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  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

81. Analysis Of Moyamoya Disease
The number indicates the strength of association to moyamoya disease. The pointsto the related MeSHD terms. Follow the green arrows to navigate MeSH-C
http://www.bork.embl-heidelberg.de/g2d/exam_disease.pl?U50960

82. References For Moyamoya Disease With The MeSH Term Moyamoya Disease
References for moyamoya disease with the MeSH term moyamoya disease, G2D Home.PMID and date. Follow the link to see the corresponding entry by PubMed
http://www.bork.embl-heidelberg.de/g2d/exam_mesh_disease.pl?Moyamoya_Disease:U50

83. RETINA - UserLogin
Morning Glory Syndrome Association With moyamoya disease, Midline Cranial Defects, moyamoya disease, derived from the Japanese word for cloud of smoke,
http://www.retinajournal.com/pt/re/retina/fulltext.00006982-200306000-00018.htm
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84. Accessory Middle Cerebral Artery And Moyamoya Disease -- KOMIYAMA And YASUI 71 (
Accessory middle cerebral artery and moyamoya disease. A rare association ofmoyamoya disease with the accessory middle cerebral artery was seen in two
http://jnnp.bmjjournals.com/cgi/content/full/71/1/129

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Accessory middle cerebral artery and moyamoya disease
A rare association of moyamoya disease with the accessory middle cerebral artery was seen in two patients. The terminal portions of bilateral internal carotid arteries and their vicinities were markedly stenotic and so-called moyamoya vessels developed at the base of the brain. The left accessory middle cerebral artery originating near the anterior communicating artery supplied the left anterior frontal lobe in both patients. Although the accessory

85. Moyamoya Disease
Postoperative Evaluation of moyamoya disease with PerfusionWeighted MR ImagingInitial Clinical and experimental pathology of moyamoya disease
http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?cat3=203

86. Moyamoya Disease
moyamoya disease presenting as Valsalva related partial seizures moyamoya disease Localized 1HMR Spectroscopy in moyamoya disease before and after
http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?offset=30&cat3=20

87. Moyamoya Disease - General Practice Notebook
moyamoya disease may present with stroke in children and young adults. The causeof the disease is unknown. It was first described in 1963; early reports
http://www.gpnotebook.co.uk/cache/939917343.htm
Moyamoya disease Moyamoya disease may present with stroke in children and young adults. The cause of the disease is unknown. It was first described in 1963; early reports were predominantly in Japanese patients although later reports include non-Japanese. It arises in the presence of bilateral occlusion of the carotid arteries resulting in the development of an extensive fine network of collateral arteries and arterioles at the base of the brain - collaterals resemble a puff of smoke. Children typically present with sudden ischaemic strokes whilst young adults more commonly present with a sub-arachnoid haemorrhage. There is no specific treatment but surgical revascularisation may be tried.
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88. %252350 MOYAMOYA DISEASE 1; MYMY1
Gadoth and Hirsch (1980) observed moyamoya disease in an Amish child who also Meschino and Hughes (1989) described moyamoya disease in monozygotic twin
http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:252350] -e

89. Persistant Diffusion Signal Over One Year Period; Moyamoya Disease
Cerebral infarction due to moyamoya disease in young adults. Stroke 1988;19826833 . Risk factors of moyamoya disease in Canada and the USA.
http://med.ege.edu.tr/norolbil/2004/NBD29204.htm

90. Persistent Diffusion Signal Over One Year Period Moyamoya Disease
Persistent diffusion signal over one year period; moyamoya disease associatedwith migraine. UT Boru, A. Kocer, A. Luleci, N. Tasali
http://med.ege.edu.tr/norolbil/2004/2004_3_35.htm

91. Entrez PubMed
OBJECTIVE Surgical revascularization of moyamoya disease can improve neurologicaloutcomes, compared with the natural history of the disease or the results
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1

92. Entrez PubMed
moyamoya disease is a progressive disorder, predominantly seen in childhood, The natural history of moyamoya disease, the options for treatment,
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=3

93. JCR: Journal Of Clinical Rheumatology - Abstract: Volume 4(6) December 1998 P 32
Systemic Lupus Erythematosus Associated with moyamoya disease Case Report and moyamoya disease is a rare chronic cerebrovascular occlusive disease
http://www.jclinrheum.com/pt/re/jcr/abstract.00124743-199812000-00006.htm
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Systemic Lupus Erythematosus Associated with Moyamoya Disease: Case Report and Review of the Literature.
JCR: Journal of Clinical Rheumatology. 4(6):328, December 1998.
Prelipcean, Vlad; Koch, Alisa E. Abstract:
Moyamoya disease is a rare chronic cerebrovascular occlusive disease diagnosed by angiogram with primary features consisting of bilateral occlusion of the internal carotid arteries and of the vessels forming the circle of Willis, and subsequent developmen development of small collateral vessels. These collateral vessels may rupture, leading to the clinical presentation of transient ischemic attacks and intracerebral hemorrhage. We describe a young Korean woman with known moyamoya disease presenting with her second major vascular event who was also found to have active, undiagnosed systemic lupus erythematosus (SLE). SLE, with or without anti-cardiolipin, or anti-cardiolipin antibody syndrome, can be associated with "pseudo-moyamoya" (unilateral central nervous system disease). SLE, anti-cardiolipin antibody syndrome, pseudo-moyamoya, or moyamoya disease can all present in young women with intracerebral events, making diagnosis difficult. Our patient presented with fatigue, anemia, leukopenia, and a positive anti-nuclear antibody. Her physicians initially entertained a diagnosis of SLE, but when she developed a thalamic infarct, this diagnosis was abandoned, because a cerebral angiogram revealed a bilateral "cigarette smoke" appearance of blood vessels characteristic of moyamoya disease rather than the similar unilateral findings more typical of pseudo-moyamoya. Subsequently, it became clear that our patient had full-blown SLE and moyamoya disease. The clinician should be aware of the diagnosis of moyamoya because patients with this disease may present with intracerebral events associated with features of autoimmune disease, even in the absence of SLE. The concurrent development of SLE may confound the diagnosis even further. (J Clin Rheumatol 1998;4:328-332)

94. Cardiovascular Diseases
Syndrome Microvascular Angina - Microvascular Angina - Mitral Valve Prolapse -moyamoya disease - moyamoya disease - moyamoya disease - Mucocutaneous
http://www.mic.ki.se/Diseases/C14.html
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Diseases and Disorders Links pertaining to Cardiovascular Diseases Alert! Patients and laypersons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. Start Page Contents: Aneurysm Angina Pectoris Angina Pectoris Angioneurotic Edema ... Wolff-Parkinson-White Syndrome
Cardiovascular Diseases The Heart and Stroke Encyclopedia , about certain Conditions and Diseases , and a collection of Medical/Scientific Statements from the American Heart Association (US) Cardiovascular Physiology Concepts [RE Klabunde] CardioVillage CME courses - free, but registration required Archives des Maladies du Coeur et des Vaisseaux [in French] - Soc. Francaise de Cardiologie (FR) Cardiovascular Examination (1st year course) - Univ of Florida (US) [D Shindler] - Robert Wood Johnson Univ. Hosp., NJ (US) An illustrated Heart Tutorial - Spencer S Eccles Libr., Univ of Utah (US)

95. Neuroguide.com - Human Neurological Diseases
moyamoya disease. * moyamoya disease Information (NINDS) moyamoya disease,Mucopolysaccharidoses, MultiInfarct Dementia, Multifocal Motor Neuropathy
http://www.neuroguide.com/cgi-bin/pdistoc.pl?file=MoyamoyaDisease

96. Korean Journal Of Radiology
Localized 1HMR Spectroscopy in moyamoya disease before and after Materials andMethods Sixteen children with moyamoya disease and eight age-matched
http://www.kjronline.org/abstract/view_articletext.asp?year=2003&page=71

97. Pediatric Neurosurgery - Moya Moya
items such as aneurysms, arteriovenous malformations and Moyamoya disease . oxygen supply to areas of the brain involved with the Moya-moya disease.
http://cpmcnet.columbia.edu/dept/nsg/PNS/moyamoya.html
Moya-moya
This page is a sub-page of the Vascular pediatric neurosurgery site which contains information on items such as aneurysms , arteriovenous malformations and Moya-moya disease.
Moya-moya is a rare disorder of uncertain cause that leads to irreversible blockage of the main blood vessels to the brain as they enter into the skull. The name comes from the Japanese and means "puff of smoke". This naming is due to the appearance of the lesion on an angiogram. This is a lesion that tends to affect children and adults in the third to fourth decades of life. In children it tends to cause strokes or seizures. In adults it tends to cause bleeding or strokes. The process of blockage (vascular occlusion) once it begins tends to continue despite any known medical management unless treated with surgery. The repeated strokes can lead to severe functional impairment or even death so that it is important to recognize these lesions and treat them early on.
Once a diagnosis is suspected by CT or MRI, the next step is usually an angiogram to confirm the diagnosis and to see the anatomy of the vessels involved. Often nuclear medicine studies such as SPECT (single photon emission computerized tomography) are used to demonstrate the decreased blood and oxygen supply to areas of the brain involved with the Moya-moya disease. The next step is for the neurosurgeon to decide what type of operation is best suited for the child. There are many operations that have been developed for the condition, but currently the most favored are:

98. Moyamoya Syndrome Associated With Congenital Heart Disease -- Lutterman Et Al. 1
moyamoya is a chronic cerebrovascular disease of unknown etiology The associationof moyamoya syndrome and congenital heart disease has two important
http://pediatrics.aappublications.org/cgi/content/full/101/1/57
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PEDIATRICS Vol. 101 No. 1 January 1998, pp. 57-60
Moyamoya Syndrome Associated With Congenital Heart Disease
Joel Lutterman Michael Scott Ruth Nass and Tal Geva From the Departments of Cardiology and Neurosurgery, Children's Hospital, Boston, Massachusetts; the Departments of Pediatrics and Surgery, Harvard Medical School, Boston, Massachusetts; and the Department of Neurology, New York University Medical Center, New York, New York.
ABSTRACT Top
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Discussion References Objective . To describe the association between moyamoya syndrome and congenital heart disease and to discuss its clinical implications.

99. CPRMap |+| Identify Specific Proteins Associated With Moyamoya Disease |+
CPRMap tracks latest proteomic news, reports, conferences, jobs, and literaturesto facilitate collaborations among researchers in the clinical proteomics
http://proteomics.cprmap.com:8090/forums/showthread.php?t=8855

100. Health/Conditions And Diseases/Rare Disorders/Moyamoya -- The Doctors Lounge(TM)
Ask the doctor. Get free medical consultation and advice. Choose a medicalspecialist and post your question! Doctors in all medical fields are available.
http://www.thedoctorslounge.net/dir/Health/Conditions_and_Diseases/Rare_Disorder
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  • report abuse/spam url: report-abuse.dmoz.org/?cat=Health/Conditions_and_D... E-Medicine: Moyamoya Disease Introduction, clinical features, differentials, work up, treatments, medication and follow up. url: www.emedicine.com/neuro/topic616.htm Moyamoya Disease Definition, clinical symptoms and radiographic finding. url: chorus.rad.mcw.edu/doc/01076.html Moyamoya Disease Diagnosis, treatment and prognosis, plus problems specific to women. url: www003.upp.so-net.ne.jp/moya-moya/ Moyamoya Disease Support group for those diagnosed with this condition and their families. Includes medical information, personal account, links and a message board. url: www.moyamoya.com NINDS: Moyamoya Disease Description, treatment and prognosis from the National Institute of Neurological Disorders and Stroke.
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