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         Moyamoya Disease:     more detail
  1. Moyamoya Disease Update
  2. Moyamoya Disease
  3. The Official Parent's Sourcebook on Moyamoya Disease: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-11
  4. Moyamoya Disease by Jiro Suzuki, 1986-06
  5. Moyamoya disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Dawn, MS, CGC Cardeiro, 2005
  6. Moyamoya disease and aortic coarctation in a patient with common brachiocephalic trunk/Moyamoya hastaligi ve aort koarktasyonunun eslik bir brakiyosefalik ... of Cardiology (Anadolu Kardiyoloji Dergisi) by Kadir Babaoglu, Tevfik Demir, et all 2007-03-01
  7. Nursing issues in caring for children with moyamoya vasculopathy and their families.(Disease/Disorder overview): An article from: Journal of Neuroscience Nursing by Selina Y.C. Hune, Gabrielle A. deVeber, et all 2007-02-01
  8. The Official Parent's Sourcebook on Moyamoya Disease A Revised and Updated Directory for the Internet Age by Icon Health Publications, 1980
  9. Tracking recovery in a case of Moyamoya-induced dysarthria.(Report): An article from: Journal of Medical Speech - Language Pathology by Cheryl L. Giddens, Glenda J. Ochsner, 2009-09-01
  10. Moyamoya: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by David, MD Greenberg, 2005

21. NINDS Moyamoya Disease Information Page
moyamoya disease information page compiled by the National Institute of NeurologicalDisorders and Stroke (NINDS). NINDS moyamoya disease Information Page.
http://accessible.ninds.nih.gov/health_and_medical/disorders/moyamoya.htm
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    NINDS Moyamoya Disease Information Page
    Reviewed 12-14-2001 Get Web page suited for printing
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    Table of Contents (click to jump to sections)
    What is Moyamoya Disease?

    Is there any treatment?

    What is the prognosis?

    What research is being done?
    ...
    Related NINDS Publications and Information

    What is Moyamoya Disease?
    Moyamoya disease is a rare, progressive cerebrovascular disorder characterized by the narrowing or occlusion of major blood vessels leading into the brain, and the formation of abnormal blood vessels called

    22. Advanced Respiratory - Airway Clearance Indications Of Moyamoya Disease
    , Reimbursed by more than 1,100 health plans nationwide. AirwayClearance Indications of moyamoya disease, Print Version. Moyamoya
    http://www.thevest.com/conditions/factsheets/moyamoya.asp?gs=patients

    23. Moyamoya Disease
    moyamoya disease. moyamoya disease is a progressive disease that affectsthe blood vessels in the brain. It is characterized by the
    http://www.hmc.psu.edu/neurosurgery/aservices/moya.htm

    24. Moyamoya
    moyamoya disease is a rare, progressive cerebrovascular disorder in which the majorblood vessels leading into the brain become closed or blocked (occlusion
    http://www.hmc.psu.edu/childrens/healthinfo/m/moyamoya.htm

    25. Thieme Medical Publishers : Product Pages: Ikezaki, Moyamoya Disease
    Ikezaki / Loftus moyamoya disease. (Distributed by Thieme for the AmericanAssociation of Neurological Surgeons) 2001 225 pp, hardcover
    http://www.thieme.com/SID2088980784223/productsubpages/pubid1021397305.html
    Thieme Medical Publishers Medical Publications
    Ikezaki
    Loftus
    Moyamoya Disease
    (Distributed by Thieme for the American Association of Neurological Surgeons)
    225 pp, hardcover
    $105.00 / EUR 119.00
    ISBN 1879284804 / 3131349719
    Product Information Author Affiliation
    Reviews

    Related Links Neurosurgery
    Order now! Add to shopping cart
    Description

    Moyamoya, a Japanese word meaning "puffy, hazy, obscure, or vague" describes the smoky appearance of the vascular collateral network this disease has on angiography. Moyamoya was first categorized by Dr. Suzuki in 1969 to describe the abnormal vascular networks at the base of the brain for which this disease is recognized worldwide. Written by the world's leading experts, this is the first text to cover this cerebrovascular occlusive disorder. Initally believed to affect patients primarilly of Japanese descent, it is now clear that moyamoya disease is not restricted certain racial genotypes or localitites. Because the etiology of this disease remains unclear, the diagnosis depends on radiographic findings through angiography, MRI, and MRA. Topics covered include: -Definitions and guidelines -Etiology of moyamoya disease -Angiographic diagnosis and magnetic resonance imaging -Clinical manifestations -Management strategies including: medical therapy, selection of surgical procedures, post-operative evaluation

    26. Thieme Medical Publishers : Book Reviews: Ikezaki, Moyamoya Disease
    Ikezaki moyamoya disease Reviews. A comprehensive accumulation of theclinical and research data that has formed the latest understanding
    http://www.thieme.com/SID2088980784223/productsubpages/bookreviews/pubid10213973
    Thieme Medical Publishers Medical Publications
    Ikezaki
    Moyamoya Disease
    Reviews
    "A comprehensive accumulation of the clinical and research data that has formed the latest understanding of moyamoya disease...contains valuable information...all of the contributors are to be commended." Journal of Neurosurgery
    Back to Product Information Page
    [top of page] [back] Thieme Medical Publishers 2003
    General information: info@thieme.com
    Technical Comments/Problems: webteam@thieme.com
    Purchase information (Rest of World): custserv@thieme.de
    Purchase information (Americas): customerservice@thieme.com
    Phone: 1-212-760-0888 * Custserv.: 1-800-782-3488 * Fax: 1-212-947-1112

    27. Radiology In Ped Emerg Med, Vol 3, Case 9
    moyamoya disease Radiology Cases in Pediatric Emergency Medicine Volume 3, Case9 Karen R. Sevigny Brown, MD Loren G. Yamamoto, MD, MPH Kapiolani Medical
    http://www.hawaii.edu/medicine/pediatrics/pemxray/v3c09.html
    Moyamoya Disease
    Radiology Cases in Pediatric Emergency Medicine
    Volume 3, Case 9
    Karen R. Sevigny Brown, MD
    Loren G. Yamamoto, MD, MPH
    Kapiolani Medical Center For Women And Children
    University of Hawaii John A. Burns School of Medicine
    L = Lateral ventricles. The anterior horns and the posterior horns are shown in this diagram. 3 = Third ventricle. CC = Corpus callosum. C = Caudate nucleus. P = Putamen G = Globus Pallidus. The putamen and globus pallidus together form the lenticular (lentiform) nucleus. T = Thalamus Arrows = Internal Capsule [anterior limb, posterior limb, genu (bend)]. O = Optic radiations. A = Auditory radiations. The corticospinal tract originates from the motor strip of the cerebral cortex. The fibers collect as they traverse through the posterior limb of internal capsule. The tract largely crosses the midline in the decussation of the pyramids. Fibers exit the spinal cord at their respective levels. View our patient's CT scan. T1 (left image) and T2 (right image) weighted axial images are shown (different levels). On the T1 image, the ventricles appear to be dark and the infarct seen in the left lenticular nucleus is dark as well. The T2 image is a lower cut through the center of the infarct. The T2 image shows the CSF within the ventricles to be white. The infarct appears as a white lesion in the caudate nucleus and the left putamen. In the T2 image, internal capsule is dark. Note the obvious distortion of the anterior limb of the left internal capsule, compared to the right. The posterior limb of the left internal capsule is also slightly distorted (compared to the right) adjacent to the infarct in the putamen. This study is read as an infarct in the left basal ganglia, the posterior limb of internal capsule, and the head of the caudate. The structures of this T2 image are labeled if you have difficulty identifying the structures.

    28. Moyamoya Disease Articles, Support Groups, And Resources
    moyamoya disease articles, support groups, and resources for patientsfrom Med Help International (www.medhelp.org). moyamoya disease.
    http://www.medhelp.org/HealthTopics/Moyamoya_Disease.html
    [Health Topics A-Z]
    A
    B C D ... Z
    Moyamoya Disease
    [Med Help Home] [Library Search] [Medical Forums] [Patient Network] Revised: 3/30/2003

    29. Moyamoya
    moyamoya disease is an idiopathic, noninflammatory vasculopathy confined to theintracranial arteries and primarily involving the major branches of the
    http://www.medhelp.org/perl6/neuro/archive/2525.html
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    Med Help International

    A not-for-profit organization Questions in The Neurology Forum are being answered by doctors from
    The Cleveland Clinic , consistently ranked one of the best hospitals in America. Subject: Moyamoya
    Topic Area: Neurology - General
    Forum: The Neurology and Neurosurgery Forum
    Question Posted By: Micheal Guest on Saturday, September 06, 1997
    Posted by CCF MD on December 06, 1997 at 10:25:03:
    In Reply to: Moyamoya posted by Robert Dodson on December 02, 1997 at 01:37:06:
    My wife was diagnosed with moyamoya in 1983. She has severe migraine headaches and is currently taking Fiornal with codeine for them. Is there another medication available which would help to control the headaches? Also, what is a general prognosis for a female currently aged 48. Any help will be appreciated. thanks, Robert Dodson Moyamoya disease is an idiopathic, noninflammatory vasculopathy confined to the intracranial arteries and primarily involving the major branches of the internal carotid artery. The hallmark of the disease is a mesh of fine vessels

    30. ClinicalTrials.gov - Linking Patients To Medical Research Search
    Query Details. No studies were found for moyamoya disease ALLFIELDS.Modify Your Search. Individual Terms, Count. moyamoya disease , None.
    http://www.clinicaltrials.gov/search/term=Moyamoya Disease

    31. ClinicalTrials.gov - Linking Patients To Medical Research Search
    Query Details. No studies were found for NINDS moyamoya disease InformationPage ALLFIELDS. NINDS moyamoya disease Information Page , None. Page , 7.
    http://www.clinicaltrials.gov/search/term=NINDS Moyamoya Disease Information Pag

    32. Health Library - Moyamoya Disease
    moyamoya disease. None. General Discussion. moyamoya disease is a progressivedisease that affects the blood vessels in the brain (cerebrovascular).
    http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=

    33. Moyamoya Disease
    moyamoya disease. This article submitted by pgamse@interaccess.com on 9/13/95. Afriend of mine has a child with a condition which may be moyamoya disease.
    http://neuro-www.mgh.harvard.edu/neurowebforum/GeneralFeedbackArticles/Moyamoyad
    Moyamoya disease
    This article submitted by pgamse@interaccess.com on 9/13/95.
    Can you help: A friend of mine has a child with a condition which may be
    Moyamoya disease. However, she says that her doctors
    understood that this disease has never been diagnosed before
    in a Caucasian patient. Can anyone comment on this, and can you recommend any
    treatment (We live in the Chicago, USA area) Thank you
    Philippa Gamse Next Article
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    34. Moyamoya Disease
    moyamoya disease. This response submitted by Neurologist on 9/13/95. moyamoya diseaseoccurs worlwide but, for unknown reasons, is more frequent in Japan.
    http://neuro-www.mgh.harvard.edu/neurowebforum/GeneralFeedbackArticles/Moyamoyad
    Moyamoya disease
    This response submitted by Neurologist on 9/13/95.
    Moyamoya disease occurs worlwide but, for unknown reasons, is more frequent in Japan. In China, most cases seem to be associated with leptospirosis infection. In America, no cause is usually found although various associated medical conditions have been reported. Treatment is not available. Revascularization procedures have been attempted but long term results are unknown. Hope this is helpful. Canadian neurologist Next Article
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    Article complete. Click HERE to return to the Neurology Web-Forum Menu.

    35. Bombay Hospital Journal - Case Reports - Moyamoya Disease
    moyamoya disease. moyamoya disease is a rare cause of recurrent and chronicstrokes, which is seen mainly in the Oriental population.
    http://www.bhj.org/journal/1998/4001_jan/cr_193.htm

    36. CJNS-Hemorrhagic Moyamoya Disease During Pregnancy
    Close Window Hemorrhagic moyamoya disease during Pregnancy Abstract BackgroundIntracranial hemorrhage in pregnant patients with moyamoya disease is rare.
    http://www.canjneurolsci.org/27febtoc/hemorrhagic.html
    Abstract
    Close Window

    Hemorrhagic Moyamoya Disease during Pregnancy
    John C.L. Sun, Margaret Yakimov, Ismail Al-Badawi, Christopher R. Honey Abstract: Background: Intracranial hemorrhage in pregnant patients with Moyamoya disease is rare. We review the case of one such patient who presented with pre-eclampsia and a catastrophic intracerebral hemorrhage in order to highlight the associated management difficulties. Methods: A case of a pregnant (31 weeks) female brought to the emergency department with hypertension and a progressive decrease in her level of consciousness is presented. She rapidly developed a dilated right pupil and left extensor posturing. A CT scan of her head showed a large putamenal intracerebral hemorrhage. She was intubated, ventilated and given intravenous mannitol and magnesium sulfate. She underwent a simultaneous craniotomy and Cesarean section. Post-operatively the patient's ICP and jugular venous saturation were monitored in the intensive care unit. Results: The patient delivered a 1185g infant who did well. The patient's ICP was well controlled until the tenth post-operative day when she developed malignant brain edema and died.

    37. Moyamoya Disease
    moyamoya disease Radiology Cases in Pediatric Emergency Medicine Volume 3, Case9 Karen R. Sevigny Brown, MD Loren G. Yamamoto, MD, MPH UserName, Password.
    http://www.pediatriconcall.com/fordoctor/CaseReports/MoyaMoya.asp
    Question of day Alternative Medicine Journals Queries ... Shopping Mall MOYAMOYA DISEASE
    Radiology Cases in Pediatric Emergency Medicine Volume 3, Case 9
    Karen R. Sevigny Brown, MD Loren G. Yamamoto, MD, MPH
    UserName Password New Register
    This is a previously healthy, right-handed 7-year old Asian female who presents to the E.D three hours after developing right sided weakness of sudden onset. She had been feeling well until noon, when she developed weakness of her right hand and was unable to feed herself. She sat up and tried to walk to her room. Her father noted that her right leg was "crooked" and she kept falling to the right. Her arm was "hanging to the
    side" and was not swinging properly. Her father also noted that her smile was "crooked." She has remained alert through this illness. There is no history of fever, trauma, seizures, loss of consciousness, headaches, migraines or palpitations. Exam: VS T37, P110, R24, BP 105/58. Weight 19 kg (10th percentile), Height 114 cm (10th percentile). She is healthy appearing, cooperative, and alert in no distress. She speaks well without dysarthria or aphasia. Head normocephalic. Optic disc margins sharp. TM's normal. Oral mucosa clear. Neck supple, no bruits. Heart regular, grade 1/6 systolic ejection murmur, vibratory in quality, at the left sternal border. Lungs clear. Abdomen benign. Color and perfusion are good.

    38. MOYAMOYA DISEASE
    References Association of the Patients and Their Families of MoyamoyaDisease (ed) Clinical investigation on moyamoya disease.
    http://www003.upp.so-net.ne.jp/moya-moya/references.htm

    39. MOYAMOYA DISEASE
    About moyamoya disease In 1950's, Japanese leading neurosurgeons at thattime began to notice the new clinical entity of moyamoya disease.
    http://www003.upp.so-net.ne.jp/moya-moya/E-Dx1.htm

    About Moyamoya Disease
    In 1950's, Japanese leading neurosurgeons at that time began to notice the new clinical entity of moyamoya disease. Since its etiology was unknown, it was named in various ways, such as moyamoya disease, chiri-chiri disease, etc. Moyamoya disease is now officially named in Japan as "the spontaneous occlusion of the circle of Willis."
    The terminal portions of the intracranial internal carotid arteries progressively become stenotic (narrowing) or occlusive. Due to reduced blood flow to the brain, tiny collateral vessels at the base of the brain enlarge to become as collateral pathways. These vessels are called "moyamoya vessels" because the angiographic appearance of these vessels resemble the "cloud" or "puff" of the cigarette smoke, which is described as "moya-moya" in Japanese language ( Suzuki J, Takaku A
    About the name of moyamoya disease

    Moyamoya Vessels (Abnormally proliferating arteries?)

    In 1960's, moyamoya disease became the main interest for the neurosurgeons and neurologists because this disease was prevalent solely in Japan and/or Japanese ethnicity. In 1994, the number of the annual patients having moyamoya disease was estimated about 3,900.
    Normal cerebral angiogram and that of moyamoya patient

    Symptoms of moyamoya disease include brain ischaemia and hemorrhage. There are two peaks in age distribution: below 10 and at 30-40 years old, with the highest peak in the first decade and lower peak in the adults. Under the age of 10, brain ischemia (transient ischemic attack and cerebral infarction) is common whilst brain hemorrhage is more common at the age of 30-40 years old.

    40. Vascular
    This includes the presentation, diagnosis, management and prognosis ofthese very tiny but potentially lethal lesions. moyamoya disease.
    http://www.health.adelaide.edu.au/paed-neuro/vascular.html
    VASCULAR DISEASE S
    ANEURYSMS
    Anterior communicating artery aneurysm
    Aneurysms are rare paediatric lesions that can affect blood vessels throughout the body. They represent a "blistering" or
    "bubble-like" protrusion off of an artery. In the brain these "bubbles" tend to occur at very predictable locations. Usually they are at
    points where a major artery is branching into smaller arteries. These sights are not in the brain substance per se, but rather in the
    deep crevices between the various lobes of the brain. Most aneurysms that are found are in older individuals, in the 4th and 5th
    decades of life, but on rare occasions they can be found in paediatrics. Some causes of aneurysms are hereditary, but most are found
    in the general population without any specific cause.
    Most aneurysms are found due to a sudden burst of blood into or around the brain because of a temporary rupture of the "bubble".
    This "bubble " will usually then seal itself off spontaneously. Usually some if not all of the blood will be found in and around these
    crevices in the brain, what are called the subarachnoid spaces. Hence the bleeding that occurs with ruptured aneurysms tends to be

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