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 27th February 2011 - New research
 THE WORST NON-MOTOR SYMPTOMS IN PARKINSON'S DISEASE
Movement Disorders [2010] 
25 (15) : 2493-2500 (Gallagher DA, Lees AJ, Schrag A.)� 
Complete abstract
Although muscular movement is the most characteristic symptom of 
Parkinson's Disease, non-motor symptoms (those that do not concern muscular 
movement) are increasingly recognised as neglected aspects of Parkinson's 
Disease. The most common non-motor symptom has been found to be urinary. In 
order of frequency the most common symptoms are : autonomic dysfunction, 
particularly urinary and gastrointestinal
symptoms 
(84%), mood (74%), fatigue (74%),� daytime somnolence (65%), pain (56%), 
nocturnal sleep problems (55%), and psychosis (55%). Motor fluctuations 
(57%) and dyskinesia (43%) were associated with worse quality of life. 
Depression had the strongest association with a lower health related quality of 
life, then fatigue, thermoregulatory, gastrointestinal, cardiovascular autonomic 
function, daytime somnolence, and urinary problems. Whilst psychiatric problems 
are increasingly documented, many symptoms, particularly those  perceived as embarrassing or unrelated, remain under reported. In order to refer to this article on its 
own 
click here. 
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� 23rd 
February 2011 - New book
 MEDIFOCUS GUIDEBOOK ON : PARKINSON'S DISEASE
 Medifocus.com (Author), Elliot Jacob (Editor) 
Publisher's 
description : You will get answers to your questions, including risk factors of 
Parkinson's Disease, standard and alternative treatment options, leading 
doctors, hospitals and medical centers that specialize in Parkinson's Disease, 
results of the latest clinical trials, support groups and additional resources, 
and promising new treatments on the horizon. This one of a kind Guidebook offers 
answers to your critical health questions including the latest treatments, 
clinical trials, and professional level information you can trust and understand 
culled from the latest peer-reviewed journals; and a unique resource to find 
leading experts, institutions, and support organizations including contact 
information and hyperlinks.
Click here for more details. 
For 
more books concerning Parkinson's Disease go to 
Parkinson's Disease Books. 
�
 21st February 2011 - New research
 ROTIGOTINE 
(NEUPRO) CLINICAL TRIAL RESULTS
Movement Disorders [2011] 
26 (1) : 90-99 (Trenkwalder C, Kies B, Rudzinska M, Fine J, Nikl J, Honczarenko 
K, Dioszeghy P, Hill D, Anderson T, Myllyla V, Kassubek J, Steiger M, Zucconi M, 
Tolosa E, Poewe W, Surmann E, Whitesides J, Boroojerdi B, Chaudhuri KR) 
Complete abstract
People
with Parkinson's 
Disease who had unsatisfactory early-morning motor symptom control were given 
either rotigotine (2mg-16mg rotigotine every 24 hours) or a placebo. 
Neupro� (Rotigotine Transdermal System) is a 
dopamine agonist that is applied to the skin in order to continuously deliver 
rotigotine over a 24-hour period. 
For more information go to
Neupro. 
Movement� symptoms improved in comparison 
to the use of a placebo, but not greatly as was claimed. 
Sleep improved in comparison to a 
placebo. The most 
frequently reported adverse events were nausea (rotigotine 21% v 9% placebo), 
application site reactions (rotigotine 15% v 4% placebo), and dizziness 
(rotigotine 10% v 6% placebo).� 
In April 2008, Neupro was withdrawn from use in the 
U.S.A. because specific batches of Neupro had deviated from their specification. 
In June 2009, UCB proposed new refrigerated storage conditions to alleviate 
crystallization on the patches. UCB has already made progress in reformulation 
and remains committed to bringing Neupro to U.S. patients. For more 
information go to the
News release. In order to refer to this article on its 
own 
click here. 
 �
 18th February 2011 - New research
 THE RISK OF COMPULSIONS IN PARKINSON'S DISEASE
Parkinsonism Related 
Disorders [2011] Feb 8 [Epub ahead of print] (Hassan A, Bower JH, Kumar N, 
Matsumoto JY, Fealey RD, Josephs KA, Ahlskog JE)� 
Complete abstract
Dopamine agonist treatment of Parkinson's Disease carries a greatly increased 
risk of compulsive behaviour. Compulsive behaviour provoked by dopamine agonists 
often goes undetected in clinical series, especially if they are not 
specifically enquired about. Of those people with Parkinson's Disease taking 
dopamine agonists 22% experienced compulsive behaviour, and 16% were pathologic. 
However, when the analysis was restricted to patients taking dopamine agonist 
doses that were at least minimally therapeutic, pathological behaviours were 
documented in 24% of people. The most common form of compulsions caused by 
dopamine agonists are : gambling (36%), hypersexuality (35%), compulsive 
spending or shopping (26%), binge eating (17%), compulsive hobbying (12%) and 
compulsive computer use (9%). The vast majority of affected cases (94%) were 
concurrently taking Sinemet or the equivalent. Among those with adequate follow 
up, compulsive behaviours completely or partly resolved when the dopamine 
agonist dose was reduced or ceased. In order to refer to this article on its own
click here. 
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	15th February 2011 - New research
 PRELADENANT 
CLINICAL TRIAL RESULTS
The Lancet Neurology, 
Early Online Publication, 10 February 2011 (Robert A Hauser, Marc Cantillon, 
Emmanuelle Pourcher, Federico Micheli, Vincent Mok, Marco Onofrj, Susan Huyck, 
Kenneth Wolski)� 
Complete abstract
Preladenant is an adenosine 2A (A2A) receptor antagonist. Researchers aimed to 
assess the efficacy and safety of Preladenant in patients with Parkinson's 
disease and motor fluctuations who were receiving L-dopa and other Parkinson's 
Disease drugs. Patients were assigned to receive 1mg, 2mg, 5mg, or 10 mg oral Preladenant twice daily, 
or matching placebo for 12 weeks. There was no significant change as a result of 
taking 1mg or 2mg of Preladenant.
Average 
daily off time was reduced by 60 minutes using 5mg Preladenant. Average daily 
off time was reduced by 72 
minutes using 10mg Preladenant. The most common adverse events for were 
worsening of Parkinson's Disease, somnolence, 
dyskinesia, nausea, constipation, and insomnia. However, the frequency of these 
adverse events was little different from those people taking the placebo. So it 
is doubtful whether they are of significance. The authors consequently believe 
that 5mg Preladenant and 10 mg Preladenant twice daily might be clinically 
useful to reduce off time in patients with Parkinson's disease and motor 
fluctuations. For more information go to the
News release. In order to refer to this 
article on its own
click here. 
 �
 12th February 2011 - New product
 DISTINGUISHING PARKINSON'S DISEASE USING THE 
EYES
EyeBrain has announced that its eye-tracking 
system, Mobile Eye Brain Tracker (EBT), is available for the detection of 
Parkinson-plus diseases. Parkinson-plus syndromes have additional features that 
distinguish them from Parkinson's Disease. 
Different areas of the brain are 
involved in producing eye movements, and abnormalities that occur can be linked 
to dysfunction in certain areas of the 
brain. Results have shown that eye movements provide a more accurate early 
diagnosis than traditional clinical examinations.� The Mobile EBT is 
non-invasive and costs less than regularly used imaging techniques, such as MRI or x-rays.� 
For more information go to 
Eye Brain Tracker.
The 
equipment 
consists of : a recording device for high-frequency, accurate eye movement 
measurement, two  screens, an introductory computer application for 
behavioural testing, and an automatic test analysis application. When an eye 
movement exam is conducted, the tests are displayed on a screen. The subject 
receives instructions on how to take the tests. The subject's eye movements are 
recorded while he takes the test. Once the tests are completed, the examiner may 
conduct a thoroughly automatic analysis, with the option of manually adjusting 
the results to enhance quality. Based on this analysis, an eye movement report 
is automatically printed to aid the examiner in diagnosing patients' possible 
illnesses. 
In order to refer to this 
article on its own
click here. 
��������������������� 
 ������������������������������������������������������������������������������������������������������������������������������������������������������ 9th February 2011 - New research
 INTRANASAL STEM CELLS FOR� PARKINSON'S 
DISEASE 
Rejuvenation Research 
[2011] February [ahead of print] 
(Lusine 
Danielyan, Richard Sch�fer, Andreas von Ameln-Mayerhofer, Felix Bernhard, 
Stephan Verleysdonk, Marine Buadze, Ali Lourhmati, Tim Klopfer, Felix Schaumann, 
Barbara Schmid, Christoph Koehle, Barbara Proksch, Robert Weissert, Holger M. 
Reichardt, Jens van den Brandt, Gayane H. Buniatian, Matthias Schwab, Christoph 
H. Gleiter, William H. Frey) 
Complete study
Stem cells have been delivered intranasally (via 
the nose), as a means of trying to treat Parkinson's Disease. Intranasal 
administration of stem cells to the brain is a proposed alternative to the 
current surgical procedures, which place stem cells directly in to the brain. 
Instead of one surgical operation, the ease of intranasal administration opens 
up the possibility of chronic stem cell treatment, which would increase the 
number of cells 
delivered 
to the brain. Many of 
the stem cells delivered intranasally survived for at least six 
months in the brain. The stem cells rapidly migrated to the damaged areas. It is 
claimed that the method substantially improved motor function in Parkinson's 
Disease. However, the study was only carried out on rats that did not actually 
have Parkinson's Disease. For years it had been claimed that stem cell therapy 
would be able to rid Parkinson's Disease. However, despite stem cell operations 
now having been carried out around the world, nobody has ever been rid of Parkinson's 
Disease using stem cell therapy. 
In order to refer to this 
article on its own
click here. 
 
�
 
7th 
February 2011 - New book
 HOW DOES THE DRILL KNOW WHEN TO STOP : LIVING 
GRACEFULLY THROUGH PARKINSON'S DISEASE 
 Perry Conrad
Publisher's 
description : At forty-one-years-old, Perry Conrad experienced a tremor in his 
left foot. Conrad consulted a neurologist who confirmed his suspicion: he had 
Parkinson's disease. In How Does the Drill Know When to Stop?, Conrad shares the 
insight that allowed him to accept and eventually overcome the limitations of 
Parkinson's disease and discusses the surgery he underwent seven years later 
that nearly eliminated his symptoms. If the cross you bear has brought you to 
your knees, or if you've ever considered your response to the unknown adversity 
that awaits us all, ask yourself, How Does the Drill Know When to Stop? and 
discover how past experience can help guide you through the hardship 
you may face tomorrow.�
Click here for more details. 
For 
more books concerning Parkinson's Disease go to 
Parkinson's Disease Books. 
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