21. Hereditary Spastic Paraplegia Hereditary spastic paraplegia (HSP), also called familial spastic paralysis,refers to a group of genetic disorders. http://neurology.health-cares.net/hereditary-spastic-paraplegia.php

22. List Of Neurological Disorders: Information From Answers.com Fabry s disease Fahr s syndrome Fainting; familial spastic paralysis;Febrile seizures; Fisher syndrome; Friedreich s ataxia http://www.answers.com/topic/list-of-neurological-disorders

showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Wikipedia Mentioned In Or search: - The Web - Images - News - Blogs - Shopping List of neurological disorders Wikipedia List of neurological disorders This is a list of major and frequently observed neurological disorders (e.g. Alzheimer's disease ), symptoms (e.g. back pain ), signs (e.g. aphasia ) and syndromes (e.g. Aicardi syndrome Contents: Top A B C ... Z A Acquired Epileptiform Aphasia Acute Disseminated Encephalomyelitis Adrenoleukodystrophy Agenesis of the corpus callosum Agnosia ... Alzheimer's disease Amyotrophic lateral sclerosis (see Motor Neurone Disease Anencephaly Angelman syndrome Angiomatosis Anoxia Aphasia Apraxia Arachnoid cyst s Arachnoiditis Arnold-Chiari malformation Arteriovenous malformation Asperger's syndrome Ataxia Telangiectasia Attention Deficit Hyperactivity Disorder Autism Auditory processing disorder Autonomic Dysfunction B Back Pain Batten disease Behcet's disease Bell's palsy Benign Essential Blepharospasm Benign Focal Amyotrophy Benign Intracranial Hypertension BFPP Binswanger's disease Blepharospasm Bloch-Sulzberger syndrome Brachial plexus injury Brain abscess Brain injury Brain tumor Spinal tumor ... Brown-Sequard syndrome C Canavan disease Carpal tunnel syndrome (CTS) Causalgia Central pain syndrome Central pontine myelinolysis Cephalic disorder Cerebral aneurysm Cerebral arteriosclerosis Cerebral atrophy Cerebral gigantism Cerebral palsy Charcot-Marie-Tooth disease Chiari malformation Chorea Chronic inflammatory demyelinating polyneuropathy

23. Alpers' Disease: Definition And Much More From Answers.com progressive cerebral poliodystrophy n. A familial spastic paralysis of theextremities occurring in infants and young children in which seizures, http://www.answers.com/topic/alpers-disease

showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Medical Wikipedia Mentioned In Or search: - The Web - Images - News - Blogs - Shopping Alpers' disease Medical progressive cerebral poliodystrophy n. A familial spastic paralysis of the extremities occurring in infants and young children in which seizures, blindness, and deafness develop during the first year of life, accompanied by progressive destruction and degeneration of neurons of the cerebral cortex. Also called Alpers' disease Christensen-Krabbe disease Wikipedia Alpers' disease Alpers' disease , also called progressive infantile poliodystrophy , is a progressive degenerative disease of the central nervous system that occurs in infants and children. It is an autosomal recessive disorder that is sometimes seen in siblings. First signs of the disease, which include intractable seizures and failure to meet meaningful developmental milestones, usually occur in infancy, after the first year of life, but sometimes as late as the fifth year. Primary symptoms of the disease are developmental delay, progressive mental retardation , hypotonia (low muscle tone), spasticity (stiffness of the limbs) possibly leading to quadriplegia , and progressive dementia . Seizures may include epilepsia partialis continua, a type of seizure that consists of repeated myoclonic (muscle) jerks.

24. Neurological Diseases And Disorders Hereditary Spastic Paraplegia (also called familial spastic paralysis).Hereditary Spastic Paraplegia Fact sheet with a description of these disease that http://home.earthlink.net/~electrikmonk/Neuro/inDis.htm

25. HEALTHMEDNET ILLNESS AND DISEASE URL DIRECTORY familial spastic paralysis. http//directory.ansme.com/health/168.html familial spastic paralysis@ (6). http//search.aol.com/aolcom/browse?id=43348 http://www.healthmednet.com/FAL-FHS.htm

26. Neurological Disorders - Medical Encyclopedia Fabry s disease; Fahr s syndrome; Fainting; familial spastic paralysis;Febrile seizures; Fisher syndrome; Friedreich s ataxia http://www.nursingstudy.com/encyclopedia/list_of_neurological_disorders.html

Medical Encyclopedia List of Topics: Anatomy Disabilities ... Surgical Procedures Neurological Disorders This is a list of major and frequently observed neurological disorders (e.g. Alzheimer's disease ), symptoms (e.g. back pain ), signs (e.g. aphasia ) and syndromes (e.g. Aicardi syndrome). A B C D ... Z A Acquired Epileptiform Aphasia Acute Disseminated Encephalomyelitis Adrenoleukodystrophy Agenesis of the corpus callosum Agnosia Aicardi syndrome Alexander disease Alpers' disease Alternating hemiplegia Alzheimer's disease Amyotrophic lateral sclerosis (see Motor Neurone Disease Anencephaly Angelman syndrome Angiomatosis Anoxia Aphasia Apraxia Arachnoid Cysts Arachnoiditis Arnold-Chiari malformation Arteriovenous malformation Asperger syndrome Ataxia Telangiectasia Attention Deficit Hyperactivity Disorder Autism Autonomic Dysfunction B Back Pain Batten disease Behcet's disease Bell's palsy Benign Essential Blepharospasm Benign Focal Amyotrophy Benign Intracranial Hypertension Binswanger's disease Blepharospasm Bloch-Sulzberger syndrome Brachial plexus injury Brain abscess Brain injury Brain tumor Spinal tumor Brown-Sequard syndrome C Canavan disease Carpal tunnel syndrome CTS Causalgia Central pain syndrome Central pontine myelinolysis Cephalic disorder Cerebral aneurysm Cerebral arteriosclerosis Cerebral atrophy

27. Encyclopedia: List Of Neurological Disorders Fabry s disease Fahr s syndrome Fainting; familial spastic paralysis Hereditary spastic paraplegia (HSP), also called familial spastic paraparesis http://www.nationmaster.com/encyclopedia/List-of-neurological-disorders

Supporter Benefits Signup Login Sources ... Pies Related Articles People who viewed "List of neurological disorders" also viewed: List of diseases starting with B List of rare diseases starting with A Williams syndrome Shy_Drager syndrome ... Canavan disease What's new? Our next offering Latest newsletter Student area Lesson plans Recent Updates Rafael Nadal Rachel Maddow RPG Maker Quinoa ... More Recent Articles Top Graphs Richest Most Murderous Most Taxed Most Populous ... More Stats Encyclopedia: List of neurological disorders Updated 54 days 15 hours 33 minutes ago. Other descriptions of List of neurological disorders This is a list of major and frequently observed neurological disorders (e.g. Alzheimer's disease ), symptoms (e.g. back pain ), signs (e.g. aphasia ) and syndromes (e.g. Aicardi syndrome Neurology is a branch of medicine dealing with disorders of the central and peripheral nervous systems. ... Back pain is pain felt in the back that may come from the spine, muscles, nerves, or other structures in the back. ... Aphasia is a loss or impairment of the ability to produce or comprehend language, due to brain damage. ...

28. List Of Neurological Disorders -- Facts, Info, And Encyclopedia Article familial spastic paralysis (Click link for more info and facts about Febrileseizures) Febrile seizures Fisher syndrome (Click link for more info and facts http://www.absoluteastronomy.com/encyclopedia/L/Li/List_of_neurological_disorder

List of neurological disorders [Categories: Psychiatric disorders, Lists of diseases] This is a list of major and frequently observed (A disorder of the nervous system) neurological disorder s (e.g. (Click link for more info and facts about Alzheimer's disease) Alzheimer's disease ), symptoms (e.g. (Click link for more info and facts about back pain) back pain ), signs (e.g. (Inability to use or understand language (spoken or written) because of a brain lesion) aphasia ) and syndromes (e.g. (Click link for more info and facts about Aicardi syndrome) Aicardi syndrome A Acquired Epileptiform Aphasia (Click link for more info and facts about Acute Disseminated Encephalomyelitis) Acute Disseminated Encephalomyelitis (Click link for more info and facts about Adrenoleukodystrophy) Adrenoleukodystrophy (Click link for more info and facts about Agenesis of the corpus callosum) Agenesis of the corpus callosum (Inability to recognize objects by use of the senses) Agnosia (Click link for more info and facts about Aicardi syndrome) Aicardi syndrome (Click link for more info and facts about Alexander disease) Alexander disease (Click link for more info and facts about Alpers' disease) Alpers' disease (Click link for more info and facts about Alternating hemiplegia) Alternating hemiplegia (Click link for more info and facts about Alzheimer's disease) Alzheimer's disease Amyotrophic lateral sclerosis (see (Click link for more info and facts about Motor Neurone Disease) Motor Neurone Disease (A defect in brain development resulting in small or missing brain hemispheres)

29. Disorders Index: National Institute Of Neurological Disorders And Stroke (NINDS) Familial Periodic Paralyses familial spastic paralysis Febrile Seizures Fisher Syndrome Floppy Infant Syndrome Friedreich s Ataxia http://accessible.ninds.nih.gov/disorders/disorder_index.htm

Disorders - National Institute of Neurological Disorders and Stroke (NINDS) Skip menus Main sections of the NINDS web site Home About NINDS Disorders-you are in this section Funding ... Jobs and Training You are here: Home Disorders Disorders section pages and search Image Description Science For the Brain The nation's leading supporter of biomedical research on disorders of the brain and nervous system. More about a disorder Clinical Trials Research Literature Press Releases NINDS Search (search help) Contact Us My Privacy NINDS is part of the National Institutes of Health Content for this page Browse All Disorders (includes synonyms and research topics) Request mailed brochures Index Disorders beginning with the letters: A to F G to L M to S T to Z A To F - Select first letter of topic: A B C D ... F G To L - Select first letter of topic: G H I J ... L M To S - Select first letter of topic: M N O P ... S T To Z - Select first letter of topic: T U V W ... Z List of disorders beginning with the letter A Absence of the Septum Pellucidum Acquired Epileptiform Aphasia Acute Disseminated Encephalomyelitis ADHD ... Return to index Select a letter to jump to the disorder or return to top of page A B C D ... Z List of disorders beginning with the letter B Back Pain Barth Syndrome Batten Disease Behcet's Disease ... Return to index Select a letter to jump to the disorder or return to top of page A B C D ... Z List of disorders beginning with the letter C Canavan Disease Carpal Tunnel Syndrome Causalgia Cavernomas ... Return to index Select a letter to jump to the disorder or return to

30. Introduction: Hereditary Spastic Paraplegia - CureResearch.com Hereditary Spastic Paraplegia Hereditary spastic paraplegia (HSP), also calledfamilial spastic paralysis, refers to a group of genetic disorders that are http://www.cureresearch.com/h/hereditary_spastic_paraplegia/intro.htm

IMPORTANT! Use of this site is subject to our Home Contents Diseases Search Search: Condition Lists By Organ By Class By Prevalence By Deaths ... Full List Current chapter: Hereditary Spastic Paraplegia Next sections Basic Summary for Hereditary Spastic Paraplegia Prognosis of Hereditary Spastic Paraplegia Symptoms of Hereditary Spastic Paraplegia Misdiagnosis of Hereditary Spastic Paraplegia ... Associated Conditions of Hereditary Spastic Paraplegia Next chapters: Porencephaly Hydrocephalus Inclusion Body Myositis Incontinentia Pigmenti ... Malpractice Introduction: Hereditary Spastic Paraplegia Hereditary Spastic Paraplegia: Genetic defect causing leg weakness and other problems. Hereditary Spastic Paraplegia: Hereditary spastic paraplegia (HSP), also called familial spastic paralysis, refers to a group of genetic disorders that are characterized by progressive weakness and spasticity (stiffness) of the legs. Researching symptoms of Hereditary Spastic Paraplegia: Further information about the symptoms of Hereditary Spastic Paraplegia is available including a list of symptoms of Hereditary Spastic Paraplegia , other diseases that might have similar symptoms in differential diagnosis of Hereditary Spastic Paraplegia , or alternatively return to research other symptoms in the symptom center Misdiagnosis and Hereditary Spastic Paraplegia: Research more detailed information about misdiagnosis of Hereditary Spastic Paraplegia , or research misdiagnosis of other diseases Treatments for Hereditary Spastic Paraplegia:

31. The World Diseases A 2 Z Names By Countrylinks And Dr Impex Familial Hypercholesterolemia. familial spastic paralysis. Fanconi Anemia.Farsightedness. Fatigue Syndrome, Chronic. Fatty Oxidation Disorders http://www.countrylinks.biz/diseases.htm

Country Links Dr Impex free on-line Services Note: search with CTRL + F A Aarskog Syndrome Aase Syndrome Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Achilles Tendonitis Achondroplasia Acoustic Neuroma Acromegaly Activated Protein C Resistance Acute Idiopathic Polyneuritis ADD and ADHD Addiction and Recovery Addison's Disease Adiposis Dolorosa Adjustment Disorders Adrenoleukodystrophy Agnosia Agoraphobia Aicardi Syndrome AIDS Alagille Syndrome Albinism Alcoholism Alexander Disease Alkaptonuria Allergies Alopecia Alpers' Disease Alpha1 Antitrypsin Deficiency Alport Syndrome Alstrom Syndrome Alternating Hemiplegia Altophobia Alzheimer's Amblyopia Amputee Amyloidosis Amyoplasia Congenita Amyotrophic Lateral Sclerosis Anal Fissures Anemia Anencephaly Aneurysm Angina Pectoris Anophthalmos Anorexia Anosmia Anterior Knee Pain Syndrome Antiphospholipid Syndrome Anxiety Aortic Valve Disease Apert Syndrome Aphasia Aplastic Anemia Apnea, Sleep Appendicitis Arrhythmia Arteriohepatic Dysplasia Arthritis Arthrogryposis Asbestosis Asperger's Syndrome Aspergillosis Asthma Atherosclerosis Athlete's Foot Atrial Fibrillation Attachment Disorder Attention Deficit Disorder Autism Auto Immune Disorders Aviophobia Aviatophobia B Bacillary Angiomatosis Back Disorders Bad Breath Balanitis Baldness Barth Syndrome Bassen Kornzweig Syndrome Batten Disease Beckwith-Wiedemann Syndrome Behcet's Syndrome Bell's Palsy Benign Breast Lumps Benign Prostatic Hyperplasia Berger's Disease Beriberi Beryllium Disease

32. Paraplegia, Hereditary Spastic familial spastic Paraplegia; FSP; HSP; spastic Spinal familial paralysis;Strumpell s familial Paraplegia; StrumpellLorrain familial Spasmodic Paraplegia http://my.webmd.com/hw/health_guide_atoz/nord398.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center XML News via RSS Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Health Tools Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map You are in Medical Library Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... For a Complete Report Paraplegia, Hereditary Spastic Important It is possible that the main title of the report Paraplegia, Hereditary Spastic 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. Synonyms Familial Spastic Paraplegia FSP HSP Spastic Spinal Familial Paralysis Strumpell's Familial Paraplegia Strumpell-Lorrain Familial Spasmodic Paraplegia Strumpell Disease Strumpell-Lorraine Syndrome Disorder Subdivisions Hereditary spastic paraplegia, complicated Hereditary spastic paraplegia, uncomplicated ("pure")

33. Clinical Trial: Characteristics Of Idiopathic Familial Voice Disorders familial vocal fold paralysis can be a lifethreatening disorder that can causedifficulty with vocal fold movement for spastic Dysphonia Voice Disorder http://www.clinicaltrials.gov/ct/gui/show/NCT00001552

Home Search Browse Resources ... About Characteristics of Idiopathic Familial Voice Disorders This study is currently recruiting patients. Verified by National Institutes of Health Clinical Center (CC) May 16, 2005 Sponsored by: National Institute of Neurological Disorders and Stroke (NINDS) Information provided by: National Institutes of Health Clinical Center (CC) ClinicalTrials.gov Identifier: Purpose The purpose the study is to determine the genetic causes of specific voice disorders that run in families. Researchers are particularly interested in two conditions; 1. Spasmodic dysphonia 2. Vocal fold paralysis Familial vocal fold paralysis can be a life-threatening disorder that can cause difficulty with vocal fold movement for breathing and voice and sometimes for swallowing. Studies are ongoing at the NIH to better understand the pathophysiology and to relate it to the genetic pattern of inheritance. Families are being recruited to participate in these studies and are being provided with further information on the disorder and genetic counseling if desired. Physician referral is requested for affected members of families with vocal fold paralysis of an unknown cause occurring over at least 2 generations. All travel, lodging, examination and counseling costs are covered for both affected and unaffected members of a family. Examinations include: voice, laryngeal, neurological, electrodiagnostic testing, genetic counseling, and radiological studies. Condition

34. Strümpell-Lorrain Disease (www.whonamedit.com) Facial spastic paraplegia, familial spastic paraplegia, familial spastic paraparesis, spastic familial paraplegia, spastic familial paralysis, http://www.whonamedit.com/synd.cfm/1759.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. A recommendation: Hypography is an open community about science and all things related Strümpell-Lorrain disease Also known as: Strümpell's familial paraplegia Strümpell-Lorrain type Strümpell-Lorrain familial spasmodic paraplegia Synonyms: Facial spastic paraplegia, familial spastic paraplegia, familial spastic paraparesis, French settlement dsease, hereditary spastic paraparesis, hereditary spastic paraplegia, paraplégie spasmodique familiale (French), spasmodic infantile paraplegia, spastic congenital paraplegia, spastic familial paraplegia, spastic familial paralysis, spastic infantile paralysis, spastic spinal familial paralysis Associated persons: Maurice Lorrain Ernst Adolf Gustav Gottfried von Strümpell Description: A familial form of paraplegia characterized by spasticity – hypertonicity and weakness - limited mainly to the lower extremities. This is followed by involvement of upper limbs, dysarthria, and dysphagia. Degeneration of the pyramidal tract of the spinal cord and of the columns of Goll is the principal histological feature. Ocular complications may include strabismus, pupillary defects, macular degeneration, and optic atrophy. Occurs in either sex, but is more common in young males. This is a very rare disease, with a frequency of about 1 in 30.000 persons. It is most common in Nordic countries. Inheritance is autosomal recessive (usually), or sex-linked.

35. Www.whonamedit.com A familial form of intermittent hypocalcaemic paralysis. spastic paraplegiaof the lower extremities and mental retardation in children with congenital http://www.whonamedit.com/syndlist.cfm/103

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. A recommendation: Hypography is an open community about science and all things related Eponyms in category: Paralysis 98 main and alternative entries found. Albert Mouchet's syndrome (Mouchet's paralysis) A historical term for a paralysis of the cubital nerve following fractures of the external condyle of the humerus in childhood. Albright-Hadorn syndrome A now obsolete eponym used to indicate the occurrence of paroxysmal hypokalemic muscular paralysis associated with osteomalacia in patients with renal tubular acidosis. Balint's syndrome A syndrome combining paralysis of visual fixation, optic ataxia, and impairment of visual fixation. Balint-Holmes syndrome (Balint's syndrome) A syndrome combining paralysis of visual fixation, optic ataxia, and impairment of visual fixation.

36. Hereditary Spastic Paraplegia Hereditary spastic Paraplegia / familial spastic Paraparesis 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

37. SPF - Spastic Paraplegia Foundation Home Page HSP is also known as Hereditary spastic Paraparesis, familial spastic Strümpell Disease, Hereditary CharcotDisease, spastic Spinal paralysis, http://sp-foundation.org/

Welcome to the Spastic Paraplegia Foundation, Inc. (SPF) Alerts and Breaking News '05 Nat'l Sept. 30 - Oct. 2, Columbus, OH Ohio TeamWalk Local TeamWalk Connections: New England Canada MidAmerica Northwest ... RGM for SPF Golf Classic, MD Quilt Raffle E-News Bulletins: Aug.-Sept. June-July April-May Meet John K. Fink, MD, SPF Medical Advisor and Teepu Siddique, MD, top researchers of HSP and PLS. Also: programs on assistive technology and adaptive equipment and more. Details here The SPF is the only non-profit organization in the Americas dedicated to neurodegenerative disorders called Primary Lateral Sclerosis (PLS) and Hereditary Spastic Paraplegia* (HSP). These diseases slowly attack one's ability to walk, causing levels of disability ranging from needing a cane to a wheelchair. In PLS, they generally also rob people of their ability to use their hands and arms, and even to speak. In very rare forms of HSP, they can cause mental retardation, dementia, epilepsy or other neurological problems. The Spastic Paraplegia Foundation is a 100% volunteer-managed and operated organization devoted to finding the causes and cures for these diseases and to providing critical information and support programs to people affected by them. We are enormously grateful to our

38. Hereditary Spastic Paraplegia familial spastic Paraplegia; spastic Spinal familial paralysis; Strumpell Disease;StrumpellLorrain familial Spasmodic Paraplegia; Strumpell-Lorraine http://www.icongrouponline.com/health/Hereditary_Spastic_Paraplegia.html

ICON Health Publications Official Health Sourcebooks Search ICON Health Titles: 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 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 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

39. Familial Spastic Paraplegia - For Patients And Families - The paraparesis (weakness), or paraplegia (paralysis), especially when similar Currently physicians use the familial spastic paraparesis/ paraplegia http://www.chg.duke.edu/patients/fsp.html

40. Genetic Localization Of A New Locus For Recessive Familial Spastic Paraparesis T OBJECTIVE To characterize a new gene locus for familial spastic paraparesis (FSP) . Infantile ascending hereditary spastic paralysis (IAHSP) Clinical http://www.neurology.org/cgi/content/abstract/53/1/50

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Figures Only Full Text Correspondence: Submit a response ... Citation Map Services Email this article 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 Murillo, F. M. Articles by Hoffman, E. P. Neurology American Academy of Neurology Articles Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15 H. Kobayashi, MD, PhD E. Pegoraro, MD, PhD G. Galluzzi, PhD G. Creel, MD C. Mariani, MD E. Farina, MD E. Ricci, MD G. Alfonso, MD R. M. Pauli, MD, PhD and E. P. Hoffman, PhD OBJECTIVE: To characterize a new gene locus for familial spastic paraparesis (FSP). BACKGROUND: FSP is a genetically heterogeneous group of upper motor neuron syndromes. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked disorder. Four loci for autosomal dominant FSP have been genetically mapped, and

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