نتایج جستجو برای: spastic limb

تعداد نتایج: 79860  

Journal: :Gait & posture 2011
Nicky Thompson Julie Stebbins Maria Seniorou Di Newham

Muscle weakness is a recognised problem in children with Cerebral Palsy (CP). Changes in the understanding of motor control, and progress in the treatment of spasticity, have led to a greater appreciation that spastic muscles are also weak. In recent years weakness has been identified in isolated muscle groups, but studies quantifying the degree and distribution of weakness in multiple muscles ...

Journal: :Clinical rehabilitation 2003
S W Blundell R B Shepherd C M Dean R D Adams B M Cahill

OBJECTIVE To determine the effects of intensive task-specific strength training on lower limb strength and functional performance in children with cerebral palsy. DESIGN A nonrandomized ABA trial. SETTING Sydney school. SUBJECTS Eight children with cerebral palsy, aged 4-8 years, seven with diagnosis of spastic diplegia, one of spastic/ataxic quadriplegia. INTERVENTION Four weeks of aft...

Journal: :caspian journal of neurological sciences 0
karim nikkhah ali ghabeli-juibary shadi zamanian resident of neurology, mashhad university of medical sciences, mashhad, iran ; [email protected]

sjogren-larsson syndrome (sls) is an inherited autosomal recessive neurocutaneous disorder with congenital ichthyosis, spastic diplegia or quadriplegia and mental retardation. we report a case of sjogren-larsson syndrome with clinical profile (mental retardation, ichthyosis, spastic diplegia) and mri findings such as seen in multiple sclerosis (ms). so this rare syndrome can be another differen...

2009
Pauline BM Aarts Peter H Jongerius Yvonne A Geerdink Alexander C Geurts

BACKGROUND In 2003 new computer software, the VOAA (Video Observations Aarts and Aarts), was designed to score and evaluate two important aspects of spontaneous upper limb use, i.e. overall duration and frequency of specific behaviours. The aim of this study was to investigate the test-retest, interrater and intrarater reliability and the construct validity of a new module, the VOAA-DDD, to det...

2017
Anne Krause Eckhard Schönau Albert Gollhofer Ibrahim Duran Anja Ferrari-Malik Kathrin Freyler Ramona Ritzmann

INTRODUCTION Individuals suffering from cerebral palsy (CP) often have involuntary, reflex-evoked muscle activity resulting in spastic hyperreflexia. Whole-body vibration (WBV) has been demonstrated to reduce reflex activity in healthy subjects, but evidence in CP patients is still limited. Therefore, this study aimed to establish the acute neuromuscular and kinematic effects of WBV in subjects...

Journal: :Pediatric neurology 2005
Wojciech Kulak Wojciech Sobaniec Joanna Smigielska-Kuzia Bozena Kubas Jerzy Walecki

The aim of this study was to compare spastic diplegic and tetraplegic cerebral palsy. Thirty-eight children had spastic diplegic cerebral palsy and 48 spastic tetraplegic cerebral palsy. Risk factors of cerebral palsy, seizures, severity of cerebral palsy, electroencephalogram, and magnetic resonance imaging findings were analyzed. Gestational history, low birth weight, and perinatal pathologie...

Journal: :iranian journal of basic medical sciences 0
ali shoeibi assistant professor of neurology, mashhad university of medical sciences mohammdmahdi etemadi professor of neurology, mashhad university of medical sciences amir moghaddam ahmadi neurologist, rafsanjan university of medical sciences mona amini resident of neurology, mashhad university of medical sciences reza boostani assistant professor of neurology, mashhad university of medical sciences

human t-cell lymphotropic virus (htlv) types 1 and 2 belong to the oncorna group of retroviridae, a large family of viruses, grouped initially by pathogenic features, but later revised on the basis of genome structure and nucleotide sequence. htlv-i was the first discovered human retrovirus to be associated with a malignancy in 1980. the malignancy, first described by uchiyama and co-workers in...

2012
Susanne T. de Bot Helenius J. Schelhaas Erik-Jan Kamsteeg Bart P.C. van de Warrenburg

Sir, The hereditary spastic paraplegias constitute a genetically and clinically heterogeneous group of disorders of which the main clinical feature is progressive lower limb spasticity due to pyramidal tract dysfunction. The cardinal signs result from a ‘dying back’ degeneration of the corticospinal tracts and dorsal column, predominantly due to disturbed axonal transport within the longest fib...

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