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Myotonic Dystrophy: more books (25)

Myotonic Dystrophy (The Facts) by Peter Harper, 2009-10-26
Myotonic Dystrophy: The Facts (Oxford Medical Publications) by Peter Harper, 2002-08-08
Myotonic Dystrophy - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-10-21
Myotonic Dystrophy: Present Management, Future Therapy
Reading and spelling impairments in children and adolescents with infantile myotonic dystrophy [An article from: Journal of Neurolinguistics] by D. Cohen, M. Plaza, et all 2006-11-01
Myotonic Dystrophy - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-18
Muscular Dystrophy Organizations: Décrypthon, Muscular Dystrophy Association, Muscular Dystrophy Campaign, Myotonic Dystrophy Foundation
Myotonic dystrophy: An entry from Thomson Gale's Gale Encyclopedia of Children's Health: Infancy through Adolescence by Tish, A.M. Davidson, Karen, M.S., C.G.C. Krajewski, 2006
Warming up improves speech production in patients with adult onset myotonic dystrophy [An article from: Journal of Communication Disorders] by B.J.M. de Swart, B.G.M. van Engelen, et all 2007-05-01
Myotonic Dystrophy: An entry from Gale's Gale Encyclopedia of Medicine, 3rd ed. by Karen, M.S., C.G.C. Krajewski, Rebecca, Ph.D. Frey, 2006
Gale Encyclopedia of Medicine: Myotonic dystrophy by C.G.C. Karen M. Krajewski M.S., 2002-01-01
Myotonic Dystrophy Medical Guide by Qontro Medical Guides, 2008-07-09
Myotonic dystrophy: An entry from Thomson Gale's Gale Encyclopedia of Genetic Disorders, 2nd ed. by Karen, MS, CGC Krajewski, 2005
CTG repeat number in the nonaffected allele of myotonic dystrophy patients is not critical for disease expression.(Brief Communication): An article from: Human Biology by M. Cipollaro, U. Galderisi, et all 1997-12-01

lists with details

Myotonic Dystrophy
MAIN SEARCH INDEX. myotonic dystrophy. myotonic dystrophy is a progressive disease in which the muscles are weak and are slow to relax after contraction.
http://www.ehendrick.org/healthy/000943.htm

Extractions: Resources Myotonic dystrophy is a progressive disease in which the muscles are weak and are slow to relax after contraction. Myotonic dystrophy (DM), also called dystrophia myotonica, myotonia atrophica, or Steinert disease, is a common form of muscular dystrophy . DM is an inherited disease, affecting males and females approximately equally. About 30,000 people in the United States are affected. Symptoms may appear at any time from infancy to adulthood. DM causes general weakness, usually beginning in the muscles of the hands, feet, neck, or face. It slowly progresses to involve other muscle groups, including the heart. DM affects a wide variety of other organ systems as well. A severe form of DM, congenital myotonic dystrophy, may appear in newborns of mothers who have DM. Congenital means that the condition is present from birth. DM occurs in about 1 of 20,000 people and has been described in people from all over the world. The most common type of DM is called DM1 and is caused by a mutation in a gene called myotonic dystrophy protein kinase (DMPK). The DMPK gene is located on chromosome 19. When there is a mutation in this gene, a person develops DM1. The specific mutation that causes DM1 is called a trinucleotide repeat expansion.
Myotonic Dystrophy
myotonic dystrophy. myotonic dystrophy is a progressive disease that keeps affected muscles from relaxing once they have been contracted or tightened.
http://www.chclibrary.org/micromed/00057650.html

Extractions: Myotonic dystrophy (DM), also called dystrophia myotonica, myotonia atrophica, or Steinert's disease, is a common form of muscular dystrophy . It affects more than 30,000 people in the United States. DM is an inherited disease, affecting men and women approximately equally. Symptoms may appear at any time from childhood to adulthood. DM causes general weakness, usually beginning in the muscles of the hands, feet, neck, or face. It slowly progresses to involve other muscle groups, including the heart. DM affects a wide variety of other organ systems as well. A rare form of DM, congenital myotonic dystrophy, may appear in newborns of mothers who have DM. Congenital myotonic dystrophy is marked by severe weakness, poor sucking and swallowing responses, respiratory difficulty, delayed motor development, and mental retardation Myotonic dystrophy is caused by an inherited gene defect, called a "triple repeat," on chromosome 19. The defective gene has not been positively identified as of early 1998. The triple repeat probably affects neighboring genes as well. Involvement of more than one gene would explain the multisystem effects of DM. The gene is inherited in an autosomal dominant pattern. In this pattern, one copy of the gene inherited from an affected parent is enough to cause the disease in the offspring. The chance of inheriting the DM gene from an affected parent is 50% for each child. This percentage is not changed by results of other pregnancies.
Disorder Information - Myotonic Dystrophy Steinert's Disease
myotonic dystrophy Steinert s disease. What is myotonic dystrophy? Who can be affected with myotonic dystrophy? Anyone can be affected by myotonic dystrophy.
http://www.mdac.ca/english/disorder-info/disorder-info-04.htm

Extractions: Steinert's disease What is myotonic dystrophy? Myotonic dystrophy, also known as Steinert's disease, is the most common form of muscle disease, affecting approximately one person in 8,000 worldwide. It is a disorder characterized by progressive muscle weakness and wasting and by myotonia (difficulty in relaxing the muscles after they have been contracted). It is a multisystem disease, typically involving a wide range of other tissues as well as muscle. Who can be affected with myotonic dystrophy? Anyone can be affected by myotonic dystrophy. It is a genetic disorder passed on to children of either either sex by one parent who has the disorder. Myotonic dystrophy can affect people at any age. The majority of people are diagnosed by the time they reach their early twenties. With each successive generation, the symptoms of myotonic dystrophy seem to get more severe, and the age at which they appear gets younger. This tendency is known as anticipation. What are the different forms of myotonic dystrophy?
Myotonic Dystrophy Volume 37, 3rd Edition
myotonic dystrophy Volume 37, 3rd Edition Major Problems in Neurology 37 Peter Harper MA DM FRCP, Professor and Consultant in Medical Genetics, University of
http://www.harcourt-international.com/catalogue/title.cfm?ISBN=0702021520
Modafinil ( Provigil ) For Myotonic Dystrophy
Reduction in excess daytime sleepiness by modafinil in patients with myotonic dystrophy by Talbot K, Stradling J, Crosby J, HiltonJones D. Department of
http://www.modafinil.com/myotonicdystrophy.html
Modafinil ( Provigil ) In The Treatment Of Myotonic Dystrophy
Modafinil reduces excessive somnolence and enhances mood in patients with myotonic dystrophy by MacDonald JR, Hill JD, Tarnopolsky MA.
http://www.modafinil.com/myotonic-dystrophy.html

Extractions: ABSTRACT O BJECTIVE: To evaluate the potential of modafinil in reducing excessive daytime somnolence (EDS) and enhancing indexes of quality of life and mood in patients with myotonic dystrophy (DM). METHODS: Forty patients with DM were randomized to receive modafinil and placebo for 14 days each, using a double-blind, cross-over design. Before and after each trial, subjects completed handgrip strength testing, spirometry, and quality-of-life measures (RAND). On days 7 and 14, each subject completed the Epworth Sleepiness Scale (ESS), the Stanford Sleepiness Scale (SSS), and the Profile of Mood States (POMS). RESULTS: ESS scores were lower while taking modafinil (mean 248 mm; 95% confidence limit 220 to 276 mm) as compared with placebo (309 mm; 281 to 336 mm) (p < 0.001). Mean SSS scores were also lower during the modafinil trial (3.05; 2.77 to 3.33) than during the placebo trial (3.45; 3.18 to 3.71) (p
Myotonic Dystrophy -- ECureMe.com
myotonic dystrophy, myotonic dystrophy is a disorder in which the relaxation of the muscles is delayed due to the defect of the muscle on the cell membrane.
http://www.ecureme.com/emyhealth/data/Myotonic_Dystrophy.asp

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Myotonic Dystrophy Support Group
myotonic dystrophy Support Group. Charity Number 1073211. ANNUAL CONFERENCE. What is myotonic dystrophy? myotonic dystrophy is one of the Muscular Dystrophies.
http://www.nottscity.co.uk/mdsg/

Extractions: Email: mdsg@tesco.net Myotonic Dystrophy is one of the Muscular Dystrophies. It is the myotonia, which is muscle stiffness. Weakness and wasting of the muscles may also occur. The myotonia or stiffness, especially in the hands, is characteristic. Other parts of the body are frequently involved, and symptoms may include cataracts, disturbance of heart rhythm, hormonal problems, learning difficulties in children and extreme tiredness. We are a self help group, willing to provide support to families affected by the neuromuscular condition Myotonic Dystrophy. The group is affiliated to the Muscular Dystrophy Group. As volunteers, we offer help and support to one another by telephone links and correspondence. We are in the process of establishing a network of contact families which will enable us to put families in touch with one another locally if they so wish.
MYOTONIC DYSTROPHY
Features Listed For myotonic dystrophy. McKusick 160900. Cataract; Club foot/hindfoot, varus; Coloboma of retina/choroid; Conjunctivitis;
http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?1192
Www.vtmednet.org/~m145037/vhgi_mem/myodys/myodys_head.htm
PILS Self Help Group S146; myotonic dystrophy Support Group myotonic dystrophy Support Group. 175A Carlton The Support Group has information which deals specifically with myotonic dystrophy. This information
http://www.vtmednet.org/~m145037/vhgi_mem/myodys/myodys_head.htm
Myotonic Dystrophy Information Diseases Database
myotonic dystrophy,Steinert s myotonia atrophica,CurschmannBatten-Steinert syndrome,Dytrophia myotonica, Disease Database Information.
http://www.diseasesdatabase.com/ddb8739.htm
Myotonic Dystrophy - Medical Dictionary Definitions Of Popular Medical Terms
MedicineNet Home MedTerms medical dictionary AZ List myotonic dystrophy. Advanced Search. myotonic dystrophy is not one genetic entity.
http://www.medterms.com/script/main/art.asp?articlekey=4494
Myotonic Dystrophy Definition Of Myotonic Dystrophy. What Is Myotonic Dystrophy?
Definition of myotonic dystrophy in the Dictionary and Thesaurus. Provides examples from classic literature, search by definition of myotonic dystrophy.
http://www.thefreedictionary.com/myotonic dystrophy

Extractions: Dictionaries: General Computing Medical Legal Encyclopedia Word: Word Starts with Ends with Definition Noun myotonic dystrophy - a severe form of muscular dystrophy marked by generalized weakness and muscular wasting that affects the face and feet and hands and neck; difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips; the onset can be any time from birth to middle age and the progression is slow; inheritance is autosomal dominant myotonia atrophica myotonic muscular dystrophy Steinert's disease dystrophy ... muscular dystrophy - any of several hereditary diseases of the muscular system characterized by weakness and wasting of skeletal muscles Legend: Synonyms Related Words Antonyms Some words with "myotonic dystrophy" in the definition: autosomal recessive defect
MYOTONIC DYSTROPHY
myotonic dystrophy. GENERAL INFORMATION What is it? Care There is no cure for myotonic dystrophy. The disease cannot be stopped or turned around.
http://www.medformation.com/ac/mm_qdis.nsf/qd/nd1625g.htm

Extractions: MYOTONIC DYSTROPHY GENERAL INFORMATION: What is it? Myotonic (mi-o-ton-ik) dystrophy (dih-strow-fee) is one of a group of diseases called muscular dystrophy. They are genetic diseases that effect muscles all over your body. A genetic disease is one that you are born with and that you may inherit from your family. Myotonic dystrophy, which is also called "DM" or Steinert's disease, is the most common type of adult muscular dystrophy. DM makes your muscles get weaker and smaller. Your muscles may also get very stiff as you use them. It then takes awhile for the muscles to relax. This is called myotonia (mi-o-to-nee-uh) and is common in the hands. Myotonic dystrophy effects more than just muscles. It causes problems in many parts of your body like the heart, eyes, brain, and more. Both men and women can get DM. People usually get DM when they are 20 to 40 years old. But, it is possible for younger children to get DM. There is no cure for DM but the symptoms can be treated. And, it is possible to live a normal life span even if you have DM. But, you may die sooner if you have very bad myotonic dystrophy. Causes: All of the muscular dystrophies are caused by problems with the information in genes and chromosomes. A gene is a little piece of information that tells your body what to do or what to make. A chromosome is like a package that holds all the genes.
Genetics Research: Myotonic Dystrophy
myotonic dystrophy. Dunne, PW, Walch, ET, and Epstein, HF Phosphorylation reactions of recombinant human myotonic dystrophy protein kinase and their inhibition.
http://www.bcm.tmc.edu/neurol/research/genes/genes9.html

Extractions: Multisystem involvement with variable clinical presentation (common clinical presentation: myotonia, distal muscle weakness and atrophy, cataracts and daytime hypersomnolence, which often accompany involvement of other organs including the gastrointestinal tract, endocrine organs, peripheral nerve and bone.) Dunne, P.W., Ma, L., Casey, D.L., Harati, Y. and Epstein, H.F. Localization of myotonic dystrophy protein kinase in skeletal muscle and its alteration with disease. Cell Motil. Cytoskel., 33:52-63, 1996. Dunne, P.W., Ma, L., Casey, D.L. and Epstein, H.F. Myotonic protein kinase expression in human and bovine lenses. Biochem. Biophys. Res. Comm. 225:281-288, 1996.
MYOTONIC DYSTROPHY
myotonic dystrophy. Specialty Definition myotonic dystrophy. Domain, Definition. Medicine. Top. Synonym myotonic dystrophy. Synonym by domain myotonic (medicine).
http://www.websters-online-dictionary.org/definition/english/My/Myotonic Dystrop

Extractions: Philip M. Parker, INSEAD. MYOTONIC DYSTROPHY Specialty Definition: MYOTONIC DYSTROPHY Domain Definition A condition presenting muscle weakness and wasting which may be progressive. Source: European Union. references Source: compiled by the editor from various references ; see credits. Top Synonym: MYOTONIC DYSTROPHY Synonym by domain: myotonic (medicine). Top Specialty definitions using "MYOTONIC DYSTROPHY" Trinucleotide Repeat Expansion references Top Commercial Usage: MYOTONIC DYSTROPHY Domain Title Source: compiled by the editor from various references ; see credits. Top Non-Fiction Usage: MYOTONIC DYSTROPHY Subject Topic Quote NIAMS is also supporting planning grants for clinical trials, including one on myotonic dystrophy references Scientists have found some clues, both for myotonic dystrophy and triplet repeat disorders in general, and research is continuing. ( references The registry, based at the University of Rochester, will recruit and classify patients, and store medical and family history data for individuals with clinically diagnosed FSHD and myotonic dystrophy references Source: compiled by the editor from ICON Group International, Inc.
TheFetus.net - Myotonic Dystrophy-Raúl Martínez, José G. Andrade
myotonic dystrophy. Br. Med J 1960; I 12848 3- Fried, K.; Pajewski, M.; Mundel, G.; Caspi, E.; Spira, R. Thin ribs in neonatal myotonic dystrophy. Clin.
http://www.thefetus.net/page.php?id=1157
UNSW Embryology-OMIM MYOTONIC DYSTROPHY
MUSCULOSKELETAL DEVELOPMENT. Embryology Home Page. myotonic dystrophy. Select Entry from OMIM. CLINICAL FEATURES. ADULTONSET myotonic dystrophy. GENERAL.
http://anatomy.med.unsw.edu.au/cbl/embryo/OMIMfind/skmus/OMIM-310200.htm
Disease Directory : Neurological Disorders : Muscle Diseases : Myotonic Dystroph
AAEM Patient Resources - myotonic dystrophy - Patient Resources - myotonic dystrophy. ?. Membership Directory. Writer s Cramp. myotonic dystrophy.
http://www.diseasedirectory.net/Neurological_Disorders/Muscle_Diseases/Myotonic_

Extractions: Muscular Dystrophies ... Muscle Diseases : Myotonic Dystrophy AAEM - Patient Resources - Myotonic Dystrophy - Patient Resources - Myotonic Dystrophy. [?]. Membership Directory. Practice Issues / Advocacy. Werdnig-Hoffman Disease. Writer's Cramp. Myotonic Dystrophy. GeneClinics - A summary of myotonic dystrophy, the diagnosis, clinical description, differential diagnosis, management, genetic counseling and resources. Genetics research: myotonic dystrophy - Myotonic Dystrophy. Dunne, PW, Walch, ET, and Epstein, HF Phosphorylation reactions of recombinant human myotonic dystrophy protein kinase and their inhibition. Introduction: Myotonic Dystrophy - WrongDiagnosis.com - Introduction to Myotonic Dystrophy as a medical condition including symptoms, diagnosis, misdiagnosis, treatment, prevention, and prognosis. Management of Myotonic Dystrophy - Management of Myotonic Dystrophy. Myotonic Dystrophy Incurable but not Unmanageable". The incidence of Myotonic Dystrophy is 1 in 8000. Myotonic Dystrophy - [ Home ] [ Up ]. Click Here! Myotonic Dystrophy. Click Here! Music-e.net Just-recipes.net EnvyMag.com Scholarships-4u.com Shesearch
Myotonic Dystrophy
myotonic dystrophy. A threegeneration family affected with myotonic dystrophy. The degree of severity increases in each generation.
http://medgen.genetics.utah.edu/photographs/pages/myotonic_dystrophy.htm

Extractions: view 10 KB version A three-generation family affected with myotonic dystrophy. The degree of severity increases in each generation. The grandmother (right) is only slightly affected, but the mother (left) has a characteristic narrow face and somewhat limited facial expression. The baby is more severely affected and has the facial features of children with neonatal-onset myotonic dystrophy, including an open, triangular-shaped mouth. The infant has more than 1000 copies of the trinucleotide repeat, whereas the mother and grandmother each have approximately 100 repeats. Examinations Photographs Movies Links ... noJava Home

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