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Alexander Disease:     more books (100)

Medical Gynecology: A Treatise On The Diseases Of Women From The Standpoint Of The Physician by Alexander J. C. Skene, 2007-07-25 Diseases of Metabolism: Detailed Methods of Diagnosis and Treatment: A Text for the Practitioner by Walter Bauer, Hugh R. Butt, et all 1947 Clostridium difficile PCR ribotypes in calves, Canada.(RESEARCH): An article from: Emerging Infectious Diseases by Alexander Rodriguez-Palacios, Henry R. Stampfli, et all 2006-11-01 Behaviour of the human ureter in health and disease, by James Alexander Ross, 1972 Handbook of Diagnosis of Avian Influenza and Newcastle Disease Human alveolar echinococcosis after fox population increase, Switzerland.(RESEARCH)(Clinical report): An article from: Emerging Infectious Diseases by Alexander Schweiger, Rudolf W. Ammann, et all 2007-06-01 Preventing and controlling disease among horses and mules (Horse and Mule Association of America. Book) by Raymond Alexander Kelser, 1946 Human metapneumovirus infection among children, Bangladesh.(DISPATCHES): An article from: Emerging Infectious Diseases by W. Abdullah Brooks, Dean Erdman, et all 2007-10-01 Neurotoxic Factors in Parkinson's Disease and Related Disorders This Long Disease My Life Alexander Pope by NicolsonMarjorie, 1968 This Long Disease My Life Alexander Pope by Marjorie Nicolson, 1968 Diseases of the newborn by Alexander J Schaffer, 1977 Uric Acid As A Factor In The Causation Of Disease V2 by Alexander Haig, 2007-04-10 Diseases of swine, with special reference to the preventive measures of disease, by Robert Alexander Craig, 1906

lists with details

41. Alexander Disease
    alexander disease. What is alexander disease? alexander disease is a rare, genetically determined degenerative disorder of the central nervous system.  
    http://www.clevelandclinic.org/health/health-info/docs/1200/1245.asp?index=6027&

42. Show-documents.asp
    alexander disease Written Information. Care Treatment. , alexander disease New Search Health Extra Menu.  
    http://www.clevelandclinic.org/healthextra/do-query.asp?TopicId=1272

43. Alexander Disease - Wikipedia, The Free Encyclopedia
    alexander disease is a slowly progressing fatal neurodegenerative disease. alexander disease belongs to leukodystrophies, a group of diseases which  
    http://en.wikipedia.org/wiki/Alexander_disease

44. Alexander Disease Information Diseases Database
    alexander disease,Fibrinoid leukodystrophy, Disease Database Information.  
    http://www.diseasesdatabase.com/ddb30685.htm

45. Hill Health Topics A-Z - Alexander Disease
    alexander disease. National Organization for Rare Disorders. Important It is possible that the main title of the report alexander disease is not the name  
    http://www.healthwise.net/hillhealth/Content/StdDocument.aspx?DOCHWID=nord56&SEC

46. Alexander('s) Disease/Syndrome
    Alexander( s) Disease/Syndrome (Dysmyelinating Disease). alexander disease Alexanders alexander disease alexander disease Alexander s Disease  
    http://www.bdid.com/alexander.htm

47. Alexander Disease - St. Joseph Mercy, Ann Arbor Michigan
    alexander disease St. Joseph Mercy Health System Hospitals serving Ann Arbor, SE Michigan, Washtenaw County, Livingston County, Wayne County,  
    http://www.sjmercyhealth.org/12386.cfm
    
    Extractions: It is possible that the main title of the report Alexander Disease is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. In infants and young children affected by Alexander Disease, associated symptoms and findings include a failure to grow and gain weight at the expected rate (failure to thrive); delays in the development of certain physical, mental, and behavioral skills that are typically acquired at particular stages (psychomotor retardation); and progressive enlargement of the head (macrocephaly). Additional features typically include sudden episodes of uncontrolled electrical activity in the brain (seizures); abnormally increased muscle stiffness and restriction of movement (spasticity); and progressive neurological deterioration. In some cases, there is hydrocephalus. In most cases, Alexander Disease appears to occur randomly for unknown reasons (sporadically), with no family history of the disease. In an extremely small number of cases, it is thought that the disorder may have affected more than one family member.

48. Short Description Of Cell Lines. Pathology: Alexander Disease *203450
    Version 4.200205. Short description of cell lines. Pathology alexander disease *203450 OMIM record. By selecting the cell line name, you will receive the  
    http://www.biotech.ist.unige.it/cldb/pat44.html

49. Alexander Disease: Diagnosis With MR Imaging -- Van Der Knaap Et Al. 22 (3): 541
    In the patient with juvenile alexander disease, three MR studies were available, one obtained Patients with an MRBased Diagnosis of alexander disease  
    http://www.ajnr.org/cgi/content/full/22/3/541
    
    Extractions: This Article Abstract Figures Only Full Text (PDF) ... Citation Map 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 van der Knaap, M. S. Articles by Powers, J. M. American Journal of Neuroradiology BACKGROUND AND PURPOSE: To date, the demonstration of Rosenthal fibers on brain biopsy or autopsy specimens is considered a prerequisite for a definitive diagnosis of Alexander disease. We initiated a multiinstitutional survey of MR abnormalities in both presumed and confirmed cases of Alexander disease to assess the possibility of an MR-based diagnosis.

50. Alexander Disease: Diagnosis With MR Imaging -- Van Der Knaap Et Al. 22 (3): 541
    Adult alexander disease With Autosomal Dominant Transmission A Distinct Entity Molecular findings in symptomatic and presymptomatic alexander disease  
    http://www.ajnr.org/cgi/content/abstract/22/3/541
    
    Extractions: This Article Figures Only Full Text Full Text (PDF) ... Citation Map 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 van der Knaap, M. S. Articles by Powers, J. M. American Journal of Neuroradiology American Society of Neuroradiology Marjo S. van der Knaap a Sakkubai Naidu a Steven N. Breiter a Susan Blaser a Hans Stroink a Stephan Springer a Jacobus C. Begeer a Rudy van Coster a Peter G. Barth a Neil H. Thomas a Jacob Valk a and James M. Powers a a BACKGROUND AND PURPOSE: To date, the demonstration of Rosenthal fibers on brain biopsy or autopsy specimens is considered a prerequisite for a definitive diagnosis of Alexander disease. We initiated a multiinstitutional survey of MR abnormalities in both presumed and confirmed cases of Alexander disease to assess the possibility of an MR-based diagnosis.

51. Alexander Disease NASET – National Association Of Special Education Teachers
    alexander disease NASET – National Association of Special Education Teachers.  
    http://www.naset.org/463.0.html

52. Alexander Disease
    Infantile alexander disease Spectrum of GFAP Mutations and GenotypePhenotype Correlation alexander disease Diagnosis with MR Imaging  
    http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?cat3=17

53. Applied Genetics News: Gene Defect For Alexander Disease
    Full text of the article, Gene Defect for alexander disease from Applied Genetics News, a publication in the field of Health Fitness, is provided free  
    http://www.findarticles.com/p/articles/mi_m0DED/is_6_21/ai_69709517
    
    Extractions: Save a personal copy of this article and quickly find it again with Furl.net. It's free! Save it. Scientists led by University of Wisconsin-Madison researcher Able Messing have pinpointed the gene responsible for a rare and devastating childhood brain disorder called Alexander disease, solving a 50-year-old mystery regarding its cause. Their work is reported in the January 3 issue of Nature Genetics. Musing's team discovered the gene after a genetic analysis of 13 cases of the disease. Because of the rarity of the disease, it took nearly two years to assemble enough cases from international sources to complete the study.

54. Alexander Disease
    alexander disease (Dysmyelogenic Leukodystrophy; Dysmyelogenic LeukodystrophyMegalobare; Federally Funded Research on alexander disease  
    http://www.icongrouponline.com/health/Alexander_Disease.html
    
    Extractions: (Dysmyelogenic Leukodystrophy; Dysmyelogenic Leukodystrophy-Megalobare; Fibrinoid Degeneration of Astrocytes; Fibrinoid Leukodystrophy; Hyaline Panneuropathy; Leukodystrophy with Rosenthal Fibers; Megalencephaly with Hyaline Inclusion; Megalencephaly with Hyaline Panneuropathy) Revised and Updated for the Internet Age P A P E R B A C K Paperback Book Paperback Book Order by phone: 800-843-2665 (within USA) 1-201-272-3651 (from outside USA) Paperback Book Shipped in 3 to 5 business days E B O O K Electronic File * E-Book version sent via e-mail in 2 business days Pages Price $28.95(USD) ISBN Published Synopsis A comprehensive manual for anyone interested in self-directed research on Alexander Disease. Fully referenced with ample Internet listings and glossary. Related Conditions/Synonyms Dysmyelogenic Leukodystrophy; Dysmyelogenic Leukodystrophy-Megalobare; Fibrinoid Degeneration of Astrocytes; Fibrinoid Leukodystrophy; Hyaline Panneuropathy; Leukodystrophy with Rosenthal Fibers; Megalencephaly with Hyaline Inclusion; Megalencephaly with Hyaline Panneuropathy Description Table of Contents Introduction Overview Organization Scope Moving Forward PART I: THE ESSENTIALS Chapter 1. The Essentials on Alexander Disease: Guidelines

55. Alexander Disease Synonyms, Eastern Carolina
    alexander disease Synonyms University Health Systems of Eastern Carolina serves tarboro, ahoskie, edento, winsor, maxhead, dear county, outebanks counties  
    http://www.uhseast.com/111946.cfm
    
    Extractions: It is possible that the main title of the report Alexander Disease is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. In infants and young children affected by Alexander Disease, associated symptoms and findings include a failure to grow and gain weight at the expected rate (failure to thrive); delays in the development of certain physical, mental, and behavioral skills that are typically acquired at particular stages (psychomotor retardation); and progressive enlargement of the head (macrocephaly). Additional features typically include sudden episodes of uncontrolled electrical activity in the brain (seizures); abnormally increased muscle stiffness and restriction of movement (spasticity); and progressive neurological deterioration. In some cases, there is hydrocephalus. In most cases, Alexander Disease appears to occur randomly for unknown reasons (sporadically), with no family history of the disease. In an extremely small number of cases, it is thought that the disorder may have affected more than one family member.

56. Demyelinating Diseases - Internet Handbook Of Neurology
    alexander disease GeneReviews; Alexander s Disease - University of Oklahoma; Childhood Leukodystrophy Presenting As Secondary Bipolar Disorder - Indian  
    http://www.neuropat.dote.hu/myelin.htm
    
    Extractions: Diseases Chapters: A Collection of High Quality Online Resources for Health Professionals Pathology see Pathology of Infectious Diseases and Disease of Myelin Overview Multiple Sclerosis Overview Multiple Sclerosis - Neurology Associates of Arlington Multiple Sclerosis - Praxis MD Multiple Sclerosis: Current Status and Strategies for the Future - National Academy Press, Multiple Sclerosis: Lectures - University of Utah, Houston ( epidemiology, pathology, etiology, laboratory findings, clinical presentation, diagnostic criteria, classification, differential diagnosis, treatment options, prognosis Multiple Sclerosis - Bhatia General Hospital, Mumbai, IN

57. Arch Neurol -- Abstract: Adult Alexander Disease With Autosomal Dominant Transmi
    Background Infantile and juvenile forms of alexander disease are well characterized and are caused by de novo mutations in the glial fibrillary acid protein  
    http://archneur.ama-assn.org/cgi/content/abstract/60/9/1307
    
    Extractions: Vol. 60 No. 9, September 2003 Featured Link E-mail Alerts Observation Article Options Full text PDF Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Stumpf E Cossette P Articles that cite this article ISI Web of Science (8) ... Contact me when this article is cited Topic Collections Neurogenetics Topic Collection Alerts Adult Alexander Disease With Autosomal Dominant Transmission A Distinct Entity Caused by Mutation in the Glial Fibrillary Acid Protein Gene Erika Stumpf, MD, MA Antoine Duquette, MD France Berthelet, MD Julia McNabb Anne Lortie, MD, FRCPC Jacques Lesage, MD, FRCPC Jacques Montplaisir, MD, PhD, CRCPC Bernard Brais, MD, MPhil, PhD Patrick Cossette, MD, MSc, FRCPC

58. Alexander Disease - Talk Medical
    Humanfriendly medical definition of alexander disease.  
    http://www.talkmedical.com/medical-dictionary/492/Alexander-Disease
    
    Extractions: Tell a friend Alexander disease: A slowly progressive and ultimately fatal brain disorder that most commonly occurs in children. The infantile form of the disease is characterized by megalencephaly (an abnormally large head), seizures, spasticity and developmental retardation. It leads to death usually within the first decade. Patients with the juvenile and adult forms of Alexander disease typically experience ataxia and spasticity and a more slowly progressive course. The classic hallmark of all forms of Alexander disease is the presence of Rosenthal fibers, abnormal inclusions in astrocytes that contain the intermediate filament protein GFAP. Mutations in the gene for GFAP (glial fibrillary acidic protein) cause Alexander disease, the first known example of a primary genetic disorder of astrocytes, one of the major cell types in the vertebrate CNS. The disease was first described by W. Stewart Alexander, a New Zealand pathologist, in 1949. Rosenthal fibers are homogeneous masses which form elongated tapered rods scattered throughout the cortex and white matter of the brain. Rosenthal fibers are located in the astrocytes. Demyelination (loss of myelin, the insulation around nerves) is also a prominent feature of the disease. Alexander disease is classified as one of the leukodystrophies, the diseases of the white matter of the brain.

59. Leucodistrofie/ALEXANDER'S DISEASE
    Histologically alexander disease is characterized by Rosenthal fibers, homogeneous eosinophilic alexander disease was proven histologically in the last.  
    http://web.peacelink.it/appeal/gianmarco/ii.html
    
    Extractions: sporadic PATHOGENESIS: 1. Background unknown etiology but thought to involve dysfunctional astrocytes PATHOLOGY: 1. Rosenthal Fibres refractile eosinophilic hyaline bodies found within the cytoplasm of astrocytes particularly in the subpial, subependymal, and perivascular regions required for definite diagnosis but not pathognomonic as seen in other disorders as well, i.e., Neurofibromatosis, MS TYPES: Type I: Infantile Form

60. Alexander Disease Topic - Unified Search Environment
    alexander disease is a progressive leukencephalopathy whose hallmark is the widespread accumulation of cytoplasmic inclusions called Rosenthal fibers.  
    http://www.use.hcn.com.au/portals/shared/subject.`Alexander Disease`/home.html
    
    Extractions: A rare inherited disorder of myelin formation. Alexander disease is a progressive leukencephalopathy whose hallmark is the widespread accumulation of cytoplasmic inclusions called Rosenthal fibers. The fibers contain GLIAL FIBRILLARY ACIDIC PROTEIN in association with ALPHA-CRYSTALLIN B CHAIN. Rosenthal fibers are found predominantly in ASTROCYTES located in the subependymal, subpial, and periventricular areas of the BRAIN. Synonyms and Source Vocabularies: Alexander Disease Neurodegenerative Diseases Olivopontocerebellar Atrophies Parkinson Disease Shy-Drager Syndrome ... Multiple System Atrophy Heredodegenerative Disorders, Nervous System Cockayne Syndrome Dystonia Musculorum Deformans Gerstmann-Straussler-Scheinker Disease Hallervorden-Spatz Syndrome ... Werner Syndrome Heredodegenerative Disorders, Nervous System Cockayne Syndrome Dystonia Musculorum Deformans Gerstmann-Straussler-Scheinker Disease Hallervorden-Spatz Syndrome ... Genetic Diseases, X-Linked

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