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Y Nagamoto, T Ishii, H Sakaura, M Iwasaki… - Spine, 2011 - journals.lww.com
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L Hong… - Journal of Spinal Disorders & …, 2011 - journals.lww.com
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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]. ...
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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. ...
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[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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