Home  - Health_Conditions - Moyamoya Disease

Books Baby Camera Phones Computers Games DVD Electronics Kitchen Magazines Music Garden Software Tools Toys Video Apparel & Accessories Jewelry & Watches Musical Instruments Health & Personal Care Beauty Sports & Outdoors Office Products

e99.com Bookstore

Images

Newsgroups

41-60 of 100    Back | 1  | 2  | 3  | 4  | 5  | Next 20

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Moyamoya Disease:     more detail

Moyamoya Disease Update Moyamoya Disease The Official Parent's Sourcebook on Moyamoya Disease: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-11 Moyamoya Disease by Jiro Suzuki, 1986-06 Moyamoya disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Dawn, MS, CGC Cardeiro, 2005 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 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 The Official Parent's Sourcebook on Moyamoya Disease A Revised and Updated Directory for the Internet Age by Icon Health Publications, 1980 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 Moyamoya: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by David, MD Greenberg, 2005

lists with details

41. Moyamoya Disease -- 23 (1): 171 -- American Journal Of Neuroradiology
    Definite moyamoya disease is the focus of the remainder of the book. Chapter 10discusses the United States experience with moyamoya disease,  
    http://www.ajnr.org/cgi/content/full/23/1/171
    
    Extractions: American Society of Neuroradiology Edited by Kiyonobu Ikezaki and Christopher M. Loftus. Rolling Meadows, IL: American Association of Neurological Surgeons; 2001. 213 pages. This multiauthored monograph provides a comprehensive review of moyamoya disease. It covers all aspects of this interesting disease, including its history, classification, epidemiology, etiology, clinical findings, diagnostic evaluation, and management. It emphasizes the various revascularization procedures that have been used to treat patients with moyamoya disease. I found this monograph very easy to read and well organized. The book can be roughly divided into two parts. The chapters

42. Angiographic Changes After Pial Synangiosis In Childhood Moyamoya Disease -- Rob
    MR Angiography of moyamoya disease Before and After EncephaloduroarteriosynangiosisAm. J. Roentgenol., January 1, 2000; 174(1) 195 200.  
    http://www.ajnr.org/cgi/content/abstract/18/5/837
    
    Extractions: This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager ... Cited by other online articles PubMed PubMed Citation Articles by Robertson, R. L. Articles by Scott, R. M. RL Robertson, PE Burrows, PD Barnes, CD Robson, TY Poussaint and RM Scott Department of Radiology, Children's Hospital Medical Center and Harvard Medical School, Boston, Mass. 02115, USA. PURPOSE: To describe the angiographic changes accompanying the surgical treatment of moyamoya disease by pial synangiosis and to compare these changes with patient outcome. METHODS: The preoperative and postoperative cerebral angiograms, MR images, and clinical records of 13 children treated with pial synangiosis for moyamoya disease were reviewed. RESULTS: After

43. Moyamoya Disease - Patient UK
    moyamoya disease Patient UK. A directory of UK health, disease, illness andrelated medical websites that provide patient information.  
    http://www.patient.co.uk/showdoc/40001992/
    
    Extractions: PatientPlus articles are written for doctors and so the language can be technical. However, some people find that they add depth to the articles found in the other sections of this website which are written for non-medical people. Recognised in Japan in the 1960's, this is a progressive occlusive cerebral arteritis affecting the distal internal carotid arteries near the Circle of Willis. Moyamoya is Japanese for "puff of smoke" and describes the appearance of the resultant network of abnormal small collateral vessels seen on angiography. Epidemiology Risk Factors More common Asians and in girls. There is a familial form which links to a gene on chromosome 17q25 - though the exact underlying cause remains unknown. Associations have also been made with leptospirosis, TB, certain anaemias, vascular disorders causing intimal thickening including hypertension and atherosclerosis, and a mixed bag of congenital syndromes (Down, Turner, Marfan, Apert) and diseases (Neurofibromatosis type I, Tuberose sclerosis, Hirschsprung) Presentation

44. UpToDate Moyamoya Disease
    INTRODUCTION — moyamoya disease is a chronic cerebrovascular disease characterizedby severe moyamoya disease was first described in Japan in 1957.  
    http://patients.uptodate.com/topic.asp?file=cva_dise/8090&title=Headaches

45. Moyamoya Disease
    Dural inversion procedure for moyamoya disease A variety of surgical procedureshave been proposed for the treatment of moyamoya disease, but few have used  
    http://www.bcm.tmc.edu/pednsurg/disorder/moyamoya.htm
    
    Extractions: MOYAMOYA SYNDROME/ STROKE IN CHILDREN A stroke occurs when an area of brain tissue becomes permanently damaged by not receiving enough blood and oxygen. This can result in various degrees of paralysis, visual loss, speech deficits, seizures, and even headaches. Multiple small strokes can erode intellectual functions as well. Once these symptoms manifest, improvement may or may not occur, depending upon many individual factors. One cause of stroke in children is inflammation of the blood vessels supplying the brain, which can occur with infections from certain viruses or other rare organisms. Treatment of this problem is directed toward the causative organism. Children with sickle cell anemia have a high risk of stroke. This occurs in about 20% of patients with this disease, and these children often have multiple strokes. Treatment of this condition involves fluid administration, blood transfusions, and oxygen. Strokes also occur in children with birth defects of the heart, as small clots that originate in the heart can escape and block blood vessels that supply the brain. This can also happen with infections of the heart valves. Treatment of these conditions includes blood thinners, repair of the heart defect itself, or antibiotics against the heart valve infections. Rarely, migraine headache can cause stroke. Surgery plays little role in the treatment of these forms of stroke. There is however, a cause of stroke in children that can be treated with surgery. This is moyamoya syndrome, which is a progressive disease of the large arteries that supply the brain. These vessels slowly occlude over time, and little, if any, blood flows though them. The body tries to compensate by drawing blood from the vessels that supply the brain's surrounding structures instead. Although this is helpful, it is frequently not enough to adequately supply the brain. The brain will either suffer many small strokes, or will be forced to function with inadequate blood supply. In addition, some children will have temporary symptoms of stroke, which clear completely later. These are called transient ischemic attacks (TIA).

46. Moyamoya Disease - OhioHealth
    moyamoya disease is a rare, progressive condition characterized by obstructionof major blood vessels at the base of the brain. It eventually leads to brain  
    http://www.ohiohealth.com/healthreference/reference/762FB9C2-CE01-4A8D-B5909C2A8

47. Moyamoya Disease
    moyamoya disease. This article submitted by pgamse@interaccess.com on 9/13/95.Can you help moyamoya disease. However, she says that her doctors  
    http://neuro-www.mgh.harvard.edu/neurowebforum/GeneralFeedbackArticles/Moyamoyad

48. 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
    
    Extractions: 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

49. The Bioline EPrints Archive - Moyamoya Disease : A Review
    Moyamoya is probably an inherited vasocclusive disease first described in Japan Keywords, Vasoocclusive disease, Moyamoya, Revascularization ni02004  
    http://bioline.utsc.utoronto.ca/archive/00000333/
    
    Extractions: @import url(http://bioline.utsc.utoronto.ca/eprints.css); @import url(http://bioline.utsc.utoronto.ca/eprints.css); @import url(http://bioline.utsc.utoronto.ca/print.css); Home About Browse Search ... Help Gosalakkal, J.A. Moyamoya Disease : A Review Neurology India pp. 6-10 Full text available as: PDF - Requires Adobe Acrobat Reader or other PDF viewer. Moyamoya is probably an inherited vasocclusive disease first described in Japan and now reported from all over the world. Genetic linkage studies and study of the factors possibly involved in its pathogenesis have shed new light on this disease. There is some suggestion that the pathogenesis may vary between races. A number of revascularization procedures have been devised. There is still controversy regarding the timing and the type of surgery. Functional MRI and PET scanning may provide more objective criterion on the outcome of these procedures. Neuropsychological studies may also be of use in judging the benefits of surgery. In this review, some of the recent advances in the study of the genetics and pathogenesis of the disease are reviewed and the clinical manifestation and the role of surgery are discussed. Relative lack of literature from outside Japan and the Korean peninsula has hampered the understanding of the disease in other countries. Item Type: Journal (Paginated) Keywords: Vaso-occlusive disease, Moyamoya, Revascularization ni02004

50. Rare Pediatric Disease Database
    WHAT moyamoya disease is a disorder involving the large blood vessels that supplythe WHO moyamoya disease affects girls more commonly than boys.  
    http://www.madisonsfoundation.org/content/3/1/display.asp?did=372

51. NewYork-Presbyterian Hospital Neuro: Moyamoya Disease
    Health information about moyamoya disease from NewYorkPresbyterian. The UniversityHospitals of Columbia and Cornell.  
    http://wo-pub2.med.cornell.edu/cgi-bin/WebObjects/PublicA.woa/5/wa/viewHContent?

52. Moyamoya Disease
    moyamoya disease (MMD) is a rare disorder of the blood vessels of the brain. moyamoya disease (MM) is characterized by progressive obstruction of the  
    http://www.thedoctorsdoctor.com/diseases/moyamoya_disease.htm
    
    Extractions: Background Moyamoya disease (MMD) is a rare disorder of the blood vessels of the brain. It is characterized by a progressive occlusive disease of the cerebral vasculature with particular involvement of the circle of Willis and the feeding arteries. The name Moyamoya is Japanese for "puff of smoke". This distinctive name describes the angiographic appearance of the abnormal vascular collateral networks that develop adjacent to the stenotic vessels. The changes may affect the major blood vessels of the brain including the anterior, middle, and posterior cerebral arteries. The symptoms and clinical course vary widely and depend upon the location and severity of the hemorrhage or damage. Thus signs and symptoms may range from asymptomatic to transient events to severe neurologic deficits. ADULTS CHILDREN Hemorrhage (intraventricular, subarachnoid, or intracerebral hemorrhage) more common Cerebral ischemic events more common

53. Moyamoya Disease By Y.Matsushima,M.D.
    EDAS? ? ?. moyamoya disease by Y. Matsushima,MD  
    http://www.geocities.co.jp/Technopolis/1023/

54. Posterior Circulation Abnormalities In Moyamoya Disease : A Radiological Study.
    Neurol India is an peerreviewed biomedical periodical of Neurological Societyof India.  
    http://www.neurologyindia.com/article.asp?issn=0028-3886;year=1999;volume=47;iss

55. Role Of Magnetic Resonance Perfusion Studies In Moyamoya Disease Khanna Paritosh
    Neurol India is an peerreviewed biomedical periodical of Neurological Societyof India.  
    http://www.neurologyindia.com/article.asp?issn=0028-3886;year=2004;volume=52;iss

56. Neurosurgery: Find A Specialist
    moyamoya disease causes blood vessels leading to the brain to narrow and close.It is rare and can occur during childhood or adulthood.  
    http://cgi.stanford.edu/dept/neurosurgery/cgi-bin/find_specialist?action=get_des

57. Arquivos De Neuro-Psiquiatria -
    ABSTRACT moyamoya disease (MMD) is a chronic occlusive cerebrovascular disease KEY WORDS moyamoya disease, adult, chronic occlusive cerebrovascular  
    http://www.scielo.br/scielo.php?pid=S0004-282X1999000300005&script=sci_arttext

58. Revista Brasileira De Anestesiologia -
    In children, moyamoya disease is primarily manifested by ischemic Approximately3800 cases of moyamoya disease were reported in 1997 5 in Japan,  
    http://www.scielo.br/scielo.php?pid=S0034-70942005000300012&script=sci_arttext&t

59. Indian Pediatrics - Editorial
    Chorea An Unusual Presenting Feature in Pediatric moyamoya disease moyamoya disease is a rare disease characterized by multiple occlusions of the  
    http://www.indianpediatrics.net/sept2000/sept-1005-1009.htm
    
    Extractions: Uday Limaye* From the Departments of Pediatrics and Radiology*, Seth G.S.Medical College and K.E.M.Hospital, Parel, Mumbai 400 012, India. Reprint requests: Dr. S.B.Bavdekar, A2-9, Worli Seaside CHS, K.A.G. Khan Road, Worli, Mumbai 400 018, India. E-mail: sandisha@bom7.vsnl.net.in Manuscript received: November 8, 1999; Revision Accepted: March 13, 2000 Moyamoya disease is a rare disease characterized by multiple occlusions of the cerebral circulation with an unusual net like system of collaterals. In Japanese, Moyamoya means ‘hazy’. The disease derives its peculiar name from the angiographic appearance of cerebral vessels in the disease that resembles a ‘puff of smoke’. In children the most common presentation is that of recurrent episodes of cerebral ischemia manifesting clinically as focal deficits, parasthesiae and seizures(13). Two cases of Moyamoya disease with uncommon present-ing features are described here. Case Report Case 1: Pre-operative digital substraction angio-graphy (DSA) revealed the classical pattern of progressive vasculopathy as seen in moyamoya disease with partial reformation of anterior circulation through the vertebro-basilar system (

60. Earth Clinic: Holistic Treatments For MOYAMOYA DISEASE
    TREATING moyamoya disease. Disclaimer The information provided on the This information on moyamoya disease was sent to us by Ted, of Bangkok, Thailand.  
    http://www.earthclinic.com/CURES/moyamoya.html
    
    Extractions: The information provided on the pages of Earth Clinic.com are intended as information only and are not a substitute for diagnosis and treatment by a physician. This website is a work-in-progress, and is our attempt to bring you reference material on the healing arts/home remedies/natural cures/etc. The ideas and information on these pages are designed to help you make informed decisions about your health. However, they are not intended as a substitute for any treatment that has been prescribed by your doctor. You must take full responsibility for your health. If you believe you have a medical or mental problem, please seek medical evaluation. Earth Clinic disclaims any responsibility for any adverse effects that may result from your use of the information contained within these pages. This information on Moyamoya Disease was sent to us by Ted, of Bangkok, Thailand. "Officially" there is no cure for Moyamoya disease. However, one of the characteristics of moyamoya disease is the lipid accumulation in the blood vessels - a clue. The treatment therefore lies in identifying various chemicals which will remove lipid accumulation which will, in turn, further delay the progression of moyamoya disease. Since this is a rare disease and adults have a 10% mortality and children have about 4%, it is therefore considered a deadly disease. "Officially" it is considered a genetic disease, however my guess is that environmental influences are making the disease appear much more apparent. I think that more people will get moyamoya and that the disease is no longer restricted to just Asian countries. My guess it is probably dietary.

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

41-60 of 100    Back | 1  | 2  | 3  | 4  | 5  | Next 20