Pages that link to "Q33588823"
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The following pages link to Idiopathic cerebellar ataxia of late onset: natural history and MRI morphology (Q33588823):
Displaying 50 items.
- Development of a 3D immersive videogame to improve arm-postural coordination in patients with TBI (Q24629010) (← links)
- Clinical signs of cerebellar dysfunction in schizophrenia, alcoholism, and their comorbidity (Q28201108) (← links)
- Progression and prognosis in multiple system atrophy: an analysis of 230 Japanese patients (Q30688673) (← links)
- Sporadic ataxia with adult onset: classification and diagnostic criteria (Q33524955) (← links)
- Multiple system atrophy: natural history, MRI morphology, and dopamine receptor imaging with 123IBZM-SPECT (Q33733062) (← links)
- Sporadic adult-onset ataxia of unknown etiology (Q34206834) (← links)
- Multiple system atrophy: pathophysiology and management (Q34432121) (← links)
- Sporadic adult onset ataxia of unknown etiology : a clinical, electrophysiological and imaging study (Q34700804) (← links)
- Diffusion tensor imaging of the cortico-ponto-cerebellar pathway in patients with adult-onset ataxic neurodegenerative disease (Q34732821) (← links)
- Population based study of late onset cerebellar ataxia in south east Wales. (Q35482433) (← links)
- Cognitive Impairment and Brain Imaging Characteristics of Patients with Congenital Cataracts, Facial Dysmorphism, Neuropathy Syndrome (Q35594692) (← links)
- High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease (Q36055058) (← links)
- Cervical dystonia in spinocerebellar ataxia type 2: clinical and polymyographic findings (Q36227397) (← links)
- Postural responses to changing task conditions in patients with cerebellar lesions (Q36318926) (← links)
- Clinical aspects of hereditary ataxias (Q36672749) (← links)
- Magnetic resonance imaging in degenerative ataxic disorders (Q36762044) (← links)
- Does use of a virtual environment change reaching while standing in patients with traumatic brain injury? (Q37070696) (← links)
- Cerebellar TMS in treatment of a patient with cerebellar ataxia: evidence from clinical, biomechanics and neurophysiological assessments (Q37633776) (← links)
- Neuropathology of degenerative ataxias (Q37914387) (← links)
- Multiple system atrophy of the cerebellar type: clinical state of the art. (Q38194974) (← links)
- Diagnosis and differential diagnosis of MSA: boundary issues (Q38348584) (← links)
- An update on the cerebellar subtype of multiple system atrophy (Q38578814) (← links)
- Comparison of cerebellar ataxias: A three-year prospective longitudinal assessment (Q39744457) (← links)
- Saccade velocity in idiopathic and autosomal dominant cerebellar ataxia (Q42121443) (← links)
- Extracerebellar MRI-lesions in ataxia telangiectasia go along with deficiency of the GH/IGF-1 axis, markedly reduced body weight, high ataxia scores and advanced age. (Q42462625) (← links)
- Proton magnetic resonance spectroscopic imaging reveals differences in spinocerebellar ataxia types 2 and 6. (Q43558052) (← links)
- Virtual reality game-based therapy for treatment of postural and co-ordination abnormalities secondary to TBI: a pilot study (Q44678527) (← links)
- The aetiology of sporadic adult-onset ataxia (Q44858419) (← links)
- Reduced cerebellar blood flow and oxygen metabolism in spinocerebellar degeneration: a combined PET and MRI study (Q48168280) (← links)
- Oculomotor abnormalities and MRI findings in idiopathic cerebellar ataxia (Q48178740) (← links)
- Proton magnetic resonance spectroscopy (1H MRS) in patients with sporadic cerebellar degeneration (Q48234826) (← links)
- Multiple system atrophy. Clinical and MR observations on 42 cases (Q48315520) (← links)
- Follow-up of neurophysiological tests and CT in late-onset cerebellar ataxia and multiple system atrophy (Q48352247) (← links)
- CT in autosomal dominant and idiopathic cerebellar ataxia (Q48381160) (← links)
- Topography of cerebral monoamine transporter availability in families with SCA2 mutations: a voxel-wise [123I]beta-CIT SPECT analysis (Q48540353) (← links)
- Physical therapy for correcting postural and coordination deficits in patients with mild-to-moderate traumatic brain injury (Q48625397) (← links)
- Contribution of cerebellum and brainstem in the control of eye movement: evidence from a functional study in a clinical model (Q48656569) (← links)
- Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus (Q48744758) (← links)
- The development of infratentorial atrophy in patients with idiopathic cerebellar ataxia of late onset: a CT study (Q48863789) (← links)
- Visuomotor learning in cerebellar patients (Q48873551) (← links)
- Improvement of upper limb ataxia and intention tremor allowing cessation of thalamic electrostimulation after four years (Q50282584) (← links)
- Decomposition of postural movements in individuals with mild TBI while reaching to intercept a moving virtual target. (Q50615228) (← links)
- A case of very rapid progressive ataxia in rehabilitation setting (Q50747876) (← links)
- Cognitive function in multiple system atrophy of the cerebellar type (Q51921379) (← links)
- Cognitive findings in spinocerebellar ataxia type 2: relationship to genetic and clinical variables. (Q52011283) (← links)
- Survival in multiple system atrophy: a study of prognostic factors in 59 cases. (Q52888623) (← links)
- Ataxia telangiectasia alters the ApoB and reelin pathway (Q57806939) (← links)
- Pre-emptive Allogeneic Hematopoietic Stem Cell Transplantation in Ataxia Telangiectasia (Q58694961) (← links)
- Cerebellar encephalitis in adults (Q72941464) (← links)
- Clinical and genetic study of a family with spinocerebellar ataxia type 1 (SCA1) and beta-thalassemia (Q74145198) (← links)