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Spinocerebellar Degenerations: more detail

Spinocerebellar degenerations: Proceedings of the International Symposium on Spinocerebellar Degenerations held October 12-14, 1978, Tokyo

Trh and Spinocerebellar Degeneration

Spinocerebellar Degenerations: The Ataxias and Spastic Paraplegias: Blue Books of Neurology Series, Volume 31 by Alexis Brice MD, Stefan-M. Pulst MD, 2007-05-23

Hereditary Neuropathies and Spinocerebellar Atrophies

The Spino-Cerebellar Degenerations by J G Greenfield, 1954-01-01

Advances in Research on Neurodegeneration.: Volume 7 (Journal of Neural Transmission Supplementum)

Handbook of Ataxia Disorders (Neurological Disease and Therapy)

lists with details

THE MERCK MANUAL, Sec. 14, Ch. 179, Disorders Of Movement
are hereditary; others are sporadic. spinocerebellar degenerations can be broadly categorized as predominantly spinal
http://www.merck.com/pubs/mmanual/section14/chapter179/179g.htm

Extractions: This Publication Is Searchable The Merck Manual of Diagnosis and Therapy Section 14. Neurologic Disorders Chapter 179. Disorders Of Movement Topics [General] Tremor Dyskinesias Drug-Induced Movement Disorders ... Idiopathic Orthostatic Hypotension And Shy-Drager Syndrome Cerebellar And Spinocerebellar Disorders Disorders of the cerebellum and its inflow or outflow pathways produce deficits in the rate, range, and force of movement. Anatomically, the cerebellum has three subdivisions. The archicerebellum (vestibulocerebellum) comprises the flocculonodular lobe, helps maintain equilibrium and coordinate eye-head-neck movements, and is closely interconnected with the vestibular nuclei. The midline vermis (paleocerebellum) helps coordinate movement of the trunk and legs. Vermis lesions result in abnormalities of stance and gait. The lateral hemispheres, which make up the neocerebellum, control ballistic and finely coordinated limb movements, predominantly of the arms. Signs of cerebellar disease are listed in Table 179-3.
1Up Health > Health Links Directory > Conditions And Diseases: Neurological Diso
Health Health Directory Conditions and Diseases Neurological Disorders Spinal Cord spinocerebellar degenerations (5)
http://www.1uphealth.com/links/spinal-cord-spinocerebellar-degenerations.html

Extractions: The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only they do not constitute endorsements of those other sites. Home Contact Us Privacy Links Directory
Olivopontocerebellar Atrophy
Cerebellar degenerations (also called spinocerebellar degenerations) can either be sporadic or heredofamilial.
http://www.medhelp.org/perl6/neuro/archive/15346.html

Extractions: : : Hello: : : Can you tell me what diagnostic test currently are used to diagnose and confirm OPCA? : : Thank you very much!! : Dear Dave: : Cerebellar degenerations (also called spinocerebellar degenerations) can either be sporadic or heredofamilial. Heredofamilial cerebellar degenerations can be either autosomal dominant (various types termed spinocerebellar ataxia = SCA 1 - 7, DRPLA, Machado-Joseph disease, etc) or autosomal recessive (Friedreich's ataxia, and some other rare types). : The syndrome of progressive ataxia (imbalance of gait, incoordination of hands, slurred speech), in association with some other characteristic abnormalities (peripheral neuropathy, optic atrophy, retinitis pigmentosa, dementia, corticospinal dysfunction, oculomotor dysfunction, etc) is seen with heredofamilial forms. Ataxia is associated with autonomic dysfunction and/or parkinsonian features in sporadic cases. Either sporadic or autosomal dominant forms of cerebellar degeneration can be associated with atrophy of the cerebellum, pons and inferior olives, either on MRI, or at autopsy. Hence, OPCA (olivopontocerebellar atrophy) is used as a descriptive term for these disorders.
BioMed Central | Abstract | Spinocerebellar Degenerations: An Update
Report spinocerebellar degenerations An Update Susan L Perlman MD Department ofNeurology, 300 UCLA Medical Plaza Suite B200, UCLA School of Medicine, Los
http://www.biomedcentral.com/1528-4042/2/331/abstract

Extractions: Over the past decade, the spinocerebellar degenerations have gone from a diverse group of loosely defined phenotypes to a family of diseases with many identifiable genotypes and the promise of gene-specific treatments. The evaluation of the spinocerebellar ataxias has been simplified, and the counseling of patients and families has been enhanced by the growing number of molecular diagnostic tests now available. Management strategies remain symptomatic and focused on rehabilitation, with empirical use of antioxidants based on research in other neuro-genetic diseases.
DIRECTORY.TERADEX.COM - Health/Fitness/Diseases/Neurological Disorders/Spinal Co
DIRECTORY / Health/Fitness / Diseases / Neurological Disorders / Spinal Cord / spinocerebellar degenerations (5)
http://directory.teradex.com/Health_Fitness/Diseases/Neurological_Disorders/Spin

Extractions: Search through: Entire site Spinocerebellar Degenerations Friedreich Ataxia DIRECTORY Health/Fitness Diseases ... Marinesco-Sjogren Syndrome - Information and a support group for families affected with this syndrome, a rare genetic disorder characterized by ataxia, cataracts, very small stature, and mental retardation.
BioMed Central | Full Text | Spinocerebellar Degenerations: An Update
Welcome guest user,
http://www.biomedcentral.com/1528-4042/2/331

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THE MERCK MANUAL, Sec. 14, Ch. 179, Disorders Of Movement
subdural hematoma, and degenerative disorders, including striatonigral degenerationand multiple systems atrophy (see spinocerebellar degenerations, below).
http://www.merck.com/pubs/mmanual/section14/chapter179/179e.htm

Extractions: (Shaking Palsy) An idiopathic, slowly progressive, degenerative CNS disorder characterized by slow and decreased movement, muscular rigidity, resting tremor, and postural instability. Etiology and Pathophysiology In primary Parkinson's disease, the pigmented neurons of the substantia nigra, locus caeruleus, and other brain stem dopaminergic cell groups are lost. The cause is not known. The loss of substantia nigra neurons, which project to the caudate nucleus and putamen, results in depletion of the neurotransmitter dopamine in these areas. Onset is generally after age 40, with increasing incidence in older age groups. Secondary parkinsonism results from loss of or interference with the action of dopamine in the basal ganglia due to other idiopathic degenerative diseases, drugs, or exogenous toxins. The most common cause of secondary parkinsonism is ingestion of antipsychotic drugs or reserpine, which produce parkinsonism by blocking dopamine receptors. Coadministration of an anticholinergic drug (eg, benztropine 0.2 to 2 mg po tid) or amantadine (100 mg po bid) may ameliorate the resulting symptoms. Less common causes include carbon monoxide or manganese poisoning, hydrocephalus, structural lesions (tumors, infarcts affecting the midbrain or basal ganglia), subdural hematoma, and degenerative disorders, including striatonigral degeneration and multiple systems atrophy (see
Spinocerebellar Degenerations
http//www.ncbi.nlm.nih.gov/genome/guide/HsChr9.shtml. 9 mutationsDysautonomia Friedreich_ataxia Torsion Dystonia 1 Fanconi_anemia,.
http://freesense.free.fr/Diseases/c/393.htm
Classes
heredodegenerative disorders, nervous system (31) muscular dystrophies(8); spinocerebellar degenerations (2). metabolism, inborn errors (25)
http://freesense.free.fr/Diseases/c/
Re: Re: Olivopontocerebellar Atrophy
The Neurology and Neurosurgery Forum ask the doctor medical forum for patients hosted by Med Help Intl. Cerebellar degenerations (also called spinocerebellar degenerations) can either be sporadic or heredofamilial.
http://www.medhelp.org/perl6/neuro/archive/15049.html

Extractions: : : Hello: : : Can you tell me what diagnostic test currently are used to diagnose and confirm OPCA? : : Thank you very much!! : Dear Dave: : Cerebellar degenerations (also called spinocerebellar degenerations) can either be sporadic or heredofamilial. Heredofamilial cerebellar degenerations can be either autosomal dominant (various types termed spinocerebellar ataxia = SCA 1 - 7, DRPLA, Machado-Joseph disease, etc) or autosomal recessive (Friedreich's ataxia, and some other rare types). : The syndrome of progressive ataxia (imbalance of gait, incoordination of hands, slurred speech), in association with some other characteristic abnormalities (peripheral neuropathy, optic atrophy, retinitis pigmentosa, dementia, corticospinal dysfunction, oculomotor dysfunction, etc) is seen with heredofamilial forms. Ataxia is associated with autonomic dysfunction and/or parkinsonian features in sporadic cases. Either sporadic or autosomal dominant forms of cerebellar degeneration can be associated with atrophy of the cerebellum, pons and inferior olives, either on MRI, or at autopsy. Hence, OPCA (olivopontocerebellar atrophy) is used as a descriptive term for these disorders.
Searchalot Directory For Spinocerebellar Degenerations
Searchalot, we search a lot, so you don't have too!
http://www.searchalot.com/Top/Health/ConditionsandDiseases/NeurologicalDisorders

Extractions: Home Search News Email Greetings Weather ... Global All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut Yahoo! Yahoo! Auctions Yahoo! News Yahooligans Zeal Sponsored Links Top Health Conditions and Diseases Neurological Disorders ... Spinal Cord : Spinocerebellar Degenerations Related Web Sites Marinesco-Sjogren Syndrome - Information and a support group for families affected with this syndrome, a rare genetic disorder characterized by ataxia, cataracts, very small stature, and mental retardation. All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut Yahoo!
Searchalot Directory For Spinal Cord
Myelitis (6). Spinal Muscular Atrophy (11); spinocerebellar degenerations (5); StiffPersonSyndrome (4); Syringomyelia (4); Tabes Dorsalis (2). Related Web Sites.
http://www.searchalot.com/Top/Health/ConditionsandDiseases/NeurologicalDisorders

Extractions: Home Search News Email Greetings Weather ... Global All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut Yahoo! Yahoo! Auctions Yahoo! News Yahooligans Zeal Sponsored Links Top Health Conditions and Diseases Neurological Disorders : Spinal Cord Related Web Sites Spinal Injuries Association - Offers a Spinal Chat Room, a Bulletin Board and factsheets for people with spinal injuries, paraplegics, tetraplegics, wheelchair users and walkers. Related Categories All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut Yahoo!
Www.nlm.nih.gov/cgi/mesh/2K/MB_cgi?term=Spinocerebellar+Degenerations
Similar pages Replaced Medical Subject Headings Sinus Thrombosis, (P), Sinus Thrombosis, Intracranial. Spinocerebellar Degeneration,(P), spinocerebellar degenerations. StiffMan Syndrome, (P), Stiff-Person Syndrome.
http://www.nlm.nih.gov/cgi/mesh/2K/MB_cgi?term=Spinocerebellar Degenerations
Conditions And Diseases: Neurological Disorders: Spinal Cord: Spinocerebellar De
Information on Conditions and Diseases, Neurological Disorders, Spinal Cord,spinocerebellar degenerations and much more Treasure Coast Health.
http://treasurecoasthealth.com/treasurecoasthealth.php/Health/Conditions_and_Dis

Extractions: Find Doctors on the Treasure Coast Select Specialty Ambulatory Care Anesthesiology Cardiology Dermatology Emergency Medicine Endocrinology Family Practice Gastroenterology Hematology/Oncology Infectious Diseases Internal Medicine Maxillofacial Surgery Neonatology Nephroology Neurology Neurosurgery Obstetrics/Gynecology Ophthalmology Orthopedic Surgery Otolaryngology Pathology Pediatics Physical Medicine Plastic Surgery Podiatry Psychiatry Psychology Pulmonary Radiation Oncology Radiology Rheumatology Surgery Thoracic Surgery Urology Vascular Surgery Select City Sebastian Palm Bay Vero Beach Fort Pierce Okeechobee Port St. Lucie Jensen Beach Stuart Palm City Hobe Sound Loxahatchee MENU Home Doctor Directory Health Resources Women Only ... About Us Ataxia Friedreich Ataxia Machado-Joseph Olivopontocerebellar Atrophy ... http://www.nutrisystem.com We have helped millions of people lose weight for more than 30 years. Lose up to 10 lbs. in your first month! Marinesco-Sjogren Syndrome - Information and a support group for families affected with this syndrome, a rare genetic disorder characterized by ataxia, cataracts, very small stature, and mental retardation.
Conditions And Diseases: Neurological Disorders: Spinal Cord | Treasure Coast He
Myelitis@ (6). Spinal Muscular Atrophy@ (11); spinocerebellar degenerations(5); StiffPerson Syndrome@ (4); Syringomyelia@ (4); Tabes Dorsalis (2).
http://treasurecoasthealth.com/treasurecoasthealth.php/Health/Conditions_and_Dis

Extractions: Find Doctors on the Treasure Coast Select Specialty Ambulatory Care Anesthesiology Cardiology Dermatology Emergency Medicine Endocrinology Family Practice Gastroenterology Hematology/Oncology Infectious Diseases Internal Medicine Maxillofacial Surgery Neonatology Nephroology Neurology Neurosurgery Obstetrics/Gynecology Ophthalmology Orthopedic Surgery Otolaryngology Pathology Pediatics Physical Medicine Plastic Surgery Podiatry Psychiatry Psychology Pulmonary Radiation Oncology Radiology Rheumatology Surgery Thoracic Surgery Urology Vascular Surgery Select City Sebastian Palm Bay Vero Beach Fort Pierce Okeechobee Port St. Lucie Jensen Beach Stuart Palm City Hobe Sound Loxahatchee MENU Home Doctor Directory Health Resources Women Only ... About Us See also: This category in other languages: Japanese Spanish http://www.nutrisystem.com
E-b-5
research is focused on diseases caused by expansions of CAG repeats encoding polyglutaminestretches, which include hereditary spinocerebellar degenerations.
http://www.nig.ac.jp/labs/AR98e/E/E-b-5.html
Volume 108 January - December 1985
Prevalence and pattern of spinocerebellar degenerations in Northeastern Libya.R . Sridharan , K . Radhakrishnan , PP . Ashok and ME . Mousa. Pages 831 - 844.
http://www3.oup.co.uk/jnls/supplements/braini/hdb/Volume_108/Issue_04/1080831.sg
Ues: Volume 108: January - December 1985: Issue 4: December 1985
Pages 817 830. Prevalence and pattern of spinocerebellar degenerations in North-easternLibya. R . Sridharan , K . Radhakrishnan , PP . Ashok and ME . Mousa
http://www3.oup.co.uk/jnls/supplements/braini/hdb/Volume_108/Issue_04/

Extractions: D Howard K Patterson S Franklin V Orchard-Lisle and J Morton Pages: R Sridharan K Radhakrishnan PP Ashok and ME Mousa Pages: CM Wiles PSJ Trend GT Spencer JA Morgan Hughes BD Lake and AD Patrick Pages: PJ Dyck JL Karnes J Daube P O'Brien and FJ Service Pages: HD Chung Pages: S Love and JM Jacobs Pages: C Kennard and AM Bronstein Pages: JZ Heckmatt CA Scurry D Hodes and V Dubowitz Pages: SC Gandevia Pages: B Williams and DW Morgan Pages: DY von Cramon N Hebel and U Schuri Pages: JA Ogden Pages: Involvement of the central nervous system in Schistosoma mansoni and Schistosoma haematobium infection. A review
Directory :: Look.com
spinocerebellar degenerations (5) Other Categories. Ataxia (10) FriedreichAtaxia (4) MachadoJoseph (6) Olivopontocerebellar Atrophy (4) Sites.
http://www.look.com/searchroute/directorysearch.asp?p=595030
Spinocerebellar Degenerations Website Results :: Linkspider UK
spinocerebellar degenerations Websites from the Linkspider UK. SpinocerebellarDegenerations Directory. Complete Results for Spinocerebellar
http://www.linkspider.co.uk/Health/ConditionsandDiseases/NeurologicalDisorders/S

Extractions: Directory Tree: Top Health Conditions and Diseases Neurological Disorders ... Spinal Cord : Spinocerebellar Degenerations (5) Add URL Advertise Here! Personalize Amazon ... Marinesco-Sjogren Syndrome - Information and a support group for families affected with this syndrome, a rare genetic disorder characterized by ataxia, cataracts, very small stature, and mental retardation.

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