland use 048 3083 2865. If calling other countries, the telephone number is +44 28 3083 2865

57. Down Syndrome: Health Issues - Medical Essays And Information
    A collection of medical essays and abstracts for parents.  
    http://www.ds-health.com
    
    Extractions: FreeFind Author's note: I'm a pediatrician and the father of Avi, 16 years old, and Nathan, 18 years old. Avi has Down Syndrome ("DS" for short) and has inspired me to write these essays about children with DS for other parents. I have put them here for general reading. You may E-mail me with any questions about these essays. I have also included some other pediatric items of interest for parents.

58. The Brain And Behavior Clinic
    Various Genetic Disorders; General Cognitive Skills (IQ) Academic Achievement (Reading, Writing, and Arithmetic) Executive Function Skills (i.e., planning/organization, inhibition, and  
    http://www.brainandbehaviorclinic.com/index.php?option=com_content&task=view

59. Mosaic Down Syndrome Information And Family Support
    Stories, message boards, and a FAQ.  
    http://www.mosaicdownsyndrome.com
    
    Extractions: Welcome to Mosaic Down Syndrome on the Web. My name is Bree Weasner, and I am the proud mommy of Morgan, my beautiful angel girl, born on July 17, 1999, and diagnosed with MDS. When my daughter was born, there was absolutely nothing on the Internet about MDS. I was devastated. It was because of this devastation and lack of information that this website now exists...so new parents won't ever have to experience what I did (and so many others). I know that this site's contents may appear "general" to many of you, but I wish I had a website such as this to go to in July, 1999, the day I found out what my daughter's diagnosis was. I do not feel alone anymore. This site continues to be updated, so do check back frequently. Thank you. To navigate through this site, use the navigation bar to your left. There is a link on the bottom of each page that will bring you back here. Be sure to check ALL the links to your left so you don't miss a thing Please do not send me your medical questions ...you'll find a link to your left where you can ask medical professionals your questions OR you can join our MosaicDS support group and post your questions there!

60. Robin Van Der Lee - Netherlands | LinkedIn
    here, including general pediatrics, infectious diseases, neurology, cardiology, nephrology, gastroenterology, pulmonology, metabolic, endocrine and genetic disorders, general and  
    http://nl.linkedin.com/in/robinvanderlee
    
    Extractions: document.body.className += " js"; Pediatrician - Fellow Neonatology at Isala Clinics Zwolle Netherlands Pediatrician - Fellow Neonatology (Medical Practice industry) January 2010 Present (11 months) (Medical Practice industry) April 2009 December 2009 (9 months) (Non-Profit; Medical Practice industry)

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