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The Japanese Journal of Antibiotics|April 18, 1998
[Pharmacokinetic, bacteriological and clinical studies on cefozopran in neonates]T Abe, M Sugiura, Y Nakazato, et al.
American Journal of Medical Genetics|May 19, 2000
Girl with accelerated growth, hearing loss, inner ear anomalies, delayed myelination of the brain, and del(22)(q13.1q13.2)Y Fujita, D Mochizuki, Y Mori, et al.
Kyobu Geka. the Japanese Journal of Thoracic Surgery|February 15, 2002
[Esophageal rupture just after the graft replacement of thoracoabdominal aorta for chronic aortic dissection]J Fukada, T Uzuka, Y Fujisawa, et al.
Neuromuscular Disorders : NMD|April 22, 2004
A novel stop codon mutation in the PMP22 gene associated with a variable phenotypeK T Abe, A M M Lino, M T A Hirata, et al.
Nuklearmedizin. Nuclear Medicine|July 30, 2009
The utility of FDG-PET for detecting multiple primary cancers in hypopharyngeal cancer patientsH Kaida, M Ishibashi, S Kurata, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 30, 1998
No deterioration in insulin sensitivity, but impairment of both pancreatic beta-cell function and glucose sensitivity, in Japanese women with former gestational diabetes mellitusH Sakamaki, H Yamasaki, K Matsumoto, et al.
The Journal of Biological Chemistry|June 8, 1999
Identification of a novel gene family encoding human liver-specific organic anion transporter LST-1T Abe, M Kakyo, T Tokui, et al.
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