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- Ascochyta imperfectan. 不全壳二胞
- Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode. 摘要牙本质形成不良是一种体染色体显性遗传的中胚层缺陷。
- Objective To evaluate the diagnostic value of X-ray in osteogenesis imperfecta of fetus. 目的评估X线对胎儿期成骨不全的诊断价值。
- Objective To summarize the experience of pamidronate for osteogenesis imperfecta. 目的总结帕米膦酸钠在成骨不全症中的应用经验。
- The causal agent identified is a species of fungi belonging to genus Asco- chyta and is named Ascochyta sp. tentatively. 经鉴定;其病原菌是一种真菌;属于半知菌亚门、球亮孢目、壳二孢属(Ascochyta sp.;)
- Methods To review the effect of intravenous pamidronate therapy on two patients with osteogenesis imperfecta in 2007. 方法对2007年我院收治的2例成骨不全症的治疗进行回顾分析。
- The geographic origin of each isolate of Ascochyta might have contributed to the genetic diversification revealed by RAPD analysis. 近年利用温室、大棚栽培甜瓜的面积逐渐扩大，采前、采后病害均比较严重。
- Dentinogenesis imperfecta type I(DGI-I) is an autosomal dominant dental disease with abnormal dentin production and mineralization. 我国科学家成功地克隆了遗传性乳光牙本质I型病的基因，为遗传性乳光牙I型病的诊断带来希望。
- The purpose of this study is the concern caregivers issue with regards to strategies and coping with adolescents who have Osteogenesis Imperfecta. 本研究的目的是探讨成骨不全症之青少年及其主要照顾者对疾病在照护过程中所关注的内容及因应的策略。
- Four new species, one new combination and nineteen Chinese new records of the genus Ascochyta are reported in this paper. The new species are Asco-chyta araliae Sun et Bai, A. 本文报告了壳二孢属(Ascochyta)新种4个:(木忽)木壳二孢(Ascochyta araliae Sun et Bai);朝鲜槐壳二孢(A.;maackiae Sun et Bai);假酸浆壳二孢(A
- Osteogenesis imperfecta is an inherited disorder of connective tissue, which affects the skeleton, ligament, skin, sclera, and dentin. 摘要骨发生不全是一种遗传性的结缔组织病变，常侵犯骨骼、韧带、皮肤、角膜及牙齿。
- We report a 20-year-old male patient with Osteogenesis imperfecta, who suffered from multiple long bone fractures and spinal kyphoscoliosis since his childhood. 本研究报告一例廿岁的男性骨发生不全患者，自幼年起即常发生四肢长骨骨折，并由于脊椎变形严重，造成心肺功能障碍。
- Joints overactive in 4 cases, 2 cases had family history.Conclusion: Osteogenesis imperfecta is an osteodysplasty X-ray examination play an important role in diagnosing the disease. 结论：本病为骨发育障碍性疾病，X线检查对本病的诊断有着十分重要的价值。
- Babies with brittle bone diseases (Ontogenesis imperfecta, OI)arereported after the launch of high calcium milk. How to explainthiscorrelation? Can it be simply commented as genetic disorder? 四.;自从有高钙奶粉上市后;玻璃娃娃也相继出现;其因何在?岂是遗传?
- Conclusion Pamidronate therapy has a positive effect on patients with osteogenesis imperfecta,while this still remains to be demonstrated in more patients with osteogenesis imperfecta. 结论帕米膦酸钠对成骨不全症有较好疗效,但需更多病例观察。
- Babies with brittle bone diseases (Ontogenesis imperfecta, OI) arereported after the launch of high calcium milk. How to explain thiscorrelation? Can it be simply commented as genetic disorder? 四.;自从有高钙奶粉上市后;玻璃娃娃也相继出现;其因何在?岂是遗传?
- ascochyta leaf spot of kidney bean 扁豆褐斑病
- osteogenesis imperfecta [abnormal bone frailty] 骨脆弱,骨发生不全
- congenital osteogenesis imperfecta 先天性成骨不全
- Neonatal lethal osteogenesis imperfecta congenita 先天性新生儿致死性成骨不全
