61. Rural Nurse Organization Clinic Digital Library kearnssayre syndrome Access document. Pathology Resources. Neuromuscular Disease Center (WUSTL) Homepage. Pathology Illustrations Table of contents http://ruralnurseorganization-dl.slis.ua.edu/clinical/metabolism/inborn/mitochon

Clinical Resources by Topic: Metabolic Disorders Kearns-Sayre Syndrome Clinical Resources Pediatrics Pathology Genetics Clinical Guidelines ... Miscellaneous Resources See also: Genetic Testing Clinical Resources General Genetic Disorders Clinical Resources General Metabolic Disorders Clinical Resources Kearns-Sayre Syndrome Patient/Family Resources The Merck Manual 17th Ed.-1999: Table of contents Chapter 184: Muscular Disorders: Table of contents Myopathies: Access document Pediatrics Resources See also General Pediatrics Resources Pediatrics (eMedicine): Table of contents Kearns-Sayre Syndrome: Access document Pathology Resources Neuromuscular Disease Center (WUSTL): Homepage Table of contents Mitochondrial Disease: Access document Cytochrome Oxidase: Access document Ragged Red Fibers: Access document SDH: Access document Ultrastructure: Access document Genetics Resources See also General Genetics Resources Online Mendelian Inheritance in Man: Homepage Kearns-Sayre Syndrome: Access document Clinical Guidelines National Guideline Clearinghouse: MeSH browse Detailed search Kearns (Keyword search): List of documents News Resources Doctor's Guide to the Internet Homepage Neurology News List of documents Brain Disease (Keyword search): List of documents Miscellaneous Kearns-Sayre Syndrome Clinical Resources YAHOO - Health:Diseases and Conditions:Metabolic Diseases Additional Metabolic Diseases resources ( These sites have not been reviewed.

62. Kearns-sayre kearnssayre syndrome. 4 Patient Support Information. PubMed Medline search on kearns-sayre syndrome Mitochondrial myopathies factsheet National http://www.ion.ucl.ac.uk/library/patient/kearnes.htm

Kearns-Sayre syndrome Patient Support Information PubMed Medline search on Kearns-Sayre Syndrome Mitochondrial myopathies factsheet: National Institute for Neurological Disorders and Stroke Support Groups Climb The Quadrangle, Crewe Hall, Weston Road, Crewe, Cheshire CW1 6UR Tel: 01270 250221 (information, advice and support to parents and professionals involved with metabolic diseases). The office is open 9.00am - 5.00pm Mondays to Fridays. Fax: 01270 250244 A national umbrella organisation working on behalf of children, young people and families affected by metabolic disease. Offers a telephone helpline for information, counselling and support; written information by post (detailed information only available following confirmed diagnosis, appropriate professional counselling and telephone contact); details of other agencies and sources of help; information about the latest research and whom to contact for specialist advice etc.

63. Syndrome De Kearns Et Sayre : Sites Et Documents Francophones kearns et sayre ; kearns et sayre, syndrome . Synonyme(s) MeSH syndrome de kearns-sayre. http://www.chu-rouen.fr/ssf/pathol/kearnsetsayresyndrome.html

Syndrome de Kearns et Sayre Synonyme(s) CISMeF KSS ; Kearns et Sayre ; kearns et Sayre, syndrome . Synonyme(s) MeSH Syndrome de Kearns-Sayre Arborescence(s) syndrome de Kearns et Sayre kearns-sayer syndrome maladies cardiovasculaires maladies de l'appareil locomoteur maladies de l'oeil maladies du système nerveux ... métabolisme et nutrition, maladies Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter toutes les ressources ou seulement les principales ou utiliser l' outil de recherche les recommandations les documents concernant l' enseignement les documents destinés aux patients Ou consulter ci-dessous une sélection des principales ressources : guide ressources Maladie de Kearns Sayre [Site éditeur SNOF Syndicat National des Ophtalmologistes de France ; définition, clinique, sites web, bibliographie ; pays : France ; langue : français ; format : html ; accès : gratuit ; non parrainé ; daté de : 2004 ; visité le : 17/08/2004]. mots clés : maladies rares signes et symptômes *syndrome de Kearns et Sayre syndrome de Kearns et Sayre /diagnostic type : guide ressources *information patient et grand public microscopie électronique ophtalmoscopie patient Kearns-Sayre, syndrome de

64. Disabilityexchange.org - Taxonomy kearnssayre syndrome. print Print this Page. What is kearns-sayre syndrome? kearns-sayre syndrome (KSS) is a rare neuromuscular disorder with onset usually http://www.disabilityexchange.org/taxonomy/index.php?fid=3&path=3_289

65. Health/Conditions And Diseases/Neurological Disorders/Ocular Motility Disorders/ url www.emedicine.com/oph/topic510.htm; NINDS kearnssayre syndrome Ryan McDonald is a 9 year old boy with kearns-sayre syndrome. http://www.thedoctorslounge.net/dir/Health/Conditions_and_Diseases/Neurological_

Advertisement Powered by Careerbuilder Search for: Home Humor Advertising Contact ... Links Specialties Cardiology Chest diseases Dermatology Endocrinology ... Urology Other Sections Membership Research Tools Medical Tutorials Medical Software ... Specialized Centers Headlines: The Medical Website Directory Popular Categories Popular Links Web Sites report abuse/spam url: report-abuse.dmoz.org/?cat=Health/Conditions_and_D... Emergency Medicine An introduction to chronic progressive external ophthalmoplegia. Includes clinical features, work up, treatment and follow up. url: www.emedicine.com/oph/topic510.htm NINDS Kearns-Sayre Syndrome Information sheet compiled by the National Institute of Neurological Disorders and Stroke. url: www.ninds.nih.gov/health_and_medical/disorders/kea... Ryan's Hope Foundation Ryan McDonald is a 9 year old boy with Kearns-Sayre Syndrome. This site is to educate the public about Ryan and his struggle with this disorder, as well as raise funds for research to cure this disease. url: www.ryanshopefoundation.org

66. ATE Responses the diagnosis of kearnssayre syndrome (KSS) in your brother is correct. kearns-sayre syndrome (KSS) is a mitochondrial deletion syndrome characterized http://www.mdausa.org/experts/viewall.cfm?id=94

67. ATE Responses My brother (age 22) was diagnosed with kearnssayre syndrome (KSS) 14 years ago. Can I develop or have in my DNA kearns-sayre syndrome (KSS)? http://www.mdausa.org/experts/question.cfm?id=4155

68. Blackwell Synergy - Cookie Absent kearnssayre syndrome A Case Report and Review of Cardiovascular Complications kearns-sayre syndrome (KSS) is a rare mitochondrial encephalomyopathy http://www.blackwell-synergy.com/doi/abs/10.1111/j.1540-8159.2005.40049.x

Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.

69. Blackwell Synergy - Cookie Absent The kearnssayre syndrome (KSS), initially described in 1958, is characterized by the triad of kearns-sayre syndrome. Association with long QT syndrome? http://www.blackwell-synergy.com/doi/abs/10.1046/j.1460-9592.2003.00292.x

Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.

70. ORPHANET - Maladies Rares - Médicaments Orphelins Translate this page MALADIE kearns-sayre, syndrome de. CIM H49.8. Le syndrome de kearns-sayre débute avant 20 ans et comporte une ophtalmoplégie, un ptosis, une rétinite http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=480

71. Kearns-Sayre, Syndrome De Translate this page Base de données sur les maladies rares et les médicaments orphelins. http://www.orpha.net/static/FR/kearnssayre.html

Accès à la base de données Orphanet Kearns-Sayre, syndrome de Accès direct aux détails Résumé Signes de la maladie OPHTALMOPLEGIE RETINITE PIGMENTAIRE TROUBLES DU RYTHME/DE LA CONDUCTION AMYOTROPHIE / MUSCLE AGENESIE ANOMALIE DE L'AUDITION/SURDITE AREFLEXIE / HYPOREFLEXIE ATAXIE / INCOORDINATION E.M.G. ANORMAL HYPOTHALAMUS-HYPOPHYSE ANOMALIE FONCTlle HYPOTONIE MUSCLE HISTOLOGIQUEMENT ANORMAL PETITE TAILLE / NANISME AGE OSSEUX RETARD DIPLEGIE/PARAPLEGIE/QUADRIPLEGIE Mise à jour : 04/09/2005 Accès à la base de données Orphanet

72. Penn State Faculty Research Expertise Database (FRED) Kearnsayre Mitochondrial Cytopathy, kearns syndrome. kearns-Sayer syndrome kearns sayre Shy Daroff syndrome, Mitochondrial Cytopathy, Kearn-sayre http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D007625

73. Publications - Clinical Medical Sciences - University Of Newcastle Submenu. Skip to content. Medical School. Publication. kearnssayre syndrome http//www.emedicine.com 2001. Posner, E; Basu, A and Turnbull, DM http://www.ncl.ac.uk/medi/publications/publication/15762

@import url("/medi/assets/css/scmsmain.css"); @import url("/medi/assets/css/scmscss.php"); Skip to main menu accessibility sitemap contact Clinical Medical Sciences University of Newcastle upon Tyne Search: Search: Main menu Skip to submenu Home Postgraduate Research ... Publications Submenu Skip to content Publication Kearns-Sayre Syndrome http://www.emedicine.com Posner, E; Basu, A and Turnbull, DM http://www.emedicine.com Staff Profiles Dr Anna Basu Telephone: +44 (0)191 202 3033 ext 43102 Email: a.p.basu@ncl.ac.uk back to top last updated: 5 July 2005 Webmaster - Catherine.McDonald@newcastle.ac.uk School of Clinical Medical Sciences Faculty of Medical Sciences University of Newcastle

74. Clinical Neuropharmacology - UserLogin Deterioration of kearnssayre syndrome Following Articaine Administration Worsening of the neuromuscular manifestations in kearns-sayre syndrome after http://www.clinicalneuropharm.com/pt/re/clnneupharm/fulltext.00002826-200505000-

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75. [DYSPHAGIA] Kern-sayre Syndrome patient with the kearnssayre syndrome and cervical dysphagia are = described. of cervical dysphagia in a patient with the=20 kearns-sayre syndrome. http://list.dysphagia.com/dysphagia/2001-April/msg00411.html

Date Prev Date Next [Chronological] [Thread] ... [Top] [DYSPHAGIA] kern-sayre syndrome Subject [DYSPHAGIA] kern-sayre syndrome From icampbelltaylor@sympatico.ca (I Campbell-Taylor) Date: Mon, 23 Apr 2001 15:01:34 -0400 000a01c0cc11$2bd280a0$912624d8@msheldon mailto:msheldon@uci.net" ;>melody = sheldon</A>=20 </DIV> <DIV style=3D"FONT: 10pt arial"><B>To:</B> <A = title=3Ddysphagia@medonline.com=20 href=3D" mailto:dysphagia@medonline.com" ;>dysphagia</A> </DIV> <DIV style=3D"FONT: 10pt arial"><B>Sent:</B> Monday, April 23, 2001 = 12:19=20 PM</DIV> <DIV style=3D"FONT: 10pt arial"><B>Subject:</B> [DYSPHAGIA] kern-sayre = syndrome</DIV> <DIV><BR></DIV> <DIV><FONT size=3D2>I was asked to evaluate a 40 y.o. gentleman with = complaints=20 of swallowing difficulty.&nbsp; He was diagnosed with a rare disease = called=20 Kerns-Sayre Syndrome.&nbsp; Is anyone familiar with the disease = process and/or=20 its affect on the swallowing = mechanism?</FONT></DIV></BLOCKQUOTE></BODY></HTML> =_NextPart_000_000E_01C0CC06.49BA7380 - To UNSUBSCRIBE from this list, please send an e-mail message to majordomo@medonline.com with the following text as a message: unsubscribe dysphagia - References [DYSPHAGIA] kern-sayre syndrome From: msheldon@uci.net (melody sheldon)

76. Neuroguide.com - Human Neurological Diseases kearnssayre syndrome. * kearns-sayre syndrome Information (NINDS) kearns-sayre syndrome, Kennedy Disease, Kinsbourne syndrome, Klippel Feil syndrome http://www.neuroguide.com/cgi-bin/pdistoc.pl?file=KearnsSayreSyndrome

77. University Medical Group - Digital Library images.MD View CollectionView Full Size, Cardiac mitochondria in kearnssayre syndrome View Full Size, Cardiac mitochondria in kearns-sayre syndrome http://umg-dl.slis.ua.edu/clinical/metabolism/inborn/mitochondrial/kearns.htm

Clinical Resources by Topic: Metabolic Disorders Kearns-Sayre Syndrome Clinical Resources Pediatrics Pathology Genetics Clinical Guidelines ... Miscellaneous Resources See also: Genetic Testing Clinical Resources General Genetic Disorders Clinical Resources General Metabolic Disorders Clinical Resources Kearns-Sayre Syndrome Patient/Family Resources The Merck Manual 17th Ed.-1999: Table of contents Chapter 184: Muscular Disorders: Table of contents Myopathies: Access document Pediatrics Resources See also General Pediatrics Resources Pediatrics (eMedicine): Table of contents Kearns-Sayre Syndrome: Access document Pathology Resources Neuromuscular Disease Center (WUSTL): Homepage Table of contents Mitochondrial Disease: Access document Cytochrome Oxidase: Access document Ragged Red Fibers: Access document SDH: Access document Ultrastructure: Access document Genetics Resources See also General Genetics Resources Online Mendelian Inheritance in Man: Homepage Kearns-Sayre Syndrome: Access document Clinical Guidelines National Guideline Clearinghouse: MeSH browse Detailed search Kearns (Keyword search): List of documents News Resources Doctor's Guide to the Internet Homepage Neurology News List of documents Brain Disease (Keyword search): List of documents Miscellaneous Kearns-Sayre Syndrome Clinical Resources YAHOO - Health:Diseases and Conditions:Metabolic Diseases Additional Metabolic Diseases resources ( These sites have not been reviewed.

78. PharmGKB: Kearns Syndrome Kearn syndrome; Kearnsayre Mitochondrial Cytopathy; kearns Sayer syndrome; kearns sayre Shy Daroff syndrome; kearns syndrome; kearns-Sayer syndrome; http://www.pharmgkb.org/do/serve?objId=PA444666&objCls=Disease

79. NORD - National Organization For Rare Disorders, Inc. NORD research award for kearnssayre syndrome Jeffrey Towbin, MD Evaluation and Treatment of Cardiac Disease in kearns-sayre syndrome http://www.rarediseases.org/research/researchgrants

Database Subscriptions Many libraries, schools, universities, and hospitals subscribe to NORD's Rare Disease Database for unlimited access to reports on more than 1,150 diseases. Index of Rare Diseases This is the list of diseases currently covered in the Rare Disease Database. Rare Disease Database Search this database for reports on more than 1,150 diseases. View sample report Index of Organizations This is the list of organizations in NORD's Organizational Database. Organizational Database Read about more than 2,000 patient organizations and other sources of help. NORD's Washington Office Read about events on Capitol Hill, funding for rare-disease research, and other topics of interest from NORD's office in Washington, DC. Research Research Grant Program Rare disease research funding opportunities being made available through NORD. Rare disease research funding opportunities being made available through NORD Member-Organizations. Read NORD's Research Program Policy to learn how NORD helps individuals, families, groups, or organizations sponsor research. October 2004 Research Awards NORD wishes to congratulate and acknowledge the individuals, families, organizations and companies who, through their generosity and commitment, have made these twenty research projects possible.

80. Kearns-Sayre Syndrome In Twins: Lethal Dominant Mutation Or Acquired Disease? -- kearnssayre syndrome in twins lethal dominant mutation or acquired disease? LP Rowland, I Hausmanowa-Petrusewicz, B Bardurska, D Warburton, http://www.neurology.org/cgi/content/abstract/38/9/1399

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Correspondence: Submit a response Alert me when this article is cited Alert me when Correspondence are posted ... 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 ... Cited by other online articles PubMed PubMed Citation Articles by Rowland, L. P. Articles by Johnson, W. G. JOURNAL ARTICLE Kearns-Sayre syndrome in twins: lethal dominant mutation or acquired disease? LP Rowland, I Hausmanowa-Petrusewicz, B Bardurska, D Warburton, I Nibroj-Dobosz, S DiMauro, M Pallai and WG Johnson Neurological Institute, Columbia-Presbyterian Medical Center, New York, NY 10032-3784. We studied twin brothers who met all diagnostic criteria for the Kearns-Sayre syndrome (KSS). The twins reinforce the view that KSS is a specific syndrome. They raise the possibility that the condition is inherited as a lethal dominant trait, a mode of inheritance that explains

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