21. F Familial Dysautonomia; @ Familial Hypercholesterolemia; @ FamilialMediterranean Fever. @ familial spastic paralysis; @ Fanconi Anemia; http://www.ad.com/Health/Conditions_and_Diseases/F/

search Top Categories: Fabry's Disease @ Facial Differences @ Facial Paralysis @ Faciocutaneoskeletal Syndrome ... @ Funnel Chest AD.COM Web Directory is based on ODP - Open Directory Project data. No proprietary software was used in the development of this web site. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor

22. Hereditary Spastic Paraplegia : Meddie Health Search (Rating 10.00 Votes 1) Rate It. MCW Healthlink HSP An article abouthereditary spastic paraplegia, also called familial spastic paralysis. http://www.meddie.com/search/Health/Conditions_and_Diseases/Genetic_Disorders/He

HOME ADD A LINK MODIFY A LINK NEW LINKS ... TOP RATED Search Meddie: the entire directory only this category More search options Home Health Conditions and Diseases ... Genetic Disorders : Hereditary Spastic Paraplegia ITEMS: LINKS: GeneClinics: An Overview In depth details about hereditary spastic paraplegia. Includes a summary, definition, categories, diagnosis, genetic counseling and resources. (Rating: 0.00 Votes: 0) Rate It Hereditary Spastic Paraplegia In depth look at this disease by John K. Fink, M.D., including genetic analysis, clinical features and FAQs. (Rating: 0.00 Votes: 0) Rate It Hereditary Spastic Paraplegia HSP information sheet compiled by the National Institute of Neurological Disorders and Stroke. (Rating: 0.00 Votes: 0) Rate It HSPinfo.org Information about hereditary spastic paraplegia, and disability resources. Includes newsletters, news, announcements, research and support. (Rating: 10.00 Votes: 1) Rate It MCW Healthlink: HSP An article about hereditary spastic paraplegia, also called familial spastic paralysis. (Rating: 6.00 Votes: 1)

23. Browsing Health Conditions And Diseases F Category V Leiden Fainting Fallen Bladder Familial Dysautonomia Familial HypercholesterolemiaFamilial Mediterranean Fever, familial spastic paralysis Fanconi Anemia http://www.uksprite.com/search/search/Health/Conditions_and_Diseases/F/

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24. Hereditary Spastic Paraplegia Website Results :: Linkspider UK counseling and resources. MCW Healthlink HSP An article about hereditaryspastic paraplegia, also called familial spastic paralysis. http://www.linkspider.co.uk/Health/ConditionsandDiseases/GeneticDisorders/Heredi

Hereditary Spastic Paraplegia Websites from Linkspider UK Keyword: Hereditary Spastic Paraplegia Linkspider UK Directory Hereditary Spastic Paraplegia Search for Directory Tree: Top Health Conditions and Diseases Genetic Disorders : Hereditary Spastic Paraplegia (6) Add URL Advertise Here! Personalize Amazon ... HSPinfo.org - Information about hereditary spastic paraplegia, and disability resources. Includes newsletters, news, announcements, research and support. Hereditary Spastic Paraplegia - In depth look at this disease by John K. Fink, M.D., including genetic analysis, clinical features and FAQs. Hereditary Spastic Paraplegia - HSP information sheet compiled by the National Institute of Neurological Disorders and Stroke. The FSP Support Group - For people suffering from Familial Spastic Paraplegia. Includes a newsletter, discussion forum, links, and contact details. GeneClinics: An Overview - In depth details about hereditary spastic paraplegia. Includes a summary, definition, categories, diagnosis, genetic counseling and resources. MCW Healthlink: HSP - An article about hereditary spastic paraplegia, also called familial spastic paralysis.

25. Katalog :  : Health : Conditions_and_Diseases : F :  - Netz-Tipp.De Familial Mediterranean Fever (*);familial spastic paralysis (*); Fanconi Anemia (*); Farsightedness http://www.netz-tipp.de/kat/Health/Conditions_and_Diseases/F/

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26. F Information Sites Familial Mediterranean Fever@; familial spastic paralysis@; FanconiAnemia@; Farsightedness@; Fatigue Syndrome, Chronic@; Fatty Oxidation http://www.medicalorg.com/ConditionsandDiseases/F/

MEDICALorg.com Search SPYorg.com (Not sure of spelling? Use first letters and * such as abc* or abcd* or abcde*) Match:.. All Any Format: Long Short Search Words: Top Health Conditions and Diseases : F Fabry's Disease Facial Differences Facial Paralysis Faciocutaneoskeletal Syndrome ... Funnel Chest Click Here for a fast ON-LINE APPLICATION Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor The content of the SPYorg.com directory is based on the Open Directory and is enhanced using Spyorg.com technology. Privacy Statement Add Your Site to SPYorg.com ADVERTISEMENT:

27. Medicalseek - Search Engine For The Healthcare Industry hspinfo.org/; MCW Healthlink HSP An article about hereditary spasticparaplegia, also called familial spastic paralysis. healthlink http://www.medicalseek.net/Conditions_and_Diseases_Genetic_Disorders_Hereditary_

CATEGORIES ADD A LINK ADVERTISE CONTACT US ... Genetic Disorders Hereditary Spastic Paraplegia Conditions and Diseases:Genetic Disorders:Hereditary Spastic Paraplegia GeneClinics: An Overview In depth details about hereditary spastic paraplegia. Includes a summary, definition, categories, diagnosis, genetic counseling and resources. geneclinics.org/profiles/hsp/ Hereditary Spastic Paraplegia HSP information sheet compiled by the National Institute of Neurological Disorders and Stroke. ninds.nih.gov/health_and_medical/disord... Hereditary Spastic Paraplegia In depth look at this disease by John K. Fink, M.D., including genetic analysis, clinical features and FAQs. med.umich.edu/hsp/ HSPinfo.org Information about hereditary spastic paraplegia, and disability resources. Includes newsletters, news, announcements, research and support. hspinfo.org/ MCW Healthlink: HSP An article about hereditary spastic paraplegia, also called familial spastic paralysis. healthlink.mcw.edu/article/921730935.html The FSP Support Group For people suffering from Familial Spastic Paraplegia. Includes a newsletter, discussion forum, links, and contact details. fspgroup.org

28. List Of Neurological Disorders - Wikipedia Encephalotrigeminal angiomatosis; Epilepsy; Erb's palsy; Essential tremor. F Fabry'sdisease; Fahr's syndrome; Fainting; familial spastic paralysis; Febrile seizures; http://www.wikipedia.org/wiki/List_of_neurological_disorders

Main Page Recent changes Edit this page Older versions Special pages Set my user preferences My watchlist Recently updated pages Upload image files Image list Registered users Site statistics Random article Orphaned articles Orphaned images Popular articles Most wanted articles Short articles Long articles Newly created articles Interlanguage links All pages by title Blocked IP addresses Maintenance page External book sources Printable version Talk Log in Help List of neurological disorders From Wikipedia, the free encyclopedia. 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 Acquired Epileptiform Aphasia Acute Disseminated Encephalomyelitis Adrenoleukodystrophy Agenesis of the corpus callosum ... Alzheimer's disease Amyotrophic lateral sclerosis (see Motor Neurone Disease Anencephaly Angelman syndrome Angiomatosis ... Autonomic Dysfunction B Back Pain Batten disease Behcet's disease Bell's palsy ... Brown-Sequard syndrome C Canavan disease Carpal tunnel syndrome CTS Causalgia ... Chronic inflammatory demyelinating polyneuropathy (CIDP) Chronic pain Chronic regional pain syndrome Coffin Lowry syndrome Coma, including Persistent Vegetative State

29. VADA GEZONDHEID En ZIEKTE - HEALTH And DISEASE SPASTIC PARAPLEGIA SP. See also HEREDITARY SPASTIC PARAPLEGIA HSP FAMILIALSPASTIC PARAPLEGIA FSP familial spastic paralysis See also PARAPLEGIA; http://www.vada.nl/medisch/medsnq.htm

VADA - GEZONDHEID en ZIEKTE HEALTH and DISEASE SN - SQ OPGELET - ATTENTION Patienten en leken die raadgevingen/adviezen/informatie zoeken via deze verzameling links wordt dringend geadviseerd de verzamelde informatie te bespreken met de (behandelend) arts/specialist/hulpverlener. Patients and lay persons 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. SNURKEN SNORING LASER ASSISTED UVULA PALATOPLASTY LAUP CONTINUOUS POSITIVE AIRWAY PRESSURE CPAP UPPER AIRWAY RESISTANCE SYNDROME UARS See also: SLAAPSTOORNISSEN See also: APNEU SLEEP APNOEA Snurken, oorzaken en behandeling Snurken Wat is: Snurken ... Snurken Veelbesproken onderwerp dat behalve de gezondheid van meer dan 300.000 Nederlanders, ook hun partners en naaste familie ongemak bezorgt Researchers Shed Light On Snoring, Stroke Risk Information about sleep and sleep disorders, including snoring and sleep apnea. Includes a self assessment quiz Sleepdisorders and Snoring Information about sleep and sleep disorders, including snoring and sleep apnea. Includes a self assessment quiz

30. DINO - Language: Englisch - Health - Conditions And Diseases - F Translate this page Dieser Link verweist auf eine Haupt-Kategorie Familial Mediterranean Fever DieserLink verweist auf eine Haupt-Kategorie familial spastic paralysis Dieser Link http://www.dino-online.de/dino_page_7d2196c29790afabc10cc0762522531b.html

Suche Profi-Suche Katalog Video ... Produkte Suchen: Web-Seiten Video Audio Bilder Produkte Schon gewusst? Hier suchen Sie in 2 Milliarden Webseiten. Live-Suche: Was suchen andere Dino-Besucher? You are here: DINO Language Englisch Health ... Conditions and Diseases F F Sprache/Language Categories Fabry's Disease Facial Differences Facial Paralysis Faciocutaneoskeletal Syndrome Faciogenitopopliteal Syndrome Factititious Disorders Factor V Leiden Fainting Fallen Bladder Familial Dysautonomia Familial Hypercholesterolemia Familial Mediterranean Fever Familial Spastic Paralysis Fanconi Anemia Farsightedness Fatigue Syndrome, Chronic Fatty Oxidation Disorders Febrile Seizure Feer Disease Female Pseudo-Turner Syndrome Fetal Alcohol Syndrome Fetal Face Syndrome Fibrocystic Breasts Fibromyalgia Fifth Disease Floating-Harbor Syndrome Flu Food Poisoning Foot Conditions Fractures Fragile X Syndrome Frey's Syndrome Friedreich Ataxia Fumarylacetoacetase Deficiency Disease Fungal Infections Funnel Chest This site is based on the Open Directory Project (ODP) Last update: 08. Jul. 2002, 18:00:37 o'clock

31. SearchUK - Finds It Fast! and support. MCW Healthlink HSP An article about hereditary spasticparaplegia, also called familial spastic paralysis. The FSP http://www.searchuk.com/104/521628.asp

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32. Familial Spastic Paraplegia - For Patients And Families - The Center For Human G is FSP/HSP? familial spastic paraparesis/paraplegia (FSP) and hereditary spastic paraparesis paraparesis (weakness), or paraplegia (paralysis), especially when similar symptoms http://www.chg.duke.edu/patients/fsp.html

For Patients and Families Familial Spastic Paraplegia/ Hereditary Spastic Paraplegia What is FSP/HSP? Genetics and HSP CHG Research Update on HSP HSP Study Participation ... Additional FSP/HSP Information What is FSP/HSP? Familial spastic paraparesis/paraplegia (FSP) and hereditary spastic paraparesis/paraplegia (HSP) are names applied to a group of degenerative neurological disorders characterized by specific walking problems. Physicians are now applying the diagnosis of hereditary spastic paraparesis/ paraplegia to patients whose leg muscles have symptoms of spasticity (stiffness and/or spasms), paraparesis (weakness), or paraplegia (paralysis), especially when similar symptoms occur in other members of the patient’s family due to inherited DNA changes (hereditary symptoms). Currently physicians use the familial spastic paraparesis/ paraplegia diagnosis for cases with similar symptoms that may result from family members’ exposure to shared environmental factors, rather than to genetic causes. FSP/HSP may vary from family to family and patient to patient.

33. HSPinfo.org - Hereditary Spastic Paraplegia Site Information about Hereditary spastic Paraplegia (familial spastic Paraparesis), and Disability Resources. Paraplegia, spastic Congenital Paraplegia, spastic Spinal familial paralysis, familial spastic Paraplegia, and French http://www.hspinfo.org/

Hereditary Spastic Paraplegia Familial Spastic Paraparesis Home E-Mail Search/Site Map Home What Is HSP? News and Announcements Research Living With HSP ... About This Site This site provides information about the disorder most commonly known as Hereditary Spastic Paraplegia or Hereditary Spastic Paraparesis (HSP) Familial Spastic Paraparesis (FSP) , or Strümpell-Lorrain . (See below for alternate names.*) There is currently no cure for HSP. However, researchers around the world are moving at a rapid pace to discover all the genes responsible for HSP and to develop effective treatments and cures. Additionally, HSP community volunteers organize meetings, conferences, fundraising events and social gatherings to help others and support researchers in the fight for a cure. Français Español Deutsch Portugese ... Italiano Select one of the languages above to translate the HSPinfo site into that language using a machine translation provided by Breaking News New HSP Gene Located: The locus of SPG20 has been mapped to chromosome 13q12.3. The mutation involves the encoding of spartin, and is responsible for a recessively inherited, complicated HSP (Troyer Syndrome) found in the Old Order Amish and associated with atrophy of hand muscles. Spartin shares similarity with spastin, a molecule that is commonly mutated in HSP. For more information, see:

34. ClinicalTrials.gov - Linking Patients To Medical Research: Study Details Spasmodic dysphonia 2. Vocal fold paralysis familial vocal fold of families with vocalfold paralysis of an Laryngeal Disease spastic Dysphonia Voice Disorder. http://www.clinicaltrials.gov/ct/gui/show/NCT00001552?order=26

35. The FSP Page - Familial Spastic Paraparesis Strümpell's familial paraplegia, spasmodic infantile paraplegia, spastic congenitalparaplegia, spastic spinal familial paralysis, hereditary spastic http://www.geocities.com/HotSprings/Spa/2847/

Welcome to the FSP Page! Familial Spastic Paraparesis Hereditary Spastic Paraplegia The FSP Page now has a new name and new location! Please vist our new site at: HSPinfo.org - http://hspinfo.org Hereditary spastic paraplegia is an inherited spinal cord disorder characterized by gradual development of muscle weakness, spasms, and stiffness of the legs. Symptoms may be first noticed in early childhood, or at any age though adulthood. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms may appear, or the weakness and stiffness may spread to other parts of the body. The terms "Hereditary Spastic Paraplegia" (HSP) and "Familial Spastic Paraparesis" (FSP) are the commonly used names in the United States for this disorder. For those in Europe, "Strumpell-Lorrain" is probably more common. These terms all refer to the same set of disorders. Other names associated with this disease are Strümpell-Lorrain familial spasmodic paraplegia, Strümpell's familial paraplegia, spasmodic infantile paraplegia, spastic congenital paraplegia, spastic spinal familial paralysis, hereditary spastic paraparesis, and familial spastic paraplegia.

36. HSPinfo.org - Hereditary Spastic Paraplegia Site Information about hereditary spastic paraplegia, and disability resources. Includes newsletters, news, Category Health Conditions and Diseases...... familial Paraplegia, Spasmodic Infantile Paraplegia, spastic Congenital Paraplegia,spastic Spinal familial paralysis, familial spastic Paraplegia, and French http://hspinfo.org/

Hereditary Spastic Paraplegia Familial Spastic Paraparesis Home E-Mail Search/Site Map Home What Is HSP? News and Announcements Research Living With HSP ... About This Site This site provides information about the disorder most commonly known as Hereditary Spastic Paraplegia or Hereditary Spastic Paraparesis (HSP) Familial Spastic Paraparesis (FSP) , or Strümpell-Lorrain . (See below for alternate names.*) There is currently no cure for HSP. However, researchers around the world are moving at a rapid pace to discover all the genes responsible for HSP and to develop effective treatments and cures. Additionally, HSP community volunteers organize meetings, conferences, fundraising events and social gatherings to help others and support researchers in the fight for a cure. Français Español Deutsch Portugese ... Italiano Select one of the languages above to translate the HSPinfo site into that language using a machine translation provided by Breaking News New HSP Gene Located: The locus of SPG20 has been mapped to chromosome 13q12.3. The mutation involves the encoding of spartin, and is responsible for a recessively inherited, complicated HSP (Troyer Syndrome) found in the Old Order Amish and associated with atrophy of hand muscles. Spartin shares similarity with spastin, a molecule that is commonly mutated in HSP. For more information, see:

37. General Informaton About HSP to) FSP familial spastic paraplegia or familial spastic paraparesis HSP DiseaseHereditary Charcot-Disease spastic Spinal paralysis Diplegia spinalis http://hspinfo.org/HSP.htm

Hereditary Spastic Paraplegia or Hereditary Spastic Paraparesis General Information Home E-Mail Search/Site Map Hereditary Spastic Paraplegia or Hereditary Spastic Paraparesis is a name used to represent a group of inherited degenerative spinal cord disorders characterized by a slow, gradual, progressive weakness and spasticity (stiffness) of the legs. Symptoms may be first noticed in early childhood, or at any age through adulthood. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the weakness and stiffness may spread to other parts of the body. Rate of progression and the severity of symptoms is quite variable even among members of the same family. Anticipation may occur in some families, with symptoms of the disorder beginning earlier and more severely in successive generations. HSP rarely results in complete loss of lower limb mobility, although mobility devices such as canes, walkers, or wheelchairs may be necessary. In some patients, the symptoms continue to increase throughout their life. For others, symptoms may begin in early childhood, worsen for a few years, then level off after adolescence. At the present time, diagnosis of HSP is generally a process of exclusion of other disorders, and observation of family history. However, a few of the gene locations have been found, and more are close to being identified. This will lead to the possibility (hopefully in the near future) of blood tests to confirm diagnosis. Blood testing for certain forms of the disorder can already be performed.

38. Strümpell-Lorrain Disease (www.whonamedit.com) French), spasmodic infantile paraplegia, spastic congenital paraplegia, spasticfamilial paraplegia, spastic familial paralysis, spastic infantile paralysis http://www.whonamedit.com/synd.cfm/1759.html

Home List categories Eponyms A-Z Biographies by country ... Contact 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. Bibliography: A. G. G. von Strümpell:

39. Erb-Charcot Paralysis (www.whonamedit.com) spastic paraplegia, spastic spinal paralysis, spastic tabes dorsalis syphilis withparaesthesia, spastic weakness, and pointed to the familial clustering of the http://www.whonamedit.com/synd.cfm/1748.html

Home List categories Eponyms A-Z Biographies by country ... Contact Erb-Charcot paralysis Also known as: Charcot-Erb disease Erb’s IV spastic spinal syphilitic paralysis Erb’s syndrome I Erb-Charcot syndrome Strümpell's disease Strümpell’s syndrome von Strümpell’s disease Synonyms: Amyotrophic syphilitic myelitis, paralysie spasmodique spinale d’Erb-Charcot (French), paralysis spinalis spastica, spastic paraplegia, spastic spinal paralysis, spastic tabes dorsalis, syphilitic poliomyelitis, vascular syphilis of the spinal cord. Associated persons: Jean-Martin Charcot Wilhelm Heinrich Erb Ernst Adolf Gustav Gottfried von Strümpell Description: A rare syndrome consisting of spinal syphilis with paraesthesia, spastic weakness, and tiredness of the legs associated with pain, sphincter disorders, exaggerated deep reflexes, muscle atrophy, sensory disorders, and paraplegia. Occurs in several forms. According to the original description, the syndrome is seen in young syphilitic patients usually six years or more after the initial infection. Onset of the paraplegia of the lower extremities is gradual. Prevalent in males. Differentiation of this condition from other neurological diseases is often impossible and is dependent upon evidence of syphilis in the blood or cerebrospinal fluid. Most cases either autosomal dominant or autosomal recessive, respectively x-linked recessive. Von Strümpell in 1886 pointed to the familial clustering of the condition.

40. Volume 67 January - December 1944 A form of familial presenile dementia with spastic paralysis. C . WorsterDrought, JG . Greenfield and WH . McMenemey. Pages 38 - 43. http://www3.oup.co.uk/jnls/supplements/braini/hdb/Volume_67/Issue_01/670038.sgm.

Volume 67: January - December 1944 Issue 1: March 1944 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

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