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         Parkinsons Disease:     more books (100)
  1. Yoga for Movement Disorders: Rebuilding Strength, Balance and Flexibility for Parkinson's Disease and Dystonia by Renée Le Verrier BS, 2008-10-30
  2. Living with Parkinson's Disease by M.D. Kathleen E. Biziere Ph.D., M.D. Matthais C. Kurth Ph.D., 1996-06-10
  3. With Shaking Hands: Aging with Parkinson's Disease in America's Heartland (Studies in Medical Anthropology) by Samantha Solimeo, 2009-05-15
  4. Parkinson's Disease (Fast Facts) by Christopher G. Clough, K. Ray Chaudhuri, et all 2007-06-30
  5. Neurodegeneration and Neuroprotection in Parkinson's Disease (Neuroscience Perspectives)
  6. Patient Education for People with Parkinson's Disease and their Carers: A Manual by Marcia Smith Pasqualini, Gwenda Simons, 2006-11-10
  7. Pathologic gambling complicating treatment of Parkinsons disease with dopamine agonists by S. Andrew Josephson, 2010-05-20
  8. Comprehensive Nursing Care for Parkinson's Disease
  9. Making the Connection Between Brain and Behavior: Coping with Parkinson's Disease by Joseph H. Friedman, 2010-10-12
  10. Handbook of Parkinson's Disease (Neurological Disease and Therapy)
  11. Health Professionals' Guide to Physical Management of Parkinson's Disease (Health Professionals Guide) by Miriam Boelen, 2009-06-24
  12. Parkinson's Disease: Questions and Answers, Fourth Edition by Robert Hauser, Kelly Lyons, et all 2003-07
  13. Treatment Decisions in Parkinson's Disease (Oxford American Pocket Notes) by Rajesh Pahwa, Kelly Lyons, 2009-12-16
  14. Deep Brain Diary: My Life as a Guy with Parkinson's Disease and Brain Surgery Volunteer by Bill Schmalfeldt, 2010-03-10

81. Parkinson's Disease - Diagnosis And Treatment Options At Mayo Clinic
Parkinson's disease and other movement disorders treatment from neurology specialists at Mayo Clinic.
http://www.mayoclinic.org/parkinsons-disease/
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Parkinson's Disease
Overview
According to the National Institute of Neurological Disorders and Stroke, at least 1 million people are believed to suffer from Parkinson's disease, and about 50,000 new cases are reported each year in the United States. These figures are expected to increase as the population ages. Nearly 4,000 patients with Parkinson's disease are treated each year by neurology and neurosurgery specialists in Mayo Clinic's movement disorders programs. Patients receive state-of-the-art treatment and have opportunities to participate in valuable research studies and clinical trials. Read more about movement disorders
Diagnosis
No specific test can diagnose Parkinson's disease. Diagnosis is usually made based on the patient's history and a comprehensive neurologic examination. Similar symptoms can be caused by certain medications and by other degenerative brain conditions.

82. Functional And Stereotactic Neurosurgery Center - GateWay To Neurosurgery @ Mass
Provides general information and links to organisations providing PD support.
http://neurosurgery.mgh.harvard.edu/Functional/default.htm
Functional Neurosurgery Neurosurgery Home - About Us - Diseases Treated - Clinical Centers - Referrals - People - Grand Rounds - Education - News, etc. - Publications - History - Support Groups - Links - Appointments - Contact Us - Search NS Web Neurosurgery Web Sites - Neurosurgery Home - Research Home - Residency Home - Alumni Home Mass General Hospital Web
Functional and Stereotactic Neurosurgery Center
Font Size: The Functional and Stereotactic Neurosurgery Center provides comprehensive evaluation and care for patients with movement disorders, epilepsy, obsessive-compulsive disorder, and certain chronic pain syndromes. The center works closely with the Partners Parkinson and Movement Disorders Treatment Center , and the MGH Epilepsy Unit Referrals Stereotactic Surgery Parkinson's Disease ... Links Currently available treatments for movement disorders include microelectrode-guided deep brain stimulation of the subthalamic nucleus, the globus pallidus or the thalamus as appropriate. The

83. Parkinsons Disease - Parkinsons Neurodegenerative Disease - Symptoms Of Parkinso
Causes, symptoms and treatments for the neurodegenerative shaking palsy known as Parkinson's disease are described. Specific genes involved in the progression of the disorder
http://biotech.about.com/od/diseases/a/Parkinsons.htm
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  • Home Biotech / Biomedical
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    By Theresa Phillips , About.com Guide
    See More About:
    zSB(3,3) is a neurodegenerative disease that appears when certain nerve cells of the brain, in a region called the substantia nigra , die or become impaired. These nerve cells are responsible for producing dopamine , which enables smooth, coordinated muscular motions throughout the body. The disease was originally called "the shaking palsy" and identified in 1817 by British Dr. James Parkinson, after whom it is now named. There are no known cures for Parkinson's, but some treatments can slow progression of the disease and help alleviate the symptoms. The treatments usually involve replacement of the missing dopamine, and drugs for this disease often contain L-dopa, the intermediate precursor in the production of dopamine from the amino acid tryptophan. Other drugs might be used to inhibit neurotransmittors or suppress MAO-B, the enzyme that degrades dopamine. Certain surgical procedures can be used to alleviate symptoms in extreme cases. Although these medications can greatly improve quality of life, many individuals are able to live and manage their disease without medication.

    84. The Parkinson S Support Center Of Kentuckiana
    Information regarding Parkinson s disease support group meetings in the Northern Kentucky/Southern Indiana areas.
    http://www.pscky.org/

    85. Deep Brain Stimulation. DBS-STN.org For DBS/STN Surgery Information Relating To
    Support and information about DBS/STN surgery for parkinson s disease for patients, relatives, caregivers and medical staff.
    http://www.dbs-stn.org
    Home About Us Contact Forum ... Links Tuesday November 16, 2010
    Welcome
    Donate now Download and Read Our Latest Survey Results . (Dec. 09)
    References from the peer-reviewed manuscripts from our Balance Report.

    Speech in Individuals with Parkinson's Disease with and without Deep Brain Stimulation
    . (Jan. 09) Info discussed in Medical Community Neuropsychiatric Symptoms in Parkinson's Disease. read more Long term biochemical changes in the Parkinsonian brain with and without deep brain stimulation using Magnetic Resonance Spectroscopy (MRS) ... read more
    Article Archive
    Current Science Review Early versus Delayed DBS Surgery: Clinical Trials needed!
    The purpose of this article was to look at the utility of a statistical model to predict the effectiveness of DBS-STN on motor functioning, cognitive abilities, and quality of life when the surgical intervention is done early or later in the disease course. Conferences and Special Events Neural Interfaces Conference: Long Beach, California June 21, 2010
    The Parkinson Alliance has been attending the Neural Interfaces Conference since 2005, and this is the first time the meeting has been held on the West coast. This particular conference kicked off the first official day with a Deep Brain Stimulation (DBS) consortium. Alliance Team visits Huntington Memorial Hospital DBS Team
    DBS in the continuum of care for PD and other movement disorders

    The Parkinson Alliance staff attended the Deep Brain Stimulation (DBS) Forum in Dallas to help educate a large group of general neurologists about DBS therapy.

    86. The Health Blog Network
    Web community designed to help PD patients and their caregivers by creating a centralized destination for helpful, personal disease information.
    http://parkinsonsblognetwork.com
    Contribute to our Parkinson's Disease blog community by completing our quick registration You'll need to register to add your Parkinson's blog or participate in our message board. If you've already registered, you can log in below. Forgot your password? Add your blog today.
    Contribute to our Parkinson's Disease community by becoming a PDBN Affiliate and adding your blog. When we work together, the whole community gets stronger.
    Remember, you need to become an affiliate to add your blog and/or participate in our message board. Parkinson Disease - My experience as a Parkinson Disease sufferer.
    Small Website About Parkinsons Disease

    Shake, Rattle and Roll: An insider's view of PD

    From the Advisors' Desk
    ...
    MOZART MOVEMENT

    Welcome to ParkinsonsDiseaseBlogNetwork.com. This Web community is designed to help Parkinson's Disease patients and their caregivers by creating a centralized destination for helpful, personal Parkinson's Disease information. The ultimate intention is for the site to serve as a real-time, virtual meeting place to exchange empowering thoughts about fighting Parkinson’s Disease. We hope you find this content valuable, and we further hope you will become an active contributor by adding a blog and/or rating on our existing blog. Chronical of living with Parkinson's: "I have now been diagnosed with Parkinson's Disease and Peripheral Neuropathy, so this will be a life long journey - coping with the medicines, nutrition, digestion problems, exercise, and no telling what else!" Blog start 8/20/2006.

    87. PDUK - For PwP
    Join the forum or chat room and share your worries and concerns about this disease, or give support to other people with PD.
    http://pduk.org

    88. Parkinsons Journey
    Offering hope and encouragement to those with Parkinson s and to those who know someone with Parkinson s.
    http://www.parkinsonsjourney.com/
    • Home About
    • November 11th, 2010 Posted in Misc No Comments These are just a handful those who I know or know of:
      Scott Signani, brother,  cousin, friend, USAF, 20 years of service;
      David Gillis, friend;
      David Kitchener, uncle, US Navy, WWII; John Francis Feldenzer, grandpa, US Navy, WWI; Rod Gard, cousin; Bob Kesson, friend; Mark Sales, friend; Dennis Feeney, friend, USMC, 3 tours in Iraq; Tom Criswell, friend, Viet Nam war; Pat Tatum, friend; Rob Kinerson, friend, fighter pilot, USAF all. Read More
      November 8th, 2010 Posted in Parkinson's Disease News No Comments
      I remember meeting my son for lunch one day and as I got out of the car, my foot was dragging somewhat.  I couldn’t raise it high enough, fast enough.  Yep, that’s right.  I fell.  Right then.  Right there.  And, mind you—I fell slowly . At least it felt that way. That fall seemed like it lasted   f-o-r-e-v-e-r .  I was sure everyone in that sandwich shop saw the woman in the jeans and red coat fall right on her toosh and then struggle to get back up.  However, either no one witnessed the dreadful sight or they were extremely good actors and kindly (or not so kindly?) turned away.  I made a mental note to myself that day that when the time deems itself necessary, get a cane. Until then, if you’re afraid of falling because your legs aren’t working properly, dropping things because your arms and hands aren’t working properly, etc., then why not build up what muscle/mobility you now have and make exercise one of the most important things you do?  I’ve already mentioned the benefits of bike riding for one man, but how about you?  What about walking?  That is what I enjoy.  (Yes, with my tennis shoes.)  Do it with someone else, which is actually safer and often more fun, but – like ‘they’ say – check with your doctor first.

    89. Welcome To CARE - For CareGivers Of People With Parkinson's
    CARE (Caregivers Are Really Essential) is a ListServ where CareGivers can let off steam in a place where they will not upset the people with parkinson s for whom they care.
    http://www.pdcaregiver.org/
    Welcome to CARE - for CareGivers of People with Parkinson's This information on this site was partially drawn from a ListServ on the Internet. The ListServ is CARE or Caregivers Are Really Essential. It is a sublist of the Parkinson's Information Exchange Network ListServ. The lion's share of the information was drawn from my personal searches on the Internet. It is especially for CareGivers (CGs) of People with Parkinson's (PWPs). The need for such a list was evident from feelings expressed on the PD (Parkinson's Disease) list that there are times when CGs need to be able to "let off steam" in a place where they will not upset their PWPs. Some of us have CareGiver support groups, where we can safely express feelings, get practical support, and share experiences but some do not.   Contents Taken From the CARE List
    Adult Day Care

    Anxiety at Bedtime

    A Story

    Assisted Living/Nursing Home Issues
    ...
    Loss of self

     Messages and Web Searches
    Loving and Sexuality

    Medicaid Eligibility

    Medications and Drugs Issues

    Movement Disorders Specialist
    ... 31 July, 2006 The contents of these pages are drawn from the messages that are posted to the CARE List as well as from search efforts by the webmaster. These are people who are CareGivers, either directly or indirectly, of people who are living with parkinson's. What is Parkinson's Disease - Condensed Version What is Parkinson's Disease - Long Version For an Alphabetical list of the Contents on both the main entry page and the Web Resources page, click

    90. Reading And West Berkshire PEPS Home Page
    Support group for people affected by Early-Onset Parkinson s living in the Reading and West Berkshire area.
    http://www.pdpeps.org/
    READING AND WEST BERKSHIRE PEPS
    AN EARLY-ONSET PARKINSON'S SUPPORT GROUP
    Reading and West Berkshire PEPS is affiliated to Parkinson's UK Next Meeting
    October 28th

    Kennett Valley Free Church PEPS Blog
    Blog Help
    Latest news and advice....
    (updated October 2nd 2010) We promote a positive perspective for early onset Parkies by:
    Supporting and befriending
    Informing and raising awareness
    Enjoying social activities and having fun
    We meet informally every month in the local area..... We would be delighted to have you contact us:
    email: briony_e_cooke@hotmail.com Please sign our Guestbook Home Diary of Events Latest News About Us Members Area ... Guestbook Last Updated:
    Reading and West Berkshire PEPS 2008 - 2010

    91. Home
    Helping those with Parkinson s and their carers and families living in East Berkshire.
    http://www.bracknellparkinsons.org/
    Bracknell Branch of Parkinson's UK
    We're here to help! Home About us Diary Evening Meetings ... Site Map Home Page for the Bracknell Branch of Parkinson's UK The aim of our Branch is to help people with Parkinson's and their carers living in and around Bracknell. A copy of our Branch Leaflet is available to download by clicking  here What's New? Next Evening Meeting is on 8th November Come find out about the Research work  that Parkinson's UK fund see Diary page for details We had a great day out on our Canal Trip  on the 9th August. The Cream Teas were fantastic (thanks Yvonne!).  Some of the services provided for Branch members are: M onthly evening meetings at which members can meet together in a friendly atmosphere to exchange views and hear a talk from a speaker on a Parkinson's issue or a general topic of interest. The services of an Information Support Worker who acts as a 'friendly contact' for members as well as advising on how to claim for benefits and obtain assistance from social services.  Access to Parkinson's Nurse Specialists ,  who are able to provide advice on medication and related matters. New members are encouraged to arrange a meeting at an early stage.

    92. WE MOVE - Worldwide Education And Awareness For Movement Disorders
    Resource for movement disorder information, including Parkinson s Disease, and disorder activities on the internet.
    http://www.wemove.org/

    93. CNS Online
    CNS is a non profit foundation in La Jolla, California, dedicated to research and treatment of neurological diseases. Parkinson s disease information is in the archives.
    http://www.cnsonline.org/
    CNS Home
    News/Events CNS News
    Monthly Lecture

    Patient Counseling

    Research News
    ...
    eNewsletter Signup

    Clinical Trials Trial Registration Signup
    Current Treatment Trials

    Patients Information
    ALS

    Alzheimer's Disease

    Multiple Sclerosis
    Parkinson's ... General Interest About CNS Mission Contact Us Our Doctors Director's Message ... CNS Publications Helping CNS How to contribute Our Donors Links Links to further resources En Espanol CNS En Espanol
    Last Updated: Sat Oct 30, 2010 CNS Update FDA approves Nuedexta which was discovered at CNS and developed by Avanir pharmaceutical corporation Dr Smith to speak at Stanford on Nov 5. At the California ALS Summit, held in San Francisco June 27-28, Dr Smith gave a talk entitled "The ALS phenotype: lost in translation" and chaired a session dealing with molecular therapy for ALS In March Dr Smith gave a series of lectures at UFM(check ufm.com) in Guatemala city and on April 14th will speak at the annual meeting of the American Academy of Neurology Family and friends of Tom Shey established a fund to support ALS research. Thus far over $6000 has been contributed. Isis pharmaceutical corporation organized a meeting in Boston in December '09 to launch a Familial ALS trial that utilizes a drug developed with UCSD and CNS. See publications.

    94. Re-Wired For Life DBS/STN | Non-profit Organization Created To Promote The Under
    An independent volunteer not-for-profit organization. Provides on-line support and information for those who have had or who are considering Deep Brain Stimulation (DBS) surgery to alleviate the symptoms of Parkinson s disease and certain other movement disorders.
    http://www.rewiredforlife.org/
    About Us Patient Forum Surgery Information Patient Stories ... Links Tuesday, November 16, 2010
    The Newsroom
    Bruce Dunwiddies Story MEDICARE COVERS COST OF DBS DIATHERMY SAFETY ALERT YOU NEED TO KNOW THIS : DBS IN THE HEALTH CARE ENVIRONMENT - Article ...
    News Archive

    from left to right: Drs. Beric ,
    Sterio, and Kelly
    Dr. Djordje Sterio
    Dr. Aleksandar Beric

    Re-Wired for Life Foundation is a non-profit organization created to promote the understanding of deep brain stimulation (DBS) among patients, their families, and medical professionals through dissemination of information, patient support meetings, medical professional meetings, and research development. This site offers assistance to patients in dealing with their day to day condition before, during, and after surgery and offers related educational and informational services as they become available.
    We are eager to share with you "The First Report" — the first summary of responses to the questions posed in the DBS/STN Patient Survey, dated July 2003. While the information presented has no constraint or standard statistically validated double-blind random protocols, we know that presenting the patients' unadulterated view is a novel and valuable approach that will benefit patients and individuals looking for more information on DBS/STN. Additionally, we believe this information will prove valuable to the scientific and medical community. Please visit our

    95. The Michael J. Fox Foundation For Parkinson's Research
    The Michael J. Fox Foundation (MJFF) for Parkinson s Research is dedicated to ensuring the development of a cure for Parkinson s disease within this decade through an aggressively funded research agenda.
    http://www.michaeljfox.org/

    96. Michigan Parkinson Foundation
    A voluntary non-profit corporation providing people with Parkinson s disease in Michigan information on support groups state-wide, current events, research news, and clinical trials. Quarterly newsletter is available on-line.
    http://www.parkinsonsmi.org

    Our web site has been developed to provide you with information about MPF and its services, to share our newsletter, The Messenger, and to help you locate and take advantage of our support groups and upcoming events. We invite you to contact us and comment, either by email, phone or mail. View the free webcast "Mind, Mood and Body: Understanding Nonmotor Symptoms of PD" that was held on July 18, 2008. The link takes you to a page to register before viewing the archived event. Interview with Alisa Z, WWJ 950 AM – Parkinson’s Disease and the Night of 1000 Stars Michigan Parkinson Foundation is proud to be an organizational partner of the World Parkinson Congress. Michigan Parkinson Foundation
    30400 Telegraph Road, Suite 150 Bingham Farms, MI 48025

    97. Northwest Parkinson's Foundation (NWPF) Improving The Quality Of Life
    A non-profit organization located in the Pacific Northwest which promotes awareness, education, care and a cure for Parkinson s Disease.
    http://www.nwpf.org

    98. PALS Front Page
    PALS Support Group has formally existed since November, 1998 and is a branch of the Parkinson s Association of Ireland. It is the brainchild of its Chairman, David Magennis, who has had PD since he was 28.
    http://gofree.indigo.ie/~pdpals

    99. Parkinson Association Of The Carolinas
    Provides support group meetings, information to the community, membership, prescription assistance to members, a swim therapy program and home health care information. Mecklenburg County, North Carolina.
    http://www.parkinsonassociation.org/
    var MenuLinkedBy="AllWebMenus [4]",awmMenuName="parkmenu",awmBN="734";awmAltUrl=""; Home Page Contact Us Type Size: A A A News Podcasts Information
    NEW DVD
    “Exercise and Parkinson’s: Questions and Answers from the Experts”

    What Causes Parkinson's Disease? "

    Michael J Fox Podcast
    Click here to listen To listen to this or any of our other podcasts, visit our Media Center
    YOU can participate in
    Clinical Trials PDTRIALS IS LED BY:

    100. Parkinson's Action Network
    PANs primary mission since its founding in 1991 has been to provide an informed, organized, and effective voice in public policy issues affecting the search for a cure for Parkinson s disease.
    http://www.parkinsonsaction.org
    Get Involved
    Size
    Current Size:
    • About PAN
      • Board of Directors Staff Grassroots Network ... more
        A Closer Look
        The mid-term elections are certainly going to create something of a sea change in the nation's capital. So, I thought it would be useful to give you a brief analysis of what the election results will mean for the Parkinson's community. Of course, how this will all settle out needs to evolve over the coming weeks – some congressional races are not even decided yet – so please take this as a quick first look at what the changes mean.
        The Department of Veterans Affairs (VA) announced on Monday, November 1, that it has begun paying disability benefits to Vietnam veterans who meet newly-enacted standards for Agent Orange exposure. The new rules, which the Parkinson's Action Network (PAN) supported, ensure that Vietnam veterans exposed to Agent Orange who later developed Parkinson’s disease, B-cell (or hairy-cell) leukemia, and ischemic heart disease, will have easier access to disability benefits.
        see all
        Latest From PAN
        Congress returns for lame-duck session on Monday, November 15

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