Home  - Health_Conditions - Prader-willi Syndrome

Books Baby Camera Phones Computers Games DVD Electronics Kitchen Magazines Music Garden Software Tools Toys Video Apparel & Accessories Jewelry & Watches Musical Instruments Health & Personal Care Beauty Sports & Outdoors Office Products

e99.com Bookstore

Images

Newsgroups

101-115 of 115    Back | 1  | 2  | 3  | 4  | 5  | 6

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

Prader-willi Syndrome:     more books (67)

Prader-willi Syndrome: Coping With the Disease - Living With Those Involved by Urs Eiholzer, 2005-05-31 Prader-Willi Syndrome: A practical guide (Resource Materials for Teachers) by Jackie Waters, 1999-07-01 Management of Prader-Willi Syndrome Prader-Willi Syndrome: Development and Manifestations by Joyce Whittington, Tony Holland, 2010-12-09 Prader-Willi Syndrome - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-04-27 Management of Prader-Willi Syndrome Prader-Willi Syndrome: Development and Manifestations by Joyce Whittington, Tony Holland, 2004-05-24 Babies and Children with Prader-Willi Syndrome: A Handbook for Parents and Carers by Jackie Waters, Margaret Gellatly, 2001-08-01 The Prader-Willi Syndrome Prader-Willi Syndrome: Selected Research and Management Issues Prader-Willi Syndrome As a Model for Obesity: International Symposium, Zurich, October 18-19, 2002 Prader-Willi Syndrome: A Handbook for Parents by Shirley Neason, 1985-06 Prader-Willi Syndrome: and Other Chromosome 15q Deletion Disorders (NATO ASI Series / Cell Biology) Prader-Willi Syndrome: Selected Research and Management Issues

lists with details

101. Prader-Willi Syndrome Definition - Medical Dictionary Definitions Of Popular Med
     Online Medical Dictionary and glossary with medical definitions.  
     http://www.medterms.com/script/main/art.asp?articlekey=5016

102. Project: National Study Into The Prader-Willi Syndrome (www.onderzoekinformatie.
     Project National study into the praderwilli syndrome. Show printer-friendly view Print View switch to nl mutation. Titel, Landelijke studie van het  
     http://www.onderzoekinformatie.nl/en/oi/nod/onderzoek/OND1296063/toon

103. CPS: CPSP Prader-Willi Syndrome
     Quality information on children s health and wellbeing, such as vaccination, pregnancy, infant care, healthy eating, common illnesses, safety,  
     http://www.cps.ca/english/cpsp/studies/prader.htm
     
     Extractions: Prader-Willi syndrome Principal investigator Glenn B. Berall, BSc, MD, FRCPC, Chief of Paediatrics, North York General Hospital, 4001 Leslie St., Toronto, ON M2K 1E1; tel.: 416-756-6222; fax: 416-756-6853; e-mail: gberall@nygh.on.ca Co-investigators Maria Virginia Desantadina, MD, Paediatrician, Research Fellow, Department of Nutritional Sciences, University of Toronto, The Hospital for Sick Children. Consultant Nita Goldband, Executive Director, Ontario Prader-Willi Syndrome Association Study publications/presentations CPSP highlights Presentations Genetic studies: A significant component of the Canadian Paediatric Surveillance Program. Challenging behavioural problems in children with genetic and rare conditions: Role of the Canadian Paediatric Surveillance Program. Public health implications of the Candadian Paediatric Surveillance Program. International Network of Paediatric Surveillance Units: A child's global village. Workshop on Puberty in CHARGE and General Endocrine Issues in CHARGE. Blake K. Presented at the 6th International CHARGE Syndrome Conference, Cleveland, Ohio, July 25 to 27, 2003. Surveillance helping patients with orphan genetic disorders. MV Desantadina, KD Blake, MJM Nowaczyk. Presented at the he 80th Annual Meeting of the Canadian Paediatric Society, Calgary, June 21, 2003.

104. Endocrine Dysfunction In Prader-Willi Syndrome: A Review With Special Reference
     The Status of Other Hormonal Axes in praderwilli syndrome. V. Endocrine Treatment of Patients with prader-willi syndrome  
     http://edrv.endojournals.org/cgi/content/full/22/6/787
     
     Extractions: HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS This Article Abstract Full Text (PDF) Alert me when this article is cited ... Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Burman, P. Articles by Lindgren, A. C. Endocrine Reviews 22 (6): 787-799 Pia Burman and Ann Christin Lindgren Pharmacia Corporation, SE-112 87 Stockholm, Sweden (P.B.) and Department of Woman and Child Health, Karolinska Institute, SE-171 76 Stockholm, Sweden (E.M.R., A.C.L.) Correspondence: Address all correspondence and requests for reprints to: Pia Burman, M.D., Ph.D., Pharmacia Corporation, Lindhagensgatan 126, SE-112 87 Stockholm, Sweden. E-mail:

105. Health.iafrica.com | Diet | Diseases Nutrition In Prader-Willi Syndrome
     But it is a fact of life for sufferers of praderwilli syndrome, prader-willi syndrome (PWS) is a complex genetic disorder that includes short stature,  
     http://health.iafrica.com/dietonline/diseases/242722.htm
     
     Extractions: Recommended Diet Are you overweight or underweight? Find out what you should be eating. Are you pregnant? Click here and we can help predict your due date. Communities: [ h o m e ] Africa Afrikaans Aids Wise Business Cars Careers Cooltech Dating Easy Money Entertainment Fun Stuff Games LifeStyle Men Motoring My Money News Property Sport Talk Travel Weather Win Women Services: Book Airtickets Blogs Car Hire Chat Online Classifieds Directories Ecards Homeloans Mobile Magic Shop Online Search RSS Feeds Diet Allergies Diseases Foodtypes ... Mind Matters Subscribe Now Monday Phenomenon

106. Behavioral Differences Among Subjects With Prader-Willi Syndrome And Type I Or T
     Key Words praderwilli syndrome • type I and type II deletions • maternal Abbreviations PWS, prader-willi syndrome • UPD, maternal disomy 15 • AS,  
     http://pediatrics.aappublications.org/cgi/content/abstract/113/3/565
     
     Extractions: Institute for Child Development, University of Kansas Medical Center, Kansas City, Kansas Objective. To determine whether phenotypic differences exist among individuals with Prader-Willi syndrome with either type I or type II deletions of chromosome 15 or maternal disomy 15 leading to a better understanding of cause and pathophysiology of this classical genetic syndrome.

107. Prader-Willi
     In 1981, the praderwilli syndrome was found to be associated with a very The genes involved in prader-willi syndrome encode proteins that are only  
     http://zygote.swarthmore.edu/chrom3a.html
     
     Extractions: In 1981, the Prader-Willi syndrome was found to be associated with a very small deletion in the long arm of human chromosome 15, between bands q11 and q13 (Ledbetter et al., 1981). However, in 1987, an identical deletion was reported in a number of patients who suffered from a very different disease, Angelman syndrome. These syndromes give quite distinct phenotypes (Figure 1). Prader-Willi syndrome is characterized by developmental delay, cryptorchidism (small or undescended testes), hyperphagia obesity (fatness due to overeating in an attempt to reach satiety), short stature, and mild retardation. Angelman syndrome is characterized by seizures, severe mental retardation, inappropriate laughter, and a characteristic face that is small with a large mouth and prominent chin. FIGURE 1. Typical phenotypes of Angelman (left) and Prader-Willi (right) syndrome patients. The difference between them belies the fact they they are caused by the same chromosomal deletion. (From Nicholls, 1994; Photographs courtesy of R. D. Nicholls). The resolution to the paradox of two different syndromes caused by the same chromosomal deletion came in 1989 when it was discovered the Prader-Willi syndrome was always caused by defects involving the paternally derived chromosome, while Angelman syndrome was always caused by deletions in the maternally derived chromosome (Knoll et al., 1989).

108. Mental Help Net
     praderwilli syndrome (PWS) is a relatively rare genetically determined This book, prader-willi syndrome follows a process of discovery that included  
     http://mentalhelp.net/poc/view_doc.php?id=2720&type=book&cn=72

109. Prader-Willi Syndrome - National Institutes Of Health (NIH)
     praderwilli syndrome - Health Information from National Institutes of Health (NIH)  
     http://health.nih.gov/result.asp/898
     
     Extractions: NLM Prader-Willi syndrome Related Topics: Genetics/Birth Defects Mental Health and Behavior Mental Health and Behavior Up to Top Look up "Prader-Willi Syndrome" in: MedlinePlus - health resources from US government agencies and other credible organizations Clinical Trials Database - research studies in which you can participate This page was last reviewed on Thursday, July 28, 2005. Career Opportunities Visitor Information FOIA

110. Prader Willi Syndrome, PWS
     diagnosis of Prader Willi syndrome, PWS common physical features are hypotonia small brachycephalic head cytogenetic pathogenesis medical intersest group  
     http://ibis-birthdefects.org/start/pwfact.htm
     
     Extractions: " ... Mothers with prior experience of normal pregnancies almost without exception report distinctly delayed onset and reduced fetal activity during the pregnancies involving PWS ... Neonates are profoundly hypotonic ... Cryptorchidism occurs with hypoplastic penis and scrotum in boys and hypoplastic labiae in girls ... hypotonia ..."

111. Prader Willi Syndrome In Children - Keep Kids Healthy
     Prader Willi syndrome is a genetic condition that can cause hypotonia (poor muscle tone), mental retardation, obestity, uncontrollable hunger and a  
     http://www.keepkidshealthy.com/welcome/conditions/prader_willi_syndrome.html
     
     Extractions: Recommend Us tell a friend about us or email this page to a friend Main Diseases and Conditions Prader Willi Syndrome is a genetic condition that is usually caused by a microdeletion (meaning a small piece of the chromosome is missing) of band q11.2 of the long arm of chromosome 15. In children with Prader Willi Syndrome, this chromosomal deletion is derived from the father. If the same microdeletion were derived from the mother, then it would cause Angelman syndrome instead. The process where a chromosomal abnormality can cause different syndromes depending on if it is inherited from the mother or father is called genetic imprinting. Although this is a genetic disorder, it is not necessarily inherited. Instead, it is usually (70% of cases) caused by the lack of genetic material that the father would have contributed to his child from chromosome 15 and this most often occurs because of a spontaneous genetic mutation around the time of conception.

112. Index
     A nonprofit group of volunteer families, friends and researchers aiming to raise funds for research into finding treatments.  
     http://www.pwsresearch.org/

113. Prader Willi Syndrome
     Prader Willi syndrome is a genetic disorder characterized by diminished muscle tone (hypotonia), feeding  
     http://webcenter.health.webmd.netscape.com/hw/heart_disease/nord14.asp
     
     Extractions: You are in All Conditions ADD/ADHD Allergies Alzheimer's Arthritis Asthma Back Pain Bipolar Disorder Breast Cancer Cancer Cholesterol Management Dental Depression Diabetes Epilepsy Eye Health Heart Disease Hepatitis HIV/AIDS Hypertension Men's Conditions Mental Health Migraines/Headaches Multiple Sclerosis Osteoporosis Parkinson's Sexual Conditions Stroke Weight Control Women's Conditions Prader-Willi syndrome is a genetic disorder characterized in infancy by diminished muscle tone (hypotonia), feeding difficulties, and failure to grow and gain weight (failure to thrive). In childhood, features of the disorder include short stature, genital abnormalities and an excessive appetite. Progressive obesity results because of a lack of feeling satisfied after completing a meal (satiety) that leads to overeating. Without appropriate treatment, individuals with severe progressive obesity may have an increased risk of cardiac insufficiency, diabetes or other serious conditions that may lead to potentially life-threatening complications. All individuals with Prader-Willi syndrome have some cognitive impairment that ranges from borderline normal with learning disabilities to mild mental retardation. Behavior problems are common and can include temper tantrums, obsessive/compulsive behavior, and skin picking.

114. Prader Willi Syndrome Center - Clinical Genetics - Department Of Molecular And H
     http://imgen.bcm.tmc.edu/molgen/cg/clinics/pwsc_index.html

115. **150 Characters**
     **150 characters** guidelines for parents guidelines for professionals growth hormone therapy ghrelin; genetics. genetics of PWS genetic forms  
     http://www.pwsa-nz.co.nz/

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

101-115 of 115    Back | 1  | 2  | 3  | 4  | 5  | 6