81. Abstracts: Molecular Analysis In Charcot-Marie-Tooth (CMT) Disease And Hereditar Abstracts Molecular analysis in charcotmarie-tooth (CMT) disease and hereditaryneuropathy with liability to pressure palsies (HNPP), September 06, 1995, http://www.hum-molgen.de/documents/abstracts/0023.html

home genetic news bioinformatics biotechnology ... next Abstracts: Molecular analysis in Charcot-Marie-Tooth (CMT) disease and hereditary neuropathy with liability to pressure palsies (HNPP) September 06, 1995 Neurogenetics K.D. Bathke(1,2), D. Lorek(1), T. Liehr(1), A. Ekici(1), E. Nelis(3), C. Van Broeckhoven(3), H. Grehl(2), D. Claus(2), B. Neundörfer(2) and B. Rautenstrauß(1) (1) lnst. for Human Genetics and (2) Dept. of Neurology, Schwabachanlage 10, 91054 Erlangen, Germany; (3) Neurogenetics Laboratory, Born Bunge Foundation, Dept. of Biochemistry (UIA), Antwerpen, Belgium 2nd Workshop Neurogenetics in Germany, Munich, October 19-21, 1995 Hereditary moto-sensory neuropathy Ia (HMSNIa, CMTlA) and hereditary neuropathy with liability to pressure palsies (HNPP) are diseases of the peripheral nervous system, caused by a duplication (CMT) or a deletion (HNPP) of 1.5 Mb at chromosomal locus 17p11.2. Acknowledgement: K.D.B., H.G. and B.R. are supported by the Deutsche Forschungsgemeinschaft, C.V.B. an E.N. are supported by the National Fund for Scientific Research in Belgium Headings Charcot-Marie-Tooth (CMT) Hereditary moto-sensory neuropathy Ia (HMSNIa, CMTlA)

82. CMTnet: Charcot-Marie-Tooth Disorders Information Exchange The purpose. CMTnet is a repository of information for research and treatmentof charcotmarie-tooth (CMT). CMT is a hereditary progressive http://users.rcn.com/smith.ma.ultranet/CMTnet.html

The purpose CMTnet is a repository of information for research and treatment of Charcot-Marie-Tooth (CMT). CMT is a hereditary progressive neuromuscular disorder that primarily effects the feet, legs and hands. CMTnet is intended to provide information for both the medical and non-medical communities. Last updated: 1/12/2000. Enter CMTnet

83. CMTnet: Charcot-Marie-Tooth Disorders Information Exchange CMTnet The purpose. CMTnet is a repository of information for researchand treatment of charcotmarie-tooth (CMT). CMT is a hereditary http://users.rcn.com/smith.ma.ultranet/CMTneto.html

The purpose CMTnet is a repository of information for research and treatment of Charcot-Marie-Tooth (CMT). CMT is a hereditary progressive neuromuscular disorder that primarily effects the feet, legs and hands. CMTnet is intended to provide information for both the medical and non-medical communities. Last updated: 1/12/2000. This information has been gather by an individual with no medical training. No claims are made about this information. The accuracy of the information must be verified by the reader. Welcome to CMTnet A. Researcher information B. Practioner information C. CMTer support information References Genetics research Orthopedics Epidemiology Warning: CMT toxic substance list - Medical Alert OMIN clinical synopsis DNA test information Physical therapy ... Support organizations

84. RLS In A 4y/o With Charcot Marie Tooth Disease RLS in a 4y/o with Charcot Marie Tooth disease. I have been trying to treat a 4 y/owith Charcot Marie Tooth disease who has a clinical history c/w with RLS. http://www.sleepnet.com/diag2/messages/192.html

Sleepnet.com's Homepage Sleep Disorders Sleep Links Search RLS in a 4y/o with Charcot Marie Tooth Disease Follow Ups Post Followup Diagnostic Dilemmas Forum2 FAQ Posted by kathleen pfeffer on March 05, 2002 at 09:11:36: I have been trying to treat a 4 y/o with Charcot Marie Tooth Disease who has a clinical history c/w with RLS. His PSG showed limb movements associated 2/hr with awakenings (some arousals), but without PLM's. Interestingly, father has the same history, but because "noone knew what to do for him" he has never been tried on medication. He also has not seen an adult sleep specialist, despite my recommendations. On the boy, I originally tried .25 - .5 mg clonipin, w/o success, then I tried codeine 60 mg, w/o success,then I tried clonidine 0.05 - 0.1 mg with transient improvement, but then a relapse. I recently (1 month ago) started mirapex 0.125 which mom says is causing him to shake and jitter (akathesia?). Dad tried his son's clonipin and it significantly helped him! Should I try other dopamine agonists and at what doses in a patient this age, weighing 15.4 kg. He had no SDB, evidence of seizure activity on the PSG. Please respond with any reference re: CMT DISEASE and RLS or on personal experiences. I find it very unnerving to try some of these dopamine agonists on kids with the known side effects. Please help with any specific ref's re: CMT and RLS or personal successful experiences with this problem in children. Thanksk.

85. Re: RLS In A 4y/o With Charcot Marie Tooth Disease Re RLS in a 4y/o with Charcot Marie Tooth disease. Follow Ups Re RLS in a 4y/owith Charcot Marie Tooth disease DeltaDoc 2057 4/17/02 (0) Post a Followup. http://www.sleepnet.com/diag2/messages/201.html

Sleepnet.com's Homepage Sleep Disorders Sleep Links Search Re: RLS in a 4y/o with Charcot Marie Tooth Disease Follow Ups Post Followup Diagnostic Dilemmas Forum2 FAQ Posted by sleepdoc on March 26, 2002 at 15:48:06: In Reply to: RLS in a 4y/o with Charcot Marie Tooth Disease posted by kathleen pfeffer on March 05, 2002 at 09:11:36: Have you measured serum ferritin levels in this child? Ferrous sulfate may help alleviate symptoms if the ferritin level is less than 45-50...(even though that's considered in the normal range)...Dopamine agonists can exacerbate or augment these symptoms, particularly in children and I would avoid them if possible...Have you thought about Tegretol? Although typically reserved for children 6 and older, if followed closely, may be helpful, starting with 100mg/5cc and give 1/2 tsp BID...good luck..... Follow Ups: Re: RLS in a 4y/o with Charcot Marie Tooth Disease DeltaDoc Post a Followup Name : (name or handle required) E-Mail : (required or use somebody@sleepnet.com to avoid spam email,etc.) Subject : Comments: PLEASE ONLY CLICK THE SUBMIT FOLLOW UP BUTTON ONCE!!. Thanks, Sandman

86. Charcot Marie Tooth Disease Related Books HOME Charcot Marie Tooth disease Related Books http://www.bdid.com/cmtbooks.htm

HOME Charcot Marie Tooth Disease Related Books Charcot-Marie-Tooth Disorders Charcot-Marie-Tooth Disorders Pathophysiology, Molecular Genetics, and Therapy Clinical and electrodiagnostic features of Charcot-Marie-Tooth syndrome Search: Books Popular Music Classical Music Video Enter keywords... Amazon.com HOME

87. Charcot Marie (Tooth) Disease HOME Charcot Marie (Tooth) disease (CMT, Hereditary Motor and Sensory Neuropathy,Peroneal Muscular Atrophy). Related Books; Short description of cell lines. http://www.bdid.com/cmt.htm

HOME Charcot Marie (Tooth) Disease (CMT, Hereditary Motor and Sensory Neuropathy, Peroneal Muscular Atrophy) Related Books Short description of cell lines. Pathology: Charcot-Marie-Tooth disease CHARCOT-MARIE-TOOTH DISEASE Charcot Marie Tooth Association ... Support Group for Horse Riding CMTs Neuronal Guadalajara Type CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE Type A CHARCOT-MARIE-TOOTH DISEASE, NEURONAL TYPE, A; CMT2A Type B CHARCOT-MARIE-TOOTH DISEASE, NEURONAL TYPE, B; CMT2B Type D CHARCOT-MARIE-TOOTH DISEASE, NEURONAL TYPE, D X-Linked CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED; CMTX1 Recessive Type 1 See Charcot Marie Tooth Disease, X-Linked Type 2 CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED RECESSIVE, 2; CMTX2 Type 3 CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED RECESSIVE, 3; CMTX3 Type 1 Charcot-Marie-Tooth Type 1 with Aplasia Cutis Congenita (Motor Sensory Neuropathy Type 1 Aplasia Cutis Congenita) Charcot marie tooth type 1 aplasia cutis congenita CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIA CUTIS CONGENITA Type 1a Charcot-Marie-Tooth Disease Type 1A Prenatal detection of Charcot-Marie-Tooth disease type 1A duplication resulting from a rare recombination event CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A; CMT1A

88. Charcot Marie Tooth Disease Charcot Marie Tooth disease. Definition. Charcot Marie Tooth disease(CMT) is the name of a group of inherited disorders of the nerves http://www.healthatoz.com/healthatoz/Atoz/ency/charcot_marie_tooth_disease.html

Encyclopedia Index C Home Encyclopedia Encyclopedia Index C Charcot Marie Tooth disease Definition Charcot Marie Tooth disease (CMT) is the name of a group of inherited disorders of the nerves in the peripheral nervous system (nerves throughout the body that communicate motor and sensory information to and from the spinal cord) causing weakness and loss of sensation in the limbs. Description CMT is named for the three neurologists who first described the condition in the late 1800s. It is also known as hereditary motor and sensory neuropathy, and is sometimes called peroneal muscular atrophy, referring to the muscles in the leg that are often affected. The age of onset of CMT can vary anywhere from young childhood to the 50s or 60s. Symptoms typically begin by the age of 20. For reasons yet unknown, the severity in symptoms can also vary greatly, even among members of the same family. Although CMT has been described for many years, it is only since the early 1990s that the genetic cause of many of the types of CMT have become known. Therefore, knowledge about CMT has increased dramatically within a short time. The peripheral nerves CMT affects the peripheral nerves, those groups of nerve cells carrying information to and from the spinal cord. CMT decreases the ability of these nerves to carry motor commands to muscles, especially those furthest from the spinal cord located in the feet and hands. As a result, the muscles connected to these nerves eventually weaken. CMT also affects the sensory nerves that carry information from the limbs to the brain. Therefore people with CMT also have sensory loss. This causes symptoms such as not being able to tell if something is hot or cold or difficulties with balance.

89. OTdirect Occupational Therapy Revision Notes: Charcot Marie Tooth Disease Occupational Therapy Revision Notes Charcot Marie Tooth disease (CMT).Please note This is a basic revision aid, not a comprehensive http://www.otdirect.co.uk/cmt.html

Occupational Therapy Revision Notes: Charcot Marie Tooth Disease (CMT) Please note: This is a basic revision aid, not a comprehensive and reliable statement of medical fact. These notes should not be used to guide treatment. For reliable information and advice, consult a qualified practitioner. [Last updated: 12 December 2002] CMT is now referred to as Hereditary Motor and Sensory Neuropathy (HMSN), sometimes also described as Peroneal Muscular Atrophy There are thought to be many different types of HMSN but primary classifications are: HMSN Type 1: demyelinating form HMSN Type 2: axonal form See table below for further details. Prevalence Epedimiological studies quote rates of 1.8:10,000 in Japan (Kurihara et.al., 2002) ; 17.5:100,100 in Central-southern Italy (Morocutti et.al., 2002) and 1:2500 in Norway . HMSN 1a is the most common form. Age at onset Variable. Some forms are symptomatic by 5 years of age. HMSN 1 is usually evident before 30 years of age, while HMSN 2 tends to appear later. Cause Cause and Pathology of HMSN Type Inheritance Pathology HMSN 1a Autosomal Dominant Demyelinating HMSN 1b Autosomal Dominant Demyelinating HMSN 1 Autosomal Dominant/Recessive?

90. Epilepsy - Charcot Marie Tooth Disease By NYERRN Epilepsy and Charcot Marie Tooth disease resources on the Web. A complete onlineguide in the field of neurology. Epilepsy and Charcot Marie Tooth disease. http://www.nyerrn.com/neuro/3.htm

Epilepsy and Charcot Marie Tooth Disease Charcot Marie Tooth Disease Charcot-Marie-Tooth Association CMTnet CMTnet provides information for both the medical and non-medical communities on Charcot-Marie-Tooth (CMT). CMT International (Charcot-Marie-Tooth Disease) Formally known as Charcot-Marie-Tooth Disease/Peroneal Muscular Atrophy International Association, Inc. This site includes information about hereditary neuropathy with liability to pressure palsies (HNPP). Family Village on Charcot-Marie-Tooth Disease Muscular Dystrophy Association Facts About Charcot-Marie-Tooth Disease (CMT) National Alliance OF The Disabled (NAOTD) CMT - Charcot Marie Tooth Disease National Center for Biotechnology Information National Institute of Neurological Disorders and Stroke Charcot-Marie-Tooth Disorder National Organization for Rare Disorders (NORD) Charcot Marie Tooth Disease Summary Neurology Channel Charcot-Marie-Tooth Disease Return to the Index of Neurology Topics Epilepsy American Epilepsy Society A professional organization of clinicians and researchers. Epilepsy Canada Epilepsy Contact Database Epilepsy Education Association Epilepsy Foundation of America Includes FAQs and a "News Desk"

91. Short Description Of Cell Lines. Pathology Charcot-Marie-Tooth Version 4.200205, Short description of cell lines. Pathology CharcotMarie-Toothdisease 118200 OMIM record. - By selecting the http://www.biotech.ist.unige.it/cldb/pat56.html

92. Health Library - Charcot Marie Tooth Disease Charcot Marie Tooth disease. Synonyms Disorder Subdivisions GeneralDiscussion Resources National Organization for Rare Disorders. http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=

93. Charcot Marie Tooth 127 PM; Cavus foot (10/8/99) 351 PM; Charcot Marie Tooth disease(Rhizotomy) (10/6/99) 1023 AM; Does my friend have CMT? (10/4/99 http://neuro-www.mgh.harvard.edu/forum/CharcotMarieToothMenu.html

Charcot Marie Tooth Menu This is a webforum to discuss and comment on Charcot Marie Tooth (CMT), HNPP, and other Hereditary Motor Sensory Neuropathies. Click here to Enter a new Neurology WebForum article... This Web Forum is not moderated in any sense. Anyone on the Internet can post articles or reply to previously posted articles, and they may do so anonymously. Therefore, the opinions and statements made in all articles and replies do not represent the official opinions of MGH and MGH Neurology. Neither is MGH or MGH Neurology responsible for the content of any articles or replies. No messages are screened for content. - Very Important Message! - Please Click Here to Read Current Posts: Oct 10, 1997 to Present Useful Websites can be found and posted here! (1/13/00) 11:11 AM CHARCOT MARIE TOOTH (1/13/00) 12:14 AM (1/8/00) 3:15 PM ... HNPP - CMT's genetic opposite (10/11/97) 7:23 PM IMPORTANT: If this page seems to be missing recently added documents, click the "Reload Page" button on your Web Browser to update the menu. Return to the main Neurology WebForum Page.

94. Charcot – Marie – Tooth Disease click For Medical Professionals only. Charcot – marie – toothdisease,, Print this article, Jean Martin Charcot, 1825–1893 http://www.amershamhealth.com/medcyclopaedia/Volume III 1/Charcot Marie Tooth

Medcyclopaedia About Medcyclopaedia Amersham Health Search for: Type a word or a phrase. All forms of the word are searchable. Advanced search Browse entry words starting with: A B C D ... Other characters Try our Medcyclopaedia Premium Edition with added tools and functionality tailored to make your working day easier. The following tools are presently available: Expanded search *For Medical Professionals only, registration required Charcot – marie – tooth disease, Jean Martin Charcot, 1825–1893, French neurologist, Pierre Marie, 1853–1940, French physician and Henry Tooth, 1856–1925, English physician), a dominantly inherited hypertrophic (type I) or neuronal (type II) form of peroneal muscle atrophy. Among the manifestations are a high plantar arch with awkward gait, hammer toe pes cavus deformity , diminished or absent tendon reflexes, and scoliosis DR The Encyclopaedia of Medical Imaging Volume III:1 Welcome to Medcyclopaedia. This site is open to a public audience, still we want to know a little more about our visitors. Please tick off the boxes that match your profile. Do you live in Europe?

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