41. Genetics Of Huntington's Disease Genetics of Huntington disease. Debra Collins, MS, CGC. Genetic diagnosis. Huntington disease is inherited as an autosomal dominant condition. http://www.kumc.edu/hospital/huntingtons/genetics.html

Genetics of Huntington disease Debra Collins, M.S., CGC Genetic Counselor Division of Endocrinology, Metabolism and Genetics University of Kansas Medical Center Huntington disease (HD) is a genetic disorder of the central nervous system with symptoms usually appearing in adults within the third or fourth decade of life, although symptoms can occur in individuals younger or older than this. Within the same family, the symptoms vary both in their rate of progression and in the age of onset. Symptoms may include involuntary movements and loss of motor control. In addition, personality changes may occur, with loss of memory and decreased mental capacity. Symptoms in individuals, as well as confirmation of diagnosis in other family members, are used to determine the diagnosis. Huntington disease is inherited as an autosomal dominant condition. The human body contains 100 trillion cells. A nucleus is inside each human cell (except red blood cells). Each nucleus contains 46 chromosome arranged in 23 pairs. One chromosome of every pair is from each parent. The chromosome are filled from each tightly coiled strands of DNA. Genes are segments of DNA that contain instructions to make proteins and other building blocks of life. An affected parent passes either the HD gene, or the other working gene, to their off spring. There is a 50% (1 in 2) chance at each pregnancy that a child of an affected parent will receive the gene for Huntington disease. The age of onset, degree and type of clinical symptoms, as well as rate of progression varies with HD.

42. Auto-forward To Hungtington's Disease Page Services of the Huntington's disease program of the University of Connecticut Health Center. http://psychiatry.uchc.edu/huntingtons.php

Click here if your browser does not support auto-forwarding Click here if your browser does not support auto-forwarding

43. Welcome To ShanaMartin.com, The Homepage Of Shana Martin!! The author is at risk for Huntington's disease, so there is a lot of information on that subject, as well as her personal story. http://www.geocities.com/CollegePark/Pool/1797/huntingtons/index.html

 Home   Daddy   Family   Huntington's Disease  ... Archives Huntingtons Disease Thank you for taking a look at this page. May of you already know, and some have no clue about how Huntington's Disease affects my life. During my birth, my mother displayed some abnormal movements. Five years later it was determined to be Huntington's Chorea. My mom was not aware she was at risk for this disease because she had been adopted. While growing up, my dad and I took care of her until eventually we could not safely leave her side. At that point we made a decision to put her in a nursing home. She is currently living at Ingleside Nursing Home in Mt. Horeb, where they take wonderful care of her. We visit her every week, and take her out as much as possible. I have a 50% chance of also getting Huntington's Disease. This is a scary thing, but I have known about this for most of my life. There is a test available, but I haven't had the guts to take it yet. I'm sure I will before I start a family though. I am very open about all of this, so if anybody has any questions about the disease, or the personal factors of it, feel free to contact me. I really do want more people to have knowledge about it, since it is such a rare disease. What is HD?

44. HD Blog - Huntington's Disease News Weblog Health Care Huntington s disease News. Huntington disease is one of nine inherited neurodegenerative disorders caused by a polyglutamine tract expansion. http://www.huntingtons.info/

HD Blog June 09, 2004 HD Writer on NPR Today Category: Community News The writer of "It's A Bird", Steven Seagle, will be on NPR's Fresh Air today. "It's A Bird" is a semi-autobiographical graphic novel about a comic book writer who is given his dream job of writing Superman at the same time he must deal with the specter of Huntington's Disease in his family. You can read more on this graphic novel here. By Dave at 05:35 AM Comments (0) TrackBack (0) Email this! June 08, 2004 More Good News Category: Genetic Research Just a few days ago I posted the 'Success' article on the University of Iowa's success with using RNAi to successfully treat a disease very similar to Huntington's disease. Today Sirna Therapeutics has announced that they are collaborating with the University of Iowa on pursuing this RNAi treatment on Huntington's Disease. They have already successfully tested this in the petri dish and are currently in the process of testing 'in-vivo' (most likely HD mice). All signs point to Sirna making this a development priority and they also appear to be financially capable to bring this therapy to market. Assuming successful in-vivo testing (very likely), we could see Phase I human tests with 18-24 months. This treatment would qualify for FDA 'fast track' testing.

45. Huntington S Disease Genetics Full size image available below. Huntington s disease Genetics They are signs of the fatal neurological disorder, Huntington s disease (HD). http://web.sfn.org/content/Publications/BrainBriefings/huntingtons.html

Login Directory Merchandise Contact Us ... Abstracts/Annual Meeting Publications Full size image available below Huntington's Disease Genetics The identification of the Huntington's disease gene in 1993 has spawned a variety of novel insights that may improve treatment or even cure this disorder. Researchers are deciphering the lethal gene's structure in order to determine how its makeup plays a role in disease development. Violent, uncontrollable movements. Repetitious fidgeting. In the 1800s clinicians compared it to a dance. But these wildly jerky movements are far from a hip hop move or tango. They are signs of the fatal neurological disorder, Huntington's disease (HD). Some 30,000 Americans are affected and another 150,000 run the risk of displaying HD. The disease, notorious for killing folk singer Woody Guthrie, ends the life of its victims within eight to 25 years. Symptoms of the disease include rapid, jerky involuntary movements, difficulty in speaking and swallowing, cognitive decline, depression, and occasionally delusions, hallucinations and obsessive compulsive disorders. Currently HD has no cure or treatment. However, researchers are developing new approaches to treat this disorder thanks to the discovery of the HD gene in 1993.

46. Glaxo Centre Alliance Charities Huntington's Disease Contact National, Head Office Huntington s disease Association. 108 Battersea High St. Merseyside, Huntington s disease Association. c/o Glaxo Neurological Centre. http://glaxocentre.merseyside.org/huntingtons.html

Charity No 296453 Contact: National Head Office Huntington's Disease Association 108 Battersea High St. London SW11 3HP England Tel: Fax: Email: info@hda.org.uk Website: www.hda.org.uk Merseyside Huntington's Disease Association c/o Glaxo Neurological Centre Norton St Liverpool L3 8LR England Tel: Fax: The Huntington's Disease Association is a national charity with the aims of promoting research, relief and treatment; disseminating knowledge about the disease; and providing information, comfort and support (including financial support where appropriate) to families and their associated professionals. The Huntington's Disease Association's Cheshire and Merseyside Regional Care Advisor holds bi-monthly advice sessions at the Glaxo Centre for people with Huntington's Disease and their carers. Please see the Glaxo Centre's newsletter to find out when the next appointment is: Glance Index . You will need to make an appointment, either ring the Glaxo Centre on 0151 298 2999 or email: mnt@gnc.u-net.com The Huntington's Disease Association - Flintshire and District Branch Tel: Ewart Cassel on 01244 534878.

47. Huntington's Disease Group Of Maine HUNTINGTON S disease GROUP of MAINE The Tapestry. Weaving Dedicated to the detection and care of those who have Huntington s disease. Website http://www.pccs-nh.com/huntingtons/

HUNTINGTON'S DISEASE GROUP of MAINE The Tapestry Weaving the threads of commons concern Meeting at 7:00 p.m. the Barron Center 1145 Brighton Ave. - Portland, ME Second Monday Each Month Exit 8, Maine Turnpike, left on Brighton Look for Barron Center on the left (Get directions from Mapquest.) Support Group Coordinator Lillian Dyhrberg 797-0566 Additional Contact Persons Southern Maine Area Steve Brantley 1-800-838-7462 166 Simpson Road Saco, ME 04072 e-mail: sjb9946@aol.com Central Maine Area Gordon Harris 1054 Lisbon Street Lewiston, ME 04240 e-mail: GHarris@megalink.net HDSA Patient Services and Information Department Concerning: Genes, genetic, markers and tests Home care/nursing/management Clinical care/evaluations/therapies Research/Videos Counseling/support/financial/legal issues Dedicated to the detection and care of those who have Huntington's Disease Website design and layout by:

48. Testing For Huntington's Disease - Part One - Suite101.com This is an article on testing for Huntington s disease. Huntington s disease Note This topic has been archived and is available for Adoption! http://www.suite101.com/article.cfm/huntingtons/30924

Topics Articles Links Courses DIRECTORY COMMUNITIES BOOK CIRCLE SUITE U ... MY SUITE Search Suite101.com Within: Huntington's Disease Health Search The Web Member Central Join Our Community! Login What's New Become a SuiteU Affiliate ... MemberUpdate Suite University About Suite University Suite University News Visit the University Course Listing ... FREE Demo Course New Topics Parenting Babies and Toddlers Views of a Young Appalachian Woman SpiritWell Travel Book Reviews ... More... Suite Events Teacher Appreciation Event 2004 Family Focus 2004 In Tune With Johann Sebastian Bach More about Suite101 About Suite101.com Advertise With Suite For more information - Select a related topic - Agoraphobia Alexander Technique Alzheimer's Disease Aromatherapy Asperger's Syndrome Asperger's Syndrome and A BodyWork Techniques Breast Cancer Canadian Health Carrie Writes About Disab Celebrating Life Child Sexual Abuse Chiropractic Health Care Clinical Nutrition Creative Therapy Depression In Women Dissociative Identity Dis Eating Disorders Fibromyalgia Friends Fitness Fluoridation Graves' Disease Health Psychology Herbal Healing Hypochondria Hypothyroidism I May Be Getting Older, B

49. Huntington's Disease - Suite101.com My topic would be on Huntington s disease. Huntington s disease Note This topic has been archived and is available for Adoption! http://www.suite101.com/welcome.cfm/huntingtons

Topics Articles Links Courses DIRECTORY COMMUNITIES BOOK CIRCLE SUITE U ... MY SUITE Search Suite101.com Within: Huntington's Disease Health Search The Web Member Central Join Our Community! Login What's New Become a SuiteU Affiliate ... MemberUpdate Suite University About Suite University Suite University News Visit the University Course Listing ... FREE Demo Course New Topics Parenting Babies and Toddlers Views of a Young Appalachian Woman SpiritWell Travel Book Reviews ... More... Suite Events Teacher Appreciation Event 2004 Family Focus 2004 In Tune With Johann Sebastian Bach More about Suite101 About Suite101.com Advertise With Suite For more information - Select a related topic - Agoraphobia Alexander Technique Alzheimer's Disease Aromatherapy Asperger's Syndrome Asperger's Syndrome and A BodyWork Techniques Breast Cancer Canadian Health Carrie Writes About Disab Celebrating Life Child Sexual Abuse Chiropractic Health Care Clinical Nutrition Creative Therapy Depression In Women Dissociative Identity Dis Eating Disorders Fibromyalgia Friends Fitness Fluoridation Graves' Disease Health Psychology Herbal Healing Hypochondria Hypothyroidism I May Be Getting Older, B

50. Research Projects - Huntington's Disease - Genetic Testing follows guidelines for testing developed by the Huntington disease Society of America and the World Federation of Neurology Research Group on huntingtons Chorea http://www.iupui.edu/~medgen/research/hd/genetic_testing/genetic_testing.html

Genetic Testing for Huntington Disease at Indiana University The Predictive Testing Program at Indiana University follows guidelines for testing developed by the Huntington Disease Society of America and the World Federation of Neurology Research Group on Huntingtons Chorea. These guidelines include a neurological examination, pretest counseling, disclosure of test results in person and followup. 1. Neurological Examination If you are interested in testing for Huntington Disease you will be scheduled for a neurological examination in the Indiana University Huntington Disease Clinic. The purpose of this visit is to see whether you are currently showing any symptoms of Huntington Disease. A diagnosis of HD is made based on the finding of clinical symptoms of HD. If you are found to be already showing symptoms of HD, you will have the option whether or not to proceed with genetic testing to confirm this diagnosis, although in many cases further testing is not necessary. HD clinic is held on Fridays 2-4 times per month. Clinics may often be booked several months ahead. To schedule an appointment for a neurological examination, call Susan Craig at 317-274-5744 or contact her by E-mail at scraig@iupui.edu. 2. Pre-test Counseling

51. Huntington's Disease - Wikipedia, The Free Encyclopedia Huntington s disease. (Redirected from huntingtons Chorea). Because of these aspects, Huntington s disease raises many of the most pressing issues of bioethics. http://en.wikipedia.org/wiki/Huntingtons_Chorea

Huntington's disease From Wikipedia, the free encyclopedia. (Redirected from Huntingtons Chorea Huntington's disease or Huntington's chorea is an inherited disorder characterized by abnormal body movements called chorea , and loss of memory . The incidence is about 1/200,000. Table of contents 1 Etiology 2 Diagnosis 3 Treatment and prevention 4 Ethical aspects ... edit Etiology The causative gene (which is one of the first identified to cause an inherited disease) is located on chromosome 4. The product of this gene is a 350KDa cytoplasmic protein called huntingtin . The continuous aggregation of huntingtin molecules in neuronal cells gives rise to cell death , especially in the frontal lobes and the basal ganglia (mainly in the caudate nucleus ) by some unknown mechanism. Huntingtin has a characteristic sequence of 40 or fewer glutamine residues in the normal form; the mutated huntingtin causing the disease has more than 40 residues. While theories as to how the mutation brings about disease remain diverse and speculative, researchers have identified many specific subcellular abnormalities associated with the mutant protein, as well as unusual properties of the protein in vitro. Just as one example, in 2001, Max Perutz discovered that the glutamine residues form a nanotube in vitro, and the mutated forms are long enough in principle to pierce

52. Huntington's Disease Association Of Ireland http://www.huntingtons.ie/

53. Huntington's Disease Association Of Ireland The Huntington s disease Association of Ireland (HDAI) provides consultation, information and individualised support to those diagnosed with Huntington s http://www.huntingtons.ie/disease.html

Huntington's Disease, there's a lot to hope for: Dr. Gill Bates. MSC Ph.D.. Professor in Neurogenetics, Guys Hospital, London. Guest Speaker at HDAI AGM on 3rd June. Marker for Huntington’s Disease (HD) gene found. Formal Launch of Huntington’s Disease Association of Ireland. Mary Robinson, President of Ireland becomes Patron of HDAI. First full-time worker employed. Scientist finds HD gene. HDAI hosts European Huntington Association meeting in Trinity College. Scientists discover HAP-1 a protein that binds to huntingtin (the protein expressed by the HD gene) and may work with it to cause HD. Dr. Gill Bates develops transgenic mouse model. Breakthrough in HD research announced in Cell and Nature publications. Dr. Andrew Greene appointed Clinical Geneticist, National Genetics Centre, Dublin. Mary McAleese, President of Ireland becomes Patron of HDAI. Home Page Association Aims Hope Newsletter Huntington's Disease ... Contact HDAI 'Eligible Charity' Serial No: 0015 Incorporated 1998. Reg. Charity No. CHY 10130. Built by Rewind Design.

54. Huntingtons Chorea approximately 1601 in huntingtons patients the ratio is reduced to 401 with a marked decrease in the number of astrocytes. The gene for this disease has been http://www.sci.uidaho.edu/med532/Huntington.htm

Med.Sci 532 Structure-Function Huntington Disease This is an autosomally-inherited, dominant disorder in which the patient begins to exhibit symptoms in the third to fourth decades. Patients with Huntington Disease (HD) initially have a tendency to fidget which over months or years develops into jerky, choreiform movements. HD usually progresses over a 10 to 25 year period. As the disease progresses it leads to dementia and usually death from incurrent infection. There is a high incidence of suicide among patients with HD. Pathologically, there is atrophy of certain forebrain structures including the entire cerebral cortex and even more notably of the caudate nucleus and putamen The head of the caudate is reduced to a narrow brownish band of tissue that is flattened or concave. In normal brain the ratio of small neurons to large neurons in the corpus striatum is approximately 160:1 in Huntingtons patients the ratio is reduced to 40:1 with a marked decrease in the number of astrocytes. The gene for this disease has been isolated to the short arm of chromosome 4. For more information concerning Huntington Disease. Please visit the web-site below.

55. $500,000,000 Market For Huntingtons' Disease Treatment New to the Huntington s disease Lighthouse Welcome, start here Beginners Search. HDL Update $500,000,000 Market For huntingtons disease Treatment, http://hdlighthouse.org/treatment-care/treatment/drugs/lax101/human/updates/0034

New to the Huntington's Disease Lighthouse: Welcome, start here Beginners Search Treatment Now ... EPA-DHA Drugs Related Haldol bench human ... human HD Lighthouse Editor's Comment: From this we can estimate the cost of LAX-101 treatment for Huntington's disease. $500,000,000/30,000=$17,000 per patient for a year. Laxdale will get about half. They deserve every penny. Jerry Posted to HDLighthouse: 04 Dec 2002 18:21 HDL Update: $500,000,000 Market For Huntingtons' Disease Treatment Investors waiting "When you cut through all the detail, this could be a drug that is very significant for the treatment of Huntington's", Rick Stewart, Amarin CEO Amarin Corp is a $25 million British company that licenses and sells drugs to treat nerve disorders, like Parkinson's Disease. Amarin's chief executive, Rick Stewart, hails from SkyePharma a British drug developer. Stewart says that Amarin's research partner, Laxdale of Scotland, will follow up any day now on preliminary findings from a Phase III study of LAX-101, a treatment for Huntington's Disease. "This is the first time we have seen anything positive for Huntington's," says Stewart, who is shaking his head about the market's treatment of the preliminary findings. A study of 83 qualifying patients took place at Harvard, Emory and Johns Hopkins universities, and in the United Kingdom and Canada. Huntington's, a genetic disorder, has been diagnosed in about 30,000 Americans and an equal number of patients in Europe. The U.S. Food and Drug Administration has granted LAX-101 a so-called fast-track designation.

56. Huntington's Disease Program Individuals who have been diagnosed with Huntington s disease can be seen in the University of Virginia s multidisciplinary HD clinic held on a monthly basis. http://www.healthsystem.virginia.edu/internet/neurology-care/huntingtons.cfm

Who We Are What We Treat A-M What We Treat I-Z Find A Doctor ... Site Index Search this site: Huntington's Disease In March 2000, the Huntington's Disease Society of America name d the University of Virginia Health System a Center of Excellence for the care of patients with HD and their families. The UVa HD Program was one of the first 10 Huntington's Centers of Excellence in the nation and is the only one in Virginia. What is Huntington's Disease? Do You Have A Genetic Risk? Our Huntington's Clinic Additional Services ... Center of Excellence Award Article What is Huntington's Disease? HD is a genetic disorder that is passed from one generation to the next. Each child of a parent with HD has a 50% chance of inheriting the gene that causes HD. Both males and females may have HD and may transmit the gene to sons and daughters. All ethnic groups are affected. The symptoms of HD usually appear during the late 30s to mid-40s, but sometimes become apparent in young children or the elderly. Symptoms vary widely, but three areas are commonly affected: personality, thinking and movement. Emotional and behavioral changes such as depression, irritability, anxiety, aggressive outbursts, mood swings and social withdrawal can occur in people with HD. Thinking abilities such as short-term memory, organizational and coping skills may be impaired. Physical symptoms such as fidgeting, twitching and difficulties in coordination may appear, gradually leading to more obvious involuntary movements of the head, trunk, and limbs as the disorder progresses. The ability to walk and maintain balance may be affected, as can speech and swallowing.

57. AllRefer Health - Huntington's Disease (Huntington Chorea) Huntington s disease (Huntington Chorea) information center covers causes, prevention, symptoms, diagnosis, treatment, incidence, risk factors, signs, tests http://health.allrefer.com/health/huntingtons-disease-info.html

AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia You are here : AllRefer.com Health Huntington's Disease Huntington's Disease Definition Prevention Treatment Expectations or Prognosis ... Go To Main Page Alternate Names : Huntington Chorea Definition Huntington's disease is an inherited condition characterized by abnormal body movements, dementia , and psychiatric problems. Huntington's disease is a progressive disorder involving wasting (degeneration) of nerve cells in the brain. The disorder was first described in 1872 by George Huntington, an American physician. Huntington's disease is inherited as a single faulty gene on chromosome #4. There is a part of the gene that is repeated in multiple copies. The greater the number of repeats, the more likely it is that the person will develop symptoms and the greater the chance they will occur at a younger age. The disease may occur earlier and more severely in each succeeding affected generation because the number of repeats can increase. Every child of a parent with the disorder has a 50% chance of inheriting Huntington's Disease. Symptoms do not usually appear until adulthood, typically between ages 35 and 50 years old but this depends on the number of repeats found in the gene so it may also appear in younger people. In children it may appear to be Parkinson's disease with rigidity, slow movements, and tremor.

58. AllRefer Health - Huntington's Disease Support Groups (Huntington Chorea) Huntington s disease (Huntington Chorea) information center covers Support Groups. for Huntington s disease. Huntington s disease. http://health.allrefer.com/health/huntingtons-disease-support.html

AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia You are here : AllRefer.com Health Huntington's Disease : Support Groups for Huntington's Disease Huntington's Disease Definition Prevention Treatment Expectations or Prognosis ... Complications Support Groups Calling Your Health Care Provider Go To Main Page Alternate Names : Huntington Chorea Huntington's Disease Support Groups Support groups for people affected by Huntington's disease are available and can help reduce the stress of dealing with this difficult diagnosis and its impact on reproductive and other life choices. See the Huntington's Disease Society of America for local information: http://www.hdsa.org/

59. PHI305: Huntington's Disease And Abortion that these treatments I have just discussed who s to say that there won t be a cure before this person start too show symptoms of huntingtons s disease. http://www.uky.edu/~cperring/hd.htm

Back to PHI 305 Home Page Huntington's Disease: Reproductive Decision-Making A Debate Bredon Jones and Cynthia Lee What is Huntington's Disease? Also called: Huntington's Chorea Lund- Huntington's Chorea Setesdal jerks An incurable , hereditary type of brain atrophy A type of "presenile dementia" Who does HD affect? Affects 1 in 10,000 150,000 are at risk in the U.S. Children of those who have HD have a 50/50 chance of inheriting the disease Anyone who has not developed the gene has no chance of passing it on to their children Mental Symptoms of HD Change in personality Loss of memory Reduced concentration Loss of initiative Irritability/ aggression Touchiness Depression Delusions Neurological Symptoms of HD Involuntary flicking movements These occur suddenly and irregularly with chance distribution all over the body Gait disturbances Slow and long- lasting muscle spasms Speech and language problems Disjoint and indistinct speech May not be able to answer questions Other Signs of HD Dysphagia Increased muscle activity often makes eating and swallowing difficult Incontinence Altered 24-hour schedule Patient may become nocturnal General lack of personal hygiene Normal Brain vs. Brain Affected by HD

60. SMD - Society For Manitobans With Disabilities - Library Services HUNTINGTON S disease BIBLIOGRAPHY. Compiled by SMD Library Staff. Aray, Alison. Genes and generations living with Huntington disease. http://www.smd-services.com/information/huntingtons.html

Wpg Adult Wpg Children Wheelchair Services Rural Services ... News Releases HUNTINGTON'S DISEASE - BIBLIOGRAPHY Compiled by SMD Library Staff For information on borrowing the following items contact the SMD library at (204) 975-3024 or email to library@smd.mb.ca Aray Alison. Genes and generations : living with Huntington Disease. New Zealand : Wellington Huntington's Disease Association, 1995. A collection of 18 interviews with people with HD, and their families, caregivers and health care professionals Dalby, Shirley . Behavioural and sexual problems in Huntington's Disease. A paper presented at the 3rd National HD conference in Australia, 1991. Folstein, Susan E Huntington's Disease : A disorder of families. Baltimore, Maryland : Johns Hopkins University Press, 1989.  This book provides an overview that will be of use to researchers and clinical professionals, including counselors who care for persons with RD and their families. While HD families will find some chapters too technical, other chapters may provide them with useful information about diagnosis, care and treatment. Gaba., Ann.

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 3     41-60 of 102    Back | 1  | 2  | 3  | 4  | 5  | 6  | Next 20