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
Extractions: Clinical Resources by Topic: Metabolic Disorders Kearns-Sayre Syndrome Clinical Resources Pediatrics Pathology Genetics Clinical Guidelines ... Miscellaneous Resources See also: Pediatrics Resources See also General Pediatrics Resources Pathology Resources Genetics Resources See also General Genetics Resources Clinical Guidelines News Resources Miscellaneous Kearns-Sayre Syndrome Clinical Resources YAHOO - Health:Diseases and Conditions:Metabolic Diseases
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
Extractions: 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.
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
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
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
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
Extractions: 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.
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
Extractions: 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.
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
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
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
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-
[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
Extractions: Date Prev Date Next [Chronological] [Thread] ... [Top] 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. He was diagnosed with a rare disease = called=20 Kerns-Sayre Syndrome. 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)
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
Extractions: Clinical Resources by Topic: Metabolic Disorders Kearns-Sayre Syndrome Clinical Resources Pediatrics Pathology Genetics Clinical Guidelines ... Miscellaneous Resources See also: Pediatrics Resources See also General Pediatrics Resources Pathology Resources Genetics Resources See also General Genetics Resources Clinical Guidelines News Resources Miscellaneous Kearns-Sayre Syndrome Clinical Resources YAHOO - Health:Diseases and Conditions:Metabolic Diseases
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
Extractions: 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.
Extractions: 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. 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
