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Toplam kayıt 9, listelenen: 1-9
Radiographic Measurement of the Sagittal Plane Deformity in Patients With Osteoporotic Spinal Fractures Evaluation of Intrinsic Error
(Springer, 2007)
Cobb method has been shown to be the most reliable technique with a reasonable measurement error to determine the kyphosis in fresh fractures of young patients. However, measurement errors may be higher for elderly patients ...
Minimum 10 Years Follow-Up Surgical Results Of Adolescent Idiopathic Scoliosis Patients Treated With Tsrh Instrumentation
(Springer, 2007)
Last two decades witnessed great advances in the surgical treatment of idiopathic scoliosis. However, the number of studies evaluating the long-term results of these treatment methods is relatively low. During recent years, ...
Embolization Of High-Flow Craniofacial Vascular Malformations With Onyx
(Amer Soc Neuroradiology, 2007)
BACKGROUND AND PURPOSE: Various techniques and materials have been used for the endovascular treatment of craniofacial high-flow arteriovenous vascular malformations, because their rarity precludes standardization of their ...
Eye Closure Sensitivity And Epileptic Syndromes: A Retrospective Study Of 26 Adult Cases
(W B Saunders Co Ltd, 2007)
Purpose: The transient, mainly generalized, together with brief changes in EEG baseline immediately after eye closure, is called 'eye closure sensitivity' (ECS) which was first reported by Robinson in 1930 and there have ...
Increased Gray Matter Density In The Parietal Cortex Of Mathematicians: A Voxel-Based Morphometry Study
(Amer Soc Neuroradiology, 2007)
BACKGROUND AND PURPOSE: The training to acquire or practicing to perform a skill, which may lead to structural changes in the brain, is called experience-dependent structural plasticity. The main purpose of this cross-sectional ...
The Myopathic Form Of Coenzyme Q10 Deficiency Is Caused By Mutations In The Electron-Transferring-Flavoprotein Dehydrogenase (Etfdh) Gene
(Oxford Univ Press, 2007)
Coenzyme Q10 (CoQ10) deficiency is an autosomal recessive disorder with heterogenous phenotypic manifestations and genetic background. We describe seven patients from five independent families with an isolated myopathic ...
Refining Genotype - Phenotype Correlations in Muscular Dystrophies with Defective Glycosylation of Dystroglycan
(Oxford Univ Press, 2007)
Muscular dystrophies with reduced glycosylation of alpha-dystroglycan (alpha-DG), commonly referred to as dystroglycanopathies, are a heterogeneous group of autosomal recessive conditions which include a wide spectrum of ...
Proton Mr Spectroscopy: Higher Right Anterior Cingulate N-Acetylaspartate/Choline Ratio in Asperger Syndrome Compared with Healthy Controls
(Amer Soc Neuroradiology, 2007)
BACKGROUND AND PURPOSE: One former study reported higher prefrontal N-acetylaspartate (NAA) levels in patients with Asperger syndrome (AS). The objective of the current study was to test the hypothesis that patients with ...
Hyperform Balloon-Assisted Endovascular Neck Bypass Technique To Perform Balloon Or Stentassisted Treatment Of Cerebral Aneurysms
(Amer Soc Neuroradiology, 2007)
We describe a technique to bypass aneurysm neck using the HyperForm balloon to perform balloon- or stent-assisted enclovascular treatment of complex large or giant aneurysms with very wide neck in which other methods would ...