【摘 要】
：
Objectives Because of the multi-systemic presentation of myotonic dystrophy (DM), many patients visit various specialists before the diagnosis of DM.A part of patients were diagnosed after perinatal o
【机 构】
：
National Hospital Organization Toneyama National Hospital
【出 处】
：
The 12th Annual Asian and Oceanian Myology Center (AOMC)Scie
论文部分内容阅读
Objectives Because of the multi-systemic presentation of myotonic dystrophy (DM), many patients visit various specialists before the diagnosis of DM.A part of patients were diagnosed after perinatal or perioperative complications.We considered that a screener for DM is essential to avoid such troubles and to introduce multidisciplinary approach smoothly.
其他文献
Generation of male germ cells in vitro could have great application for treating male infertility.Currently there is no effective method for generating haploid sperm in vitro from human testes.Cryptor
Multiple gestations carry significant maternal and neonatal risks and are considered an adverse outcome of assisted reproductive technology.Appropriate selection of a single blastocyst for transfer de
前言·人的出生原本屬於「天擇」 (by chance),但由於生殖醫療科技的發達,越來越趨近於科學家們可以精心策劃的「人擇」 (by Choice).·法律的内容常常落後於社會的變遷,更永遠趕不及科技的發展.胚胎在台灣法體系的地位·胚胎的地位一向是生命倫理學者舆法律學者探討的重點.一般而言共有三種學說:人的模式、物的模式、以及尊敬模式.
近年来出现的胚胎延时摄像技术(time-lapse)能够对胚胎体外发育过程进行全程监控,获取胚胎发育的动态信息,建立胚胎行为学指标对胚胎发育潜能进行更有效的评估,选择发育潜能最佳的胚胎进行移植.以往的研究主要关注卵裂时间、卵裂同步性等形态动力学(morphokinetics)指标,而我们的研究主要致力于探讨卵裂行为与胚胎发育潜能及染色体异常的关系,并且将异常卵裂模式根据卵裂时期进行划分,希望发现不
After a period of heated debate on the efficacy of PGS(Preimplantation Genetic Screening), followed by a cautious decline of the use of PGS, recent enthusiasm in PGS is evident.This renewed interest i
在体外受精治疗中,胚胎发育潜能的正确评价是得到良好妊娠结局的基本保障.目前胚胎质量的评价仍以形态学为主要依据.卵裂期胚胎的形态学评分目前国内大多数中心采用的是第3天卵裂期移植的方式,采用以细胞数和碎片含量为主要指标的形态学评价方法,挑选优质的胚胎进行移植或冷冻,较差的胚胎则丢弃.但是由于胚胎移植入体内后着床、妊娠与多种因素相关,因此这种形态学的选择方法是否与胚胎的发育潜能是否一致难以判断.而体外进
玻璃化冷冻任何一项工作都是为了:保存人类珍贵的生命:卵子/胚胎没有损伤,没有风险直到患者的梦想成为现实Cryotec玻璃化冷冻的历史第一例体外受精胚胎(牛)第一例卵母细胞的体外成熟(牛)猪卵母细胞(最困难的细胞)
Introduction Long exercise test is helpful for diagnosis of hypokalemic periodic paralysis.After exercise, the CAMP amplitude of the studied muscle decreased accompanied by decrease of muscie strength
We report the case of a 40-year-old woman developed generalized muscle weakness without fluctuation in two months, Physical examination revealed a mobile mass in the right upper arm.Serum creatine pho
Introduction CMT1A is the most common hereditary neuropathy character by distal weakness and atrophy in limbs clinical and Pes Cavus.The electronic character is markedly decreased in nerve conduction.