61. Articles Martial Arts, mcardles disease, Medical Conditions, Medicine Ball Training,Meditation, Menopause, Mental Conditioning, Metabolism, Mind Body Training http://www.ptonthenet.com/articles.aspx

home membership newsletters testimonials ... register member's access username password forgotten your password? downloads contact us welcome visitors Articles We now have almost 1000 articles across 14 categories , written by a wide variety of internationally renowned Authors In the article library, you’ll find in depth features on functional training, core training, program design, sports training, performance nutrition, Pilates, injury prevention and personal training sales and marketing – to name just a few! PTontheNET.com members can access the entire article database 24 hours a day. Visitors are welcome to browse and search topics and view excerpts of each article! Browse the last 3 months topics , or use the search below to refine your search. Search here! How to Use Search Type in word or phrase or use any of the search fields below to hone your search! To complete your search, please

62. ~MC // Medical-Conditions.org // Medical Conditions MC 1288 MC1288 MC1288 MCA Infarction McArdle Disease mcardles disease MCC GeneMCC Genes MCF Virus MCF Viruses MCGF-2 McGill Pain Questionnaire McGill Pain http://www.medical-conditions.org/?q=~Mc

63. EVALUATING MUSCLE SYMPTOMS -- Petty 74 (Supplement 2): 38 -- Journal Of Neurolog In glycolytic defects such as mcardles disease it is clearly related toexercise—severe pain with contracture develops often within one minute of ischaemic http://jnnp.bmjjournals.com/cgi/content/full/74/suppl_2/ii38

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS Author Keyword(s) Vol Page [Advanced] This Article Extract Full Text (PDF) Submit a response ... Alert me if a correction is posted Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Petty, R. Related Collections Neurology in Practice Neuromuscular disease Journal of Neurology Neurosurgery and Psychiatry BMJ Publishing Group EVALUATING MUSCLE SYMPTOMS Richard Petty Correspondence to: Dr Richard Petty, Department of Neurology, Southern General Hospital, 1345 Govan Road, Glasgow G51 4TF, UK; Keywords: muscular disease; muscle symptoms The correct interpretation of neuromuscular symptoms is critical, with terms such as fatigue or weakness rarely being used with their medical sense. The

64. McArdle´s, Morbus McArdle, Glykogenose Typ 5, Phosphorylase Kinase Defizienz, P Translate this page mcardles disease, Private Seite eines McArdle Betroffenen in den USA (spezielleInfo). Australien Homepages Australien http://www.morbus-pompe.de/mp/html/wissenschaftliches/glyko_typ5/mcardle_info.ht

Muskelglykogenose Glykogenose Typ V (McArdle Krankheit, Myophosphorylase Defizienz) Inhalt Beschreibung der Erkrankung 1. McArdle- und andere Muskelspezialisten in Deutschland 2. Deutsche Selbsthilfegruppen und Hilfsorganisationen 3. Internationale Links von Selbsthilfegruppen ... 5. Englischsprachige Literatur 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 1. McArdle- und andere Muskelspezialisten in Deutschland Homepages (deutschsprachig) Ansprechpartner, Adresse, E-Mail Muskelzentrum Ruhrgebiet spezielle Info Anschrift und Ansprechpartner: Herr Dr. Matthias Vorgerd Muskelzentrum Ruhrgebiet Kliniken Bergmannsheil D-44789 Bochum Tel.: 0234/302-6806

65. 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.

Page last modified Archaeological Chemistry Soil chemistry and element cycling Palaeoenvironmental and palaeoclimate reconstruction Biomolecular palaeontology ... Industrial forensic science Publications PUBLISHED WORKS OF EVERSHED Overview: A: 179 listed full papers B: 19 invited chapters and reviews in edited works C: 29 contributions to refereed conference volumes D: 11 extended abstracts E: 5 contributions to other research media Total of 233 items 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

66. 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

67. 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/

LOW GRAPHICS VERSION HELP 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 2005 AGSD(UK) Annual Conference The 2005 AGSD(UK) Annual Conference will be held on Sunday 16th October 2005 in Milton Keynes, UK.

68. AMPK Activity And Isoform Protein Expression Are Similar In Muscle Of Obese Subj kinase in exercise regulation of glucose utilization and glycogen synthaseactivity in skeletal muscle; insights from patients with mcardles s disease. http://ajpendo.physiology.org/cgi/content/full/286/2/E239

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: Am J Physiol Endocrinol Metab 286: E239-E244, 2004. First published October 7, 2003; doi:10.1152/ajpendo.00326.2003 This Article Abstract Full Text (PDF) All Versions of this Article: most recent Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed ... Cited by other online articles Search for citing articles in: ISI Web of Science (4) PubMed PubMed Citation Articles by Wojtaszewski, J. F. P. AMPK activity and isoform protein expression are similar in muscle of obese subjects with and without type 2 diabetes 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

69. 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

70. 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

Glycogen Storage disease I (glucose-6-phosphatase deficiency, Von Gierke) II (alpha glucosidase deficiency, Pompe) III (debrancher enzyme deficiency, Cori) IV (brancher enzyme deficiency, Anderson) V (muscle glycogen phosphorylase deficiency, McArdle) VII (muscle phosphofructokinase deficiency, Tauri) VI (liver phosphorylase deficiency, Hers) IX (liver glycogen phosphorylase kinase deficiency) Association for Glycogen Storage (AGSD) PO Box 896 Durant, IA 52747-9769 Phone: 563.785.6038 (also fax) Web site: www.agsdus.org Association for Glycogen Storage Disease (UK) Pompe Disease Page , United Kingdom Association Francophone des Glycogenoses (French Glycogen Storage Disease Association) Rue G. Guynemer 37390 La Membrolle S/Choiselle Tel et Fax: 02.47.87.03.18 E-mail: ahugon@infonie.fr Acid Maltase Deficiency Association (GSD type II) P.O. Box 700248 San Antonio, Texas 78270-0248 Phone: 210-494-6144 or 210-490-7161 Fax: 210-490-7161 or 210-497-3810 E-mail: tianrama@aol.com

71. 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

72. 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

73. 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

74. 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

75. 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

Socialstyrelsen 106 30 Stockholm Socialstyrelsen klassificerar sin utgivning i olika dokumenttyper McArdles sjukdom Glykogenos typ V Myofosforylasbrist Sjukdom/skada/diagnos Orsak till sjukdomen/skadan Symtom Diagnostik ... Dokumentinformation Dokumentdatum: 2003-02-03 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. Sjukdom/skada/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.

76. 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

Socialstyrelsen 106 30 Stockholm Socialstyrelsen klassificerar sin utgivning i olika dokumenttyper McArdles sjukdom Glykogenos typ V Myofosforylasbrist Sjukdom/skada/diagnos Orsak till sjukdomen/skadan Symtom Diagnostik ... Dokumentinformation Dokumentdatum: 2003-02-03 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. Sjukdom/skada/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.

77. 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

78. 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

79. 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

80. 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

1300 (bekende) Metabole ziekten (van Research Trust for Metabolic Dieases in Children) De lijst... Abetalipopprotinaemia Achondroplasia Adenosine Deaminase Deficiency Adrenal Hyperplasia Adrenal Hypoplasia Aicardi-Goutieres Syndrome Alagille Syndrome Alcaptonuria Alpers Disease Alpha One Antitrypsin Deficiency 5 Alpha Reductase Deficiency Alports Syndrome Alstroni s Disease Amyloidosis Androgen Insensitivity Arachidonic Acid, Absence of: Arginase Deficiency Arginosuccinic Aciduria (ASA) Aromatic amino acid decarboxylase deficiency Arterial Calcification of Infancy Occlusive Infantile Arteriopathy Arylsulphatase A Deficiency Aspartyl Glucosaminuria Ataxia Telangiectasia Bartters Syndrome Batten's Disease Berardinelli Lipodystrophy Syndrome Beta Ketothiolase Deficiency 2 Methylacetoacetyl CoA Thiolase Deficiency Beta-Methylcrotonylglycinuria Biliary Hypoplasia Biotin Deficiency CI Esterase Deficiency Carbamyl Phosphate Synthetase Deficiency (CPS) Carbohydrate Deficient Glycoprotein Syndrome Carnitine Deficiency Carnitine Palmitoyltransferase Deficiency Cerebrotendinous Xanthomatosis Chondrodysplasia Punctata Citrullinaemia Cobalamin C/G Deficiency Cockayne Syndrome Crigler Najjar Syndrome type I Cystinosis Cystinuria Cytochrome C Oxidase Deficiency Diabetes Insipidus Dysmyelination Endocardial Fibroelastosis Ethylmalonic Aciduria Ethylmalonic Adipic Aciduria Farbers Disease Fabry's Disease Fanconi's Syndrome Fish Odour Syndrome (Trimethylamineuria) Fructose Intolerance, hereditary

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