• 参予者类型新生儿出生体重小于2500公克,出生24小时证实有代谢性酸血症动脉血液气体分析)。

    Types of participants Newborn infants with birth weight <2500g and less than 24 hours of age with proven metabolic acidaemia (on arterial blood gas).

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  • 篇文献主要目的评估对于出生体重(<2500公克新生儿早期(在出生后24小时内)代谢酸血症快速矫正后产生的短期长期效应

    The main objective was to assess the short and long-term effects of the rapid correction of early (first 24 hours) metabolic acidaemia in LBW (<2500g birth weight) neonates.

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  • 同样地,高磷血症液过多症、蛋白尿存在依靠试验模型饮食方式可能使人误解并且无法其扩展表现出的准确测量

    Likewise, the presence of hyperphosphatemia, acidosis, and proteinuria may be misleading depending on the experimental model and diet and may not represent a precise measure of progression.

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  • 甲基丙二血症由于甲基丙二酰辅酶A变位酶辅酶腺苷钴胺素缺陷所致遗传代谢疾病

    Methylmalonic acidemia is an inherited metabolic disorder, which is caused by deficiency of methylmalonyl-coenzyme a mutase or its cofactor adenosylcobalamin.

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  • 粒细胞胃肠炎一种原因不明疾病其特征胃肠道弥漫局限柱细胞浸润同时伴有周围的嗜粒细胞增多症。

    Eosinophilic gastroenteritis is a disease of unknown cause, characterized by diffuse or localized gastrointestinal eosinophil infiltration, often accompanied by peripheral blood eosinophilia syndrome.

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  • 粒细胞胃肠炎一种原因不明疾病其特征胃肠道弥漫局限柱细胞浸润同时伴有周围的嗜粒细胞增多症。

    Eosinophilic gastroenteritis is a disease of unknown cause, characterized by diffuse or localized gastrointestinal eosinophil infiltration, often accompanied by peripheral blood eosinophilia syndrome.

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