41. Volume 63 January - December 1940 A form of familial presenile dementia with spastic paralysis. C . WorsterDrought, JG . Greenfield and WH . McMenemey. Pages 237 - 254. http://www3.oup.co.uk/jnls/supplements/braini/hdb/Volume_63/Issue_03/630237.sgm.

Volume 63: January - December 1940 Issue 3: September 1940 Abstract A form of familial presenile dementia with spastic paralysis C Worster-Drought JG Greenfield and WH McMenemey Pages: Part of the OUP Brain WWW service General Information Click here to register with OUP. This page is maintained by OUP admin Last updated 13 May 97 Part of the OUP Journals World Wide Web service Oxford University Press, 1997

42. Dorlands Medical Dictionary syndrome. hereditary cerebrospinal paralysis, hereditary spastic paraplegia.hyperkalemic periodic paralysis, see familial periodic p. http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocszSzuszS

43. Bibliography Refsum S, Skillicorn SA (1954) Amyotrophic familial spastic paraplegia. Neurology4407. Rhein J (1914) Family spastic paralysis. J Nerv Ment Dis 44115-44. http://www.med.umich.edu/hsp/bibliography.htm

Hereditary spastic paraplegia Bibliography Baraitser M. ; Motulsky AG, Bobrow M, Harper PS, Scriver C, editors.The Genetics of Neurological Disorders. 2nd ed. New York: Oxford University Press, 1990; 15, Spastic paraplegia/HSP. p. 275-90. Behan W, Maia M (1974) Strumpell's familial spastic paraplegia: genetics and neuropathology. J Neurol Neurosurg Psychiatry 37:8-20. Boustany RN, Fleischnick E, Alper CA, Marazita ML, Spense MA, Martin JB, Kolodny EH (1987) The autosomal dominant form of "pure" familial spastic paraplegia. Neurology 37:910-5. Bruyn RPM, van Deutekom J, Frants RR, Padberg GW (1993) Hereditary spastic paraparesis: clinical and genetic data from a large Dutch family. Clin Neurol Neurosurg 95:125-9. Cambi F, Tartaglino L, Lublin FD, McCarren D (1995) X-linked pure familial spastic paraparesis: characterization of a large kindred with magnetic resonance imaging studies. Arch Neurol 52:665-9. Cartlidge N, Bone G (1973) Sphincter involvement in hereditary spastic paraplegia. Neurology 23:1160-3. Claus D, Waddy HM, Harding AE (1990) Hereditary motor and sensory neuropathies and hereditary spastic paraplegia: a magnetic stimulation study. Ann Neurol 28:43-9.

44. Health Library - Paraplegia, Hereditary Spastic covered by this report. Synonyms. familial spastic Paraplegia; FSP; HSP;spastic Spinal familial paralysis; Strumpell's familial Paraplegia; http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=

45. Health Library - Fahr's Disease with increased muscle stiffness (rigidity) and restricted movements (spastic paralysis). reportsin the medical literature, Fahr's Disease is often familial. http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=

46. FSP:Patient-Informations accepted · FSP familial spastic paraplegia · HSP - Hereditary spastic paraplegia· SPG - spastic paraplegia · SSP - spastic spinal paralysis Division http://www.fsp-info.de/engl/infopat.htm

Disease History Name of the Disease The two Frenchmen Lorrain and Charcot made the same experience what is an explanation for the following names the disease was first given: Later the following definitions were added: The abbreviations which are mainly used still today can partly be lead back to the above names. However, the English designations have been widely accepted: Division and Classification Thanks to Anita Harding from London we have now a classification of this clinically heterogeneous clinical picture. Basically, the disease is divided into a "pure" and a "complicated" form, whereas the "complicated" form additionally to the spastic shows other symptoms like epilepsy or dernence. In the order of their discovery the forms of "pure" spastic are genetically divided into SPG1 to SPG7. These designations stand for externally similar clinical pictures, which however have to be attributed to different genes or devolution forms. Genetics Because of the growing importance of genetics and molecular biology various researcher (groups) try to find out, whether the different forms of this illness can be attributed to one or several genes (carrier of genetic information). And they want to find which ways the devolution runs within the families. There is a dominant and a recessive characteristic and a difference is made between sex-specific and neutral transmission.

47. Hereditary Spastic Paraplegia The Official Patient's Sourcebook on HEREDITARY spastic PARAPLEGIA (familial spasticParaplegia; spastic Spinal familial paralysis; Strumpell Disease; Strumpell http://www.icongrouponline.com/health/Hereditary_Spastic_Paraplegia.html

ICON Health Publications Official Health Sourcebooks The Official Patient's Sourcebook on HEREDITARY SPASTIC PARAPLEGIA (Familial Spastic Paraplegia; Spastic Spinal Familial Paralysis; Strumpell Disease; Strumpell-Lorrain Familial Spasmodic Paraplegia; Strumpell-Lorraine Syndrome; Strumpell's Familial Paraplegia) Revised and Updated for the Internet Age Paperback Book Order by phone: 800-843-2665 (within USA) 1-201-272-3651 (from outside USA) 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 Hereditary Spastic Paraplegia. Fully referenced with ample Internet listings and glossary. Related Conditions/Synonyms Familial Spastic Paraplegia; Spastic Spinal Familial Paralysis; Strumpell Disease; Strumpell-Lorrain Familial Spasmodic Paraplegia; Strumpell-Lorraine Syndrome; Strumpell's Familial Paraplegia Description Table of Contents Introduction Overview Organization Scope Moving Forward PART I: THE ESSENTIALS Chapter 1. The Essentials on Hereditary Spastic Paraplegia: Guidelines

48. Paralysis Resources for paralysis. familial spastic paraplegia. Published by CaFDirectory. info@cafamily.org.uk. paralysis the loss of muscle power. http://www.nhsdirect.nhs.uk/innerpage2.asp?Code=FB&Topic=303

49. Hereditary Spastic Paraplegia Spasmodic Paraplegia, Strumpell's familial Paraplegia, Spasmodic Infantile Paraplegia,spastic Congenital Paraplegia, spastic Spinal familial paralysis). http://www.kumc.edu/gec/support/hsp.html

Hereditary Spastic Paraplegia / Familial Spastic Paraparesis (Strumpell-Lorrain Familial Spasmodic Paraplegia, Strumpell's Familial Paraplegia, Spasmodic Infantile Paraplegia, Spastic Congenital Paraplegia, Spastic Spinal Familial Paralysis) Hereditary Spastic Paraplegia / Familial Spastic Paraparesis - web page: http://www.geocities.com/HotSprings/Spa/2847/ To locate a genetic counselor or clinical geneticist in your area: Professional Genetics Societies Genetic clinics, centers, departments Genetic Societies Clinical Resources ... Search Genetics Education Center Debra Collins, M.S. CGC , Genetic Counselor, dcollins@kumc.edu This site subscribes to the principles of the HONcode (Health on the Net, Code of Conduct for Medical and Health Web Sites) of the Health On the Net Foundation

50. NORD - National Organization For Rare Disorders, Inc. Synonyms of Paraplegia, Hereditary spastic FSP; familial spastic Paraplegia;HSP; spastic Spinal familial paralysis; Strumpell Disease; http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Paraplegia, H

51. HEALTHMEDNET familial Non Hemolytic Non Obstructive Jaundice. familial Periodic paralysis.familial Polyposis. familial spastic Paraparesis. familial Tremor. Family Health. http://www.epscorp.com/healthmednet/f.htm

Directory Index HEALTHMEDNET Example Report Request ... DataBase Note: The names were derived from the specific illness/disease source directories. Therefore, there are some variations in the names. When ordering a list of URLs for your illness/disease, where possible, include the general usage, technical, acronym, and/or abbreviation names. Fabry Disease Facelifts Facet Degeneration (Low Back Pain) Facet Joint Problems Facial and Head Injuries Facial Asymmetry Facial Dermatoses Facial Hemiatrophy Facial Infection Facial Injuries (Cheek, Chin, or Jaw) Facial Injury: First Aid Facial Nerve Paralysis Facial Nerve Problems Facial Nerve Weakness or Paralysis (Bell's Palsy) Facial Neuralgia (Tic Douloureux) Facial Pain Facial Pain and Sinus Pain Facial Palsy Facial Paralysis Facial Tics Facioscapulohumeral Facioscapulohumeral Muscular Dystrophy (Landouzy-Dejerine) Facio-Scapulo-Humeral-Muscular D. Factitious Disorders Factitious Hyperthyroidism Factitous Disorder Factor II Deficiency Factor IX Deficiency Factor IX Hemophilia Factor V Deficiency Factor VII Deficiency Factor VIII Deficiency Hemophilia Factor X Deficiency Factor XII (Hageman Factor) Deficiency Factor XIII Deficiency Fahr's Disease Fahr's Syndrome Failure failure to thrive Fainting Fainting and Dizziness Fainting- What Causes It Fainting: Action Fainting: First Aid Fairbank Disease Falciparum Malaria Fall Allergies Fallopian Tube Fallopian tube procedures [in Infertility] Fallot's Tetrology Falls Falls and Hip Fractures Falls, Old Age

52. Full Listing DEFECTS AND ABNORMALITIES, BRACHIAL PLEXUS paralysis, BRAIN INJURED familial HYPERCHOLESTEROLAEMIA,familial HYPERLIPIDAEMIA, familial spastic PARAPLEGIA, FAMILY http://www.doctor.gp/help/full_listing.htm

DIRECTORY OF BRITISH SELF HELP GROUPS AND SUPPORT ORGANISATIONS by Steve and Julie Garrill Home

53. SPF - Home Page are Hereditary spastic Paraplegia, familial spastic Paraparesis (or Disease, HereditaryCharcotDisease, spastic Spinal paralysis, Diplegia Spinalis http://www.sp-foundation.org/

Welcome to the Spastic Paraplegia Foundation, Inc. We are under construction. Basic information is provided in the interim. Send Dollars To Research When You Shop Online NEW: Cookbook! Info Here 2003 Research Grant Program The SPF is a non-profit organization dedicated to neurological disorders Hereditary Spastic Paraparesis* (HSP) and Primary Lateral Sclerosis (PLS). Information on the SPF here and on the disorders here SPF VISION: The day where all individuals with HSP or PLS are diagnosed, treated and cured. SPF MISSION: We are committed to: *Discovering the cures for HSP and PLS by promoting research *Providing accurate information about these disorders *Creating opportunities for mutual support and sharing Get information about HSP and PLS and about the SPF Information about the Disorders (PDF Format) Basic information English En español En français What's Happening in My Body? English En español To make a tax-deductable donation: Click here. To get involved, please use the email link below. Subscribe To The SPF E-News!

54. Encyclopedia F-Fm (Search FastHealth.com) Encyclopedia F-Fm deficiency familial Mediterranean Fever familial non hemolytic non obstructivejaundice familial Periodic paralysis familial spastic Paraparesis familial http://www.jacksonfasthealth.com/encyclopedia/encyclopedia_F-Fm.php

Email This! A-Am An-Az B-Bm ... Z F-Fm Face pain Facelift Facial edema Facial Exercise ... Dead Links

55. Keywords Encephalomyelitis Ependymoma Epilepsy Erectile dysfunction Erythromelalgia F Fabry'sDisease Facial paralysis Fahr's Syndrome familial spastic Paraplegia Fecal http://www.ion.ucl.ac.uk/library/patient/keywords.html

A B C D ... P Q R S T U ... W X Y Z General A Acoustic Neuroma Adrenolukodystrophy (see leukodystrophy Agnosia Aicardi Syndrome AIDS Alexanders Disease (see leukodystrophy Alper's Disease Alzheimer's Disease Amyotrophic Lateral Sclerosis ... Autism B Behcet's Disease Batten Disease Bell's Palsy Binswanger's Disease ... Brown-Sequard Syndrome C Canavan Disease Carpal Tunnel Syndrome Cancer Cauda Equina ... Cerebral Aneurysm Cerebral Arteriosclerosis (see stroke Cerebral Atrophy Cerebral Palsy Charcot-Marie-Tooth Disease ... Continence problems Corticobasal degeneration Craniosynotosis Creutzfeldt-Jacob Disease Cushing's Syndrome D Dandy Walker Syndrome Deafness Dementia (see also Alzheimer's disease and CJD) DeMorsiers Syndrome Depression Dermatomyositis Devic's Syndrome Diabetic Neuropathy ... Dystonia E Ehlers Danlos Syndrome Encephalitis Encephalomyelitis E pendymoma ... Epilepsy Erectile dysfunction Erythromelalgia F Fabry's Disease Facial paralysis Fahr's Syndrome Familial Spastic Paraplegia Fecal Incontinence Fibromyalgia ... Friedrich's ataxia G Gaucher's Disease Gerstmann's Syndrome Gilles de la Tourette (see Tourette) Gliomas Glossopharyngeal Neuralgia Guillain Barre Syndrome H Haemangioblastoma Hallervorden-Spatz Disease Head Injury Headache ... Hemifacial Spasm Hereditary Motor and Sensory Neuropathy Hereditary Spastic Paraplegia Holoprosencephaly Huntington's Disease Hydrocephalus ... Hypotonia and Hypertonia I Inclusion Body Myositis Incontinence Intracranial Aneurysm Isaac's Syndrome J Joubert Syndrome K Kearns-Sayre Syndrome Kennedy's Disease Kleine-Levin Syndrome Klippel-Feil Syndrome Klippel-Trenaunay-Weber Syndrome Kluver-Bucy Syndrome ... Kuru L

56. THE LIGHTNING HYPERTEXT OF DISEASE. Packet No. 6 40257 175780 PORENCEPHALY, familial HEMIPLEGIA, INFANTILE infantilecerebral palsy 343 cerebral congenital spastic paralysis (cerebral) 343 http://www.pathinfo.com/cgi-bin/lh.cgi?tx=hemiplegia

57. THE LIGHTNING HYPERTEXT OF DISEASE. No. 8 15737 SYNONYMS familial spastic paraplegia syndrome Hereditary spastic paraplegiaStrumpellLorrain SYNONYMS Lower paraplegia paralysis of both http://www.pathinfo.com/cgi-bin/lh.cgi?tx=paraplegia

58. ENLmedical.com: Conditions And Concerns: Medical Encyclopedia: Familial Periodic and Tests The health care provider may suspect familial periodic paralysis basedon a Weakness is flaccid rather than spastic and is greater in the http://www.enlmedical.com/article/000312.htm

Medical Dictionary Naturapathic Glossary Aphrodisiacs Immune System ... Table of content Familial periodic paralysis Causes and Risks: Familial periodic paralysis is a condition of intermittent episodes of paralysis or muscle weakness that occurs in multiple members of a family group. Many (but not all) cases of familial periodic paralysis are termed "hypokalemic" periodic paralysis. Hypokalemic periodic paralysis occurs as an inherited condition. In most cases, it is inherited as an autosomal dominant disorder (only one parent must transmit the gene). In other cases, the disorder appears sporadically in a family group. The disorder involves attacks of muscle weakness or paralysis alternating with periods of normal muscle function. Attacks usually begin in adolescence but can occur before age 10. Attacks of intermittent weakness that do not begin until adulthood are rare and usually caused by other disorders. The frequency of attacks varies from daily to yearly. Episodes of muscle weakness may last for a few hours or persist for several days. During an attack of muscle weakness, there is a low level of potassium in the bloodstream (serum).

59. Neurologic Manifestations Cure paralysis Now; Worlds Wheelchair Culture; Spinal Cord Injury Univ of Michigan(US); Hereditary spastic Paraplegia/familial spastic Paraperesis C http://www.mic.ki.se/Diseases/c10.597.html

search help staff Neurologic Manifestations 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. Communication Disorders Int'l Dyslexia Association, IDA , including the What is Dyslexia? Children and Adults with Dyslexia - Educational Issues - ERIC-EC The British Dyslexia Association - (UK) Dyslexia - The Gift Dyslexia Teacher JM Kuster Dyslexia Resources G Row ] - (UK) The British Dyslexia Association The American Hyperlexia Association The Canadian Hyperlexia Association Hyperlexia and Language Disorders C Miller Learning disabilities in mathematics (Dyscalculia) - LD Online Dyscalculia .org Communication Issues Associated with Aging D Kergil ]- Puget Sound Univ. About the Brain and Language Earles et al. ] - Furman College (US) Speech Disorders - Healthtouch , a few chapters online from the book [ TD Kehoe Stuttering Home Page [ ] - via Mankato State Univ. The Stuttering Foundation of America Information on Stuttering SD Thiele The National Center for Stuttering - (US) The Stuttering Page at East Carolina University (US) The British Stammering Association - (UK) The Association for Research into Stammering in Childhood CAPS - Canadian Assoc. for People Who Stutter (CA)

60. Birth Disorder Information Directory - P Paroxysmal NonKinesigenic Dyskinesia See Choreoathetosis, familial Paroxysmal. PowellVenencie Gordon Syndrome (Keratoderma Palmoplantar spastic paralysis) http://www.bdid.com/defectp.htm

HOME P P-4 Deletion Syndrome A nationally recognized not-for-profit pre-school and therapeutic center for children with and without developmental delays ages 18 months to five years p47-PHOX, Deficiency of See Granulomatous Disease, Chronic, Autosomal Cytochrome-b-Positive Form, Type I p67-PHOX, Deficiency of See Granulomatous Disease, Chronic, Autosomal Cytochrome-b-Positive Form, Type II Pachydermopreiostosis (Hypertrophic Osteoarthropathy, Primary or Idiopathic) PACHYDERMOPERIOSTOSIS; PDP Pachyonychia Congenita See Jadassohn Lewandowsky Syndrome Pagod Syndrome See Kennerknecht Sorgo Oberhoffer Syndrome Pagon Bird Detter Syndrome (Anemia Sideroblastic Spinocerebellar Ataxia) Anemia sideroblastic spinocerebellar ataxia ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA; ASAT Pagon Syndrome See Walker Warburg Syndrome Pallister Syndrome See Schinzel Syndrome Pallister Hall Syndrome (Hypothalamic Hamartoblastoma, Hypopituitarism, Imperperforate Anus, and Postaxial Polydactyly) Pallister Hall syndrome:early diagnosis and natural history PALLISTER-HALL SYNDROME; PHS Also see McKusick Kaufman Syndrome Pallister Killian Syndrome V-KI-RAS2 KIRSTEN RAT SARCOMA 2 VIRAL ONCOGENE HOMOLOG; KRAS2

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 3     41-60 of 92    Back | 1  | 2  | 3  | 4  | 5  | Next 20