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- 家族性C5補體無能症Lenier syndrome
- 肥胖性生殖無能症dystrophia adiposogenitalis
- 目的探討慢性肺源性心臟病患者血清補體C1q、C5、C9水平的變化及臨床意義。Objective To study the change and the clinical significance of complement C1q and C5 and C9 on serum in the chronic cor pulmonale patients.
- 家族性高膽固醇血症患者低密度脂蛋白受體基因新突變一例Identification of one novel mutation of the low density lipoprotein receptor gene in Chinese patients with familial hypercholesterolemia
- 青島地區新生兒臍血膽固醇測定早期篩查家族性高膽固醇血症Early screening familial hypercholesterolemia through infant umbilical blood cholesterol testing
- 人血漿補體C_9的純化Purification of the Ninth Component of Human Complement (C9)
- 家族性高膽固醇血症家系低密度脂蛋白受體基因剪接突變的研究Identification of a novel splice mutation of low density lipoprotein receptor gene in a Chinese family with familial hypercholesterolemia
- 特發性低補體血症essential hypocomplcmeatemia
- "別繼續以這種節奏節生活：你會得神經衰弱症的。""Don't carry on living this pace: You'll wind up with a nervous breakdown"
- 適體fit
- 次Schur補Sub-Schur complement
- 親和配體affinity ligand
- 肥胖性生殖無能綜合征dysdrophia adiposogenitalis
- 肥粒體[機] ferrite
- 白便症white feces syndrome
- 原孢子體protosporophore
- 原子性atomicity
- 主智能體main agent
- 原卟啉症protoporphyria
- 性價比高high performance cost ratio; highly cost effective
