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Machado-joseph Disease: more detail

The Official Patient's Sourcebook on Machado-Joseph Disease: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-09
Machado-Joseph disease
Origins of a mutation: population genetics of Machado-Joseph disease in the Azores (Portugal).: An article from: Human Biology by Manuela Lima, Francine M. Mayer, et all 1998-12-01
Machado-Joseph disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Sandra Galeotti, 2005
Prevalence, geographic distribution, and genealogical investigations of Machado-Joseph disease in the Azores (Portugal).: An article from: Human Biology by Manuela Lima, Francine Mayer, et all 1997-06-01
Machado-Joseph disease (SuDoc HE 20.3520:M 18) by U.S. Dept of Health and Human Services, 2001

lists with details

Hereditary Disease Foundation Home Page
dystrophy, Kennedy's disease (spinobulbar muscular dystrophy), Haw River Syndrome, 3 types of hereditary ataxia, SCI1, Machado Joseph disease
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
OMIM - MACHADO-JOSEPH DISEASE; MJD
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=109150
Entrez PubMed
Expanded polyglutamine in the machadojoseph disease protein induces cell death in vitro and in vivo. Ikeda H, Yamaguchi M, Sugai S, Aze Y, Narumiya S,
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=8
Central Nervous System Diseases
Machado Joseph Disease (and the Jewish connction) MazorNet About the Gene for machado-joseph disease - Neurobiology of Disease (US)
http://www.mic.ki.se/Diseases/C10.228.html

Extractions: Diseases and Disorders Links pertaining to Central Nervous System 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: Alzheimer Disease Arachnoiditis Brain Abscess Brain Abscess ... Uveomeningoencephalitic Syndrome Central Nervous System Diseases Nerve Cells [Lodish et al.] - Molecular Cell Biol., Chap 21, via NLM (US) Pathol. Images of the Central Nervous System - Univ of Utah (US) The Human Brain [JD MacArthur] How brain cells work [Cardoso et al.] EEG Course and Glossary [S Louis] About Normal EEG Variants [S Louis] - eMedicine The Global Brainstem '97 , the Cerebellum '97 , the Thalamus '97 , the Spinal Cord '97 - Univ. of Wisconsin (US) Mental Disorders Links
Potential Therapeutic Role For The Ataxin-3 Protein For Machado-Joseph Disease
Potential therapeutic role for the ataxin3 protein for machado-joseph disease. Medical Research News. Published Sunday, 3-Apr-2005
http://www.news-medical.net/?id=8883
Machado-Joseph Disease - Information & News
machadojoseph disease - Information News Potential therapeutic role for the ataxin-3 protein for machado-joseph disease. // Medical Research News
http://www.news-medical.net/?keyword=Machado-Joseph disease
Machado-Joseph Disease
machadojoseph disease (MJD-III), also called spinocerebellar ataxia type III, is a rare, inherited, ataxia (lack of muscular control) affecting the central
http://www.bchealthguide.org/kbase/nord/nord110.htm

Extractions: It is possible that the main title of the report Machado-Joseph 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. Machado-Joseph Disease (MJD-III), also called spinocerebellar ataxia type III, is a rare, inherited, ataxia (lack of muscular control) affecting the central nervous system and characterized by the slow degeneration of particular areas of the brain called the hindbrain. Patients with MJD may eventually become crippled and/or paralyzed but their intellect remains intact. The onset of symptoms of MJD varies from early teens to late adulthood.
Machado-joseph Disease - Definition From Biology-Online.org
Definition and other additional information on machadojoseph disease from Biology-Online.org dictionary.
http://www.biology-online.org/dictionary/machado-joseph_disease

Extractions: Directory ... M machado-joseph disease A progressive degenerative disease of the central nervous system occurring in portuguese -azorean families , having a variety of forms and inherited as an autosomal dominant trait . There are four major types : type I: with pyramidal and extrapyramidal deficits ; type II: with cerebellar , pyramidal and extrapyramidal deficits; type III: with cerebellar deficits and distal sensorimotor neuropathy ; type IV : with parkinsonism and distal sensory neuropathy. It was originally reported in two portuguese-azorean families in massachusettes (machado), then in another portuguese family ( thomas ), and later in a third family in california ( joseph , who settled there in 1845). It has been reported also in japanese families.
Hill Health Topics A-Z - Machado-Joseph Disease
machadojoseph disease. National Organization for Rare Disorders. Important It is possible that the main title of the report machado-joseph disease is not
http://www.healthwise.net/hillhealth/Content/StdDocument.aspx?DOCHWID=nord110&SE
NORD - National Organization For Rare Disorders, Inc.
machadojoseph disease (MJD-III), also called spinocerebellar ataxia type III Three forms of machado-joseph disease are recognized Types MJD-I, MJD-II,
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Machado-Josep
Machado-Joseph Disease
What Are the Different Types of machadojoseph disease? What Causes machado-joseph disease? How Is machado-joseph disease Diagnosed?
http://www.icongrouponline.com/health/Machado-Joseph_Disease.html

Extractions: (Autosomal Dominant Spinocerebellar Degeneration; Azorean Neurologic Disease; Machado Disease; Machado-Joseph Disease; Nigrospinodentatal Degeneration; Spinocerebellar Ataxia Type III; Striatonigral Degeneration, Autosomal Dominant Type) 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 Machado-Joseph Disease. Fully referenced with ample Internet listings and glossary. Related Conditions/Synonyms Autosomal Dominant Spinocerebellar Degeneration; Azorean Neurologic Disease; Machado Disease; Machado-Joseph Disease; Nigrospinodentatal Degeneration; Spinocerebellar Ataxia Type III; Striatonigral Degeneration, Autosomal Dominant Type Description Table of Contents Introduction Overview Organization Scope Moving Forward PART I: THE ESSENTIALS Chapter 1. The Essentials on Machado-Joseph Disease: Guidelines
Brazilian Journal Of Genetics - Molecular Characteristics Of Machado-Joseph Dise
Molecular characteristics of machadojoseph disease mutation in 25 newly described machado-joseph disease (MJD) is a form of autosomal dominant
http://www.scielo.br/scielo.php?pid=S0100-84551997000400026&script=sci_arttext&t
Arquivos De Neuro-Psiquiatria -
machadojoseph disease VERSUS HEREDITARY SPASTIC PARAPLEGIA CAG expansions in a novel gene for machado-joseph disease at chromosome 14q32.1.
http://www.scielo.br/scielo.php?pid=S0004-282X2001000500030&script=sci_arttext&t
Machado-Joseph Disease
machadojoseph disease. Azorean neurologic disease Spinocerebellar ataxia type 3 (machado-joseph disease) severe destruction of the lateral reticular
http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?cat3=679
NeuroRx -- Sign In Page
CAG expansions in a novel gene for machadojoseph disease at chromosome The genomic structure and expression of MJD, the machado-joseph disease gene.
http://www.neurorx.org/cgi/content/full/2/3/480

Extractions: This Article Summary Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Similar articles in this journal Alert me to new issues of the journal Download to citation manager PubMed Articles by Colomer Gould, V. F. To view this item, select one of the options below: Sign In User Name Sign in without cookies. Purchase Short-Term Access Pay per Article - You may access this article (from the computer you are currently using) for 1 day for US$10.00 Pay for Admission - You may access all content in NeuroRx Online (from the computer you are currently using) for 24 hours for US$20.00. Regain Access - You can regain access to a recent Pay per Article or Pay for Admission purchase if your access period has not yet expired.
Mouse Models Of Machado-Joseph Disease And Other Polyglutamine Spinocerebellar A
Summary machadojoseph disease (MJD), also called spinocerebellar ataxia type 3, is caused by mutant ataxin-3 with a polyglutamine expansion.
http://www.neurorx.org/cgi/content/abstract/2/3/480

Extractions: This Article Full Text Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Similar articles in this journal Alert me to new issues of the journal Download to citation manager PubMed Articles by Colomer Gould, V. F. Veronica F. Colomer Gould Department of Psychiatry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287 Summary: Machado-Joseph disease (MJD), also called spinocerebellar ataxia type 3, is caused by mutant ataxin-3 with a polyglutamine expansion. Although there is no treatment available at present to cure or delay the onset of MJD, mouse models have been generated to facilitate the development of a therapy. In this review, the published reports on mouse models of MJD and other polyglutamine spinocerebellar ataxias are compared. Based on these studies, the following approaches will be discussed as candidate treatments for MJD: 1) interfering with the formation of the mutant ataxin-3 cleavage fragment and possibly aggregate or inclusions, 2) reducing
Machado-Joseph Disease - General Practice Notebook
machadojoseph disease is an autosomal dominant neuromuscular degenerative disease. machado-joseph disease is also termed spinocerebellar ataxia type 3.
http://www.gpnotebook.co.uk/cache/-234487767.htm
Treatment Of Machado-Joseph Disease With Trimethoprim-sulphamethoxazole Followin
machadojoseph disease, also known as spino-cerebellar atrophy type 3, is a progressive, autosomal-dominant disorder. Originally described in individuals of
http://www.nzma.org.nz/journal/117-1191/819/

Extractions: Machado-Joseph disease, also known as spino-cerebellar atrophy type 3, is a progressive, autosomal-dominant disorder. Originally described in individuals of Portuguese extraction, it has subsequently been identified worldwide, possibly derived from Portuguese travellers. The disease is caused by a (CAG)n trinucleotide repeat in the MJD1 gene, located on chromosome 14q32. Unexpectedly, trimethoprim-sulphamethoxasole has shown benefit in this disease. This has been attributed to increasing central nervous system biopterin levels. Disappointingly, however, a recent double-blind crossover trial failed to demonstrate a significant effect of trimethoprim-sulphamethoxasole in Machado-Joseph disease.
Machado-Joseph Disease - St. Joseph Mercy, Ann Arbor Michigan
machadojoseph disease - St. Joseph Mercy Health System Hospitals serving Ann Arbor, SE Michigan, Washtenaw County, Livingston County, Wayne County,
http://www.sjmercyhealth.org/14430.cfm

Extractions: It is possible that the main title of the report Machado-Joseph 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. Machado-Joseph Disease (MJD-III), also called spinocerebellar ataxia type III, is a rare, inherited, ataxia (lack of muscular control) affecting the central nervous system and characterized by the slow degeneration of particular areas of the brain called the hindbrain. Patients with MJD may eventually become crippled and/or paralyzed but their intellect remains intact. The onset of symptoms of MJD varies from early teens to late adulthood.
Machado-Joseph Disease Presenting As Severe Asymmetric Proximal Neuropathy -- Va
machadojoseph disease should be considered in progressive axonal neuropathy. Keywords neuropathy; machado-joseph disease; SCA3; trinucleotide repeat
http://www.jnnp.com/cgi/content/abstract/63/4/534

Extractions: Vol Page [Advanced] This Article Full Text Full Text (PDF) Submit a response ... Citation Map Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by van Schaik, I N Articles by de Visser, M J Neurol Neurosurg Psychiatry 534-536 ( October ) Machado-Joseph disease presenting as severe asymmetric proximal neuropathy I N van Schaik, M Vermeulen, H Keizers, P A Bolhuis, M de Visser Department of Neurology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands

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