21. MeSH-D Terms Associated To MeSH-C Term Cerebellar Diseases MeSHD terms associated to MeSH-C term cerebellar diseases, G2D Home the strength of the association of the corresponding term to cerebellar diseases. http://www.bork.embl-heidelberg.de/g2d/c2d.pl?Cerebellar_Diseases:unknown

22. References For Joubert Syndrome-1 With The MeSH Term Cerebellar References for Joubert syndrome1 with the MeSH term cerebellar diseases,G2D Home. PMID and date. Follow the link to see the corresponding entry by PubMed http://www.bork.embl-heidelberg.de/g2d/exam_mesh_disease.pl?Cerebellar_Diseases:

23. CEREBELM Cerebellar disease are recognized in the patient s inability to perform coordinated cerebellar diseases often lead to hypotonia of the muscles. http://www2.umdnj.edu/~paneuweb/cerebelm.htm

Maintained by David P. Crockett . E-mail suggestions to crockett@umdnj.edu (Revised 2/12/97) David P. Crockett, M.A., Ph.D. Department of Neuroscience and Cell Biology UMDNJ-Robert Wood Johnson Medical School Room R-306, Telephone: 235-3404 Notes on the cerebellum PA Neuroscience Home Page I. Introduction: 1. Cerebellum = 'little brain'; by weight is only 10% of the total brain and yet it contains more than half of all the neurons in the brain. 2. Highly regular, almost crystalline organization. 3. Cerebellar functions: The cerebellum acts as a 'comparator'; i.e., a device that compensates for errors by comparing intention with performance. The cerebellum is said to compare the central commands for movement with the actual movements themselves. Three features are important to keep in mind: a. The cerebellum receives information from brain sites that are involved in the planning of movements and commands for movements: corollary discharge b. The cerebellum receives information about motor performance; i.e., the results of the movement command, through sensory feedback arising in the periphery during the course of movement: reafference. The cerebellum is then in a position to compare the corollary discharge with reafference (the sensory feedback associated with the movement); if there is a mismatch, corrections may be made.

24. Margolis, Russell L. Psychopathology in degenerative cerebellar diseases A comparison to HuntingtonÆsdisease and normal controls, American Journal of Psychiatry, http://www.hopkinsmedicine.org/Psychiatry/Faculty/Margolis.html

Russell L. Margolis , M.D. Professor of Psychiatry and Neurology Director, Laboratory of Genetic Neurobiology Director, Neurogenetic Testing Laboratory Main Office Add. Administrative Assistant Education and Government Service ... Selected Publications Main Office Address Division of Neurobiology Department of Psychiatry and Behavioral Sciences CMSC 8-121 The Johns Hopkins Hospital 600 North Wolfe St. Baltimore, MD 21287-5371 Phone 410-614-4262 / Fax 410-614-0013 E-mail: rmargoli@jhmi.edu Administrative Assistant Marie Sonderman Phone: 410-955-1536 E-mail: ssonder1@jhmi.edu Education and Government Service A.B. Princeton University M.D. Johns Hopkins University School of Medicine Medicine-Psychiatry Internship Francis Scott Key Hospital Psychiatry Residency Johns Hopkins Neurobiology Fellowship National Institute of Mental Health Government Service Public Health Service Professional Interests My research interests focus on the interface of psychiatry, neurology, and genetics. A major emphasis is determining the etiology and pathogenesis of neurodegenerative disorders affecting the cerebellum and basal ganglia, and describing the psychiatric aspects of such disorders. A second emphasis is on determining the genetic risk factors for bipolar disorder, schizophrenia, and autism. My clinical interests include affective disorders, geriatric psychiatry, and neuropsychiatry. Selected Publications Holmes SE, O'Hearn E, McInnis MG, Kwak NG, Gorelick-Feldman DA, Kleiderlein JK, Callahan C, Sherr M, Sharp AH, Sumner AJ, Ashworth RG, Ananth U, Seltzer W, Vieria-Saecker AM, Epplen JT, Reiss O, Ross CA, Margolis RL. Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12. Nature Genetics, 1999:23:391-392.

25. Cerebellar artery ? Cerebellar Ataxia ? Cerebellar Cortex ? cerebellar diseases ?cerebellar ectopia ? Cerebellar Neoplasms ? Cerebellar Nuclei ? cerebellar http://www.websters-online-dictionary.org/definition/english/Ce/Cerebellar.html

Philip M. Parker, INSEAD. Cerebellar Definition: Cerebellar Cerebellar Adjective . Relating to or associated with the cerebellum; "cerebellar artery". Source: WordNet 1.7.1 Specialty Definitions: Cerebellar Domain Definitions Health Pertaining to the cerebellum. ( references Source: compiled by the editor from various references ; see credits. Top Crosswords: Cerebellar English words defined with "cerebellar" cerebellar artery cerebellar vein hereditary cerebellar ataxia inferior cerebellar artery ... references Specialty definitions using "cerebellar" Carbohydrate-Deficient Glycoprotein Syndrome Cerebellar Diseases cerebellar ectopia Cochlear Nucleus ... references Non-English Usage: Cerebellar " is also a word in the following language with the English translation in parentheses. Danish (cerebellar). Top Commercial Usage: Cerebellar Domain Title Books Angiographic Anatomy of the Anterior Inferior Cerebellar Artery (Advances in Anatomy, Embryology, and Cell Biology, Vol 92) ( reference Atlas of Cerebellar Development In The ( reference Cerebellar Degenerations: Clinical Neurobiology (Foundations of Neurology) ( reference Pdgf in Cerebellar reference The Cerebellum: Recent Developments in Cerebellar Research ( reference (more book examples) Source: compiled by the editor from various references ; see credits.

26. Ataxia Motor ataxia may be associated with cerebellar diseases; cerebral cortex diseases; Friedreich s disease ? locomotor ataxia ? Marie s cerebellar ataxia http://www.websters-online-dictionary.org/definition/english/At/Ataxia.html

Philip M. Parker, INSEAD. Ataxia Definition: Ataxia Ataxia Noun . Inability to coordinate voluntary muscle movements; unsteady movements and staggering gait. Source: WordNet 1.7.1 Specialty Definition: Ataxia Domain Definition Unsteady or irregular gait resulting from incoordination of the muscles, which can be caused by a variety of lesions throughout the nervous system. Source: European Union. references Health Impairment of the ability to perform smoothly coordinated voluntary movements. This condition may affect the limbs, trunk, eyes, pharnyx, larnyx, and other structures. Ataxia may result from impaired sensory or motor function. Sensory ataxia may result from posterior column injury or peripheral nerve diseases. Motor ataxia may be associated with cerebellar diseases; cerebral cortex diseases; thalamic diseases; basal ganglia diseases; injury to the red nucleus; and other conditions. ( references Medicine An inability to co-ordinate muscular movements. Source: European Union. references Source: compiled by the editor from various references ; see credits.

27. Brain Diseases - Brain Pathology - Information Page With HONselect Brain Neoplasms cerebellar diseases Cerebrovascular Disorders Dementia Encephalitis Encephalomalacia http://www.hon.ch/HONselect/Selection/C10.228.140.html

InitBulle("navy","#F8F8F8","#000066",1); HONcode sites All Web sites HONselect News ... Images HONselect Search English French German Spanish Portuguese the word the part of word in MeSH term in MeSH term and description Information on "Brain Diseases": Medical hierarchy and definition Research Articles Web resources Medical Images Medical News Medical Conferences Clinical Trials Hierarchy English French German Spanish Portuguese Brain Diseases Definition: Pathologic conditions affecting the BRAIN , which is composed of the intracranial components of the CENTRAL NERVOUS SYSTEM . This includes (but is not limited to) the CEREBRAL CORTEX ; intracranial white matter; BASAL GANGLIA THALAMUS HYPOTHALAMUS BRAIN STEM ; and CEREBELLUM Synonym(s): Brain Pathology / Intracranial Central Nervous System Disorders / Brain Disorders / CNS Disorders, Intracranial / Narrow term(s): Auditory Diseases, Central Basal Ganglia Diseases Brain Abscess Brain Damage, Chronic ... Thalamic Diseases See Related: Brain Cerebellum Brain Stem Central Nervous System ... New search Web resources for "Brain Diseases" English French = Site with HON description - = Site with a robot description info: enter the site: (click below) domain of the site: HONcode - NORD - National Organization for Rare Disorders, Inc.

28. Machado-Joseph Disease - Azorean Disease - Information Page With HONselect Spinal Cord Diseases Spinocerebellar Degenerations Spinocerebellar Ataxias Brain Diseases cerebellar diseases Spinocerebellar Degenerations http://www.hon.ch/HONselect/RareDiseases/EN/C10.228.140.252.700.700.500.html

InitBulle("navy","#F8F8F8","#000066",1); HONcode sites All Web sites HONselect News ... Images HONselect Search English French German Spanish Portuguese the word the part of word in MeSH term in MeSH term and description Information on "Machado-Joseph Disease": Medical hierarchy and definition Research Articles Web resources Medical Images Medical News Medical Conferences Clinical Trials Hierarchy English French German Spanish Portuguese Machado-Joseph Disease Definition: A dominantly-inherited ataxia first described in people of Azorean and Portuguese descent, and subsequently identified in Brazil, Japan, China, and Australia. This disorder is classified as one of the SPINOCEREBELLAR ATAXIAS (Type 3) and has been associated with a mutation of the MJD1 gene on chromosome 14. Clinical features include progressive ataxia, dysarthria, postural instability, nystagmus, eyelid retraction, and facial fasciculations. Dystonia is prominent in younger patients (referred to as Type I Machado-Joseph Disease). Type II features ataxia and ocular signs; Type III features muscle atrophy and a sensorimotor neuropathy; and Type IV features extrapyramidal signs combined with a sensorimotor neuropathy. (From Clin Neurosci 1995;3(1):17-22; Ann Neurol 1998 Mar;43(3):288-96) Synonym(s): Azorean Disease / Joseph Disease / Spinocerebellar Ataxia Type 3 / Striatonigral Degeneration, Autosomal Dominant /

29. FA INFO The Handbook of cerebellar diseases, Ed. Richard Lechtenberg (Marcel Dekker,Inc., New York, 1993) It covers anatomy, history, examination, http://mypage.direct.ca/s/slogan/fa.html

FRIEDREICH'S ATAXIA (FA) Index What is Friedreidrich's Ataxia? What are the major symptoms of FA? What other symptoms might occur? How is FA passed on the family? ... National Ataxia Foundation What is Friedreich's ataxia? Friedrich's ataxia (FA) is a very rare neurological genetic disorder, that affects speech, balance and coordination. In some respects it is similar to multiple sclerosis. It is an inherited genetic disease in which a person is born with. Most people who have Friedreich's Ataxia, eventually need support to walk, like a scooter, walker or wheelchair. Although, not deemed terminal, it is progressive and as a result, complications can occur to the respiratory systems, (heart and lungs ect.) Friedreich's ataxia was the first form of hereditary ataxia to be distinguished from other forms of ataxia. It is named after the German doctor, Nikolaus Friedreich, who first described it in 1863. Presently there is no known cure, but please don't fret or become discouraged, because with the advancement of all the recent genetic discoveries and research, there is great deal of hope indeed! Back up to Index What are the major symptoms of Friedreich's ataxia?

30. Mood Disorder Rate In HD cerebellar diseases, compared with 21 patients with Huntington s 77% in thepatients with degenerative cerebellar diseases, http://endoflifecare.tripod.com/juvenilehuntingtonsdisease/id300.html

Juvenile-HD HOME INDEX Page Tools For Viewing 10 The Most Commonly Asked Questions ... Mania/OCD~Physician's Guide Mood Disorder Rate In HD Myoclonus (Movements) Nails-What To Look For Night Terrors Obsessive Compulsive OCD ... GUESTBOOK Mood Disorder Rate In HD INDEX Page Aug 2002 A m J Psychiatry 2002 Aug;159(8):1306-14 Psychopathology in Patients With Degenerative Cerebellar Diseases: A Comparison to Huntington's Disease Authors : Leroi I, O'Hearn E, Marsh L, Lyketsos CG, Rosenblatt A, Ross CA, Brandt J, Margolis RL. HD Researchers Christopher Ross and group compaired HD patients to others. Here is what they found. Compaired to neurologicaly healthy subjects, HD patients have: less than twice the incidence of non-cognitive disorders. about three times the incident of mood disorders. OBJECTIVE: This study estimated the psychiatric morbidity of patients with degenerative cerebellar diseases. METHOD: The study included a series of 31 patients with degenerative cerebellar diseases, compared with 21 patients with Huntington's disease and 29 neurologically healthy comparison subjects. Comprehensive psychiatric evaluations, including the Structured

31. Arch Neurol -- Abstract: Double-blind Crossover Study With Physostigmine In Pati DESIGN A doubleblind crossover study with physostigmine was performed in 19patients with degenerative cerebellar diseases. http://archneur.ama-assn.org/cgi/content/abstract/54/4/397

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA (1998-2004) JAMA CareerNet For The Media Meetings Peer Review Congress Vol. 54 No. 4, April 1997 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Wessel K Kompf D Contact me when this article is cited Double-blind crossover study with physostigmine in patients with degenerative cerebellar diseases K. Wessel, K. Langenberger, M. F. Nitschke and D. Kompf Department of Neurology, Medical University of Lubeck, Germany. OBJECTIVE: To determine whether treatment with physostigmine can improve the conditions of patients with ataxia. DESIGN: A double-blind crossover study with physostigmine was performed in 19 patients with degenerative cerebellar diseases. SETTING: Patients were selected from an ongoing

32. Arch Neurol -- Abstract: Double-blind Crossover Study With Levorotatory Form Of DESIGN A doubleblind crossover study with the levorotatory form of hydroxytryptophanwas performed in 39 patients with degenerative cerebellar diseases. http://archneur.ama-assn.org/cgi/content/abstract/52/5/451

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA (1998-2004) JAMA CareerNet For The Media Meetings Peer Review Congress Vol. 52 No. 5, May 1995 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Wessel K Ziegler W Contact me when this article is cited Double-blind crossover study with levorotatory form of hydroxytryptophan in patients with degenerative cerebellar diseases K. Wessel, J. Hermsdorfer, K. Deger, T. Herzog, G. P. Huss, D. Kompf, N. Mai, K. Schimrigk, A. Wittkamper and W. Ziegler Department of Neurology, Medical University of Lubeck, Germany. OBJECTIVE: To determine whether treatment with the levorotatory form of hydroxytryptophan (L-5-hydroxytryptophan), a controversial experimental drug, can improve the conditions of patients with ataxia. DESIGN: A

33. Entrez PubMed cerebellar diseases/etiology; cerebellar diseases/physiopathology; CerebellarDiseases/rehabilitation*; Cerebellar Neoplasms/complications http://www.jneuroengrehab.com/pubmed/9149763

My NCBI [Sign In] [Register] All Databases ... Books Search PubMed Protein Nucleotide Structure Genome Books CancerChromosomes Conserved Domains 3D Domains Gene Genome Project GENSAT GEO Profiles GEO DataSets HomoloGene Journals MeSH NCBI Web Site NLM Catalog OMIA OMIM PMC PopSet Probe PubChem BioAssay PubChem Compound PubChem Substance SNP Taxonomy UniGene UniSTS for Limits Preview/Index History Clipboard Details About Entrez Text Version Entrez PubMed Overview FAQ Tutorial New/Noteworthy ... E-Utilities PubMed Services Journals Database MeSH Database Single Citation Matcher Batch Citation Matcher ... Cubby Related Resources Order Documents NLM Mobile NLM Catalog NLM Gateway ... PubMed Central Display Summary Brief Abstract Citation MEDLINE XML UI List LinkOut ASN.1 Related Articles Cited Articles Cited in Books CancerChrom Links Domain Links 3D Domain Links GEO DataSet Links Gene Links Gene (GeneRIF) Links Genome Links Project Links GENSAT Links GEO Profile Links HomoloGene Links Nucleotide Links OMIA Links OMIM Links BioAssay Links Compound Links Compound via MeSH Substance Links Substance via MeSH PMC Links Cited in PMC PopSet Links Probe Links Protein Links SNP Links Structure Links UniGene Links UniSTS Links Show Sort by Author Journal Pub Date Send to Text File Clipboard E-mail Order All: 1 Review: Phys Ther.

34. FAMILIAR CEREBELLUM DEGENERATION There are a variety of cerebellar degenerative diseases which run in families . For a small fraction of cerebellar diseases, there are genetic tests (for http://www.medhelp.org/forums/neuro/archive/7551.html

Questions in The Neurology Forum are being answered by doctors from The Cleveland Clinic , consistently ranked one of the best hospitals in America. Forum: The Neurology and Neurosurgery Forum Topic: Neurology - General Subject: FAMILIAR CEREBELLUM DEGENERATION Does any one know where one could go to get help for the above subject? My father has had this for 10 years now, and it is getting worst. The main problem is that he is having problems walking and keeping his balance. Docyors her in Canada have diagnosed him withthe familiar cerebellum degeneration disease and claim that not enough is know about the disease to treat it. As I know that there are ohters who have this, I am wondering if any one is aware of any treatment for this. There are a variety of cerebellar degenerative diseases which run in families. The common symptom produced by damage to the cerebellum (of whatever cause) is ataxia, that is, incoordination. Ataxia can affect gait, causing people to walk like they're drunk (alcohol affects the cerebellum, so that's actually why you walk like that if you drink too much). Ataxia can also affect limb function, so that use of the hands is incoordinated. Familial cerebellar system degenerative diseases can be inherited in dominant or recessive patterns, depending on the specific disease. Dominant is when you have it, a parent has it, and a grandparent has it, as well as assorted brothers, sisters, aunts, uncles, and cousins. Recessive is when two siblings have it but no one else in the family has it.

35. MDVU Resource Library - Parkinson's Disease - Differential Diagnosis Patients exhibiting cerebellar signs such as dysmetria, ataxia, nystagmus,titubation, or gait ataxia need to be evaluated further for cerebellar diseases. http://www.mdvu.org/library/disease/pd/par_dd.html

WE MOVE 204 West 84th Street New York, NY 10024 E-mail: wemove@wemove.org Resource Library Movement Disorders Introduction Epidemiology ... References Resource Library Parkinson's Disease Rating Scales and Data Forms Search the E-MOVE Archives Parkinson's Disease Support Organizations Campus Store Parkinson's Disease Slide Set (PowerPoint) Multimedia Center Parkinson's Disease Slide Set (Online Presentation) Our Mission Professional Services Make a Donation ... Contact Us Parkinson's Disease Differential Diagnosis There are a number of factors useful in separating an atypical form of parkinsonism from idiopathic Parkinson's disease. Patients with early-onset or rapidly progressive dementia coupled with parkinsonian features are more likely to have diffuse Lewy body disease (also called Lewy body dementia) or Alzheimer's disease. In addition, a history of a rapidly progressive course should trigger the clinician to look for other parkinsonian syndromes. The presence of supranuclear gaze palsy, especially a downgaze palsy, suggests progressive supranuclear palsy (PSP), a parkinsonism-plus syndrome. Evidence of upper motor neuron involvement, such as Babinski's sign and pathological hyperreflexia, suggests corticospinal pathway involvement. Patients exhibiting cerebellar signs such as dysmetria, ataxia, nystagmus, titubation, or gait ataxia need to be evaluated further for cerebellar diseases. Patients with early onset of urinary incontinence should be evaluated for normal pressure hydrocephalus or other possible symptomatic or secondary causes of parkinsonism.

36. Independent Research In a neuroimaging study of patients with cerebellar diseases, researchers foundimpariments of verbal fluency, abstract reasoning and working memory; http://www.dyslexiaonline.com/evidence/independent.html

FORUMS SEARCH SITE MAP CONTACT US SEARCH Home Evidence Developmental trajectories of brain volume abnormalities in children and adolescents with attention-deficit/hyperactivity disorder. JAMA 1740-8. Castellanos FX, et al Various anatomic brain abnormalities have been reported for attention-deficit/hyperactivity disorder (ADHD), with varying methods, small samples, cross-sectional designs, and without accounting for stimulant drug exposure. The objective of this study was to compare regional brain volumes at initial scan and their change over time in medicated and previously unmedicated male and female patients with ADHD and healthy controls. The researchers concluded that Developmental trajectories for all structures, except caudate, remain roughly parallel for patients and controls during childhood and adolescence, suggesting that genetic and/or early environmental influences on brain development in ADHD are fixed, nonprogressive, and unrelated to stimulant treatment. [abstract] Deficits of motion transparency perception in adult developmental dyslexics with normal unidirectional motion sensitivity.

37. Central Nervous System Diseases Facing Huntington s Disease , A Handbook for Families and Friends Caring forPeople with Huntington s Disease Kansas Univ. cerebellar diseases http://www.mic.ki.se/Diseases/C10.228.html

search search staff sitemap ABOUT KAROLINSKA INSTITUTET ... print this page Diseases and Disorders Links pertaining to Central Nervous System Diseases Alert! 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. Start Page Contents: Alzheimer Disease Arachnoiditis Brain Abscess Brain Abscess ... Uveomeningoencephalitic Syndrome Central Nervous System Diseases Nerve Cells [Lodish et al.] - Molecular Cell Biol., Chap 21, via NLM (US) Pathol. Images of the Central Nervous System - Univ of Utah (US) The Human Brain [JD MacArthur] How brain cells work [Cardoso et al.] EEG Course and Glossary [S Louis] About Normal EEG Variants [S Louis] - eMedicine The Global Brainstem '97 , the Cerebellum '97 , the Thalamus '97 , the Spinal Cord '97 - Univ. of Wisconsin (US) Mental Disorders Links Brain Diseases Brain Functions and Map - Centre for Neuro Skills The Whole Brain Atlas - Atlas Project/Harvard Medical School et al. (US) Dissections of the Real Brain [Williams et al] - Univ of Iowa (US) Anatomy of the Brain - AANS Hallervorden-Spatz Syndrome HSSA: Hallervorden-Spatz Syndrome Association - (US) Genetic aspects of Hallervorden-Spatz Syndrome - OMIM/NLM (US) A nineteen year old boy ... (Hallervorden-Spatz Syndrome)

38. Data Suggest It S Time To Rethink The Cerebellum Arehart Patients with cerebellar diseases may experience not just deterioration in Thirtyone had degenerative cerebellar diseases—spinocerebellar ataxia or http://pn.psychiatryonline.org/cgi/content/full/37/16/17

39. Study Finds Psychiatric Disorders Are Common In People With Cerebellar Degenerat The study suggests that patients with cerebellar diseases may benefit fromscreening and treatment of psychiatric symptoms. http://accessible.ninds.nih.gov/news_and_events/news_articles/news_article_cereb

News and Events - National Institute of Neurological Disorders and Stroke (NINDS) Skip menus Main sections of the NINDS web site Home About NINDS Disorders Funding ... Jobs and Training You are here: Home News and Events News Articles News and Events 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. News Press Releases News Articles - you are in this section Funding News Events Calendar of Events Proceedings Online Events Congressional Testimony NINDS Search (search help) Contact Us My Privacy NINDS is part of the National Institutes of Health Content for this page Study Finds Psychiatric Disorders are Common in People with Cerebellar Degeneration For release: Wednesday, September 25, 2002 Overview Get Web page suited for printing Email this to a friend or colleague For decades, researchers have known that the cerebellum, a fist-sized structure at the back of the brain, helps to coordinate the body and to fine-tune movements. A growing body of research conducted during the last decade supports the notion that the cerebellum also plays a role in cognition, emotion, and other non-motor symptoms. Now, a new study shows that most patients with movement disorders caused by damage to the cerebellum also have psychiatric symptoms. The study suggests that patients with cerebellar diseases may benefit from screening and treatment of psychiatric symptoms.

40. Temporal Organization Of "Internal Speech" As A Basis For Cerebellar Modulation A speaking task analysis of the dysarthria in cerebellar disease. Handbook ofcerebellar diseases. New York Marcel Dekker. Levelt, WJM (1989). http://bcn.sagepub.com/cgi/content/refs/3/1/14

JOURNAL HOME HELP CONTACT US SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: Behavioral and Cognitive Neuroscience Reviews, Vol. 3, No. 1, 14-22 (2004) DOI: 10.1177/1534582304263251 This Article Abstract Full Text (PDF) References ... Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager ... Reprints and Permissions PubMed PubMed Citation Articles by Ackermann, H. Articles by Ivry, R. B. Temporal Organization of "Internal Speech" As a Basis for Cerebellar Modulation of Cognitive Functions Hermann Ackermann Klaus Mathiak University of Tuebingen Richard B. Ivry University of California The sequencing of smooth and rhythmically "sculptured" words to 6 Hz) critically depends on the cerebellum. Besides overt performance, the cerebellum also seems to organize the syllabic is, a prearticulatory but otherwise fully elaborated and temporally organized representation of verbal utterances. As a consequence

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