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Extractions: (McArdle Krankheit, Myophosphorylase Defizienz) Inhalt Beschreibung der Erkrankung: McArdle, was ist das? Medizinischer Text (* = Quelle: Muskelerkrankungen, Felix Jerusalem und Stephan Zierz, Georg Thieme Verlag Stuttgart, 2. Auflage, 1991) Deutsch Englisch McArdle Krankheit McArdle Disease Glykogenspeicherkrankheit Typ V Glycogen Storage Disease Typ V Glykogenose Glycogenosis Myophosphorylase Mangel Myophosphorylase Deficiency Auf der DGM-Homepage: http://www.dgm.org/muskelk/letters/letter3/kilimann.html http://www.ruhr-uni-bochum.de/pressemitteilungen-1996/msg00135.html
Richard Evershed Research phosphorylase and pyridoxal phosphate implications in mcardles disease, InAdvances in Food and Nutrition Research 40, 135-147, Academic Press Inc. http://www.chm.bris.ac.uk/org/evershed/research/evershed/richard_e_publications.
Extractions: A) Papers in primary journals [ top 1. E.D. Morgan, R.P. Evershed and R.C. Tyler (1979) Gas chromatographic and structure analysis of volatile pheromons in insects. J. Chromatogr. R.P. Evershed and E.D. Morgan (1980) A chemical study of the Dufours glands of two Attine ants. Insect. Biochem. R.P. Evershed and E.D. Morgan (1981) Chemical investigations of the Dufours gland of Attine ants. Insect. Biochem
Entrez PubMed Impairment of muscle glycogenolysis in McArdle s disease Impairment of musclemitochondrial oxidative metabolism in mcardles s disease. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=8
AGSD UK Site : Home Page The Association for Glycogen Storage disease (UK) was founded in 1986 to provide 734 mcardles 485.00 180.76 665.76 29 Type III 748.20 33.59 781.79 http://www.agsd.org.uk/home/
Extractions: Registered Charity No. 327841 Home Email How we can help Join ... About us Fri Sep 9 What we do How can we help? What is Glycogen Storage Disease? Forums ... Enter administration section Welcome to AGSD! The Association for Glycogen Storage Disease (UK) was founded in 1986 to provide support and help for famlies affected by GSD by providing information, issuing Newsletters and holding Conferences and Workshops. Glycogen Storage Disease (GSD) occurs when there is an absence or deficiency of the enzyme needed to produce or break down glycogen in the body. GSD primarily affects the liver and/or muscles. Below, you can read news and updates concerning AGSD (UK). On the left, is a navigation bar where you can click on a link to move around the site. On the right, is a voting poll and quicklinks. Posted : 05 August 2005
Extractions: ISI Web of Science (4) PubMed PubMed Citation Articles by Wojtaszewski, J. F. P. Kirsty J. Mustard, D. Grahame Hardie, Henning Beck-Nielsen, Erik A. Richter, and Department of Human Physiology, Copenhagen Muscle Research Centre, Institute of Exercise and Sport Sciences, University of Copenhagen, DK-2100 Copenhagen; Diabetes Research Centre, University of Southern Denmark and Department of Endocrinology, Odense University Hospital, DK-5000 Odense, Denmark; and
Muscular Dystrophy Campaign McArdle s disease does not affect life expectancy. mcardles s disease is inheritedin an autosomal recessive pattern. Back to the McArdle s disease home http://www.muscular-dystrophy.org/about_your_condition/mcardles_disease/introduc
Glycogen Storage Disease Glycogen storage disease information, links to national and international Liver Foundation, Type I Glycogan Storage disease Pamphlet; mcardles Page, http://www.kumc.edu/gec/support/glycogen.html
McArdle S Disease Information Source This site provides useful information on McArdle s disease, a Glycogen Storagedisease. It contains a description of McArdle s disease (lack of the http://home.nyc.rr.com/samdave/mcardles/mcdisclaimer.html
McArdle S Disease Information Source This site provides useful information on McArdle s disease, a Glycogen Storage disease.It contains a description of McArdle s disease (lack of the myophosphorylase http://home.nyc.rr.com/samdave/mcardles/mcheader.html
Rare Diseases Terms - Office Of Rare Diseases Glycogen storage disease type 5. mcardles type glycogen storage disease. Links todisease information are being added on a regular basis, so please check http://ord.aspensys.com/asp/diseases/diseaseinfo.asp?ID=6528
Rarelink.net - Diagnoselisten Glykogen Storage Disease Type V Glycogen storage disease V; McArdle disease, mcardles sjukdom; Glykogenos typ V;Myofosforylasbrist, Glykogen storage disease type V; Glykogenose type V http://www.rarelink.dk/diagnosedetail.jsp?diagnoseId=168
McArdles Sjukdom - Små Och Mindre Kända Handikappgrupper Flodmark B, Ockander L. Misstänk mcardles sjukdom vid muskelsmärta. Läkartidningen1995; 92 20202022. Haller RG. Treatment of McArdle disease. http://www.sos.se/SMKH/2003-29-167/2003-29-167.htm
Extractions: HTML-version:1.0 Socialstyrelsen Detta är ett utdrag ur Socialstyrelsens kunskapsdatabas om små och mindre kända handikappgrupper. Med små och mindre kända handikappgrupper avses ovanliga sjukdomar/skador som leder till omfattande funktionshinder och som finns hos högst 100 personer per miljon invånare. Syftet med databasen är att ge aktuell information om små och mindre kända handikappgrupper och om det stöd och den service som dessa grupper behöver. För ytterligare information om aktuell diagnos hänvisas till informationsmaterial, litteratur och databaser som anges under resp diagnos. myofosforylasbrist fosforylas Orsak till sjukdomen/skadan Fosforylas myofosforylas fosfokreatinkinas (CK). Enstaka personer med McArdles sjukdom har endast delvis avsaknad av myofosforylas . Dessa personer kan ha lindrigare symtom. myofosforylas.
McArdles Sjukdom - Små Och Mindre Kända Handikappgrupper mcardles sjukdom är en av fem kända glykogenomsättningssjukdomar. Creatinetherapy in myophosphorylase deficiency (McArdle disease) a http://www.sos.se/smkh/2003-29-167/2003-29-167.htm
Extractions: HTML-version:1.0 Socialstyrelsen Detta är ett utdrag ur Socialstyrelsens kunskapsdatabas om små och mindre kända handikappgrupper. Med små och mindre kända handikappgrupper avses ovanliga sjukdomar/skador som leder till omfattande funktionshinder och som finns hos högst 100 personer per miljon invånare. Syftet med databasen är att ge aktuell information om små och mindre kända handikappgrupper och om det stöd och den service som dessa grupper behöver. För ytterligare information om aktuell diagnos hänvisas till informationsmaterial, litteratur och databaser som anges under resp diagnos. myofosforylasbrist fosforylas Orsak till sjukdomen/skadan Fosforylas myofosforylas fosfokreatinkinas (CK). Enstaka personer med McArdles sjukdom har endast delvis avsaknad av myofosforylas . Dessa personer kan ha lindrigare symtom. myofosforylas.
Q Describe The Structure Of Chromatin. A Condensed By A deficiency of debranching enzyme alpha1,6-glucosidase Q What are the findingsin mcardles s disease and what is the problem A increased glycogen in http://umed.med.utah.edu/palm/supermemo/sm_1st_Aid__Biochem.txt
Rarelink.net - Diagnoslistan McArdles Sjukdom Du är här Hem Diagnoslistan mcardles sjukdom Glycogen storage disease V;McArdle disease, mcardles sjukdom; Glykogenos typ V http://www.rarelink.se/diagnosedetail.jsp?diagnoseId=168
Rarelink.net - Diagnoslistan McArdles Sjukdom (Glykogenos Typ V) Du är här Hem Diagnoslistan mcardles sjukdom (Glykogenos typ V) Glycogen storage disease V; McArdle disease, mcardles sjukdom; Glykogenos typ V http://www.rarelink.se/diagnosedetail.jsp?diagnoseId=168&synonymId=335
1300 Ziekten Glycogen Storage disease Type 5 (mcardles) Glycogen Storage disease Type 9Hallervorden Spatz Hartnup disease (Tryptophan Malabsorption) http://boks.be/nl_site/html/1300dis.htm
