Current status of hypothermia treatment for neonatal hypoxic-ischemic encephalopathy in Taiwan.

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Published in Pediatr Int on October 01, 2012

Authors

Bai-Horng Su, Takashi Igarashi

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Short-term and long-term outcomes of octogenarians after off-pump coronary artery bypass surgery. Gen Thorac Cardiovasc Surg (2010) 0.83

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Prefrontal activation during inhibitory control measured by near-infrared spectroscopy for differentiating between autism spectrum disorders and attention deficit hyperactivity disorder in adults. Neuroimage Clin (2013) 0.81

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Survival in a neonate with complete urorectal septum malformation sequence after fetal vesico-amniotic shunting for a prominently dilated cloaca. Fetal Diagn Ther (2008) 0.80

Children's toxicology from bench to bed--Drug-induced renal injury (1): The toxic effects of ARB/ACEI on fetal kidney development. J Toxicol Sci (2009) 0.79