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         Charcot-marie-tooth Disease:     more books (25)
  1. 21st Century Complete Medical Guide to Charcot-Marie-Tooth Disease (CMT), Hereditary Motor and Sensory Neuropathy (HMSN), Peroneal Muscular Atrophy, Authoritative ... for Patients and Physicians (CD-ROM) by PM Medical Health News, 2004-03
  2. Coping with Charcot Marie Tooth Disease (Volume 1) by Diane M Gracely, 2010-06-16
  3. Charcot-Marie-Tooth Disease - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-09-16
  4. Charcot-Marie-Tooth disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Karen, MS, CGC Krajewski, 2005
  5. Charcot-Marie-Tooth Disease: A Practical Guide. Also Known as Hereditary Motor and Sensory Neuropathy and Peroneal Muscular Atrophy. by (No Author), 2000
  6. Charcot-Marie-Tooth Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-20
  7. Charcot-Marie-Tooth disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Christine Kelly, 2006
  8. Gale Encyclopedia of Medicine: Charcot Marie Tooth disease by CGC Karen M. Krajewski MS, 2002-01-01
  9. CHARCOT-MARIE-TOOTH DISEASE: A PROCTICAL GUIDE.
  10. Charcot-Marie-Tooth disease and multiple malignant melanomas: a case report.(Case study): An article from: Journal of Drugs in Dermatology by Ritu Saini, Stephanie Lehrhoff, et all 2010-02-01
  11. Charcot Marie Tooth Disease: An entry from Gale's <i>Gale Encyclopedia of Medicine, 3rd ed.</i> by Karen, MS, CGC Krajewski, 2006
  12. Charcot-Marie-Tooth Disorders (Annals of the New York Academy of Sciences)
  13. 2009 Conquering Charcot-Marie-Tooth (CMT) Disease - The Empowered Patient's Complete Reference - Diagnosis, Treatment Options, Prognosis (Two CD-ROM Set) by PM Medical Health News, 2009-04-04
  14. Charcot-Marie-Tooth (CMT) Disease Toolkit - Comprehensive Medical Encyclopedia with Treatment Options, Clinical Data, and Practical Information (Two CD-ROM Set) by U.S. Government, 2009-04-04

61. FIRSTConsult - Sdfdsf
FIRSTConsult, charcotmarie-tooth disease (Patient Education File). Published for medical students and primary healthcare providers by Elsevier.
http://www.firstconsult.com/?action=view_article&id=1037325&type=103&bref=1

62. FIRSTConsult - Sdfdsf
FIRSTConsult, charcotmarie-tooth disease (Medical Condition File). Published for medical students and primary healthcare providers by Elsevier.
http://www.firstconsult.com/?action=view_article&id=1014455&type=101&bref=1

63. Charcot-Marie-Tooth Disease - Definition Of Charcot-Marie-Tooth Disease By The F
Definition of charcotmarie-tooth disease in the Online Dictionary. Meaning of charcot-marie-tooth disease. What does charcot-marie-tooth disease mean?
http://www.thefreedictionary.com/Charcot-Marie-Tooth disease
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Charcot-Marie-Tooth disease
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Cite / link Email Feedback Thesaurus Legend: Synonyms Related Words Antonyms Noun Charcot-Marie-Tooth disease - a form of neuropathy that can begin between childhood and young adulthood; characterized by weakness and atrophy of the muscles of the hands and lower legs; progression is slow and individuals affected can have a normal life span; inheritance is X-linked recessive or X-linked dominant hereditary motor and sensory neuropathy neuropathy - any pathology of the peripheral nerves Mentioned in References in classic literature No references found No references found Dictionary/thesaurus browser Full browser Charcoal drawing charcoal gray charcoal grey Charcoal point ... Charcot Charcot-Marie-Tooth disease charcuterie chard chard plant Chardonnay ... Charcot, Jean Baptiste

64. ANNALS ONLINE -- Collected Resources : Charcot-Marie-Tooth Disease
Overview of charcotmarie-tooth disease Type 1A PK THOMAS X-linked charcot-marie-tooth disease and Connexin32 KENNETH H. FISCHBECK, ANNETTE ABEL,
http://www.annalsnyas.org/cgi/collection/charcot

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Charcot-Marie-Tooth Disease
Citations 1-10 of 43 total displayed. Most recent content (14 Sep 1999):
Part I. Clinical and Pathological Review of What Constitutes CMT
Overview of Charcot-Marie-Tooth Disease Type 1A
P. K. THOMAS
Ann. N.Y. Acad. Sci. 1999; 883: 1-5. [Abstract] [Full text] [PDF]
Part I. Clinical and Pathological Review of What Constitutes CMT
Historical Perspective of Defining Charcot-Marie-Tooth Type 1B
THOMAS D. BIRD
Ann. N.Y. Acad. Sci. 1999; 883: 6-13. [Abstract] [Full text] [PDF]
Part I. Clinical and Pathological Review of What Constitutes CMT
Overview of Hereditary Neuropathy with Liability to Pressure Palsies
PHILIP F. CHANCE
Ann. N.Y. Acad. Sci. 1999; 883: 14-21. [Abstract] [Full text] [PDF]
Part I. Clinical and Pathological Review of What Constitutes CMT
Molecular Mechanisms for CMT1A Duplication and HNPP Deletion
C. F. BOERKOEL, K. INOUE, L. T. REITER, L. E. WARNER, and J. R. LUPSKI
Ann. N.Y. Acad. Sci. 1999; 883: 22-35.

65. Charcot-Marie-Tooth Disease
Usual course chronic; progressive. CAUSES. hereditary. Synonyms peroneal muscular atrophy ICD-9-CM 356.1 charcot-marie-tooth disease
http://www.5mcc.com/Assets/SUMMARY/TP0187.html
Charcot-Marie-Tooth disease
DESCRIPTION: Progressive neuropathic (peroneal) muscular atrophy, usually autosomal dominant. Characteristics - cramps, paresthesias, leg and hand weakness, difficulty in walking. Usual course - chronic; progressive.
CAUSES:
  • hereditary
Synonyms: peroneal muscular atrophy
ICD-9-CM:
356.1 Charcot-Marie-Tooth disease
Author(s):
Mark R. Dambro, MD

66. || DukeMedNews || Genetic Testing For Charcot-Marie-Tooth Disease
DURHAM, NC – Duke University Medical Center researchers have identified mutations in a protein they believe is directly related to an inherited form of
http://www.dukemednews.org/news/article.php?id=5152

67. EPodiatry
charcotmarie-tooth disease. Comments charcot-marie-tooth disease. URL http//www.curtin.edu.au/curtin/dept/physio/podiatry/encyclopedia/ciecle/
http://www.epodiatry.com/education_sub3.asp?topic=Pediatrics&sub1=Learning resou

68. Charcot-Marie-Tooth Disease - Neurologychannel
CharcotMarie-Tooth (CMT) disease is an inherited, degenerative peripheral nerve disorder that causes muscle weakness and atrophy in the feet, legs, hands,
http://www.neurologychannel.com/charcot/
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TOOTH DISEASE
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Alzheimer's Disease Autism ... Carpal Tunnel Syndrome Cephalic Disorders Cerebral Palsy Charcot-Marie-Tooth Disease Chronic Pain Dementia Encephalitis Epilepsy ... Guillain-Barre Syndrome Headache Huntington's Disease Hydrocephalus Lou Gehrig's Disease ... Traumatic Brain Injury Vertigo DIAGNOSTIC TESTS CT Scan MRI Scan TREATMENT OPTIONS
Botulinum Toxin Therapy Epidural Injection Trigger Point Injection Vagus Nerve Stimulation RESOURCES Clinical Trials Glossary Links MDLocator ... What Is a Neurologist? Videos FOR DOCTORS ONLY Website Services Get Listed in MDLocator CME ABOUT US Healthcommunities.com Testimonials print this email this Overview Charcot-Marie-Tooth (CMT) disease, also known as hereditary motor and sensory neuropathy (HMSN), is an inherited, degenerative nerve disorder that causes muscle weakness and atrophy in the feet, legs, hands, and forearms. It is characterized by progressive loss of use and sensation in the limbs. Charcot, Marie, and Tooth are the names of the physicians who identified the disease and described its symptoms. It is not the same as

69. NINDS Forwarding Page
How is charcotmarie-tooth disease treated? What research is being done? charcot-marie-tooth disease (CMT) is one of the most common inherited
http://www.ninds.nih.gov/health_and_medical/pubs/cmt.htm
NINDS has redesigned its website and the URL for the page you were seeking has changed. The new URL for this page is /disorders/charcot_marie_tooth/detail_charcot_marie_tooth.htm . Please update your bookmark to this page. You will be automatically taken to this page in 5 seconds, or you can click the link to go there now.

70. Charcot-Marie-Tooth Disease Information Page: National Institute Of Neurological
CharcotMarie-Tooth Disorder information page compiled by the National Institute of Neurological Disorders and Stroke (NINDS).
http://www.ninds.nih.gov/disorders/charcot_marie_tooth/charcot_marie_tooth.htm
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Condensed from Charcot-Marie-Tooth Disease Fact Sheet Get Web page suited for printing Email this to a friend or colleague Table of Contents (click to jump to sections) What is Charcot-Marie-Tooth Disease? Is there any treatment? What is the prognosis? What research is being done? ... Additional resources from MEDLINEplus What is Charcot-Marie-Tooth Disease? Is there any treatment? There is no cure for CMT, but physical therapy, occupational therapy, braces and other orthopedic devices, and orthopedic surgery can help patients cope with the disabling symptoms of the disease. What is the prognosis?

71. AllRefer Health - Charcot-Marie-Tooth Disease (Hereditary) (Hereditary Motor And
charcotmarie-tooth disease (Hereditary) (Hereditary Motor and Sensory Neuropathy, Hereditary Peroneal Nerve Dysfunction, Neuropathy - Peroneal (Hereditary)
http://health.allrefer.com/health/charcot-marie-tooth-disease-hereditary-info.ht

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Alternate Names : Hereditary Motor and Sensory Neuropathy, Hereditary Peroneal Nerve Dysfunction, Neuropathy - Peroneal (Hereditary), Progressive Neuropathic (Peroneal) Muscular Atrophy Definition Charcot-Marie-Tooth disease defines a group of inherited, slowly progressive disorders that result from progressive damage to nerves. Symptoms include numbness and wasting of muscle tissue, first in the feet and legs, then in the hands and arms.

72. ► Charcot-Marie-Tooth Disease (hereditary)
A medical encycopedia article on the topic charcot-marie-tooth disease (hereditary)
http://www.umm.edu/ency/article/000727.htm
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Charcot-Marie-Tooth disease (hereditary)
Overview Symptoms Treatment Prevention Definition: Charcot-Marie-Tooth disease defines a group of slowly progressive, inherited disorders that result from progressive damage to nerves. In addition to loss of sensation, there is wasting of muscle tissue in the feet and legs, then hands and arms.
Alternative Names: Progressive neuropathic (peroneal) muscular atrophy; Hereditary peroneal nerve dysfunction; Neuropathy - peroneal (hereditary); Hereditary motor and sensory neuropathy
Causes, incidence, and risk factors: Charcot-Marie-Tooth diseases involve damage to nerves (neuropathy), usually from demyelination or loss of the electrical insulation around nerve fibers. All nerves are affected, but motor nerves are disproportionately so. The nerves in the legs are affected first and most severely. Symptoms usually begin between mid-childhood and early adulthood. The disorder is inherited, with autosomal dominant and recessive as well as X-linked recessive inheritance patterns. At least four genes have been discovered to be the cause of this group of diseases.
Charcot-Marie-Tooth disease causes destruction (degeneration) of the covering of the nerve cells ( myelin sheath) in some people. In other people, the

73. Charcot-Marie-Tooth Disease - Genetics Home Reference
What other names do people use for charcotmarie-tooth disease? charcot-marie-tooth disease is a group of progressive disorders affecting peripheral
http://ghr.nlm.nih.gov/condition=charcotmarietoothdisease
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Charcot-Marie-Tooth disease
On this page:
What is Charcot-Marie-Tooth disease?
Charcot-Marie-Tooth disease is a group of progressive disorders affecting peripheral nerves. These nerves connect the brain and spinal cord to muscles as well as sensory cells that detect sensations such as touch, pain, heat, and sound. The different types of Charcot-Marie-Tooth disease are distinguished by genetic cause, pattern of inheritance, and nerve abnormality. Genetic changes are related to the following types of Charcot-Marie-Tooth disease.

74. Charcot-Marie-Tooth Disease, Type 2 - Genetics Home Reference
Type 2 charcotmarie-tooth disease is a progressive disorder that affects You may find the following resources about charcot-marie-tooth disease,
http://ghr.nlm.nih.gov/condition=charcotmarietoothdiseasetype2
Home What's New Browse Handbook ... Search Charcot-Marie-Tooth disease, type 2
Charcot-Marie-Tooth disease, type 2
On this page:
What is Charcot-Marie-Tooth disease, type 2?
Type 2 Charcot-Marie-Tooth disease is a progressive disorder that affects peripheral nerves. These nerves connect the brain and spinal cord to muscles as well as sensory cells that detect sensations such as touch, pain, heat, and sound. Type 2 is characterized by mutations in particular genes and abnormalities in the fiber, or axon, that extends from a nerve cell. Charcot-Marie-Tooth disease, type 2 is a subtype of

75. Charcot-Marie-Tooth Syndrome
charcotmarie-tooth disease (CMT) disease is named after its three discoverers, who first noted the disease around the turn of the century.
http://www.ncbi.nlm.nih.gov/disease/Charcot.html
This Genes and Disease page has been moved to:
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on chromosome 17
Databases
PubMed

the literature
LocusLink

collection of gene-related information
OMIM

catalog of human genes and disorders Information Charcot-Marie-Tooth Association patient support, education and research Charcot-Marie-Tooth International run by and for people who have CMT disease GeneClinics a medical genetics resource CHARCOT-MARIE-TOOTH disease (CMT) disease is named after its three discoverers, who first noted the disease around the turn of the century. It is the most common inherited peripheral neuropathy in the world, characterized by a slowly progressive degeneration of the muscles in the foot, lower leg, hand and forearm, and a mild loss of sensation in the limbs, fingers and toes. Full expression of CMT's clinical symptoms generally occurs by age 30. CMT is not a fatal disease, however, and the disorder does not affect normal life expectancy. CMT is a genetically heterogeneous disorder, in which mutations in different genes can produce the same clinical symptoms. In CMT, there are not only different genes but different patterns of inheritance. One of the most common forms of CMT is Type 1A. The gene for Type 1A CMT maps to chromosome 17 and is thought to code for a protein (PMP22) involved in coating peripheral nerves with myelin, a fatty sheath that is important for their conductance. Other types of CMT include Type 1B, autosomal-recessive and X-linked.

76. Short Description Of Cell Lines. Pathology: Charcot-Marie-Tooth Disease #118200
Pathology charcotmarie-tooth disease 118200 OMIM record. - By selecting the cell line name, you will receive the detailed description of the cell line
http://www.biotech.ist.unige.it/cldb/pat56.html
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Pathology: Charcot-Marie-Tooth disease
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By selecting the cell line name , you will receive the detailed description of the cell line
By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines
You can search any term of the list by using the 'Find' utility of your browser
human, Caucasian
skin, fibroblast GEIMM
human, Caucasian
...
By Beatrice...

77. Charcot-Marie-Tooth Disorders - For Patients And Families - The
What is charcotmarie-tooth disease? New CMT2 Gene Found Mitofusin 2 charcot-marie-tooth disease (CMT) is the most common inherited disease that
http://www.chg.duke.edu/patients/cmtd.html

78. What Is Charcot-Marie-Tooth Disorder? - For Patients And Families
charcotmarie-tooth disease (CMT) is the most common inherited disease that affects the peripheral nerves in humans. These nerves carry signals from the
http://www.chg.duke.edu/patients/cmtwhat.html

79. Yahoo! Search Results
charcotmarie-tooth disease Information Exchange - a hereditary progressive neuromuscular disorder that primarily effects the feet, legs and hands.
http://www.ability.org.uk/Charcot_Marie_Tooth_Disease.html
Our Aims Services Stats ... Z Charcot-Marie-Tooth Disease CMT International UK - Support group for people with Charcot Marie Tooth disease Ask Noah About: Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Disease ... Information Exchange - a hereditary progressive neuromuscular disorder that primarily effects the feet, legs and hands. Charcot-Marie-Tooth International - self-help, consumer run organization providing information for people with CMT around the world. Charcot-Marie-Tooth Association Webmaster . Site Design by Ability "see the ability, not the disability" Acknowledgments

80. Log In Problems
A collection of MEDLINE abstracts from the editors of Medscape.
http://www.medscape.com/viewarticle/431507
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