يعرض 1 - 20 نتائج من 72,608 نتيجة بحث عن '"MOVEMENT disorders"', وقت الاستعلام: 1.08s تنقيح النتائج
  1. 1
    Academic Journal
    Postmovement Beta Rebound in Real and Imagined Movement.

    المؤلفون: Sisti, Helene M., Beebe, Annika, Gabrielsson, Elias, Bishop, Mercedes

    المصدر: Motor Control; Jan2025, Vol. 29 Issue 1, p53-68, 16p

    مصطلحات موضوعية: AMYOTROPHIC lateral sclerosis, MOTOR imagery (Cognition), SENSORIMOTOR cortex, MOTOR learning, MOVEMENT disorders


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  2. 2
    Dissertation/ Thesis
    Enfermedades minoritarias causantes de trastornos del movimiento y degeneración de ganglios basales en la infancia

    المؤلفون: Baide Mairena, Heidy

    Thesis Advisors: Pérez Dueñas, Belén, Moreno Galdó, Antonio

    المصدر: TDX (Tesis Doctorals en Xarxa)

    مصطلحات موضوعية: Ganglis basals, Ganglios basales, Basal ganglia, Trastorns del moviment, Trastornos del movimiento, Movement disorders, Malalties rares, Enfermedades raras, Rare diseases, Ciències de la Salut

    وصف الملف: application/pdf

    URL الوصول: http://hdl.handle.net/10803/690099

    View record in TDX

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  3. 3
    Academic Journal
    Total functioning capacity scale in Huntington's disease: natural course over time.

    المؤلفون: van der Zwaan, K. F.1 (AUTHOR) k.f.van_der_Zwaan@lumc.nl, Feleus, S.1,2 (AUTHOR), Dekkers, O. M.2 (AUTHOR), Roos, R. A. C.1 (AUTHOR), de Bot, S. T.1 (AUTHOR)

    المصدر: Journal of Neurology. Feb2025, Vol. 272 Issue 2, p1-11. 11p.

    مصطلحات موضوعية: *HUNTINGTON disease, *MOVEMENT disorders, *FUNCTIONAL status, *DISEASE progression, *CLINICAL trials


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  4. 4
    Academic Journal
    Molecular basis of the development of Parkinson's disease.

    المؤلفون: Absalyamova, Margarita1 (AUTHOR), Traktirov, Dmitrii1,2 (AUTHOR) ds.traktirov@gmail.com, Burdinskaya, Viktoria2 (AUTHOR), Artemova, Valeria1 (AUTHOR), Muruzheva, Zamira2 (AUTHOR), Karpenko, Marina1 (AUTHOR)

    المصدر: Neuroscience. Jan2025, Vol. 565, p292-300. 9p.

    مصطلحات موضوعية: *PARKINSON'S disease, *MOVEMENT disorders, *DOPAMINERGIC neurons, *SYMPTOMS, *OXIDATIVE stress, *CALPAIN


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  5. 5
    Academic Journal
    The Overaction of the Inferior Oblique Muscle and Associated Vertical Strabismus: Prevalence, Etiology and Diagnosis.

    المؤلفون: Khorrami-Nejad, Masoud1,2, Karim, Huda2, Hatem, Wisam2, Abdullah, Mustafa2, Gheibi, Ali3 aligheibi79@yahoo.com, Boromand, Mohammad Ghasemi4

    المصدر: Journal of Modern Rehabilitation. Jan2025, Vol. 19 Issue 1, p14-20. 7p.

    مصطلحات موضوعية: *EYE movement disorders, *SYMPTOMS, *STRABISMUS, *CONVERGENT strabismus, *DIAGNOSTIC examinations


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  6. 6
    Academic Journal
    Assessment der Kognition: Demenz und Delir: Unter Berücksichtigung der AWMF-Leitlinien 038-013 und 084-002LG.

    Alternate Title: Assessment of cognition: dementia and delirium: In consideration of the AWMF guidelines 038-013 and 084-002LG.

    المؤلفون: Krupp, Sonja1 (AUTHOR) krupp@geriatrie-luebeck.de, Iglseder, Bernhard2 (AUTHOR)

    المصدر: Der Nervenarzt. Jan2025, Vol. 96 Issue 1, p97-104. 8p.

    مصطلحات موضوعية: *COGNITION disorders, *MOVEMENT disorders, *COGNITIVE testing, *DELIRIUM, *DEMENTIA


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  7. 7
    Academic Journal
    Movement Disorders and Smart Wrist Devices: A Comprehensive Study.

    المؤلفون: Caroppo, Andrea1 (AUTHOR) gabriele.rescio@cnr.it, Manni, Andrea1 (AUTHOR) andrea.caroppo@cnr.it, Rescio, Gabriele1 (AUTHOR), Carluccio, Anna Maria1 (AUTHOR), Siciliano, Pietro Aleardo1 (AUTHOR), Leone, Alessandro1 (AUTHOR)

    المصدر: Sensors (14248220). Jan2025, Vol. 25 Issue 1, p266. 50p.

    مصطلحات موضوعية: *MEDICAL personnel, *MOVEMENT disorders, *GAIT disorders, *CEREBRAL palsy, *SEIZURES (Medicine)

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  8. 8
    Academic Journal
    Consolidating the Role of Mutated ATP2B2 in Neurodevelopmental and Cerebellar Pathologies.

    المؤلفون: Stehr, Antonia M.1 (AUTHOR), Lenberg, Jerica2 (AUTHOR), Friedman, Jennifer2,3,4,5 (AUTHOR), Dobbelaere, Dries6,7 (AUTHOR), Imbard, Apolline8,9 (AUTHOR), Levy, Jonathan9,10 (AUTHOR), Donoghue, Sarah11,12 (AUTHOR), Derive, Nicolas9 (AUTHOR), Stoeva, Radka13 (AUTHOR), Gueguen, Paul9,14,15 (AUTHOR), Zech, Michael1,16,17 (AUTHOR) michael.zech@mri.tum.de

    المصدر: Clinical Genetics. Jan2025, Vol. 107 Issue 1, p91-97. 7p.

    مصطلحات موضوعية: *MOVEMENT disorders, *HEARING disorders, *DEVELOPMENTAL delay, *CELL membranes, *INTELLECTUAL disabilities


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  9. 9
    Academic Journal
    Gait pattern differences in unilaterally affected children with cerebral palsy and children with acquired brain insult.

    المؤلفون: Salazar-Torres, Jose1 jose.salazar@nemours.org, Church, Chris1, Miller, Freeman1, Lennon, Nancy1, Howard, Jason J.1, Shields, Thomas1, Owens, Laura1, Zhang, Ran2, Shrader, M. Wade1

    المصدر: Gait & Posture. Jan2025, Vol. 115, p116-121. 6p.

    مصطلحات موضوعية: *CHILDREN with cerebral palsy, *MOVEMENT disorders, *KINEMATICS, *ADOLESCENCE, *LEG


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  10. 10
    Academic Journal
    Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability.

    المؤلفون: Sabeh, Pascale1 (AUTHOR), Dumas, Samantha A.1,2 (AUTHOR), Maios, Claudia3 (AUTHOR), Daghar, Hiba3 (AUTHOR), Korzeniowski, Marek2 (AUTHOR), Rousseau, Justine1 (AUTHOR), Lines, Matthew4 (AUTHOR), Guerin, Andrea5 (AUTHOR), Millichap, John J.6 (AUTHOR), Landsverk, Megan7 (AUTHOR), Grebe, Theresa8 (AUTHOR), Lindstrom, Kristin9 (AUTHOR), Strober, Jonathan10 (AUTHOR), Ait Mouhoub, Tarik11 (AUTHOR), Zweier, Christiane12 (AUTHOR), Steinraths, Michelle13 (AUTHOR), Hebebrand, Moritz14 (AUTHOR), Callewaert, Bert15 (AUTHOR), Abou Jamra, Rami16 (AUTHOR), Kautza-Lucht, Monika17 (AUTHOR)

    المصدر: American Journal of Human Genetics. Jan2025, Vol. 112 Issue 1, p75-86. 12p.

    مصطلحات موضوعية: *MOVEMENT disorders, *EXOCRINE pancreatic insufficiency, *AUTISM spectrum disorders, *DEVELOPMENTAL delay, *ANGELMAN syndrome, *PROTEOLYSIS, *UBIQUITINATION

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  11. 11
    Academic Journal
    Examination and Imaging Correlates of Visual Symptoms in Mild TBI.

    المصدر: Neurology Alert. Jan2025, Vol. 44 Issue 5, p1-14. 14p.

    مصطلحات موضوعية: *EYE movement disorders, *EYE physiology, *VISION disorders, *BRAIN injuries


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  12. 12
    Academic Journal
    STUB1‐Associated Autosomal‐Recessive Spinocerebellar Ataxia Type 16 (SCAR16) Presenting with Gordon–Holmes Syndrome Caused by Maternal Uniparental Isodisomy.

    المؤلفون: Agianda, Habibah A.P.1 (AUTHOR), Tam, Amy1 (AUTHOR), Kunta, Avaneesh2 (AUTHOR), Zubair, Umar1 (AUTHOR), Saffari, Afshin1 (AUTHOR), Rong, Joshua1 (AUTHOR), Crough, Michelle1 (AUTHOR), Srouji, Rasha1 (AUTHOR), Quiroz, Vicente1 (AUTHOR), Yang, Kathryn1 (AUTHOR), Schierbaum, Luca1 (AUTHOR), Ebrahimi‐Fakhari, Darius1 (AUTHOR) darius.ebrahimi-fakhari@childrens.harvard.edu

    المصدر: Movement Disorders Clinical Practice. Dec2024, p1. 4p. 4 Illustrations.

    مصطلحات موضوعية: *MOVEMENT disorders, *HEREDITY, *SEIZURES (Medicine), *FAMILIAL spastic paraplegia, *GENETIC disorders


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  13. 13
    Academic Journal
    Measurements of Objective Cyclotorsion in a Population of Healthy Children.

    المؤلفون: Lin, Hsu-Ying1,2 (AUTHOR), Wu, Wei-Chi2,3 (AUTHOR), Sun, Ming-Hui2,3 (AUTHOR), Lin, Jui-Yen2,4 (AUTHOR), Huang, Ping-Hsuan5 (AUTHOR), Liu, Chun-Hsiu2,3 (AUTHOR) cdeegg@gmail.com, Monteiro, Mário (AUTHOR)

    المصدر: Journal of Ophthalmology. 12/18/2024, Vol. 2024, p1-8. 8p.

    مصطلحات موضوعية: *TORSION abnormality (Anatomy), *EYE movement disorders, *RESEARCH funding, *EYE movement measurements, *PREMATURE infants, *OPTICAL coherence tomography, *PHOTOGRAPHY, *DESCRIPTIVE statistics, *GESTATIONAL age, *RETINA, *COMPARATIVE studies, *RETROLENTAL fibroplasia, *CHILDREN

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  14. 14
    Academic Journal
    The First Case of Autosomal Recessive Cerebellar Ataxia with Prominent Paroxysmal Non‐kinesigenic Dyskinesia Caused by a Truncating FGF14 Variant in a Turkish Patient.

    المؤلفون: Türkdoğan, Dilşad1 (AUTHOR), Smolina, Natalia2 (AUTHOR), Tekgül, Şeyma2 (AUTHOR), Gül, Tuğçe2 (AUTHOR), Yeşilyurt, Ahmet3 (AUTHOR), Houlden, Henry4 (AUTHOR), Zuchner, Stephan5 (AUTHOR), Brais, Bernard6,7 (AUTHOR), Pellerin, David4,5,6 (AUTHOR), Başak, Ayşe Nazlı2 (AUTHOR) nbasak@ku.edu.tr

    المصدر: Movement Disorders. Dec2024, p1. 6p. 2 Illustrations.

    مصطلحات موضوعية: *CEREBELLAR ataxia, *MOVEMENT disorders, *TURKS, *CONSANGUINITY, *GENETIC variation


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  15. 15
    Academic Journal
    Genetic Analysis of GCA Repeats in the GLS Gene: Implications for Undiagnosed Ataxia and Spinocerebellar Ataxia 3 in Mainland China.

    المؤلفون: Lei, Lijing1 (AUTHOR), Peng, Linliu1 (AUTHOR), Wan, Linlin1,2,3,4,5 (AUTHOR), Chen, Zhao1,2,3,6 (AUTHOR), Wang, Chunrong7 (AUTHOR), Peng, Huirong1 (AUTHOR), Qiu, Rong8 (AUTHOR), Tang, Beisha1,2,3,6 (AUTHOR), Jiang, Hong1,2,3,5,6,9,10,11 (AUTHOR)

    المصدر: Movement Disorders. Dec2024, p1. 11p. 5 Illustrations.

    مصطلحات موضوعية: *SPINOCEREBELLAR ataxia, *MOVEMENT disorders, *CAPILLARY electrophoresis, *POLYMERASE chain reaction, *CHINESE people


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  16. 16
    Academic Journal
    Diagnostic Utility of Clinical Neurophysiology in Jerky Movement Disorders: A Review from the MDS Clinical Neurophysiology Study Group.

    المؤلفون: Latorre, Anna1 (AUTHOR) a.latorre@ucl.ac.uk, Ganos, Christos2 (AUTHOR), Hamada, Masashi3 (AUTHOR), Phielipp, Nicolas4 (AUTHOR), Rocchi, Lorenzo5 (AUTHOR), Merchant, Shabbir6 (AUTHOR), Tijssen, Marina A.7,8 (AUTHOR), Veen, Sterre7,8 (AUTHOR), Chen, Robert9,10 (AUTHOR)

    المصدر: Movement Disorders Clinical Practice. Dec2024, p1. 13p.

    مصطلحات موضوعية: *STARTLE reaction, *MOVEMENT disorders, *MYOCLONUS, *RELIABILITY in engineering, *CHOREA


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  17. 17
    Academic Journal
    Eye movement disorders: A new approach to preliminary screening of Parkinson's disease.

    المؤلفون: Li, Han1 (AUTHOR), Li, Chengqian1,2 (AUTHOR), Ma, Wenqi1 (AUTHOR), Qin, Kunpeng1 (AUTHOR), Wang, Zihan1 (AUTHOR), Hou, Binghui1 (AUTHOR), Xie, Anmu1,3 (AUTHOR) xieanmu@163.com

    المصدر: Neuroscience. Dec2024, Vol. 563, p202-211. 10p.

    مصطلحات موضوعية: *EYE movement disorders, *PARKINSON'S disease, *VISUAL perception, *RECEIVER operating characteristic curves, *LOGISTIC regression analysis, *SACCADIC eye movements, *NOMOGRAPHY (Mathematics)


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  18. 18
    Academic Journal
    A Population‐Wide Exploration of the THAP11 CAG Repeat Size and Structure in the 100,000 Genomes Project and UK Biobank.

    المؤلفون: Clarkson, Chris1,2 (AUTHOR), Chen, Zhongbo3,4 (AUTHOR), Rocca, Clarissa2 (AUTHOR), Jadhav, Bharati5 (AUTHOR), Ibañez, Kristina1 (AUTHOR), Ryten, Mina6 (AUTHOR), Sharp, Andrew J.5 (AUTHOR), Houlden, Henry2 (AUTHOR), Tucci, Arianna1,7 (AUTHOR) a.tucci@qmul.ac.uk

    المصدر: Movement Disorders. Dec2024, p1. 6p. 2 Illustrations.

    مصطلحات موضوعية: *FRIEDREICH'S ataxia, *MOVEMENT disorders, *SPINOCEREBELLAR ataxia, *NEURODEGENERATION, *DATABASES


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  19. 19
    Academic Journal
    The use of eye tracking in supporting individuals with dyslexia: a review.

    المؤلفون: Nguyen, Thi Kieu Chinh1 (AUTHOR), Le, Duc Duy1 (AUTHOR), Le, Thanh Ha1 (AUTHOR), Nguyen, Thi Cam Huong2 (AUTHOR), Ngo, Thi Duyen1 (AUTHOR) duyennt@vnu.edu.vn

    المصدر: Disability & Rehabilitation: Assistive Technology. Dec2024, p1-16. 16p. 2 Illustrations.

    مصطلحات موضوعية: *EYE movement disorders, *EYE tracking, *LEARNING disabilities, *RESEARCH personnel, *DYSLEXIA, *ASSISTIVE technology


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  20. 20
    Academic Journal
    KCNMA1‐Related Episodes of Behavioral Arrest and Loss of Postural Reflexes: A Critical Reappraisal.

    المؤلفون: Roze, Emmanuel1 (AUTHOR), Silveira‐Moriyama, Laura2,3 (AUTHOR), Leu‐Semenescu, Smaranda4 (AUTHOR), Villeneuve, Nathalie5,6 (AUTHOR), Lecardonnel, Bérénice7 (AUTHOR), François‐Heude, Marie‐Céline7 (AUTHOR), Meyer, Pierre7,8 (AUTHOR), Gusmao, Claudio M.9,10 (AUTHOR), Roubertie, Agathe7,11 (AUTHOR) a-roubertie@chu-montpellier.fr

    المصدر: Movement Disorders Clinical Practice. Dec2024, p1. 11p. 2 Illustrations.

    مصطلحات موضوعية: *MOVEMENT disorders, *EPILEPSY, *CATAPLEXY, *ATAXIA, *DYSKINESIAS


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