81. Roche Lexikon Medizin (4. Aufl.) - Hallervorden*-Spatz* Syndrom Translate this page Hallervorden*-Spatz* Syndrom. engl. hallervorden-spatz syndrome Biogr. JULIUS H., 1882–1965, Neurologe, Gießen HUGO SP. autosomal http://www.gesundheit.de/roche/ro15000/r15041.html

Hallervorden*-Spatz* Syndrom engl.: Hallervorden-Spatz syndrome Biogr.: J ULIUS UGO S P Hyperkinesen Tremor Palilalie Athetose ... Hirnatrophie betrifft v.a. das Pallidum u. die Substantia nigra u. ist verbunden mit Ablagerung von rostbraunem Pigment u. Pseudokalk. Verwandte Themen Athetose, Athetosis Hirnatrophie Hyperkinese, -kinesie, -kinesis Palilalie ... Tremor

82. Karger Publishers 2 Sethi KD, Adams RJ, Loring DW, EI Gammal T hallervordenspatz syndrome Clinical and magnetic resonance imaging correlations. Ann Neurol 1988;24692-694. http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowFulltext&ProduktNr=

83. Alexa Web Search - Subjects > Health > ... > Neurological Disorders > Brain Dise OMIM National Center for Biotechnology Information. A clinical synopsis of hallervordenspatz syndrome. Avg. User Review 5.0 of http://www.alexa.com/browse/categories?catid=595050

84. Membres De La SENP Pediatr Neurol 2001;25(2) Striatal and pontocerebellar hypoperfusion in hallervordenspatz syndrome. Castelnau P, Zilbovicius M, Ribeiro http://www.senp-neuropediatrie.org/Annuaire_des_membres/Liste_des_Membres_de_la_

PARU Annuaire de la SENP France CASTELNAU Pierre Adresse : Téléphone : Fax : Abstracts : Hôpital Clocheville Neuropédiatrie 49 Boulevrad Béranger 37044 TOURS Cede p.castelnau@clocheville.chu-tours.fr Epileptic Disord 2003;4(3) Epilepsy and neuroprotection: an illustrated review. Arzimanoglou A, Hirsch E, Nehlig A, Castelnau P, Gressens P, Pereira de Vasconcelos A Epilepsy Unit, Child Neurology and Metabolic Diseases Departmentand INSERM E9935, University Hospital Robert-Debré, Paris, France. alexis.arzimanoglou@rdb.ap-hop-paris.fr PMID: 12446219[PM] Am J Perinatol 2002;19(6) Akinesia, arthrogryposis, craniosynostosis: a presentation of neonatal myasthenia with fetal onset. Cantagrel S, Maury L, Yamamoto AM, Maheut J, Toutain A, Castelnau P Pediatric and Neonatal Intensive Care Unit, Clocheville Children's Hospital, Tours, France. Major akinesia with arthrogryposis and craniosynostosis at birth mimics irreversible disorders of the nervous system of pejorative outcome. In this context, the early detection of anti-acetylcholine fetal receptor antibodies in the mother may allow rapid diagnosis of transient neonatal myasthenia of favorable prognosis. PMID: 12357420[PM] Pediatr Neurol 2001;25(2)

85. GREENSEEK hallervordenspatz syndrome Association (HSSA) OMIM National Center for Biotechnology Information. - A clinical synopsis of hallervorden-spatz syndrome. http://www.greenseek.de/internet/index.php/Health/Conditions_and_Diseases/Neurol

SEITE ANMELDEN NEUZUGÄNGE IM KATALOG FORUM UND COMMUNITY WETTERBERICHTE ... WEBDESIGN-VORLAGEN an abmelden im Katalog deutschem Web gesamten Web internationaler Katalog KATALOG Health Hallervorden-Spatz_Syndrome See also: Health: Conditions and Diseases: Genetic Disorders Health: Conditions and Diseases: Rare Disorders Hallervorden-Spatz Disease - Information sheet compiled by NINDS. Hallervorden-Spatz Syndrome Association (HSSA) - Contains news, research information, family pages with personal stories, publications and resources, details of fund-raising efforts and association history. MCW HealthLink - An article about Hallervorden-Spatz disease, with an explanation, the symptoms and prognosis. NORD: Neurodegeneration with Brain Iron Accumulation Type 1 - Offers synonyms, a general discussion and further resources for the disorder formerly known as Hallervorden-Spatz Syndrome. OMIM National Center for Biotechnology Information. - A clinical synopsis of Hallervorden-Spatz syndrome. Help build the largest human-edited directory on the web.

86. Health Library - Founded 1996.Provides emotional support to families affected by hallervordenspatz syndrome, a rare, progressive neurological disorder, resulting in iron http://yalenewhavenhealth.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29h

87. LikeALS hallervordenspatz syndrome Adult hallervorden-spatz syndrome simulates amyotrophic lateral sclerosis. http//www.als.net/alstdf http://home.goulburn.net.au/~shack/likeals.htm

DIAGNOSING ALS ALS LIKE DISEASES In many countries, ALS is regarded as just one form of several related Motor Neurone Diseases. In these countries the broader (and perhaps more accurate) term "Motor Neurone Disease" is used instead of ALS. There are some symptoms that occur in "textbook" cases of ALS that can differentiate it from other Motor Neurone disorders. The diagnosis of typical or so called "sporadic" ALS requires the presence of upper motor neuron signs (spasticity, rigidity, abnormal reflexes), lower motor neuron signs (weakness, atrophy) and progression. The pattern of upper and lower motor neuron signs that a neurologist detects are usually found in certain patterns commonly spread throughout several regions of the body. EMG and nerve conduction studies are helpful in identifying lower motor neuron problems in areas where there may not be much weakness. There are a large number of other illnesses that share some or many features of ALS and they must be evaluated or ruled out before a definite diagnosis can be made. An experienced practitioner who is familiar with the many presentations of ALS can make an accurate diagnosis with appropriate diagnostic testing and time to ensure that "look-alike" diseases have been excluded. OTHER MOTOR NEURON DISEASES Primary Lateral Sclerosis This motor neuron disease is similar to ALS but only the upper motor neurons are degenerating. Although rare, some lower motor neurons may appear to be involved with mild atrophy. PLS patients have most problems with spasticity and stiffness. The disease can progress slowly over many years. Patients often respond well to medical therapy to reduce their spasticity and stiffness.

88. BBC NEWS | Health | Gene Test For Rare Brain Disease area of the brain. Prof Jane Gitschier. The genetic disease, known as hallervordenspatz syndrome (HSS), affects the basal ganglia. http://news.bbc.co.uk/2/hi/health/2617337.stm

NEWS SPORT WEATHER WORLD SERVICE ... A-Z INDEX SEARCH You are in: Health News Front Page Africa Americas ... Programmes SERVICES Daily E-mail News Ticker Mobile/PDAs Text Only ... Help EDITIONS Change to UK Thursday, 2 January, 2003, 01:12 GMT Gene test for rare brain disease One form of the disease surfaces in later life Scientists have developed a new test for a rare brain disorder similar to Parkinson's Disease. They have found that all patients have a distinctive pattern of brain changes which can be detected by scanning. We are now working to figure out why these defects lead to cell death and iron accumulation in this very specific area of the brain Prof Jane Gitschier The genetic disease, known as Hallervorden-Spatz Syndrome (HSS), affects the basal ganglia. A number of neurological disorders, including Parkinson's, Huntingdon's disease and Tourette's syndrome, are also believed to arise from problems in this part of the brain. Researchers hope the test could lead to a better understanding of what goes wrong as well as improved diagnosis of the rare condition. Slow progression HSS is an inherited, neurological movement disorder marked by a progressive decline of the nervous system.

89. Hallervorden-Spatz (syndrome D’) syndrome. http://www.vulgaris-medical.net/texth/hallervo.html

Hallervorden-Spatz (syndrome d’) Voir également hypertonie, globus pallidus, locus niger, pigment. En anglais : Hallervorden-Spatz's syndrome. Affection familiale rare, débutant dans l'enfance par des troubles de la marche qui sont secondaires à un excès de tonicité musculaire (hypertonie) des membres inférieurs et de tout le corps. Au cours de ce syndrome, en rapport avec la dégénérescence d'une zone du cerveau (le globus pallidus et le locus niger) qui est envahie par des pigments contenant du fer, la parole et la déglutition (avaler quelque chose) sont très difficiles. Il s'y ajoute d'autre part une agitation psychique et des mouvements involontaires. Cause Affection récessive autosomique dont on ne connaît pas l'origine. La transmission génétique de nature récessive autosomique signifie qu'il est nécessaire que les deux parents portent l'anomalie génétique pour que l'enfant ait la maladie. Symptômes Début entre 5 à 12 ans (chez quelques malades, la maladie survient plus tôt). Le premier signe de la maladie est un trouble de la marche Rigidité Tension musculaire (hypertonie) importante, se caractérisant par des spasmes de torsion

90. Hallervorden-Spatz Disease hallervorden spatz syndrome. nausea hallervordenspatz Disease. hallervorden-spatz Disease syndrome. hallervorden-spatz Disease detectors. http://www.icongrouponline.com/health/Hallervorden-Spatz_Disease.html

ICON Health Publications Official Health Sourcebooks The Official Patient's Sourcebook on HALLERVORDEN-SPATZ DISEASE (Hallervorden-Spatz Syndrome; late infantile neuroaxonal dystrophy; Neuroaxonal Dystrophy, Late Infantile; Pigmentary Degeneration of Globus Pallidus, Substantia Nigra, Red Nucleus; pigmentary pallidal degeneration syndrome; Progressive Pallid Degeneration Syndrome; progressive pallidal degeneration syndrome) 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 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 Hallervorden-Spatz Disease. Fully referenced with ample Internet listings and glossary. Related Conditions/Synonyms Hallervorden-Spatz Syndrome; late infantile neuroaxonal dystrophy; Neuroaxonal Dystrophy, Late Infantile; Pigmentary Degeneration of Globus Pallidus, Substantia Nigra, Red Nucleus; pigmentary pallidal degeneration syndrome; Progressive Pallid Degeneration Syndrome; progressive pallidal degeneration syndrome Description Table of Contents Introduction Overview Organization Scope Moving Forward PART I: THE ESSENTIALS Chapter 1. The Essentials on Hallervorden-Spatz Disease: Guidelines

91. Ha : On Medical Dictionary Online syndrome Hallermann s syndrome HallermannStreiff syndrome Hallermanns syndrome Hallervorden Spatz Disease Hallervorden Spatz syndrome hallervorden-spatz http://www.online-medical-dictionary.org/?q=~Ha

92. Hallervorden-spatz, Maladie : Arborescences MeSH Translate this page du motclef page CISMeF du motclef hallervorden-spatz, maladie C10.228.140.079.493 page PubMed du motclef page CISMeF du motclef meige, syndrome C10.228.140 http://www.chu-rouen.fr/navimesh/H/navihallervordenspatzmaladie.html

Hallervorden-spatz, maladie : arborescences MeSH Menu général CISMeF Vous pouvez aussi consulter toutes les arborescences des mots clés utilisés dans CISMeF système nerveux, maladies système nerveux central, maladies encéphalopathies noyaux gris centraux, maladies ... Unverricht-Lundborg, syndrome 27 janvier 2004 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

93. Rare Disorders - Information / Diagnosis / Treatment / Prevention Subtopics Rare Disorders Agnosia, Rare Disorders Aicardi syndrome. Rare Disorders Alstrom syndrome, Rare Disorders Barth syndrome. http://www.healthcyclopedia.com/rare-disorders.html

Home Health cyclopedia All Topics by Category The Good Health Search Engine Health Conditions A-Z Gurus ... Contact Us Rare Disorders Information / Diagnosis / Treatment / Prevention External links (marked with an arrow ) open in a new window. This site is a web directory and does not offer medical advice. We cannot take responsibility for information found on listed sites. This Page Subtopics Related Topics Message Boards Health News ... Web Directory: Subtopics: Rare Disorders > Agnosia Rare Disorders > Aicardi Syndrome Rare Disorders > Alstrom Syndrome Rare Disorders > Barth Syndrome Rare Disorders > Cerebrocostomandibular Syndrome Rare Disorders > Cleidocranial Dysplasia Rare Disorders > Cystinosis Rare Disorders > Degos Rare Disorders > Erythromelalgia Rare Disorders > Jacobsen Syndrome Rare Disorders > Melorheostosis Rare Disorders > Moyamoya Rare Disorders > Ollier Disease Rare Disorders > Pemphigoid Rare Disorders > Pemphigus Rare Disorders > Phenylketonuria Rare Disorders > Pierre Robin Syndrome Rare Disorders > Progeria Rare Disorders > Rubinstein-Taybi Syndrome Rare Disorders > Tyrosinemia Rare Disorders > VATER Syndrome Rare Disorders > Wegener's Granulomatosis Related Topics: Aarskog Syndrome Aase Syndrome Abetalipoproteinemia Ablepharon-Macrostomia Syndrome ... Zollinger-Ellison Syndrome Message Boards and Online Support Groups: iVillage.com - The Women's Network

94. ORPHANET - Rare Diseases - Orphan Drugs Printing version, DISEASE hallervordenspatz disease, Synonym(s) Neuroaxonal dystrophy, late infantile Pantothenate kinase-associated neurodegeneration, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=385

95. Hallervorden-Spatz Disease - Eurorad - Clinical Case 1804 - Resident Neuroradiology Miscellaneous Case 1804 hallervordenspatz disease S. Cakirer, H. Toroslu, I. Celebi, M. Basak Diagnosis. hallervorden-spatz disease. http://www.eurorad.org/case.cfm?uid=1804

96. Neurology -- Abstracts: Ching Et Al. 58 (11): 1673 is a rare syndrome with many clinical similarities to pantothenate kinase–associated neurodegeneration (PKAN, formerly Hallervorden–Spatz syndrome). http://www.neurology.org/cgi/content/abstract/58/11/1673

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: Full Text of this Article PDF Version of this Article Citation Map Email this article to a friend Correspondence: Submit a response to this article Similar articles found in: Neurology Online PubMed PubMed Citation This Article has been cited by: other online articles Search PubMed for articles by: Ching, K. H.L. Hayflick, S. J. Alert me when: new articles cite this article Download to Citation Manager Collections under which this article appears: Hematologic Metabolic disease (inherited) All Movement Disorders Neurology American Academy of Neurology Brief Communications K. H.L. Ching, BS S. K. Westaway, PhD J. Gitschier, PhD J. J. Higgins, MD and S. J. Hayflick, MD From the Departments of Molecular and Medical Genetics (Drs. Hayflick and Westaway, and K. Ching), Pediatrics and Neurology (Dr. Hayflick), School of Medicine, Oregon Health and Science University, Portland; Howard Hughes Medical Institute and Departments of Medicine and Pediatrics (Dr. Gitschier), University of California, San Francisco; and Center for Human Genetics and Child Neurology (Dr. Higgins), Mid Hudson Family Health Institute, New Paltz, NY. Address correspondence and reprint requests to Dr. S. Hayflick, Department of Molecular and Medical Genetics, OHSU, L-103a, Portland, OR 97201-3098; e-mail:

97. Gimenei >> Health >> Conditions_and_Diseases >> Neurological_Disorders >> Brain_ Gimenei.com, Search for Scope All Words, Results per page 10. Request Timeout 2, http://www.gimenei.com/directory/top/Health/Conditions_and_Diseases/Neurological

Search for: Scope: All Words Any Word Phrase Results per page: Request Timeout: Search Depth: Gimenei Health Conditions and Diseases Neurological Disorders ... Basal Ganglia Hallervorden Spatz Syndrome DVD:

98. OMIM - PANTOTHENATE KINASE-ASSOCIATED NEURODEGENERATION; PKAN http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=234200

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