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Early transition from insulin to sulfonylureas in neonatal diabetes and follow-up: Experience from China.

Xiuzhen LiAijing XuHuiying ShengTzer Hwu TingXiaojian MaoXinjiang HuangMinyan JiangJing ChengLi Liu
Published in: Pediatric diabetes (2017)
Molecular genetic diagnosis is recommended in all patients with NDM. However, if genetic testing results are delayed, sulfonylurea therapy should be considered before such results are received, even in infants with newly diagnosed NDM.
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