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         Dystonia Musculorum Deformans:     more detail
  1. Dystonia Musculorum Deformans: A Genetic and Clinical Population Study of 121 Cases. Acta Neurologica Scandinavica Supplement 17 by Tage & Sjogren, [Karl Gustav] Torsten Larsson, 1966-01-01
  2. Dystonia musculorum deformans;: A genetic and clinical population study of 121 cases, (Acta neurologica Scandinavica) by Tage Larsson, 1966
  3. Dystonia Musculorum Deformans: A Genetic and Clinical Population Study of 121 Cases. Acta Neurologica Scandinavica Supplement 17 by Tage & Sj"gren, Torsten (born 1896) Larsson, 1966
  4. Dystonia Musculorum Deformans by Tage Larsson and Torsten Sjogren and Gota Sjogren, 1966
  5. Living Well with Dystonia: A Patient Guide by M.D. Daniel Truong, M.D. Mayank Pathak, et all 2010-04-13
  6. Dystonia, 2 (Advances in Neurology) (Vol 50) by Stanley Fahn, C. David Marsden, 1988-02
  7. The Victim Is Always the Same (Norton Library) by Irving Spencer Cooper, 1976-07-17

61. Clinical Research - Personal Accounts
generalised dystonia deformans. Why did you undertake a clinical research project on dystonia musculorum deformans? In November 1996
http://www.chu-montpellier.fr/gb/rc-temoi02.html
Personal accounts Generalised dystonia deformans: Prof. Philippe Coubes of Neurosurgery describes his research project on generalised dystonia deformans. Why did you undertake a clinical research project on dystonia musculorum deformans? The team in your unit is working on several subjects. What are these? The research topics are: - Agathe Roubertie: pheno-genotypical characterisation of dystonic syndromes, DOPA receptor mapping, creation of an international database of generalised dystonic syndromes; - Nathalie Vayssieres: validation of stereotactic neurosurgery using MRI (detection and treatment of distortions, 3D modelling of basal ganglia, introduction of framed fusion imaging); - Simone Hemm: study of variations in brain impedance in stimulated dystonic children, influence on the choice of target, influence of the effects of therapy; - Laura Cif: development and assessment of a computer scale for clinical rating of dystonia. 25 patients have so far been treated within the framework of a Huriet Act protocol. Results are very encouraging. Montpellier CHU is in a pioneer position and is the only centre providing this treatment which is highly restrictive in terms of equipment and costs. French medical teams refer their patients to us. Foreign patients cannot be treated. What pitfalls did you meet with during the project?

62. Liste Des Résumés De Langue Anglaise
B., FREREBEAU P. Bilateral chronic stimulation of the internal globus pallidus as a treatment of idiopathic dystonia musculorum deformans case report.
http://www.urma-montpellier.org/francais/popup/resumes_anglais.html
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COUBES P., HUMBERTCLAUDE V., BAUCHET L., CAMBONIE G., TRABAUD V., ECHENNE B., FREREBEAU P. Bilateral chronic stimulation of the internal globus pallidus as a treatment of idiopathic Dystonia musculorum deformans : case report. Stereotactic and Functional Neurosurgery, 1997, 67:70
COUBES P., ROUBERTIE A., HUMBERTCLAUDE V., BAUCHET L., CAMBONIE G., TRABAUD V., ECHENNE B., FREREBEAU P. Stimulation chronique bilatérale du pallidum interne dans un cas pédiatrique de dystonie musculaire déformante. Proceedings of the Société de Neurochirurgie de Langue Française, Paris, 1-3 décembre, 1997.
COUBES P., HUMBERTCLAUDE V., BAUCHET L., CAMBONIE G., TRABAUD V., ECHENNE B., FREREBEAU P. Bilateral chronic stimulation of the internal globus pallidus as a treatment of idiopathic dystonia musculorum deformans : case report. Proceedings of The International Society for Pediatric Neurosurgery. XXV Annual Congress, Verona, 13-18 septembre, 1997.
HUMBERTCLAUDE V., COUBES P., BAUCHET L., CAMBONIE G., TRABAUD V., ECHENNE B., FREREBEAU P.

63. :: Ez2Find :: Dystonia
URL http//www.angelfire.com/ca6/Tnippy; Medicine Net Site Info - Translate - Open New Window A description of dystonia musculorum deformans.
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64. UVA Neurogram - Dystonia
This term includes inherited dystonias (eg, dystonia musculorum deformans associated with the DYT1 gene on chromosome 9) along with idiopathic dystonias (the
http://www.healthsystem.virginia.edu/internet/neurogram/neurogram2_1_dystonia.cf
Neurogram Newsletter Neuroscience Service Center Homepage Neurology Neurosurgery ... Site Index Search this site:
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Dystonia
Dystonia is a neurologic syndrome characterized by involuntary, sustained, patterned and often repetitive muscle contractions of opposing muscles, causing twisting movements or abnormal postures. Dystonia is a fairly common neurological disorder with a prevalence of approximately 1 in 3,400 for focal dystonia and 1 in 29,400 for generalized dystonia.(1) If patients with drug-induced tardive dystonia related to neuroleptic medications and secondary dystonia related to brain injury are added to this group, the prevalence figure can probably be doubled and approaches that of multiple sclerosis.(2) All gender, ethnic, and socioeconomic groups are equally affected.
Clinical presentation
If one dichotomizes movement disorders to those with reduced movement (akinetic-rigid syndromes) versus those with excessive movement (hyperkinetic syndromes), dystonia falls into the hyperkinetic disorder category. However, distinguishing dystonia from other hyperkinetic movement disorders may be challenging. The clinical characteristic of dystonia that helps differentiate it from other hyperkinetic movement disorders is that dystonic movements are repetitive and stereotyped, with involvement of the same group of muscles. For instance, a patient with idiopathic cervical dystonia or spasmodic torticollis with involuntary right-head rotation will continue to have right-head rotation throughout the duration of his disorder. By comparison

65. An Excerpt
The playwright is afflicted with generalized dystonia, (dystonia musculorum deformans), the most severe and painful form of this disorder.
http://www.newsun.com/stormreadingSept.html
"STORM READING" a play by Neil Marcus
Neil Marcus, the author and lead actor of the play, has a condition called dystonia. In this excerpt, the Dystonia Medical Research Foundation wants to place an advertisement in the playbill which defines Neil's illness from their point of view. Neil has a different point of view. Pictured from top to bottom: Kathyrn Voice, Neil Marcus, Matthew Ingersoll. Matt: Neil, the Dystonia Medical Research Foundation is interested in your show. Kathryn: They think you are a great role model. Matt: They see STORM READING as a great vehicle to tell the world about your condition. Kathryn: They want to put an ad in your playbill. It reads, (Ad appears on the screen and Matt reads it)
The Dystonia Medical Research Foundation:
Playwright Neil Marcus suffers from dystonia, a rare neurological disorder in which powerful involuntary muscle spasms twist and jerk the body into unusual postures. The playwright is afflicted with "generalized dystonia," (dystonia musculorum deformans), the most severe and painful form of this disorder. It denies his ability to speak, stand, walk and/or control sudden and sometimes bizarre movements. (Neil interrupts Matt here) Neil: Wait a minute. If they think that they can say anything they want, think again. For years I've been under the medical microscope. I've been called: twisted, paralyzed, tortured, afflicted, horribly disabled, disfigured, unintelligible and confined to a wheelchair.

66. Untitled Document
Dyslexia Dysmenorrhea (Menstrual Cramps) Dysmotility Syndrome Dyspepsia and Heartburn Dysphagia (Swallowing) Dystonia dystonia musculorum deformans (Dystonia).
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67. Dy_hist
dystonia musculorum deformans , eine Bezeichnung die heute
http://www.kgu.de/znn/neurologie/epbs/dy_hist.htm
Kurze Geschichte der Dystonie
Die Dystonie ist zwar noch relativ wenig bekannt, jedoch keineswegs eine neue Erkrankung. Aus der Antike gibt es Berichte, die den Schluss zulassen, dass der Redner Demosthenes an einem Torticollis spasmodicus sowie an einer spasmodischen Dysphonie gelitten haben könnte. Es ist nämlich überliefert, dass er sich beim Einüben seiner Reden eine Schwertspitze an das Kinn gehalten habe, um seinen Kopf an den unwillkürlichen Seitwärtsdrehungen zu hindern und auch, dass er versuchte, mit einem Kieselstein auf der Zunge seine nicht näher charakterisierte Sprachstörung zu heilen.
Im 16. Jahrhundert malte Pieter Brueghel d.Ä. ein Porträt eines Mannes mit zusammengekniffenen Augen und wie zwanghaft geöffnetem Mund und nannte es "Der Gähner" (s. Abb.). Aus zeitgenössischen Berichten lässt sich schließen, dass es sich hier um einen Patienten handelte, der an einem Blepharospasmus in Verbindung mit einer orofazialen Dystonie vom Kieferöffnungstyp litt. Diese Erkrankung, die bei uns auch nach einem französischen Neurologen der Jahrhundertwende Meige-Syndrom (MEIGE; 1910) genannt wird, heißt im englischen und amerikanischen Sprachraum daher auch oft nach dem Maler "Brueghel-Syndrom".

68. SearchBug Directory: Health: Conditions_and_Diseases: Neurological_Disorders: Mo
Neurosurgery http//www.neurosurgery.medsch.ucla.edu/Diagnoses/Movement/MovementDis_7.html An article explaining what dystonia musculorum deformans is, the
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Related Categories: Web Pages - ranked by popularity Dystonia Dialogue http://www.dystonia-foundation.org/

69. MDVU Library - Essential Tremor - Differential Diagnosis
tremor and lipofuscinosis; RamsayHunt syndrome (progressive myoclonic ataxia); dystonia musculorum deformans; DOPA-responsive dystonia
http://www.mdvu.org/library/disease/et/et_mdd.html
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Movement Disorders Library Multimedia Center Essential Tremor Differential Diagnosis The differential diagnosis of ET includes a number of hereditary and idiopathic disorders, metabolic conditions, cerebral diseases, and peripheral neuropathies that may be characterized by postural, intention, or rest tremors or combinations of such tremor elements. (For a listing of such conditions, please refer to table 4.) Table 4. Differential Diagnosis of ET
  • Parkinson's disease (PD) Multiple system atrophy (MSA) (e.g., olivopontocerebellar atrophy [OPCA], striatonigral degeneration) Huntington's disease (HD) Benign hereditary chorea Wilson's disease Fahr's disease Paroxysmal dystonic choreoathetosis (PDC) Ataxia-telangiectasia (AT) Familial intention tremor and lipofuscinosis Ramsay-Hunt syndrome (progressive myoclonic ataxia) Dystonia musculorum deformans DOPA-responsive dystonia (Segawa syndrome) Spasmodic torticollis (cervical dystonia) Meige syndrome Task- or position-specific tremors (e.g., primary writing tremor, isolated voice tremor)

70. Entrez PubMed
Dopamine/analysis; Dopamine/metabolism*; dystonia musculorum deformans/metabolism*; dystonia musculorum deformans/pathology; Human; Membrane
http://www.facultyof1000.com/pubmed/12177384
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Neurology. 2002 Aug 13;59(3):445-8. Related Articles, Links
Dopamine transmission in DYT1 dystonia: a biochemical and autoradiographical study. Augood SJ, Hollingsworth Z, Albers DS, Yang L, Leung JC, Muller B, Klein C, Breakefield XO, Standaert DG. Center for Aging, Genetics, and Neurodegeneration, Massachusetts General Hospital and Harvard Medical School, 114 16th Street, Charlestown, MA 02129, USA. augood@helix.mgh.harvard.edu

71. Dystonia-support4u.co.uk
Sometimes the dystonia is more widespread Segmental and Generalised Dystonia (dystonia musculorum deformans). The majority of cases
http://www.dystonia-support4u.co.uk/info.php?page=forms

72. Dystonia-support4u.co.uk
from 2050%, occurred in patients with both focal (Meige s syndrome; spasmodic torticollis) and generalized (dystonia musculorum deformans; levodopa-induced
http://www.dystonia-support4u.co.uk/spotlight.php
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Pianomap : Dystonia
Dystonia is distinct from injuries like tendonitis that affect muscles and tendons. In dystonia the brain's capacity to control movement is impaired.
Muscles may tighten involuntarily, producing awkward, jerky movements. Hands or fingers may fail to respond to conscious commands, or respond in unintended ways. Fingers may clench involuntarily instead of touching the intended key. The condition may not be painful, but the emotional stress and frustration endured by musicians suffering from dystonia is immense. Dystonia has ended the careers of some famous and wonderful musicians.
Dystonia can affect any part of the body, and it takes many forms. Some dystonias are devastating conditions that affect large areas of the body, distort posture and speech, make driving, walking, talking or eating difficult or impossible. Some dystonias seem to be congenital, perhaps genetic. The cause of these conditions is not well understood, nor is there any reliable cure.
Other forms of dystonia are not congenital but appear later in life. Acquired dystonia often affects only a specific part of the body, perhaps just one finger, which may uncontrollably clench or freeze or shoot out to the side. Dystonia of this sort is called "focal dystonia" and it is the sort that most often occurs in pianists. Focal dystonia usually affects parts of the body that are subject to constant use in an activity like writing or piano playing. Sometimes the affected part, a finger, for example, responds normally in other activities and becomes uncontrollable only in the context of the specific activity of writing or piano playing.

73. Atlantoaxial Dislocation In Idiopathic Cervical Dystonia Kanekar S Neurol India
4. 5. Oppenheim H. Dysbasia lordotica progressiva, dystonia musculorum deformans. Neurol centrabl 1911;3010907. Back to cited text no. 5.
http://www.neurologyindia.com/article.asp?issn=0028-3886;year=2004;volume=52;iss

74. DMRF: Forms Of Dystonia: Early-Onset Generalized Dystonia
Historically, earlyonset generalized dystonia has also been referred to as idiopathic torsion dystonia and dystonia musculorum deformans. Back to top.
http://www.dystonia-foundation.org/defined/early.asp
To view specific content on this page, click on a category above. Early-Onset Generalized Dystonia Cable/T1 (Get RealPlayer)
What is it?
Early-onset generalized dystonia, the most common hereditary form of dystonia, is characterized by the twisting of the limbs, specifically the foot/leg or hand/arm. The spasms may spread to involve twisting contractions of other parts of the body.
Back to top
Symptoms
Symptoms in early-onset generalized dystonia can range from twisted postures, turning in of the foot or arm, muscle spasms, unusual walking with bending and twisting of the torso, rapid, sometimes rhythmic, jerking movements; and progression of symptoms leading to sustained or fixed postures. Because the legs and trunk are so commonly affected in early-onset generalized dystonia, abnormal gait may be common. Factors such as age and site play a significant role in the progression of early-onset generalized dystonia. The younger the age of onset, the more likely the dystonic symptoms will begin in one of the legs, spread upward to other areas, and possibly become generalized. Symptoms commonly begin with a specific action, that is, the abnormal movements appear with a specific action, and are not present at rest. For example, if it begins in one leg, the symptoms may only be present when walking and disappear when the child runs or walks backwards.

75. The Dystonias Fact Sheet
Some patterns of dystonia are defined as specific syndromesTorsion dystonia, previously called dystonia musculorum deformans or DMD, is a rare, generalized
http://www.healthieryou.com/dystonia.html
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The Dystonias Fact Sheet
What are the dystonias? The dystonias are movement disorders in which sustained muscle contractions cause twisting and repetitive movements or abnormal postures. The movements, which are involuntary and sometimes painful, may affect a single muscle; a group of muscles such as those in the arms, legs, or neck; or the entire body. Diminished intelligence and emotional imbalance are not usually features of the dystonias. What are the symptoms? Early symptoms may include a deterioration in handwriting after writing several lines, foot cramps, and a tendency of one foot to pull up or drag after running or walking some distance. The neck may turn or pull involuntarily, especially when tired. Other possible symptoms are tremor and voice or speech difficulties. The initial symptoms can be very mild and may be noticeable only after prolonged exertion, stress, or fatigue. Over a period of time, the symptoms may become more noticeable and widespread and be unrelenting; sometimes, however, there is little or no progression.

76. Parkinson's Disease Page 1
unknown causes idiopathic torsion dystonia; dystonia musculorum deformans. Tics sudden, abnormal coordinated movements Characteristics
http://www.pharmacology2000.com/Central/Parkinson/park1.htm
Parkinson's Disease Definitions Tremor Chorea Athetosis ... Impaired cognition Drug Treatment
  • Levodopa-Overview
    • Dopamine L-DOPA Receptor Classification ...
      • Treatments Definitions:
        • Tremor: rhythmic/oscillatory movement around a joint
          • Resting tremor (Parkinson's disease): , associated with:
            • rigidity impairment of volitional movement
            Essential Tremor:
            • postural tremor (clearly observable)
            Intentional Tremor:
            • brain stem/cerebellar lesion (particularly with superior cerebellar peduncle involvement May be associated with alcohol/other drug toxicities Chorea: involuntary muscle jerks; unpredictable

77. Search By Disease
143 Dystonia 3, torsion, Xlinked (DYT3). 144 Dystonia 5 (DYT5). 145 dystonia musculorum deformans 1. 146 Dystonia, dopa-responsive, autosomal dominant (DRD).
http://www.eddnal.com/directory/disease.php?letter=D&page=10

78. »»Dystonia Reviews««
studies that Dr. Cooper uses to illustrate his point of view have to do with a condition called muscular dystonia (dystonia musculorum deformans), because the
http://www.health-issue-books.com/Dyspnea/Dystonia/
Dystonia Reviews
Related Subjects: Dyspnea
More Pages: Dystonia Page 1 Book reviews for "Dystonia" sorted by average review score: The Victim Is Always the Same Author: Irving Spencer Cooper Amazon base price:
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Reveiw of "The Victim is Always the Same" Dystonia Is... a personal poem Published in Paperback by The Dystonia Foundation (01 April, 1999) Author: Rebecca Serdans Amazon base price: Average review score: No reviews found. Holding the Hope: A Parent's Guide to Living with Dystonia Published in Paperback by The Dystonia Foundation (01 November, 1996) Author: Karen K. Ross PhD Amazon base price: Average review score: No reviews found. Dystonia 3 (Advances in Neurology, Vol 78) Authors: Stanley Fahn and C. David Marsden Amazon base price:
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No reviews found. Dystonia 4 (Advances in Neurology, Vol. 94) Authors: Stanley, Md. Fahn, Mark, Md. Hallett, Mahlon R., Md. Delong, and Stantey Fahn Amazon base price:
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79. Volume 97 January - December 1974
Idiopathic torsion dystonia (dystonia musculorum deformans) a review of forty-two patients. CD . Marsden and MJG . Harrison. Pages 793 - 811.
http://www3.oup.co.uk/jnls/supplements/braini/hdb/Volume_97/Issue_04/970793.sgm.
Volume 97: January - December 1974
Issue 4: December 1974
Abstract
  • Idiopathic torsion dystonia (dystonia musculorum deformans) - a review of forty-two patients
  • CD Marsden and MJG Harrison 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 14 May 97 Part of the OUP Journals World Wide Web service Oxford University Press, 1997

    80. OMIM - DYSTONIA MUSCULORUM DEFORMANS 4; DYT4

    http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?cmd=framedSynopsis&id=128101

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