81. Diabetes: Subcellular Localization Of ALMS1 Supports Involvement Of Centrosome A alstrom syndrome is a rare autosomal recessive disorder characterized by Interestingly, the phenotype of alstrom syndrome overlaps with that of http://www.findarticles.com/p/articles/mi_m0922/is_5_54/ai_n13681108

@import url(/css/us/style1.css); @import url(/css/us/searchResult1.css); @import url(/css/us/articles.css); @import url(/css/us/artHome1.css); Advanced Search Home Help IN free articles only all articles this publication Automotive Sports 10,000,000 articles - not found on any other search engine. FindArticles Diabetes May 2005 Content provided in partnership with 10,000,000 articles Not found on any other search engine. Related Searches Type 2 diabetes / Genetic aspects Type 2 diabetes / Research Centrosomes / Evaluation Obesity / Research ... Obesity / Genetic aspects Featured Titles for AAACN Viewpoint ABNF Journal, The AIDS Treatment News AMAA Journal ... View all titles in this topic Hot New Articles by Topic Automotive Sports Top Articles Ever by Topic Automotive Sports Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes Diabetes May, 2005 by Tom Hearn Cosma Spalluto Victoria J. Phillips Glenn L. Renforth ... David I. Wilson Save a personal copy of this article and quickly find it again with Furl.net. It's free! Save it.

82. Statesman.com alstrom syndrome. Overview Symptoms Treatment. Alternative names.AlstromHallgren syndrome; Alstroem s retino-otodiabetic syndrome. Definition http://www.statesman.com/health/healthfd/shared/health/adam/ency/article/001665.

@import url(http://alt.coxnewsweb.com/statesman/css/display_template_more.css); /*Adds styles that break page in NN 4.78.*/ var cxType = ""; Home Page Site Map Search Last 7 Days ... Log in Search Site/Web Yellow Pages Classifieds Jobs Cars Homes ... Advertise With Us Resources Customer Service Archives Corrections Member Center ... For Sale E-MAIL THIS PAGE MOST E-MAILED ARTICLES Illustrated Health Encyclopedia Important notice Ency. home Disease A Alstrom syndrome Overview Symptoms Treatment Alternative names: Alstrom-Hallgren syndrome; Alstroem's retino-otodiabetic syndrome Definition: an inherited disease characterized by progressive blindness juvenile onset diabetes mellitus, obesity deafness , and normal mental capacity. Causes and Risks This is an autosomal recessive , inherited disorder. It is extremely rare. The syndrome has a higher incidence in Holland and Sweden. Ency. home Disease A The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. For further information click here E-MAIL THIS PAGE MOST E-MAILED ARTICLES Back to top Advertise Online or in Print Subscribe to the Newspaper Make us your Homepage Presented by The Austin American-Statesman Contact us Corrections Site Requirements Please read our Privacy Policy . By using this site, you accept the terms of our

83. PharmGKB: ALMS1 ALMS1 alstrom syndrome 1. Alternate Names, None Details. Cytogenetic Location,2p13. OMIM Phenotype, alstrom syndrome. Product Name, ALMS1 http://www.pharmgkb.org/do/serve?objId=PA24721&objCls=Gene

84. About BBC Children In Need £16670. Medical Conditions alstrom syndrome UK, Devon Families with childrensuffering from serious medical conditions can sometimes need extra support. http://www.bbc.co.uk/foi/docs/community_involvement/charities/About_BBC_Children

Freedom of Information About BBC Children in Need BBC Children in Need started in 1980, and has raised more than £325 million. Every penny has been used to improve the lives of British children who have experienced problems or hardships, such as abuse, serious illness and poverty. History The BBC Children in Need Appeal is the most important single event in the BBC calendar and the only occasion when the whole of the BBC joins together in support of a single project on TV, radio and online. The BBC's first broadcast appeal for children took place in 1927, in the form of a five-minute radio broadcast on Christmas Day. It raised about £1,143 which equates to about £27,150 by today's standards. The first televised appeal took place in 1955 and was called the Children's Hour Christmas Appeal, with Sooty and Harry Corbett fronting it. The Christmas Day Appeals continued on TV and radio right up until 1979, with stars such as Terry Hall, Eamonn Andrews, Leslie Crowther and Michael Aspel. During that time a total of £625,836 was raised. Terry Wogan first appeared during this five-minute appeal in 1978 and again in 1979. The appeal in 1980 was broadcast for the first time as a telethon. This event, hosted by Terry Wogan, Sue Lawley and Esther Rantzen, captured the public's imagination to such an extent that the amount raised increased dramatically to more than £1 million.

85. Alström Syndrome UK info@alstrom.org.uk. Who is it for. alstrom syndrome patients, their carers andprofessionals. How to Contact. Call direct. Accessibility http://www.guide-information.org.uk/guide/search_index_detail.lasso?RecID=G30256

86. Impaired Glucose Tolerance Leads To Delayed Diagnosis Of Alstrom Syndrome -- Hol OBJECTIVETo emphasis the need for timely diagnosis of alstrom syndrome. CASEWereport a case of latedetected alstrom syndrome in a boy 15 1/2 years of http://care.diabetesjournals.org/cgi/content/abstract/18/5/698

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Request Permissions PubMed PubMed Citation Articles by Holder, M. Articles by Gilli, G. ARTICLES Impaired glucose tolerance leads to delayed diagnosis of Alstrom syndrome M Holder, W Hecker and G Gilli Olgahospital, Department of Pediatrics, Stuttgart, Germany. OBJECTIVETo emphasis the need for timely diagnosis of Alstrom syndrome. CASEWe report a case of late-detected Alstrom syndrome in a boy 15 1/2 years of age who was admitted because of poor wound healing and hyperglycemia. RESULTSDiagnosis was made and the patient's impaired glucose tolerance improved by diet. CONCLUSIONSRegular follow-ups are needed to recognize and possibly prevent late-appearing complications. This article has been cited by other articles: D. Richardson, M. Shires, and A. M. Davison

87. HONcode: Principles - Quality And Trustworthy Health Information alstrom syndrome is in compliance with the HONcode. Title of the site,alstrom syndrome. Web address, http//www.jax.org/alstrom/ http://www.hon.ch/HONcode/Conduct.html?HONConduct424846

88. Report On The Rare Diseases And Conditions Research Activities Of The National I alstrom syndrome is a rare autosomal recessive disorder that causes progressive Identification of the gene mutation causing alstrom syndrome may aid in http://rarediseases.info.nih.gov/html/reports/fy1998/nichd.html

Report on the Rare Diseases and Conditions Research Activities of the National Institutes of Health 1998 National Institute of Child Health and Human Development (NICHD) Overview of Rare Diseases Research Activities The mission of the National Institute of Child Health and Human Development is to conduct and support research on the reproductive, physiologic and behavioral processes that determine the health of individuals and populations. The Institute's programs are based on the concept that adult health and well-being are determined in part by episodes early in life and that human development continues throughout the life span. Diseases or conditions that interfere with healthy development are of concern to the Institute and thus, the NICHD supports research in the prevention, diagnosis, evaluation and treatment of many rare diseases and disorders. Recent Scientific Advances in Rare Diseases Research Familiar Hyperinsulinemia Familiar hyperinsulinemia, also known as nesidioblastosis, is characterized by unregulated insulin secretion in the neonatal period despite the presence of severe, life-threatening, hypoglycemia. NICHD-supported investigators have currently found two different mutations in the sulfonylurea receptor gene in individuals affected with this disorder. Mutational analyses will be undertaken on blood samples obtained from 50 affected individuals of various ethnic backgrounds and clinical symptoms. These studies will enable the investigators to establish the frequency of the gene mutations in a variety of ethnic groups and to correlate clinical status of patients with their genetic make-up. These investigations may help to predict which individuals will respond to medical therapy and which ones will require surgical intervention to resolve their severe hypoglycemia.

89. Annual Report On The Rare Diseases And Conditions Research Activities Of The Nat alstrom syndrome is a rare autosomal recessive disorder. Fewer than 100 caseshave been diagnosed since the disorder was first reported in 1959. http://rarediseases.info.nih.gov/html/reports/fy2000/nichd.html

Annual Report on the Rare Diseases and Conditions Research Activities of the National Institutes of Health FY 2000 National Institute of Child Health and Human Development (NICHD) Overview of NICHD Rare Diseases Research Activities Recent Scientific Advances in Rare Diseases Research Polycystic Ovarian Syndrome (PCOS) Clomiphene citrate (CC) is a drug successfully used to induce ovulation in women with PCOS; however, many women are resistant to the drug. To determine if hyperinsulinemia may be involved in the resistance to CC, metformin, an insulin-sensitizer, has been administered to CC-resistant women while they are being treated with CC. Seventy-five percent of the participants given metformin ovulated, compared to 27% given placebo. Furthermore, 55% given metformin conceived, compared to less than 10% given placebo. This study provides compelling evidence that hyperinsulinemia of PCOS is associated with resistance to CC and suggests a therapy for ovulation induction. PCOS symptoms have been noted to vary with racial and ethnic groups. Because the metabolic abnormalities may increase the risk for cardiovascular diseases, these differences are a health disparity issue that is worth pursuing. Due to higher levels of low-density lipoproteins (LDLs) in their blood, Hispanic women have a higher risk of developing blocked arteries than Caucasian women. Differences in serum lipids of Hispanic women with PCOS and weight-matched Hispanic controls have been demonstrated. The elevated levels of androgen of PCOS along with the higher level of lipids in Hispanic women may have an adverse effect on cardiovascular risk.

90. Dilated Cardiomyopathy And Sensorineural Hearing Loss : A Heritable Syndrome Tha Homozygosity mapping at alstrom syndrome to chromosome 2p. Natural historyof alstrom syndrome in early childhood onset with dilated cardiomyopathy. http://circ.ahajournals.org/cgi/content/full/101/15/1812

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 ... Request Permissions PubMed PubMed Citation Articles by Seidman, C. E. Related Collections Congestive Myocardial cardiomyopathy disease Genetics of cardiovascular disease Heart failure - basic studies Circulation. Clinical Investigation and Reports Dilated Cardiomyopathy and Sensorineural Hearing Loss Hara Levy, MD Somkiat Sangwatanaroj, MD Diane Fatkin, MD Calum MacRae, MBChB Christopher Halpin, PhD Roland Eavey, MD Edward F. Philbin, MD Hugo Katus, MD J. G. Seidman, PhD Christine E. Seidman, MD Correspondence to Christine E. Seidman, MD, Dept of Genetics/Alpert Room 533, Harvard Medical School, 200 Longwood Avenue, Boston MA 02115. E-mail Abstract Top Abstract Introduction Methods Results Discussion References Background hearing loss (SNHL) are prevalent disorders that occur alone or as components of complex multisystem syndromes. Multiple

91. Arch Pediatr Adolesc Med -- Abstract: Growth Hormone Deficiency In Two Siblings PARTICIPANTSTwo siblings with alstrom syndrome who were referred to the Endocrine alstrom syndrome confirmation of linkage to chromosome 2p1213 and http://archpedi.ama-assn.org/cgi/content/abstract/147/1/97

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA (1998-2004) JAMA CareerNet For The Media Meetings Peer Review Congress Vol. 147 No. 1, January 1993 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager Articles in PubMed by Alter CA Moshang T Articles that cite this article Contact me when this article is cited Growth hormone deficiency in two siblings with Alstrom syndrome C. A. Alter and T. Moshang Jr Department of Pediatrics, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine 19104-4399. OBJECTIVETo investigate if there is an endocrinologic explanation for the short stature in patients with Alstrom syndrome. DESIGNPatient reports. SETTINGThe Children's Hospital of Philadelphia, Pa. PARTICIPANTSTwo siblings with Alstrom syndrome who were referred to the Endocrine Division for evaluation of obesity, growth, and glucose metabolism.

92. Primary Identified Etiology - Deafblind 101 Aicardi syndrome. 102 Alport syndrome. 103 alstrom syndrome. 104 Apertsyndrome (Acrocephalosyndactyly, Type 1). 105 BardetBiedl syndrome (Laurence http://www.tsbvi.edu/Education/db-etiology.htm

Home Site TOC Site Search Education Primary Identified Etiology - Deafblind Links about Syndromes and Rare Diseases Hereditary/Chromosomal Syndromes and Disorders 101 Aicardi syndrome 102 Alport syndrome 103 Alstrom syndrome 104 Apert syndrome (Acrocephalosyndactyly, Type 1) 105 Bardet-Biedl syndrome (Laurence Moon-Biedl) 106 Batten disease 107 CHARGE association 108 Chromosome 18, Ring 18 109 Cockayne syndrome 110 Cogan Syndrome 111 Cornelia de Lange 112 Cri du chat syndrome (Chromosome 5p- syndrome) 113 Crigler-Najjar syndrome 114 Crouzon syndrome (Craniofacial Dysotosis) 115 Dandy Walker syndrome 116 Down syndrome (Trisomy 21 syndrome) 117 Goldenhar syndrome 118 Hand-Schuller-Christian (Histiocytosis X) 119 Hallgren syndrome 120 Herpes-Zoster (or Hunt) 121 Hunter Syndrome (MPS II) 122 Hurler syndrome (MPS I-H) 123 Kearns-Sayre syndrome 124 Klippel-Feil sequence 125 Klippel-Trenaunay-Weber syndrome 126 Kniest Dysplasia 127 Leber congenital amaurosis 128 Leigh Disease 129 Marfan syndrome 130 Marshall syndrome 131 Maroteaux-Lamy syndrome (MPS VI) 132 Moebius syndrome 133 Monosomy 10p 134 Morquio syndrome (MPS IV-B) 135 NF1 - Neurofibromatosis (von Recklinghausen disease) 136 NF2 - Bilateral Acoustic Neurofibromatosis 137 Norrie disease 138 Optico-Cochleo-Dentate Degeneration 139 Pfieffer syndrome 140 Prader-Willi 141 Pierre-Robin syndrome 142 Refsum syndrome 143 Scheie syndrome (MPS I-S) 144 Smith-Lemli-Opitz (SLO) syndrome 145 Stickler syndrome 146 Sturge-Weber syndrome 147 Treacher Collins syndrome 148 Trisomy 13 (Trisomy 13-15, Patau syndrome)

93. Oklahoma Deaf-Blind Technical Assistance Project - Major Causes Of Deaf-Blindnes Aicardi Syndrome; Alport Syndrome; alstrom syndrome; ApertSyndrome (Acrocephalosyndactyly, Type 1); BardetBiedl Syndrome (Laurence Moon-Biedl) http://www.ou.edu/okdbp/mcauses.htm

Oklahoma Deaf-Blind Technical Assistance Project Home Project Abstract Project Staff Who is Eligible? ... Training Major Causes Referral Form Advisory Board Links Major Causes of Deaf-Blindness Etiology: Indicate the etiology code that best represents the mahor identified cause of deaf/blindess for the individual from one of the following five areas. Please specify etiologies not listed. Hereditary Syndromes and Disorders Aicardi Syndrome Alport Syndrome Alstrom Syndrome Apert Syndrome (Acrocephalosyndactyly, Type 1) Bardet-Biedl Syndrome (Laurence Moon-Biedl) Batten disease CHARGE Association Chromosome 18, Ring 18

94. Alstrom-Hallgren Syndrome Definition - Medical Dictionary Definitions Of Popular Online Medical Dictionary and glossary with medical definitions. http://www.medterms.com/script/main/art.asp?articlekey=39605

95. Alstrom's Syndrome - St. Joseph Mercy, Ann Arbor Michigan alstrom s syndrome St. Joseph Mercy Health System Hospitals serving Ann Arbor,SE Michigan, Washtenaw County, Livingston County, Wayne County, http://www.sjmercyhealth.org/12416.cfm

@import url(default.css); Online Health Information Health Information - Support Groups Back to Health Library Print This Page Email to a Friend Self Help Clearinghouse Alstrom's Syndrome Alstrom Syndrome International This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site. Alstrom Syndrome International International network. 4 affiliated groups (Canada, France, Brazil and UK). Founded 1995. Provides support and networking for families affected by Alstrom syndrome. Supports medical research initiatives to more fully understand the complexities of Alstrom syndrome and develop better therapies for Alstrom patients. Publishes a quarterly newsletter. Provides information resources to families, educators, researchers and physicians. WRITE: Alstrom's Syndrome International 14 Whitney Farm Rd.

96. Print Manager alstrom s syndrome. Table of Contents. alstrom s syndrome alstrom s syndromeInternational 14 Whitney Farm Rd. Mount Desert, ME 04660 http://yalenewhavenhealth.org/WebApps/PrintFriendly/PrintManager.aspx?URL=/libra

97. Alstrom's Syndrome, Eastern Carolina alstrom s syndrome University Health Systems of Eastern Carolina serves tarboro,ahoskie, edento, winsor, maxhead, dear county, outebanks counties in http://www.uhseast.com/117515.cfm

Health News Health Library Health Topics Healthy Living ... Nutrition Self-Help Resources Information about national and local self-help organizations and support groups. Alstrom's Syndrome This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site. Alstrom Syndrome International International network. 4 affiliated groups (Canada, France, Brazil and UK). Founded 1995. Provides support and networking for families affected by Alstrom syndrome. Supports medical research initiatives to more fully understand the complexities of Alstrom syndrome and develop better therapies for Alstrom patients. Publishes a quarterly newsletter. Provides information resources to families, educators, researchers and physicians. WRITE: Alstrom's Syndrome International 14 Whitney Farm Rd.

98. Research Findings Register: Summary Number 425 alstrom s syndrome, inborn errors of metabolism, MeckelGruber syndrome, Goutiere syndrome - 1 locus,Fraser syndrome - 1 locus,alstrom s syndrome http://www.refer.nhs.uk/ViewRecord.asp?ID=425

99. Alström Syndrome Of Canada cheap printer toner,Cheap toner for laser printers and ink listing. Find thetoner refill and inket cartridges you need for cheap price and top quality. http://alstromsyndrome.ca/

used laser printer abord?ent the top carefully, and the carpet was posed on the ground for y d?oser. Here, a crat?e entour?par snow?ait filled of one?aisse black mud which bubbled. In his medium, a character?l' malevolent air, the malignant glance and the long claws and libert?lorsque gamekeeper to used laser printer emerges derri?e she. The man holds up a dagger; he threatens White-Snow of it. But?l' urgent to strike it, its arm weakens. It l?he its weapon and falls?genoux to the feet from the Princess?ouvant?. "Forgive me, g?it it. it to you, procreate you, ridges of new followers of the newspaper SHOCK, embryos d?une next civilization where only kindnesses will reign, orgasmes literary, intense crises of SHOCK procreating a soft harmonious joy after design, and finally agree to go on holiday in such a place, but only apr? to have made the purchase of a cellular thone, d?une chart modem and of a portable. All of which you r?ez, it is a speed of connection faster. used laser printer The night, you fa?es of the r?es in HTML. You add "COM"?chaque time that you type a point by using your text processing. When you go to the toilet, you say:

100. MedlinePlus Medical Encyclopedia: Alström Syndrome Alström syndrome is an inherited disease characterized by progressive blindness,deafness, earlyonset There is no specific treatment for this syndrome. http://www.nlm.nih.gov/medlineplus/ency/article/001665.htm

@import url(/medlineplus/images/advanced.css); Skip navigation Medical Encyclopedia Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Alstr¶m syndrome Contents of this page: Definition Causes, incidence, and risk factors Symptoms Signs and tests ... Calling your health care provider Definition Alstr¶m syndrome is an inherited disease characterized by progressive blindness deafness , early-onset type 2 diabetes mellitus , and obesity . Intelligence is not affected. Causes, incidence, and risk factors Alstr¶m syndrome is an autosomal recessive inherited disorder, which means that a person must inherit a copy of the defective gene from both parents in order to be affected. It is extremely rare, but is more common in Holland and Sweden than in the United States. The mutated gene, , was recently identified, but it is not yet known how this gene causes the disorder. Symptoms Blindness or severe vision impairment in infancy Symptoms of childhood-onset or type 2 diabetes Obesity Deafness Dark patches of skin (acanthosis nigricans) Growth retardation Impaired heart function ( cardiomyopathy ), which may lead to heart failure

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