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The Journal of Clinical Endocrinology and Metabolism|November 30, 2000
Rare somatic inactivation of the multiple endocrine neoplasia type 1 gene in secondary hyperparathyroidism of uremiaH Tahara, Y Imanishi, T Yamada, et al.
Acta Crystallographica. Section D, Biological Crystallography|October 27, 2001
Crystals of ternary protein-DNA complexes composed of DNA-binding domains of c-Myb or v-Myb, C/EBPalpha or C/EBPbeta and tom-1A promoter fragmentT H Tahirov, M Sasaki, T Inoue-Bungo, et al.
Journal of Human Genetics|May 17, 2001
Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis: a common mutation, R179XT Miyamoto, N Kanazawa, S Kato, et al.
Hiroshima Journal of Medical Sciences|April 21, 2001
Characteristic magnetic resonance imaging for neurological assessment in HELLP syndrome with eclampsia: a case reportS Fukuhara, K Migita, K Iida, et al.
Clinical Nephrology|January 26, 2008
Reversible primary hypothyroidism in Japanese patients undergoing maintenance hemodialysisT Sanai, T Inoue, K Okamura, et al.
Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|January 1, 1992
[An elderly case of hypertension with persistent orthostatic hypotension]Y Nakata, A Otsuka, M Oishi, et al.
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