نتایج جستجو برای: spondylo
تعداد نتایج: 77 فیلتر نتایج به سال:
increase haemoglobin synthesis and erythro-poiesis. Further clinical and fundamental research is warranted to establish the possible beneficial effects of (oral) iron chelation treatment on RA activity and the anaemia of chronic disease. of hydroxyl radicals in the presence of ferritin and hemosiderin. Is hemosiderin formation a biological protective mechanism? Biochem J 1986; 234: 727-31. Iron...
OBJECTIVE The purpose of this cross-sectional survey was to obtain and analyze data on self-perceived efficacy of different types of complementary alternative medicine (CAM) by patients with various rheumatologic conditions. METHODS Patients followed in rheumatology outpatient clinics were screened for the use of CAM. Patients reporting the use of CAM were asked to participate in face-to-face...
La spondylodiscite tuberculeuse est la localisation la plus fréquente des tuberculoses ostéo-articulaires et parmi-celle-ci l'atteinte dorsolombaire est prédominante. Les formes associées à d'autres localisations de la tuberculose restent rares chez les immuno-compétants. Les auteurs rapportent une observation d'un patient présentant des signes radiologiques majeurs d'une tuberculose multiviscé...
Spondylolisthesis has always fascinated orthopaedist and others concerned with the treatment of low back disease. Spondylo means Vertebra and Olisthesis to slip or slide down a slippery path.In this orticle.the history of spondylolisthesis has been described,followed by the recent classification of different types of the condition.There are Sdifferent types of spondylolisthesisdysplastic,Isth...
Spondylo-meta-epiphyseal dysplasia (SMED) with short limbs and abnormal calcifications (SMED-SL) is a rare, autosomal recessive human growth disorder, characterized by disproportionate short stature, short limbs, short broad fingers, abnormal metaphyses and epiphyses, platyspondyly and premature calcifications. Recently, three missense mutations and one splice-site mutation in the DDR2 gene wer...
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