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Hereditary Sensory Motor Neuropathy:     more detail

Hereditary Motor and Sensory Neuropathy: Webster's Timeline History, 1980 - 2007 by Icon Group International, 2009-04-16 Genetics of hereditary motor and sensory neuropathy and the Costa Rican contribution.(Charcot-Marie-Tooth (CMT)): An article from: Revista de Biología Tropical by Alejandro Leal, 2004-09-01 Charcot-Marie-Tooth Disease: A Practical Guide. Also Known as Hereditary Motor and Sensory Neuropathy and Peroneal Muscular Atrophy. by (No Author), 2000 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 Lipidoses: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Tish, A.M. Davidson, Altha Edgren, 2006

lists with details

101. Entrez PubMed
     hereditary motor and sensory Neuropathies/complications hereditary motor and sensory Neuropathies/diagnosis* hereditary motor and sensory  
     http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=9

102. Entrez PubMed
     hereditary motor and sensory Neuropathies/diagnosis hereditary motor and sensory Neuropathies/genetics* Human Male Menkes Kinky Hair Syndrome/genetics  
     http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1

103. Painful Feet: The Small Fiber Neuropathies - CNI Review Medical Journal - Online
     Patients with large fiber neuropathies, such as demyelinating hereditary sensory motor neuropathies complain of numbness, tingling, and weakness.  
     http://www.thecni.org/reviews/13-2-p07-treihaft.htm
     
     Extractions: Volume 13, Number 2 This Issue Contents Next Article Small fiber neuropathy is a relatively common disorder often associated with systemic conditions, such as diabetes, HIV, and vasculitis. Painful burning feet with diminished pain and temperature perception, and in some cases autonomic dysfunction, characterize this syndrome. Despite the magnitude of the symptoms there are few objective measures to identify and quantify these neuropathies. Skin biopsy and new immunohistochemical staining techniques have facilitated the evaluation of this syndrome. Introduction . Peripheral neuropathies involve different populations of nerve fibers. Most patients present with large fiber neuropathies characterized by numbness, tingling, weakness, loss of deep tendon reflexes, and abnormal electrophysiologic studies. A more enigmatic group of patients present with severe pain and a paucity of findings on clinical examination and electrophysiologic studies. Many of these patients have small fiber neuropathies. The disparity of subjective sensory complaints to objective signs sometimes leads to an erroneous diagnosis of psychogenic pain. Patients with these syndromes are often difficult to treat. Thus, prompt evaluation and accurate identification of these syndromes is important. Clinical Presentation

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