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Human Genetics|September 1, 1995
Molecular basis of phenotypic variation in patients with argininemiaT Uchino, S E Snyderman, M Lambert, et al.
The European Journal of Neuroscience|August 8, 2001
Roles of the glutamate receptor epsilon2 and delta2 subunits in the potentiation and prepulse inhibition of the acoustic startle reflexT Takeuchi, Y Kiyama, K Nakamura, et al.
Human Genetics|February 1, 1997
The R40H mutation in a late onset type of human ornithine transcarbamylase deficiency in male patientsA Nishiyori, M Yoshino, H Kato, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 24, 1999
Mass screening for Wilson's disease: results and recommendationsY Yamaguchi, T Aoki, S Arashima, et al.
Clinical Chemistry|November 1, 1987
Four methods compared for measuring des-carboxy-prothrombin (PIVKA-II)J Widdershoven, P van Munster, R De Abreu, et al.
Pharmacology & Therapeutics|January 1, 1992
Activation of lymphokine genes in T cells: role of cis-acting DNA elements that respond to T cell activation signalsN Arai, Y Naito, M Watanabe, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|November 1, 1996
A new blood compatible and permselective hollow fiber membrane for hemodialysisS Yamashita, A Mochizuki, T Nakazaki, et al.
European Journal of Neurology|June 4, 2013
p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small-vessel occlusion in elderly Japanese malesK Nakamura, Y Sekijima, K Nakamura, et al.
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