Geometry.Net - Health_Conditions: Myopathies

Aventis Pharma France - Association FranÃ§aise Contre Les Myopathies (AFM)
les myopathies (AFM). Association Française contre les myopathies (AFM).
http://www.aventispharma.fr/main/0,1003,FR-FR-26821-43738--,00.html

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Myopathies | Ahealthyme.com
myopathies Turkington, Carol A. Definition. myopathies are diseases ofskeletal muscle which are not caused by nerve disorders.
http://www.ahealthyme.com/article/gale/100083738

Extractions: There are many different types of myopathies, some of which are inherited, some inflammatory, and some caused by endocrine problems. Myopathies are rare and not usually fatal. Typically, effects are mild, largely causing muscle weakness and movement problems, and many are transitory. Only rarely will patients become dependent on a wheelchair. However, muscular dystrophy (which is technically a form of myopathy) is far more severe. Some types of this disease are fatal in early adulthood. Causes and symptoms Genetic myopathies Among their many functions, genes are responsible for overseeing the production of proteins important in maintaining healthy cells. Muscle cells produce thousands of proteins. With each of the inherited myopathies, a genetic defect is linked to a lack of, or problem with, one of the proteins needed for normal muscle cell function. There are several different kinds of myopathy caused by defective genes: Central core disease Centronuclear (myotubular) myopathy Myotonia congenita Nemaline myopathy Paramyotonia congenita Periodic paralysis (hypokalemic and hyperkalemic forms)
Myopathies | Ahealthyme.com
You are here Home Health A to Z myopathies. myopathies. Definition myopathiesare diseases of skeletal muscle which are not caused by nerve disorders.
http://www.ahealthyme.com/topic/topic100587191

Extractions: There are many different types of myopathies, some of which are inherited, some inflammatory, and some caused by endocrine problems. Myopathies are rare and not usually fatal. Typically, effects are mild, largely causing muscle weakness and movement problems, and many are transitory. Only rarely will patients become dependent on a wheelchair. However, muscular dystrophy (which is technically a form of myopathy) is far more severe. Some types of this disease are fatal in early adulthood. Causes and symptoms Genetic myopathies Among their many functions, genes are responsible for overseeing the production of proteins important in maintaining healthy cells. Muscle cells produce thousands of proteins. With each of the inherited myopathies, a genetic defect is linked to a lack of, or problem with, one of the proteins needed for normal muscle cell function.
Myopathies
myopathies. Progressive Proximal Weakness. Click here to return.
http://daffodil.uthscsa.edu/faculty/dumitru/emgs/myopathies/Default.htm
OUP USA: Evaluation And Treatment Of Myopathies
by Subject $139.95 (05) 0803644108 Add to My Basket 1995 In Stock S H Standard ContemporaryNeurology Series 44, Evaluation and Treatment of myopathies ROBERT C
http://www.oup-usa.org/isbn/0803644108.html
Myopathies
myopathies. The obtained. In myopathies this technique has revealedsilent areas indicating focal loss of fibres in the motor unit.
http://www.neurofys.uu.se/v1/Document/emg/expmyopathy.htm

Extractions: Myopathies The EMG shows typical changes in cases of myopathy. The classical EMG abnormalities have been interpreted as beeing signs of loss of muscle fibres but also other changes take place in the motor unit in myopathies. SFEMG recordings indicate that local concentration of muscle fibres in a given motor unit, the so called fibre density is increased . At the same time the total size of the motor unit, investigated with Macro EMG is unchanged or small. These findings indicate that also regenerative processes are present. This picture changes with time related to the dynamic changes in the motor unit. In early stages of myopathy there is increased signal amplitudes in some type of EMG recordings (Macro EMG). This may be due to compensatory fibre hypertrophy and subsequent splitting in inherently weak muscle fibres, or hypertrophy after overuse of noninvolved muscle groups. In later stages, findings compatible desynchronisation of the electrical acitivity (polyphasic and complex MUPs) may reflect fibre diameter variation, a typical biopsy findings. With progression, many parameters indicate more profound changes in motor unit topography such as loss of fibres in certain areas of the motor unit (Scanning EMG) and local regenerative processes with splitting, innervation of sequestered muscle fibres or regenerating muscle fibres. In Scanning EMG, in which an electrode, e.g a concentric needle electrode is pulled through the muscle in small steps (50um), the electrical cross section of the motor unit is obtained. In myopathies this technique has revealed silent areas indicating focal loss of fibres in the motor unit.
USC Events Calendar - Myopathies/Peripheral Nerve
myopathies/Peripheral Nerve. Neuroscience Conference. Margaret Burnett andCarol Miller of USC will be speaking on myopathies/Peripheral Nerve.
http://www.usc.edu/calendar/events/16305.html
Neuromuscular Disorders Inflammatory Myopathies
Translate this page Neuromuscular Disorders Inflammatory myopathies. Évaluateur Marie-HélèneIglesias Date de publication 12 avril 1999 Produit
http://medes3.med.umontreal.ca/MedWeb/Cyberm/inflammyopath.htm
PAG-VII GENETIC STUDIES OF EQUINE MYOPATHIES
1999. W93 GENETIC STUDIES OF EQUINE myopathies. recessive. In conclusion,many myopathies in horses appear to have a genetic basis.
http://www.intl-pag.org/7/abstracts/pag7151.html
French Association For Myopathies
French Association for myopathies. Type of Document, Type of File, LastUpdated. Application, RTF, December 2001. Instructions, RTF, December2001.
http://www.biu.ac.il/RA/www/forms/AFM.html
Colloquium On Mitochondria And Myopathies/Halle - MITONET Meeting
Neurologische Klinik der MartinLuther Universität Halle-Wittenberg. 2 nd Colloquiumon Mitochondria and myopathies in Halle/Saale. March 31- April 2, 2000.
http://www.kms.mhn.de/mitonet/pages/halle.htm
CAC
Fact Sheet myopathies. WHAT ARE myopathies? Autoimmune myopathies THE RHEUMATOLOGISTSROLE IN TREATING myopathies. Rheumatologists specialize
http://www.columbusarthritis.com/muscle.html

Extractions: Ankylosing Spondylitis Back Pain Fibromyalgia ... Rheumatologist Fact Sheet Myopathies WHAT ARE MYOPATHIES? Autoimmune myopathies are a group of diseases that involve inflammation of the muscles and may be associated with diseases of internal organs. Diseases affecting muscles include polymyositis, dermatomyositis and inclusion body myositis. The main symptom is muscle weakness in the upper arms, upper legs and neck, muscle pain, fatigue, joint pain and swelling, rashes over the face and knuckles, fevers, swallowing difficulty and shortness of breath. CAUSE The cause of myopathies is unknown, but environmental factors (such as viral infections) and genetic predisposition are felt to be important in some cases. HEALTH IMPACT DIAGNOSIS Diagnosis is attained through a history and physical exam, certain laboratory tests, muscle biopsy and electromyography (a study of the electrical activity of muscle). Other diseases or conditions such as hypothyroidism, toxin exposure, drug reactions and genetic disorders may also affect muscles and need to be ruled out.
Association Française Contre Les Myopathies
Translate this page
http://afm-front.heb.fr.colt.net/jsp/index.jsp
Anesthésie Des Enfants Atteints De Myopathies
Translate this page Médecins anesthésistes pouvant conseiller les collègues ayant à prendreen charge l'anesthésie d'enfants atteints de myopathies et de maladies
http://www.sfar.org/myopathieanesth.html

Extractions: Tel: 02 99 28 24 2 http://www.sfar.org/hyperrthermmal.html http://www.orpha.net/ Site Inserm sur les maladies orphelines http://www.neuro.wustl.edu/neuromuscular/index.html http://www.ncbi.nlm.nih.gov/Omim/searchomim.html Online Mendelian Inheritance In Man - National Intitute of Health US http://telethon.bio.unipd.it/
AFM (association Française Sur Les Myopathies) : Compte D'emploi Pour 1993 Des
Translate this page Liste des rapports. L'Association Française sur les myopathies. Aucunrésumé n'est disponible pour ce document. Merci de vous
http://www.ccomptes.fr/Cour-des-comptes/publications/rapports/afm/cdc83.htm
Myopathies | Principal Health News
myopathies. myopathies. Turkington, Carol A. Definition. myopathies are diseasesof skeletal muscle which are not caused by nerve disorders. These
http://www.principalhealthnews.com/topic/topic100587191

Extractions: There are many different types of myopathies, some of which are inherited, some inflammatory, and some caused by endocrine problems. Myopathies are rare and not usually fatal. Typically, effects are mild, largely causing muscle weakness and movement problems, and many are transitory. Only rarely will patients become dependent on a wheelchair. However, muscular dystrophy (which is technically a form of myopathy) is far more severe. Some types of this disease are fatal in early adulthood. Causes and symptoms Genetic myopathies Among their many functions, genes are responsible for overseeing the production of proteins important in maintaining healthy cells. Muscle cells produce thousands of proteins. With each of the inherited myopathies, a genetic defect is linked to a lack of, or problem with, one of the proteins needed for normal muscle cell function.
Sharelook: Myopathies
Translate this page Régions Autres. myopathies, Retour à sharelook.fr Santé Maladies Affections articulaires . Associations et organismes. AFM
http://www.sharelook.fr/sante/maladies/affections_articulaires/myopathies.html

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S000522d - Polymyositis And Inflammatory Myopathies - Laboratory Assessment
Polymyositis and Inflammatory myopathies Laboratory Assessment. Inflammatorymyopathies polymyositis, dermatomyositis, inclusion body myositis.
http://www.emory.edu/WHSCL/grady/amreport/litsrch99/s000522d.html

Extractions: [litsrch99/page_header.html] Polymyositis and Inflammatory Myopathies - Laboratory Assessment 5/22/00 (Doyle) Group: Monday Residents RE: A 29 year old male with vitamin b12 deficiency who presented with hand and foot weakness. Question: What tests can be used to confirm the diagnosis of polymyositis or other inflammatory myopathies? Comprehensive Therapy. 24(10):494-502, 1998 Oct. Inflammatory myopathies [polymyositis, dermatomyositis, inclusion body myositis]. [Review] [35 refs] British Journal of Rheumatology. 36(6):656-60, 1997 Jun. Elevated serum levels of neopterin in adult patients with polymyositis/dermatomyositis. Baillieres Clinical Rheumatology. 9(3):497-514, 1995 Aug. Inflammatory myopathies. [Review] [57 refs] Annals of the New York Academy of Sciences. 756:410-3, 1995 Jul 7. The alpha beta T-cell receptor repertoire in idiopathic inflammatory myopathies: distinct patterns of gene expression by: muscle-infiltrating lymphocytes in different clinical and serologic groups. Annals of the Rheumatic Diseases. 52(12):857-61, 1993 Dec.
CJNS-Myopathies In The Intensive Care Unit
Abstract, Close Window myopathies in the Intensive Care Unit DouglasZochodne. Abstract myopathies that occur in the intensive care
http://www.canjneurolsci.org/25febsuppltoc/myop.html

Extractions: Myopathies in the Intensive Care Unit Douglas Zochodne Abstract: Myopathies that occur in the intensive care unit can be divided into preexisting myopathies or newly acquired myopathies that develop in the intensive care unit. Myotonic dystrophy is an example of a preexisting myopathy that may render patients susceptible to acute respiratory failure following surgical procedures and anaesthesia. A group of myopathies that develop within the intensive care unit have been labelled acute necrotizing myopathy of intensive care, thick filament myopathy and acute steroid myopathy. Corticosteroids and nondepolarizing muscle blocking agents may play a role in their development. Can. J. Neurol. Sci. 1998; 25: S41 - S42
Arch Neurol -- Page Not Found
Arch Neurol. 56;758, June 1999, InclusionBody Myositis and myopathies, AnthonyA. Amato, MD. Section 2 is a historic perspective into these myopathies.
http://archneur.ama-assn.org/issues/v56n6/ffull/nbk0699-1.html

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