1. Adult Outpatient Programs And Services Muscular Dystrophy Association Clinic Metabolic Diseases of the Muscle. Phosphorylase deficiency(mcardles disease). Acid Maltase Deficiency (Pompe's disease) http://www.njrehab.org/MDA.htm

Adult Outpatient Programs and Services Muscular Dystrophy Association Clinic The JFK Johnson Rehabilitation Institute's Muscular Dystrophy Association (MDA) Clinic provides a multidisciplinary approach to the diagnosis and treatment of over 40 muscular dystrophies. Adult and pediatric clinics are held once a month throughout the year. Services consist of examination, testing and counseling performed by a physiatrist, physical, occupational and speech therapist. A social worker and registered nurse also assist in assessing the patient's/family's needs. After establishing the diagnosis and treatment plan, the patient is monitored two to three times a year through follow-up clinic visits. The clinic, partially supported by the Muscular Dystrophy Association through a grant, is one of 230 hospital-based clinics affiliated with the MDA. If you suspect that you or your child may have the diagnosis of muscular dystrophy, you may call for a clinic appointment. Appointments for the adult clinic can be made by calling (732) 321-7733 and the pediatric clinic can be reached at (732) 548-7610. Diseases treated through the MDA clinic include: Muscular dystrophies Myotonic Dystrophies Duchenne's Becker's Limb-Girdle Facioscapularhumeral Congenital Distal Emery-Dreifus Motor neuron diseases Amyotrophic lateral sclerosis(ALS) Infantile progressive spinal muscular atrophy (Type 1 Werdnig Hoffman disease) Intermediate Spinal Muscular Atrophy (Type 2)

2. McArdle's Disease And Exercise I can provide a lot more information about my life with mcardles disease, if requested. http://neuro-www.mgh.harvard.edu/neurowebforum/NeuromuscularArticles/McArdlesDis

McArdle's Disease and Exercise This response submitted by David W. Brock, Ph.D. on 2/16/97. Author's Email: dbrock1111@aol.com I was diagnosed with McArdle's disease through a muscle biopsy as the University of Colorado Medical Center in 1975. I then volunteered to participate in an extensive series of research experiments in McArdle's disease. One set of experiments showed that I could do all of the exercise I wanted as long as I stayed below the cramp threshhold. I would ride a stationary bicycle with blood samples taken immediately before and after the workout. The samples showed that there was no rise in the level of creatine phosphokinase in my blood before or after the exercise, indicating that there was no muscle damage, as long as I eased off on the exertion at the first sign of cramping. Walking is probably one of the best exercises for a person with McArdle's disease, since it circulates the blood through the muscles. The main problem for a person with this disorder is that the muscles cannot burn their stored fuel, glycogen, so that their muscles must extract all of their fuel from the blood. Yesterday, I went on a vigorous five mile walk, and I did not have any problems. I did not see my urine turn brown, which would indicate myoglobinuria. The worst type of exertion for a person with this disorder to engage in is lifting heavy objects, such as moving furniture. I have often given myself severe cramps followed by myoglobinuria this way. This is because the muscles are stationary during heavy lifting and the blood flow is limited. I have found that I can lift heavy objects if I do some exercise to warm the involved muscles up first. The exact reasons why this helps are not known to medical science.

3. Mioti: Medical Condition Maxillofacial Dysostosis, • Maxillofacial Surgery. • May Hegglin Anomaly,• mcardles disease. • McCune Albright Syndrome, • McKusick Syndrome. http://www.mioti.com/cat/condition/results.asp?Alpha=M

4. Mioti: Medical Condition Condition mcardles disease. MEDLINEplus McArdle Syndrome. MEDLINEplus,a goldmine of good health information from the world's http://www.mioti.com/cat/condition/condition.asp?Cat=McArdlesDisease

5. 5 Listing Of Potential Topics Coris Disease Galactosemia McArdles Coris disease. Galactosemia. mcardles disease. Von Gierkes Disease. Pompes Disease http://www.uwlax.edu/faculty/weaver/pdfs/writing_emphasis.pdf

6. McArdle´s, Morbus McArdle, Glykogenose Typ 5, Phosphorylase Kinase Defizienz, P Translate this page Info). mcardles disease, Private Seite eines McArdle Betroffenen inden USA (spezielle Info). Homepages Australien, Erläuterung. MDA http://www.morbus-pompe.de/glyko_typ5/mcardle_info.html

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 Homepage (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

7. Untitled An English physician named Dr. Brian McArdle diagnosed the first case of mcardles disease in 1951. At that time he reported on a 30 year old man who experienced pain followed by weakness and stiffness after exercise. also known as Glycogen Storage Disease Type V . Myophosphorylase Deficiency, McArdle Glycogenesis, McArdles Myopathy or http://webportfolio.csuohio.edu/~ekutchman/Artifacts/ARTIFACT8/stand_8_mcardlepa

8. Page 17 Neuromuscular Disorders, Dystrophic Cardiomyopathy, mcardles disease, General Paediatricsand Paediatric Neurology General Paediatrics Muscular Dyshophy and http://www.keele.ac.uk/depts/rjah/yearbook/Consultants_Services/consultants__ser

Back Up Next QUINLIVAN Dr Rosaline BSc. (Hons), MB, BS, DCH, MRCP, FRCP Consultant Paediatrician with an Interest in Paediatric Neurology Secretary: Outpatient Clinics: Clinical Interests: Publications In the Following Topics: Qualification: Consultant Appointments: Sarah Evans 01691 404376 Friday all day Neuromuscular Disorders, Dystrophic Cardiomyopathy, McArdles Disease, General Paediatrics and Paediatric Neurology General Paediatrics Muscular Dyshophy and Congenital Neuropathies PET Scanning in Paediatric Cardiology Peripheral Neuropathies Congenital and Acquired McArdles disease Hereditary and congenital peripheral neuropathy, muscular dystrophy and dystrophic cardiomyopathy. Invited reviews on Becker cardiomyopathy and cardiac PET scanning in Paediatrics 1985 UCH, London 1995 Oswestry and Shrewsbury RAY Dr Sumeeta FRCA Consultant Anaesthetist Secretary: Clinical Interests: Publications: Qualification: Consultant Appointments: Mandie Owen 01691 404246 Cardio-pulmonary Resuscitation Management of Difficult Airways 1991 London 1995 Oswestry REDFORD Mr David MB FRCS FRCOG Consultant Gynaecologist Obstetrician Secretary: Outpatient Clinics: Clinical Interests: Publications: Qualification: Consultant Appointments: Jeanne McKay 01691 404302 Alternate Tuesday am Endoscopic vaginal surgery, medical complications of pregnancy

9. AGSD - UK Site - Guest Book I was diagnosed with mcardles disease in 1999 after suffering all my life never knowing what was wrong with me. http://www.agsd.org.uk/home/guestbook.asp

LOW GRAPHICS VERSION HELP Registered Charity No. 327841 Home Email How we can help Join ... About us Mon Mar 31 Guest Book Welcome to our Guest Book Please leave us a message click here Posted by Jack on the love you E-mail: dumexz5000@juno.com Posted by Vicky on the My father was diagnosed with GSD in 1961. At the time, we were told that he was only the 3rd person to be diagnosed with this disease. While doing research on Dad, my brothers and I had to undergo a lot of testing, also. My mother was told that two of us showed symptons, but the doctors refused to tell her which two. For over 40 years, we have lived with this cloud hanging over us. It's been like waiting for a bomb to explode. Since my father was in a Veterans Hospital for three years and this was where the testing was done, I tried for several years after Dad died to track down his records. Apparently, the physician in charge took them with him when he left and has since died. I did track down one of the other doctors briefly. He remembered the case, but did not know the outcome. Because of Dad's delicate health, they convinced him the second tests proved the first tests wrong and this became a giant family secret. Only now is truth finally starting to come out as my youngest brother and I are unable to keep our strength up and our children are starting to show symptoms. Unfortunately, the scarcity of information only complicates the problem. When asking for help, I have been told I am "crazy,"; "What makes you so special?"; and, "You should just let your whole family die out!"

10. Curt Rogers Curt Rogers. Disability mcardles disease, My name is Curt Curtis M .Rogers ,butjust Curt does fine. My online name is Gambit. I have mcardles disease . http://www.withoutwheels.org/Profiles/crogers/

Curt Rogers Disability: McArdles Disease My name is Curt "Curtis M .Rogers" ,but just Curt does fine. My online name is Gambit. As Paul does, I also play Golf Online and that is how I came across his site here "Without Wheels", and decided to write him and tell him my story. I have "McArdles Disease". Basically McArdles disease is a muscle disease that affects the skeletal muscles, which in turn if over stressed can affect the kidneys. In extreme cases as mine, they can completely shut down the kidneys. Well, I remember the days in elementary school, as far back has kindergarten. My School was about a mile and a half walk from home. Well, that walk would take me almost an hour to do. All through elementary school, I could not walk more then 50 yards without having to stop and sit down and rest. My legs would get this burning in them and they would feel like they weighed more then ten times then they actually were. The muscles wouldn't just move them anymore until I sat and rested. Running was out of the question. I remember them days in elementary school when we had them 40 yard dash's and stuff "Field Day" I think they called it. Well I would get up to them lines to run them dash's just knowing I could beat everyone and I did....for about 10 steps. I would push so hard that my muscles would completely lock up on me, but I would keep pushing "Something that I did not know could really hurt me then" until I made it to that finish line "Last every time I might add". Even the girls would beat me and I'm only talking about a lousy 40 yards. Needless to say, I would collapse just about when I crossed the line. Somehow I would manage to keep my feet under me and try to recover quickly. I hid it very well because it was embarrassing, at least to a 6 to 11 year old it was.

11. MEMBER TRIVIA Answer. 1. mcardles disease 2. I loved sports and loved baseball. 3. I cando anything they can do. . 4. God was giving me my kidneys back! Answer. http://www.withoutwheels.org/gazette/MemberTrivia/member_trivia.htm

MEMBER TRIVIA 1. Born in Livermore, California. 2. "Chase the Boy Down" 3. Received 14 Bowling trophies. 4. Quadriplegic, C-6 incomplete, C-7 complete Answer 1. "Lost soul" 2. "I am not a professional counselor or therapist. 3. I am a "work in progress" 4. A Recovering Co-Dependent Answer 1. Oldest out of 5 boys. 2. Played golf, racquetball, and a martial artist. 3. "I am a Happy & Lucky Man." 4. Reflex Sympathetic Dystrophy Answer 1. Loving foster home. 2. New Bedford Vocational High School 3. Planning on getting married in the future. 4. Right side paralysis Answer 1. Lives in Maine. 2. "A Disabled Soul" 3. “I spent my entire time as a professional counselor/therapist.” 4. Has a rare form of cancer. Answer 1. Born and raised in a small Texas town. “ I have not, will not let that stop me from being the best me I have ever been.” 3. I have decided to go to school to become a High School English teacher.

12. Mda I have mcardles disease. I would like to talk to others who have this. http://www.mda.org.au/services/gbarchive/mar99.html

"Welcome to The MDA Guest Book" "March 1999" Name Tom Albrecht Website Referred by : Just Surfed In! From : Pueblo West, CO 81007 Time Comments : Just purchased computer and learning how to use it. Found this site because I was looking for someone else who has Acid Maltase Deficiency. I was diagnosed in 1977 as having Limb-girdle dystrophy. Later changed to AMD. Would like to have someone to talk to about how they cope with this disease. Name carol tibus Website Referred by : Just Surfed In! From : POSEN IL Time Comments Name Tammy S. Alessandro Website Referred by : Just Surfed In! From : South Carolina, USA Time Comments : I am looking for information on a book titled Journey of Love: A Parent's Guide to Duchenne's MD My brother has Duchenne's. This website is very informative! Name Nancy Website Referred by : Just Surfed In! From : Phoenix, AZ Time Comments : We just found out my husband has Myotonic Dystrophy. He is 38 years old. We are looking for any information on things that help delay the disease. Any information would be great. Name Julie Website Referred by : Just Surfed In!

13. Glycogen And Other Sugar Pathways mutation f1) all organs affected f2) increased glycogen f3) Cardiorespiratory failure,death before 2 g) mcardles disease mutation in phosphorylase g1) muscle http://umed.med.utah.edu/MS1/biochem/study/glycogen.html

Sugar Utilization A) There are basically 4 disaccharides we are concerned about 1) Maltose a) Cleaved by maltase into 2 glucose b) glucose enters glycolysis directly 2) trehalose a) Cleaved by trehalase into 2 glucose b) glucose enters glycolysis directly 3) Sucrose a) Cleaved by sucrase into fructose and glucose b) glucose enters glycolysis directly c) fructose must undergo distinct metabolic modification for utilization in glycolysis 4) lactose a) cleaved by lactase into galactose and glucose b) glucose enters glycolysis directly c) galactose must undergo distinct metabolic modification for utilization in glycolysis d) lactase defficiency is the most common defect in disaccharide metabolism d1) 10% of public is affected to some degree d2) lactase is in the brush border of the small intestine d3) undigested lactose has an osmotic effect causing cramps and diarhea d4) undigested lactose is utilized by bacteria to generate methane, CO2 and H2 B) Fructose metabolism 1) Fructose has a non insulin depedent uptake by cells. This uncontrolled utilization can lead to increased glycolytic activity: lactate acidosis.

14. New Alabama Chapter It was then that I was diagnosed with Muscular Dystrophy a veryrare form called mcardles disease (phosphorylase deficiency). http://www.vhl.org/newsletter/vhl2001/01coalab.htm

Basic Facts About VHL Managing Your Health Information for Health Care Professionals Research ... Press Room Families, Friends, Physicians, and Researchers working together to improve diagnosis, treatment, and quality of life for people affected by von Hippel-Lindau disease. New Alabama Chapter Linda D. is our new chapter chairperson for Alabama. She shares her story, and her goals for the chapter. I am 48 years of age, one of seven children, with me being number seven and twin to number six. There are 4 boys and 3 girls in our family. I graduated High School and went into the paramedic program at the University of Alabama, Birmingham, Alabama. I worked for Carraway Hospital in the emergency room at the time and wanted to train for the Life Saver Helicopter that was just being introduced. In my second level of paramedic training I was sent to NIH in Bethesda, Maryland, for evaluation of muscle problems. It was then that I was diagnosed with Muscular Dystrophy a very rare form called McArdles Disease (phosphorylase deficiency). This ended my dream of becoming a flight medic or even a paramedic. Since I could not be a paramedic, I worked as an office manager with several companies, and then started my own cleaning business approximately 8 years ago. I have two children. My son, Patrick, is a Staff Sgt. in the Air Force in Louisiana. My daughter-in-law, Brandy, graduated from the Police Academy in June. My daughter, Candi, lives near me and helps me with my cleaning business. I have two grandsons, Justin (5) and Hunter (1), the joy of my life.

15. Definitions Of Genetic Disorders -P disease/pgam.html. Phosphorylase Deficiency (MPD) (mcardles disease)http//www.mdausa.org/disease/mpd.html. Phosphorylase 6 Kinase http://www.icomm.ca/geneinfo/def-p.htm

The GAPS INDEX to Information on the Internet about Genetic Disorders and Birth Defects Genetic Information and Patient Services, Inc. (GAPS) HOME DISORDERS GLOSSARY Definitions of Genetic Disorders beginning with the letter P Click on the link next to the disorder to view its definition. P-V congheart.html PA amenor.htm PAC arrhythm.htm Pachyonychia Ichtyosiforme pachon.htm Pachyonychia Congenita with Natal Teeth pachon.htm Pachyonychia Congenita ed.htm Pachyonychia Congenita Keratosis Disseminata Circumscripta (follicularis) pachon.htm Pachyonychia Congenita Jadassohn-Lewandowsky Type pachon.htm PAF with MSA shydrager.htm Paget's Disease paget.htm Paget's Disease of Bone paget.htm Paget's Disease of the Breast pagetbr.htm Paget's Disease of the Nipple pagetbr.htm Paget's Disease of the Nipple and Areola pagetbr.htm Pagon Syndrome walkerwar.htm Painful Ophthalmoplegia tolosahunt.htm PAIS androgen.htm Palatal Myoclonus myoclonus.htm

16. Creatine FAQ's Creatine has also been used successfully to improve patients with neuromusculardiseases such as mcardles disease, neuropathic disorders, inflammatory http://www.nutrasense.com/nutrasense/creatinefaqs.html

How Effective is creatine? Studies have shown that Creatine, when supplemented with proper diet, exercise and adequate hydration, can increase lean muscle mass and strength. It has also been shown to aid in recovery after workouts. How Safe is creatine? To date there have been well over 75 research articles published about creatine in various journals, as well as a number of papers presented at various meetings such as the National Strength and Conditioning Associations Symposium. These studies reported no negative side effects. The only consistent side effect has been an average water weight gain of 3-5 lbs. Simply put, with the exception of carbohydrates, creatine is the most extensively studied nutritional sports supplement available to today's athlete. Olympic Committee Supports Use of Creatine Who can benefit from creatine supplementation? Even though creatine supplementation is most common with athletes it has a multitude of uses ranging from infants to the elderly. Creatine has been used successfully to treat infants with extrapyramidal movement disorders and creatine deficiencies in the brain. Creatine has also been used successfully to improve patients with neuromuscular diseases such as McArdles disease, neuropathic disorders, inflammatory myopathies, diomyopathy, mitochondrial cytopathy, dystrophies/congenital myopathies, and ALS - Lou Gehrigs disease. Study Shows Creatine Strengthens Elderly and Patients with Neuromuscular Disease - USA Today Creatine has also been used successfully on reducing muscle fatigue in elderly men.

17. THE LIGHTNING HYPERTEXT OF DISEASE. McArdle Disease, McArdle's Diseases, McArdle Diseases, McArdle's Glycogenosis 5sMcArdle Diseases McArdle's Diseases mcardles disease Muscle Phosphorylase http://www.pathinfo.com/cgi-bin/lh.cgi?tx=mcardles

18. Personal Training On The Net - Newsletter Polycystic Ovary Syndrome. Strength for Rowing (click to view). mcardles disease.mcardles disease and Exercise. Niacin. Shin Splints. Clicking Hip (click to view). http://www.ptonthenet.com/newsletter/june_02.htm

19. Department Of Kinesiology [FACULTY MEMBERS - Martin Gibala] ranged from young healthy volunteers to special populations including neuromusculardisease patients (eg, myoadenlyate deaminase deficiency, mcardles disease). http://kinlabserver.mcmaster.ca/kf/mg.html

Martin Gibala (Ph.D., Guelph Location Ivor Wynne Centre, Room AB122 Telephone (905) 525 - 9140 Ext. 23591 Email gibalam@mcmaster.ca Fax M Recent Publications: Gibala, M.J. Regulation of skeletal muscle amino acid metabolism during exercise. Int. J. Sports Nutr. Exerc. Metab. Gibala, M.J., S.A. Interisano, M.A. Tarnopolsky, B. Roy, J.R. MacDonald, K.E. Yarasheski, and J.D. MacDougall. Myofibrillar disruption following acute concentric and eccentric resistance exercise in strength-trained men. Can. J. Physiol. Pharmacol. Pharmacol. 78: 656-661, 2000. Gibala, M.J. Nutritional supplementation and resistance exercise: What is the evidence for enhanced skeletal muscle hypertrophy? Can. J. Appl. Physiol. Gibala, M.J., and B. Saltin. PDH activation by dichloroacetate reduces TCA cycle intermediates at rest but not during exercise in humans. Am. J. Physiol. Endocrinol. Metab. Gibala, M.J., M. Lozej, M.A. Tarnopolsky, C. McLean, and T.E. Graham. Low glycogen and branched-chain amino acid ingestion do not impair anaplerosis during exercise in humans. J. Appl. Physiol

20. Muscular Dystrophy Association | What's New Treatment of mcardles disease by Dr. Ronald Haller 5/23/01; JerryLewis MDA Telethon 2000 Broadcast Journalism Awards 5/15/01; http://www.mdausa.org/whatsnew/con_archive01.html

Archive of Past News Stories The following items originally appeared on the What's New at MDA page. For more in-depth information, please visit the Research section of this Web site; or search the site for your topic of interest. MDA News: Caution with Anesthesia Urged for Children With Mitochondrial Myopathies President Signs MD-CARE Act Mandating More NIH Emphasis on MD Research MDA Web Feature: Life Imitates Art and Vice Versa for Filmmaker With Dejerine-Sottas Disease Research News: Study Finds Increased Risk of ALS Among Gulf War Veterans ... Mattie’s on a Roll! Book Hits #10 on NYT Best Seller List Research News: Neuroscience Conference to Explore Advances In Neuromuscular Disease Research News: New Clues to Muscle Atrophy In ALS, SMA, CMT Research News: SMA Drug Search Gains Ground Mattie Stepanek to Appear on Oprah Winfrey Show ... Stress and Neuromuscular Disease What to Watch for in the Aftermath of Tragedy MDA Offers Flu Shots For People With Neuromuscular Diseases Research News: ALS-Like Disease Attributed to HIV Infection House Passes MD-CARE Act Research News: Gene Therapy Offers Hope for Congenital Muscular Dystrophy ... Mattie Stepanek and where to find his book of poems, "Heart Songs."

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 1     1-20 of 78    1  | 2  | 3  | 4  | Next 20