BAHA B CASTELNAU P., ZILBOVICIUS M., RIBEIRO MJ, HERTZPANNIER L., OGIER H., EVRARD P. Striatal and pontocerebellar hypoperfusion in hallervorden-spatz syndrome. http://www.necker.fr/irnem/Unites 2001/01radioped.htm
Extractions: Intestinal occlusion occurs in approximately 1 in 3000 births. Its diagnosis can be made in utero with ultrasound however, determination of its precise location is difficult to achieve. We report herein the feasibility of diagnosing and locating a fetal small-intestine occlusion with the use of magnetic resonance imaging. [References: 5] BRUNELLE F.
LONGSTANDING deep brain stimulation (DBS) has appeared as an a Pallidal deep brain stimulation for longstanding severe generalized dystonia in hallervordenspatz syndrome. http://mind-brain.com/abstracts.php?qa=longstanding
²Ä¤Q¥|¨÷²Ä¤T´ÁVolume 14Number 3 Magnetic Resonance Imaging of hallervordenspatz syndromeA Case Report I-Hao Su, Andy Shau-Bin Chou1, Chau-Chin Lee1, Pao-Sheng Yen1 Department of Diagnostic http://www.tzuchi.com.tw/tcmj/92-2/8.htm
Extractions: A 48-year-old man had suffered from progressive involuntary movement of bilateral arms since the age of 24 years. Clinical examination revealed acanthocytosis and optic nerve atrophy. Cranial magnetic resonance imaging (MRI) demonstrated abnormal hypointensity in the globus pallidus with central zones of hyperintensity on T2-weighted and Proton-weighted images, producing the "eye of the tiger" sign. Based on the clinical features and MRI findings, Hallervorden-Spatz syndrome was diagnosed. (Tzu Chi Med J 2003; 15:131-134)
Hallervorden-Spatz, Maladie : Sites Et Documents Francophones Translate this page associée à la . Arborescence(s) du thesaurus MeSH contenant le mot-clé Hallervorden-Spatz, maladie hallervorden-spatz syndrome http://www.chu-rouen.fr/ssf/pathol/hallervordenspatzmaladie.html
Pediatric Neurology, Volume: 25, Issue: 2, August, 2001 First scientific workshop on hallervordenspatz syndrome executive summary. Hayflick, Susan J. pp. 99-101. hallervorden-spatz syndrome. Swaiman, Kenneth F. pp. http://else.hebis.de/cgi-bin/sciserv.pl?collection=journals&journal=08878994&iss
Other Brain Conditions There is an article on cluster headaches that is particularly recommended reading by OUCH UK. hallervordenspatz syndrome back to top. http://www.nervecentre.org.uk/Other Conditions.htm
Extractions: Supporting people in Caithness and North Sutherland affected by neurological disorders www.nervecentre.org.uk info@nervecentre.org.uk Other Neurological Conditions up Brachial plexus injury Lambert-Eaton syndrome Brain tumour, haemorrhage and AVM Mal De Debarquement syndrome (MDDS) Benign essential tremor Migraine Cluster headaches Neuromuscular conditions ... Tuberous Sclerosis Full (?) List of Neurological conditions The US National Institute for Neurological Disorders and Stroke has a fairly comprehensive listing of neurological conditions from which you can find out more on each one. Click here to find the page you need to start your search. Brachial Plexus injury Brain Tumour, Haemorrhage and AVM (arterio venous malformations) Brain Tumour Action is an organisation set up to support and help people diagnosed with brain tumours, in direct and useful ways such as through their Befrienders scheme. The site has a lot of information on brain tumours and statistics on their incidence in the population.
Rare Disease Catalog H-K This page last updated November 13, 2000. H. Disease Name, Omim , Organizations/Sites. hallervordenspatz syndrome, 234200, hallervorden-spatz syndrome Association. http://www.med.nyu.edu/rgdc/dis_hijk.htm
Extractions: Heriditary Angiodema Heriditary Hemorrhagic Telangiectasia Heriditary Multiple Exostoses Many: Search Omim Heriditary Neuropathies Many: Search Omim Hermansky-Pudlak Syndrome Hirshsprung Disease Holoprosencephaly Holt-Oram Syndrome Hunter Syndrome Associazione Italiana per le Mucopolisaccaridosi Ethan's Feeling Switch Canadian MPS Society Gesellschaft für Mukopolysaccharidosen e. V.
PhatNav Directory - Health/Conditions_and_Diseases/P Porencephaly. Health/Conditions and Diseases/Neurological Disorders/Brain Diseases/Basal Ganglia/hallervordenspatz syndrome. Health http://www.phatnav.com/directory/Health/Conditions_and_Diseases/P.cat
Extractions: Scroll to see all. Related Categories Health/Conditions and Diseases/Musculoskeletal Disorders/Congenital Anomalies/Pectus Excavatum Health/Conditions and Diseases/Rare Disorders/Phenylketonuria Health/Conditions and Diseases/Neurological Disorders/Brain Diseases/Intracranial Hypertension Health/Conditions and Diseases/Cardiovascular Disorders/Heart Disease/Pericarditis ... Top of this directory. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor PhatNav and Diagonal Media Group Inc.
Ô˶¯ÕÏ°ÐÔ¼²²¡---www.sunbinmd.com 8? 1 Pena JA,PrietoCarrasquero M,Gonzalez-Ferrer S. hallervorden-spatz syndrome in 2 Venezuelan patients. hallervorden-spatz syndrome. http://www.sunbinmd.com/newsinfo.asp?nid=114
Extractions: UniProt ensEMBL Entrez RZPD ... EBI-Hinxton-"Uniprot-Swissprot-TrEMBL" database General information Entry name Accession number Created TrEMBLrel. 17, 1-JUN-2001 Sequence update TrEMBLrel. 17, 1-JUN-2001 Annotation update TrEMBLrel. 22, 1-OCT-2002 Description and origin of the Protein Description Hypothetical protein (Fragment). Organism source Homo sapiens (Human). Taxonomy Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Primates; Catarrhini; Hominidae; Homo. NCBI TaxID References Strausberg,R., Submitted AUG-2001 to the EMBL GenBank DDBJ databases Position SEQUENCE FROM N.A. Comments TISSUE=Placenta; Database cross-references EMBL Keywords Hypothetical protein Features Key Begin End Length Description UniGene LocusLink OMIM GenAtlas ... Genome Browser Chromosomal Location Chromosome/Cytoband Microarray Gene Expression Data Data available Show Gene Expression Data LocusLink Information Locus Link Summary This gene encodes a protein belonging to the pantothenate kinase family. Pantothenate kinase is a key regulatory enzyme in the biosynthesis of coenzyme A (CoA) in bacteria and mammalian cells. It catalyzes the first committed step in the universal biosynthetic pathway leading to CoA and is itself subject to regulation through feedback inhibition by CoA. Mutations in this gene are associated with HARP syndrome and pantothenate kinase-associated neurodegeneration (PKAN), formerly Hallervorden-Spatz syndrome. Alternative splicing has been observed at this locus, including the use of 4 alternate first exons. Six transcript variants have been identified, encoding four distinct isoforms.
Brain Diseases - 114 Of The Best Sites Selected By Humans NORD Neurodegeneration with Brain Iron Accu MCW HealthLink -hallervorden-spatz syndrome Association (HSSA) Basal_Ganglia -Sydenhams Chorea and Chorea http://www.cbel.com/brain_diseases/?order=alpha
Brain Diseases - 114 Of The Best Sites Selected By Humans 1 NORD Neurodegeneration with Brain Iron Accu 1 -MCW HealthLink 1 -hallervorden-spatz syndrome Association (HSSA) 1 Basal_Ganglia 6 -Sydenhams http://www.cbel.com/brain_diseases/?order=pop
ASENT | NeuroRx Newsletter - Role Of Iron In Neurodegeneration hallervordenspatz syndrome Gene Defect Identified hallervorden-spatz syndrome (HSS) is a progressive, autosomal neurodegenerative disorder of childhood and http://www.asent.org/newsletter/2001/september/
Extractions: What's Inside Role of Iron in Neurodegeneration A Vaccine for Prion Disease? and Related Articles Industry News News from Other Countries ... Employment Opportunities The Role of Iron in Neurodegeneration Excessive iron accumulation has been reported in the brains of patients with Parkinsons or Alzheimers disease, and it has been postulated that abnormal iron accumulation in the brain is neurotoxic through the generation of free radicals. However, it remains unclear whether iron-induced oxidative stress is a primary or a secondary event in the process that leads to neuronal death. Two recent reports suggest that - at least in some cases - iron toxicity may be a primary event in neurodegeneration. Neuroferritinopathy Causative Gene Identified In recent years, Curtis et al have described a previously unrecognized adult-onset neurodegenerative disease that affects the basal ganglia and is associated with iron accumulation. The disease is dominantly inherited and presents with extrapyramidal symptoms and low ferritin serum levels. Histopathology is characterized by lesions in the globus pallidus with abundant spherical inclusions containing aggregates of ferritin and iron. Additionally, axonal swellings are found throughout the brain and are immunoreactive for ubiqutin and tau. Within the brain, only the basal ganglia appear to be affected. Outside the brain, organs such as the pancreas, liver, and heart that are typically affected in iron accumulation disease, appear to function normally.
Blackwell Synergy - Cookie Absent hallervordenspatz syndrome. Pediatric Neurology 2001;25 102-108. hallervorden-spatz syndrome clinical and magnetic resonance imaging correlations. http://www.blackwell-synergy.com/links/doi/10.1034/j.1600-0447.2003.00159.x/abs/
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