Y Nagamoto, T Ishii, H Sakaura, M Iwasaki… - Spine, 2011 - journals.lww.com Wolters Kluwer Health may email you for journal alerts and information, but is committed to maintaining your privacy and will not share your personal information without your express consent. For more information, please refer to our Privacy Policy. ... Skip Navigation Links Home > Current ... Related articles - All 6 versions
L Hong… - Journal of Spinal Disorders & …, 2011 - journals.lww.com Wolters Kluwer Health may email you for journal alerts and information, but is committed to maintaining your privacy and will not share your personal information without your express consent. For more information, please refer to our Privacy Policy. ... Skip Navigation Links Home > Current ... Related articles - All 3 versions
A Onda, S Kikuchi, S Yabuki, K Otani… - Journal of Orthopaedic …, 2011 - Springer Alkaptonuria is a rare autosomal recessive metabolic dis- ease of the aromatic amino acids phenylalanine and tyro- sine. The disease is characterized by deficient homogentisic acid oxidase in the liver and kidneys and the subsequent excretion of homogentisic acid (HGA) in the urine [1, 2]. ... Related articles - All 2 versions
Q Guo, X Bi, B Ni, X Lu, J Chen, J Yang… - European Spine Journal, 2011 - Springer Abstract The purpose of this article is to compare the outcomes of three different anterior approaches for three- level cervical spondylosis. The records of 120 patients who underwent anterior approaches because of three-level cer- vical spondylosis between 2006 and 2008 were reviewed. ... Related articles - All 2 versions
[PDF] from nagasaki-u.ac.jpH Baba, A Tagami, S Adachi… - Acta Medica …, 2011 - naosite.lb.nagasaki-u.ac.jp Recent advances in hemodialysis have prolonged patient lifespan and increased the number of hemodialysis patients. However, the incidence of complications has increased. Destructive spondyloarthropathy (DSA) complicating chronic hemodialysis was defined by Kuntz et ...
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