101. Spinal Muscular Atrophy - HUM-MOLGEN Author, Topic spinal muscular atrophy. marivicervera I have recently seen a 6 years old boy whith spinal muscular atrophy confirmed by biosy. The http://www.hum-molgen.de/bb/Forum2/HTML/000107.html

home genetic news bioinformatics biotechnology ... DIAGnostics - Clinical Research (professional requests) Spinal Muscular Atrophy profile register preferences faq ... next oldest topic Author Topic: Spinal Muscular Atrophy marivicervera Member posted 08-13-2002 06:48 PM I have recently seen a 6 years old boy whith spinal muscular atrophy confirmed by biosy. The familiy is interested in molecular studies. I would like to know if anyone is working on this studies. Thank you. Marivi Cervera M.D. IP: 152.163.201.187 All times are ET (US) next newest topic next oldest topic Administrative Options: Close Topic Archive/Move Delete Topic Hop to: Select a Forum or Archive List of Forums: Biotechnical requests and sources DIAGnostics - Clinical Research (professional requests) Ethical, legal and social implications Open Topic Forum List of Archives: Genetic News DIAGnostics - Clinical Research Contact Us HUM-MOLGEN HUM-MOLGEN Powered by: Ultimate Bulletin Board, Version 5.44a By posting requests at HUM-MOLGEN you reach more than 9.500 mailing list subscribers and a 6 digit number of www users. Therefore post high quality messages only, including full name and institutional address.

102. :: Ez2Find :: Spinal Muscular Atrophy Guide spinal muscular atrophy, Global Metasearch Any Language Guides, spinal muscular atrophy. ez2Find Home Directory Health http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas

Guide : Spinal Muscular Atrophy Global Metasearch Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode All Words Any Word Phrase Results Timeout Depth Adult Filter Add to Favorites Other Search Web News Newsgroups Images Guides Spinal Muscular Atrophy ez2Find Home Directory Health Conditions and Diseases ... Muscle Diseases : Spinal Muscular Atrophy Related Categories Health: Conditions and Diseases: Neurological Disorders: Spinal Cord Web Sites Families of SMA (Spinal Muscular Atrophy) [Site Info] [Translate] [Open New Window] International support group and resource center for this disease, includes current research. URL: http://www.fsma.org Families of Spinal Muscular Atrophy Canada [Site Info] [Translate] [Open New Window] Canadian charity supports research into a cure for SMA. URL: http://www.fsma.org/canada/

103. Spinal Muscular Atrophy - ABC Homeopathy Forum Homeopathy and Health Forum. spinal muscular atrophy. Post ReplyPOST REPLY. Re spinal muscular atrophy, From DRVenugopal, on 200302-06. http://www.abchomeopathy.com/forum2.php/202/

Homeopathics Homeopathy Software Homeopathic Remedies Store ABC Homeopathy Homeopathic medicine Homeopathy Forum Materia Medica Links: Aceticum Acidum Phosphorus Plumbum Metallicum NOTE: Due to spelling variations not all remedies mentioned in the forum are included as links above. To find others, go to the home page and follow the alphabetical links in the shop section. Forum Archive: Homeopathy and Health Forum Spinal Muscular Atrophy From starfighter-n [Log on to view profile] on 2003-02-01 5 replies 158 views My condition results in weakness and wasting of the main sceletal muscules and I use a wheelchair - I would like to get stronger as present I am getting weaker - I am 31year old Re: Spinal Muscular Atrophy From DRVenugopal [Log on to view profile] on 2003-02-06 Laboratory investigations would reveal if the problem is genetic or not. Seeing the same we can say whether we can slow down the progress of this disease. In any case Homoeopathy can surely give more relief . Dr.Venugopal Gouri. drvenugopal@hotmail.com

104. Entrez PubMed Click here to read Acute onset of infantile spinal muscular atrophy. SMN protein (spinal muscular atrophy). PMID 11516612 PubMed indexed for MEDLINE http://www.biomedcentral.com/pubmed/11516612

Entrez PubMed Nucleotide Protein ... Books Search PubMed Protein Nucleotide Structure Genome Books CancerChromosomes 3D Domains Domains Gene GEO GEO DataSets HomoloGene Journals MeSH NCBI Web Site OMIM PMC PopSet SNP Taxonomy UniGene UniSTS for Limits Preview/Index History Clipboard ... Text Version Entrez PubMed Overview FAQ Tutorial New/Noteworthy ... E-Utilities PubMed Services Journals Database MeSH Database Single Citation Matcher Batch Citation Matcher ... Cubby Related Resources Order Documents NLM Gateway TOXNET Consumer Health ... PubMed Central Summary Brief Abstract Citation ASN.1 MEDLINE XML UI List LinkOut Related Articles Cited in Books CancerChrom Links Domain Links 3D Domain Links GEO DataSet Links Gene Links Genome Links GEO Links HomoloGene Links Nucleotide Links OMIM Links PMC Links Cited in PMC PopSet Links Protein Links SNP Links Structure Links UniSTS Links Show: Sort Author Journal Pub Date Text File Clipboard E-mail Order Pediatr Neurol. 2001 May;24(5):371-2. Related Articles, Links Acute onset of infantile spinal muscular atrophy. Ravid S, Topper L, Eviatar L. Division of Pediatric Neurology, Schneider Children's Hospital, New Hyde Park, NY 11040, USA. Two patients with acute generalized weakness and areflexia are presented. The electrophysiologic studies in both revealed evidence of decreased conduction velocity and mixed axonal and demyelinating neuropathy, suggestive of the diagnosis of Guillain-Barre syndrome. The young ages of the patients and their failure to respond to immunoglobulin therapy were the major clues to the final diagnosis of spinal muscular atrophy type I. Blood for DNA study revealed homozygous deletion mutation in exons 7 and 8 of the survival motor neuron gene. This diagnosis should be considered in every child under 1 year of age who presents with acute weakness because Guillain-Barre syndrome in this age group is rare.

105. Spinal Muscular Atrophy Spermagglutination. spinal muscular atrophy. Spinocerebellar Ataxia. SS A Antibodies (Ro) \. spinal muscular atrophy. Source, Blood. Mnemonic, MISCMDL. http://www.calgarylabservices.com/LabTests/AlphabeticalListing/S/Spinal-Muscular

Home Contact Us Useful Links Site Map ... Z List All Test Names Beginning With: A B C D ... Cytopathology Spinal Muscular Atrophy Source Blood  Mnemonic MISCMDL  Specimen Requirements Adults : 3 x 5 mL (or 2 x 7 mL) lavender top EDTA tube - whole blood Pediatric : 2 x 3 mL tubes Infants : 2 to 3 mL Newborns : 1 mL May be collected at any Patient Service Center Monday-Thursday only. Specimen Handling DO NOT centrifuge or separate specimen. DO NOT freeze. Transport specimen, along with ACH Molecular Diagnostic Lab requisition if available, at room temperature without delay to DSC. If overnight storage cannot be avoided, store in refrigerator. Additional Information Testing Location ACH Molecular Diagnostic Lab  Testing Frequency Alternate Name(s) Back Page updated on Apr 28, 2004 at 12:59 PM. Please read our

106. »»Spinal-Muscular-Atrophy Reviews«« SpinalMuscular-Atrophy Reviews. Current Concepts in Childhood spinal muscular atrophy. Published in Hardcover by Springer-Verlag Telos (November, 1989). http://www.health-issue-books.com/Soft-Tissue-Sarcoma/Spinal-Muscular-Atrophy/

Spinal-Muscular-Atrophy Reviews Related Subjects: Soft-Tissue-Sarcoma Book reviews for "Spinal-Muscular-Atrophy" sorted by average review score: The Me in the Mirror Published in Paperback by Seal Press (May, 1994) Author: Connie Panzarino Amazon base price: List price: that's off! Used price: Collectible price: Buy one from zShops for: Average review score: A must read... As a disabled woman, I really loved this book, and could identify with many aspects of Connie's life. An educating book to those who are not disabled. Honest and Funny I read this book a few years a go and loved it. I think it was an honest book. I know it is because I have SMA like the author so I am a good judge of the subject. This book is not "Preachy" or filled with religious meaning like some disabled books. Nor does it make the disabled look needy or helpless. It's just about her life. It's not supposed to go in to great detail of specific disability issues...that's what essays and textbooks are for. Even so, I do think it does give the average "walkie-talkie" insight of disabled culture. Everything from care, school, career and romance. The writing is in everyday language and shows her humor in dealing with her struggles. The main flaw is the poor edit job. I didn't find it too distracting (if you can handle reading a personal journal you should be OK with this book) and the book is a quick read. There is a great need for books on adults with born with disabilities and disabled women. I'm glad this book made it!

107. SPINAL MUSCULAR ATROPHY-DIAPHRAGMATIC PARALYSIS Features Listed For spinal muscular atrophyDIAPHRAGMATIC PARALYSIS. McKusick Tongue fasciculations; Diaphragm, general abnormalities; http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?6067

108. (11[2]: 231-247) Spinal Muscular Atrophy: Present State (112 231247) spinal muscular atrophy Present State Henning Schmalbruch and Georg Haase spinal muscular atrophy (SMA) is a hereditary neurodegenerative http://brainpath.medsch.ucla.edu/abstracts/vol11/1102/112a9.htm

Spinal Muscular Atrophy: Present State Henning Schmalbruch and Georg Haase Spinal muscular atrophy (SMA) is a hereditary neurodegenerative disease caused by homozygous deletions or mutations in the SMN1 gene on Chr.5q13. SMA spans from severe Werdnig-Hoffmann disease (SMA 1) to relatively benign Kugelberg-Welander disease (SMA 3). Onset before birth possibly aggravates the clinical course, because immature motoneurons do not show compensatory sprouting and collateral reinnervation, and motor units in SMA 1, in contrast to those in SMA 3, are not enlarged. Genetic evidence indicates that SMN2, a gene 99% identical to SMN1, can attenuate SMA severity: in patients, more SMN2 copies and higher SMN protein levels are correlated with milder SMA. There is evidence that SMN plays a role in motoneuron RNA metabolism, but it has also been linked to apoptosis. Several mouse models with motoneuron disease have been successfully treated with neurotrophic factors. None of these models is, however, homologous to SMA. Recently, genetic mouse models of SMA have been created by introducing human SMN2 transgenes into Smn knockout mice or by targeting the Smn gene knockout to neurons. These mice not only provide important insights into the pathogenesis of SMA but are also crucial for testing new therapeutic strategies. These include SMN gene transfer, molecules capable to up-regulate SMN expression and trophic or antiapoptotic factors. (

109. GeneReviews: Spinal And Bulbar Muscular Atrophy Your browser does not support HTML frames so you must view spinal and Bulbar muscular atrophy in a slightly less readable form. http://www.geneclinics.org/profiles/kennedy/

Your browser does not support HTML frames so you must view Spinal and Bulbar Muscular Atrophy in a slightly less readable form. Please follow this link to do so.

110. The Jennifer Trust Site Has Moved To Http://www.jtsma.org.uk/ The Jennifer Trust site has moved. The Jennifer Trust site is now at http//www.jtsma.org.uk/. Please change your bookmarks to the new URL. http://www.jtsma.demon.co.uk/

The Jennifer Trust site has moved The Jennifer Trust site is now at: http://www.jtsma.org.uk/ Please change your bookmarks to the new URL The new entry page should load itself in a moment (or click on the logo).

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