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         Hereditary Spastic Paraplegia:     more detail
  1. The Official Patient's Sourcebook on Hereditary Spastic Paraplegia: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-09
  2. Hereditary spastic paraplegia: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Chitra, MBBS, MD Venkatasubramanian, 2005
  3. Hereditary spastic paraplegia: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Sandra Galeotti, 2005
  4. On hereditary ataxia and spastic paraplegia (The treasury of human inheritance) by Julia Bell, 1939

41. Hereditary Spastic Paraplegia - General Practice Notebook
hereditary spastic paraplegia. This is a hereditary neurodegenerative disorderwhich in its simple form results in a progressive spastic paraplegia.
http://www.gpnotebook.co.uk/cache/825557023.htm
hereditary spastic paraplegia This is a hereditary neurodegenerative disorder which in its simple form results in a progressive spastic paraplegia. Patients present at any time from childhood to old age. There are two main forms of the disease:
  • early onset with a very indolent course later onset, 40-60 yrs, with occasional complicating features such as cerebellar ataxia, dementia and epilepsy
There is an important differential diagnosis.
Click here for more information...

42. NeuroCAST - SPG3A (atlastin) And SPG4 (spastin): Hereditary Spastic Paraplegia
hereditary spastic paraplegia (HSP) is a clinically and genetically heterogeneousgroup of inherited disorders characterized by insidiously progressive, often
http://www.neurocast.com/site/content/sessions_08_2003.asp
Hereditary spastic paraplegia (HSP) is a clinically and genetically heterogeneous group of inherited disorders characterized by insidiously progressive, often severe, lower extremity weakness and spasticity. Symptom severity, age of onset and rate of disease progression may vary widely among patients. It is estimated that three in every 100,000 people are affected with HSP in the U.S. HSPs are classified by clinical presentation, as either uncomplicated or complicated, and by inheritance pattern. Uncomplicated (or pure) HSP is the most common form and is characterized by progressive lower extremity spastic weakness, accompanied by hypertonic urinary bladder disturbances, and often, mildly impaired vibration sensation. Uncomplicated HSP can be disabling, but it does not shorten life span. HSP is classified as complicated if the impairments of the uncomplicated form are accompanied by additional neurologic abnormalities that are not attributable to other co-existing disorders. Researchers estimate that uncomplicated HSP represents 90% of all HSP cases, while complicated HSP accounts for 10%.
HSP's inheritance pattern may be autosomal dominant (the most common), autosomal recessive or X-linked. Recent advances in molecular genetic testing now enable the identification of at least 50% of uncomplicated autosomal dominant hereditary spastic paraplegia (ADHSP) cases.

43. NeuroCAST - References - SPG3A (atlastin) And SPG4 (spastin): Hereditary Spastic
hereditary spastic paraplegia. In Emery and Rimoin’s Principles and Practice ofMedical Genetics, 4th Edition, eds. Fink, JK hereditary spastic paraplegia.
http://www.neurocast.com/site/content/references_08_2003.asp
  • Fink, J. Hereditary spastic paraplegia. In: , 4th Edition, eds. David L. Rimoin et al., 3124-45. 2001. London:Churchill Livingstone. Muglia, M. et al., A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. J Neurol Stapley, C. Spastic Paraplegia or Hereditary Spastic Paraparesis General Information. In: HSPinfo.org http://hspinfo.org/HSP.htm Fink, J.K. Hereditary spastic paraplegia. Neurol Clin N Am Tessa, A. et al., SPG3A, An additional family carrying a new atlastin mutation. Neurology Zhao, X. et al., Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia. Nat Genet Fink, J. Hereditary Spastic Paraplegia: The Pace Quickens. Ann Neurol Patel, H. SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia. Nat Genet Hazan, J. et al., Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Nat Genet Fink, J. Hereditary spastic paraplegia: Clinical features. In: Hereditary Spastic Paraplegia (HSP) Research http://www.med.umich.edu/hsp/clinfeatures.htm
  • 44. Diagnosing Hereditary Spastic Paraplegia
    Subject Diagnosing hereditary spastic paraplegia Topic Area Neurology GeneralForum The Neurology and Neurosurgery Forum Question Posted By Cheryl on
    http://www.medhelp.org/forums/neuro/archive/1298.html
    Questions in The Neurology Forum are being answered by doctors from
    The Cleveland Clinic , consistently ranked one of the best hospitals in America. Subject: Diagnosing Hereditary Spastic Paraplegia
    Topic Area: Neurology - General
    Forum: The Neurology and Neurosurgery Forum
    Question Posted By: Cheryl on Monday, July 28, 1997
    Posted by CCF MD on August 15, 1997 at 09:41:49:
    In Reply to: Diagnosing Hereditary Spastic Paraplegia posted by Cheryl on July 28, 1997 at 13:03:46:
    : I am trying to verify whether or not a blood test exists to diagnose
    Hereditary Spastic Paraplegia (or Familial Spastic Paraparesis). I
    have heard that there may be a blood test available for the X-linked
    gene, but have not been able to verify that, or find out if tests are currently available for any of the other genes. Tough question. This is not an active area of research in our institution so I'm not sure how much help I can be. I've asked around and the word I hear is that the gene locus is being looked at in the various subtypes but I think that any testing is still experimental. I will give you some reference articles

    45. Diagnosing Hereditary Spastic Paraplegia
    Subject Diagnosing hereditary spastic paraplegia Forum The Neurology and NeurosurgeryForum Topic Area Posted by Cheryl on July 28, 1997 at 130346
    http://www.medhelp.org/forums/neuro/archive/1188.html
    Questions in The Neurology Forum are being answered by doctors from
    The Cleveland Clinic , consistently ranked one of the best hospitals in America. Subject: Diagnosing Hereditary Spastic Paraplegia
    Forum: The Neurology and Neurosurgery Forum
    Topic Area:
    Posted by Cheryl on July 28, 1997 at 13:03:46:
    I am trying to verify whether or not a blood test exists to diagnose
    Hereditary Spastic Paraplegia (or Familial Spastic Paraparesis). I
    have heard that there may be a blood test available for the X-linked
    gene, but have not been able to verify that, or find out if tests
    are currently available for any of the other genes.
    The Neurology Forum Neurology Forum Archives Med Help Home If you would like to make an appointment at the Cleveland Clinic, please call 1-800-CCF-CARE or inquire online by using the Neurology Dept. website. The website contains a directory of the staff that can be used to select the physician best suited to address your neurological or neurosurgical problem. Information contained within this forum is intended solely for general educational purposes and is not intended nor implied to be a substitute for professional medical advice relative to your specific medical condition or question. Always seek the advice of your physician or other health provider for any questions you may have regarding your medical condition. Only your physician can provide specific diagnoses and therapies. By using this site you agree to the following

    46. :: Ez2Find :: Hereditary Spastic Paraplegia
    Guide hereditary spastic paraplegia, Global Metasearch Any Language Guides,hereditary spastic paraplegia. ez2Find Home Directory Health
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    47. ClinicalTrials.gov - Information On Clinical Trials And Human Research Studies:
    1. Completed, Nuclear Magnetic Spectroscopy Imaging to Evaluate Primary LateralSclerosis, hereditary spastic paraplegia and Amyotrophic Lateral Sclerosis
    http://www.clinicaltrials.gov/search/term=Hereditary Spastic Paraplegia
    Home Search Browse Resources ... About Search results for Hereditary Spastic Paraplegia [ALL-FIELDS] are shown below.
    Include trials that are no longer recruiting patients.
    1 study was found. Completed Nuclear Magnetic Spectroscopy Imaging to Evaluate Primary Lateral Sclerosis, Hereditary Spastic Paraplegia and Amyotrophic Lateral Sclerosis
    Conditions: Primary Lateral Sclerosis; Hereditary Spastic Paraplegia; Amyotrophic Lateral Sclerosis U.S. National Library of Medicine Contact NLM Customer Service National Institutes of Health Privacy ... Freedom of Information Act

    48. Clinical Trial: Nuclear Magnetic Spectroscopy Imaging To Evaluate Primary Latera
    Nuclear Magnetic Spectroscopy Imaging to Evaluate Primary Lateral Sclerosis,hereditary spastic paraplegia and Amyotrophic Lateral Sclerosis.
    http://www.clinicaltrials.gov/ct/show/NCT00023075?order=1

    49. Conditions And Diseases: Genetic Disorders: Hereditary Spastic Paraplegia
    Health and Home. hereditary spastic paraplegia. http//www.fspgroup.org.hereditary spastic paraplegia. Last Update Mon May 10 2004.
    http://www.health-home.net/Conditions_and_Diseases/Genetic_Disorders/Hereditary_
    Health and Home
    Hereditary Spastic Paraplegia
    HOME LOGIN ADD A LINK MODIFY A LINK ... PARTNER
    Looking for something in particular? the entire directory only this category Home Conditions and Diseases Genetic Disorders : Hereditary Spastic Paraplegia LINKS:
    • GeneClinics: An Overview
      In depth details about hereditary spastic paraplegia. Includes a summary, definition, categories, diagnosis, genetic counseling and resources.
      http://www.geneclinics.org/profiles/hsp/
    • Hereditary Spastic Paraplegia
      In depth look at this disease by John K. Fink, M.D., including genetic analysis, clinical features and FAQs.
      http://www.med.umich.edu/hsp/
    • Hereditary Spastic Paraplegia
      HSP information sheet compiled by the National Institute of Neurological Disorders and Stroke.
      http://www.ninds.nih.gov/health_and_medical/disorders/hereditarysp.htm
    • MCW Healthlink: HSP An article about hereditary spastic paraplegia, also called familial spastic paralysis. http://healthlink.mcw.edu/article/921730935.html
    • Spastic Paraplegia Foundation Supports on the upper motor neuron disorders hereditary spastic paraplegia and primary lateral sclerosis. Information about these conditions, disability resources, newsletters, news, announcements, research and support. http://sp-foundation.org/

    50. Hereditary Spastic Paraplegia
    The New Health Directory, Directory, Home Health Conditions and DiseasesGenetic Disorders hereditary spastic paraplegia (6). HSPinfo
    http://www.thenewhealthfind.com/Health/ConditionsandDiseases/GeneticDisorders/He
    Directory Home Health Conditions and Diseases Genetic Disorders : Hereditary Spastic Paraplegia (6)
      HSPinfo.org - Information about hereditary spastic paraplegia, and disability resources. Includes newsletters, news, announcements, research and support. Hereditary Spastic Paraplegia - In depth look at this disease by John K. Fink, M.D., including genetic analysis, clinical features and FAQs. Hereditary Spastic Paraplegia - HSP information sheet compiled by the National Institute of Neurological Disorders and Stroke. The FSP Support Group - For people suffering from Familial Spastic Paraplegia. Includes a newsletter, discussion forum, links, and contact details. GeneClinics: An Overview - In depth details about hereditary spastic paraplegia. Includes a summary, definition, categories, diagnosis, genetic counseling and resources. MCW Healthlink: HSP - An article about hereditary spastic paraplegia, also called familial spastic paralysis.

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    51. The FSP (Familial Spastic Paraplegia) Group
    Familial Spastic Paraplegia (FSP) is also known as hereditary spastic paraplegia(HSP), Familial Spastic Paraparesis or StrumpellLorrain Syndrome.
    http://www.fspgroup.org/
    The FSP Group
    Moving Forward Together
    What is Familial Spastic Paraplegia?
    Familial Spastic Paraplegia (FSP) is also known as Hereditary Spastic Paraplegia (HSP), Familial Spastic Paraparesis or Strumpell-Lorrain Syndrome. The condition is rare and is caused by the inheritance of an abnormal gene from an affected parent. It has been diagnosed where no family history of the condition is known. FSP describes a group of disorders characterised by progressive stiffness (spasticity) of the legs associated with varying degrees of weakness. A number of symptoms are associated with this condition including stiffness and leg cramps which often precede the emergence of a scissoring spastic gait.
    What does the FSP Group do?
    • A quarterly newsletter which updates members on current topics. A national meeting which includes an Annual General Meeting, lectures by FSP specialists and subsequent discussion groups. A help-line which offers advice to new members and those with problems. A library of information articles on FSP.

    52. Hereditary Spastic Paraplegia
    hereditary spastic paraplegia. disease marie strumpell. nausea HereditarySpastic Paraplegia. hereditary spastic paraplegia bleeding.
    http://www.icongrouponline.com/health/Hereditary_Spastic_Paraplegia.html
    ICON Health Publications
    Official Health Sourcebooks The Official Patient's Sourcebook
    on
    HEREDITARY SPASTIC PARAPLEGIA

    (Familial Spastic Paraplegia; Spastic Spinal Familial Paralysis; Strumpell Disease; Strumpell-Lorrain Familial Spasmodic Paraplegia; Strumpell-Lorraine Syndrome; Strumpell's Familial Paraplegia) Revised and Updated for the Internet Age P A P E R B A C K Paperback Book Paperback Book Order by phone: 800-843-2665 (within USA) 1-201-272-3651 (from outside USA) Paperback Book Shipped in 3 to 5 business days
    E B O O K Electronic File * E-Book version sent via e-mail in 2 business days Electronic File *E-Book version sent via e-mail in 2 business days Pages Price $28.95(USD) ISBN Published Synopsis A comprehensive manual for anyone interested in self-directed research on Hereditary Spastic Paraplegia. Fully referenced with ample Internet listings and glossary. Related Conditions/Synonyms Familial Spastic Paraplegia; Spastic Spinal Familial Paralysis; Strumpell Disease; Strumpell-Lorrain Familial Spasmodic Paraplegia; Strumpell-Lorraine Syndrome; Strumpell's Familial Paraplegia Description Table of Contents Introduction Overview Organization Scope Moving Forward PART I: THE ESSENTIALS Chapter 1. The Essentials on Hereditary Spastic Paraplegia: Guidelines

    53. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Genetic_Disorders/
    Click Here. Top Health Conditions and Diseases Genetic Disorders HereditarySpastic Paraplegia (6 links). News about hereditary spastic paraplegia
    http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Genetic_Dis
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    54. Hereditary Spastic Paraplegia
    hereditary spastic paraplegia. hereditary spastic paraplegia (HSP),also called familial spastic paraparesis (FSP), refers to a group
    http://www.sciencedaily.com/encyclopedia/hereditary_spastic_paraplegia
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    Hereditary spastic paraplegia
    Hereditary spastic paraplegia (HSP), also called familial spastic paraparesis (FSP), refers to a group of inherited disorders that are characterized by progressive weakness and stiffness of the legs. Though the primary feature of HSP is severe, progressive, lower extremity spasticity , in more complicated forms it can be accompanied by other neurological symptoms. These include optic neuropathy, retinopathy (diseases of the retina), dementia ataxia (lack of muscle control), icthyosis (a skin disorder resulting in dry, rough, scaly skin), [[mental retardation]

    55. NORD - National Organization For Rare Disorders, Inc.
    General Discussion hereditary spastic paraplegia (HSP) is a group of inherited neurologicaldisorders characterized by progressive weakness (paraplegia) and
    http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Paraplegia, H

    56. University Of Miami School Of Medicine - Glossary - Autosomal Dominant Hereditar
    Autosomal dominant hereditary spastic paraplegia. Autosomal dominant hereditaryspastic paraplegia can result from changes in a number of different genes.
    http://www.med.miami.edu/patients/glossary/art.asp?articlekey=10971

    57. Yes Medical Information On Ailments, Personal And Family Health Matters - Yes Me
    ailments, personal and family health matters. Top Health Conditionsand Diseases Genetic Disorders hereditary spastic paraplegia (6),
    http://www.yes-medical.com/dir/pg/Health/Conditions_and_Diseases/Genetic_Disorde
    Yes Medical Yes Medical Information on ailments, personal and family health matters Yes Medical Information on ailments, personal and family health matters Yes Medical Home
    Yes Medical Information on ailments, personal and family health matters
    Top Health Conditions and Diseases Genetic Disorders : Hereditary Spastic Paraplegia
    • The FSP Support Group - For people suffering from Familial Spastic Paraplegia. Includes a newsletter, discussion forum, links, and contact details.
    • GeneClinics: An Overview - In depth details about hereditary spastic paraplegia. Includes a summary, definition, categories, diagnosis, genetic counseling and resources.
    • Hereditary Spastic Paraplegia - HSP information sheet compiled by the National Institute of Neurological Disorders and Stroke.
    • Hereditary Spastic Paraplegia - In depth look at this disease by John K. Fink, M.D., including genetic analysis, clinical features and FAQs.
    • MCW Healthlink: HSP - An article about hereditary spastic paraplegia, also called familial spastic paralysis.
    • Spastic Paraplegia Foundation - Supports on the upper motor neuron disorders hereditary spastic paraplegia and primary lateral sclerosis. Information about these conditions, disability resources, newsletters, news, announcements, research and support.

    58. SPG20 Is Mutated In Troyer Syndrome, An Hereditary Spastic
    ng937 volume 31 no. 4 pp 347 348 SPG20 is mutated in Troyer syndrome,an hereditary spastic paraplegia Heema Patel, Harold Cross
    http://www.nature.com/cgi-taf/DynaPage.taf?file=/ng/journal/v31/n4/full/ng937.ht

    59. SPG20 Is Mutated In Troyer Syndrome, An Hereditary Spastic
    Published online 22 July 2002, doi10.1038/ng937 volume 31 no. 4 pp 347 348SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia
    http://www.nature.com/cgi-taf/DynaPage.taf?file=/ng/journal/v31/n4/abs/ng937.htm

    60. PharmGKB: Spastic Paraplegia, Hereditary
    Alternate Names Autosomal Dominant hereditary spastic paraplegia; Autosomal DominantSpastic Paraplegia Hereditary; Autosomal Recessive Hereditary Spastic
    http://www.pharmgkb.org/do/serve?objId=PA446141&objCls=Disease

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