神經病遺傳 的英文怎麼說
中文拼音 [shénjīngbìngyízhuàn]
神經病遺傳
英文
neuropathic heredity- 神 : Ⅰ名詞1 (神靈) god; deity; divinity 2 (精神; 精力) spirit; mind 3 (神氣; 神情) expression; l...
- 經 : 經動詞[紡織] (把紡好的紗或線梳整成經紗或經線) warp
- 病 : Ⅰ名詞1 (疾病; 失去健康的狀態) illness; sickness; disease; malum; nosema; malady; morbus; vitium...
- 遺 : 遺動詞[書面語] (贈與) offer as a gift; make a present of sth : 遺之千金 present sb with a gener...
- 傳 : 傳名詞1 (解釋經文的著作) commentaries on classics 2 (傳記) biography 3 (敘述歷史故事的作品)...
- 神經病 : 1. (神經系統中的疾病) neuropathy; nervous disease2. (精神病的俗稱) mental disorder
- 神經 : nerve; nervus
- 遺傳 : [生物學] heredity; hereditary; inheritance; inherit
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We concluded that ( 1 ) motion asymmetry correlates closely with early - onset eye disorders that hinder the normal development of binocular vision ; ( 2 ) motion asymmetry correlates less with pure amblyopia ; ( 3 ) motion asymmetry is not unique to infantile esotropia syndrome ; ( 4 ) persisted motion asymmetry in adult is acquired rather than gene - determined ; ( 5 ) motion asymmetry may not be the cause of strabismus ; ( 6 ) motion asymmetry my not be secondary to disorganized nondecussated optic pathway and ( 7 ) motion asymmetry is an overall immaturity of sensory - motor pathway
我們的結論是: ( 1 )任何早發性眼科疾病,假如阻礙了正常的雙眼視覺發育,則造成不對稱的運動覺; ( 2 )運動覺不對稱並不直接和弱視本身相關聯; ( 3 )運動覺不對稱並非幼兒型內斜視專有的特徵; ( 4 )成人的運動覺若不對稱,是視覺發育過程中受到阻礙造成,而非遺傳而來的; ( 5 )運動覺不對稱並非斜視的原因; ( 6 )運動覺不對稱的原因並非來自視覺神經路徑上太多的非交叉視覺神經; ( 7 )運動覺不對稱是向感覺到運動總體視路徑發育不全所造成的結果。Hereditary motor and sensory neuropathy
遺傳性運動感覺性神經病One particularly bad gene leads to huntington ' s disease, which progressively destroys key nerve cells
一個壞基因可以導致遺傳性慢性舞蹈病的發生,此病能逐漸破壞人體中關鍵性的神經細胞。Huntington ' s disease is a genetic disease marked by a decline in cognitive functions, including memory loss and disorientation, the onset of uncontrolled movements and impaired motor skills
亨廷頓癥是一種遺傳病,其典型癥狀是認知機能出現衰退,具體包括記憶丟失,方向知覺喪失,無序行為發作以及運動神經機能衰退。When someone with a susceptible genetic background encounters certain environmental factors, such as pesticides or other chemicals [ see box on this page ], the cells in that individual ' s substantia nigra suffer more stress and accumulate more misfolded proteins than do the same cells in other people
當易發病遺傳體質的人碰了上某些環境因子,例如殺蟲劑或其他化學物質(見右欄環境元凶) ,這些人的黑質神經元,會比其他人更容易受逆境所傷害,摺疊錯誤的蛋白質也堆積得更多。Alternatively, they could generate healthy specialized cells from patients who had donated their genetic material, and transplant them into tissues - - without the risk of prompting immune rejection - - to treat failing hearts, neurological diseases such as parkinson ' s disease and amyotrophic lateral sclerosis, spinal cord injury and diabetes
上述二者中,他們可從被診為患遺傳疾病的病人中生成指定的健康細胞,並將其移植培養為組織不存在排斥免疫方面的風險可治療心臟衰竭,神經疾病如帕金森癥,肌萎縮性(脊髓)側索硬化癥,骨髓病癥和糖尿病。In the meantime, congenital amblyopia resulted from optic nerve lesion was observed in the crested ibis, with an incidence rate of 3 - 5 %. since the epilepsy and congenital amblyopia are both hereditary, it is feasible to perform genetic engineering studies on the correlative genes, which could protect neurons from the damages of excitation toxin and vision sickness, in order to cure the diseases at gene level
由於癲癇和視神經病變類疾病均屬于遺傳性疾病,因此,利用分子生物學技術,對因癲癇和遺傳性弱視癥導致的神經元損傷具有保護及再生作用,以及視神經通路的發育、分化和受損視覺通路具有修復作用的相關基因,開展克隆、表達和活性鑒定之研究,將為通過基因工程技術實現其疾病治療之目標奠定基礎。A male patient of 10 years old gave his chief complaint of slow movement and unclear vision in the xishan department of neural regeneration and functional reconstruction in beijing shijingshan district in october 16th 2005
0引言x -連鎖腎上腺腦白質營養不良是一種遺傳性代謝疾病,由於飽和極長鏈脂肪酸在過氧化酶體內-氧化障礙,以致飽和極長鏈脂肪酸在血、腦白質、腎上腺皮質等器官和組織大量積聚,引起中樞神經系統脫髓鞘和腎上腺皮質萎縮或發育不良。Discuss the cause of these two diseases in terms of their anatomical, genetic and neurotransmitter basis
請就解剖學、遺傳學以及神經傳導物質方面討論這兩種疾病的成因。The study of motor nerve conduction of the stroke sequela models of rats which are lack of qi and with blood silted
中風后遺癥氣虛血瘀大鼠病證模型運動神經傳導的研究" it seems that physical activity had an even more pronounced effect among those with the susceptibility gene apoe4, the most important risk factor for alzheimer ' s disease and dementia, " kivipelto added
報道說,這項發表在新一期柳葉刀:神經病學雜志上的研究結果顯示,那些對癡呆癥具有遺傳易感性的人受到的效果最為明顯。To deal with the two - class classification problem, a new strategy of integrating the genetic algorithm and the lvq artificial networks is adopted to reduce the dimensions in high dimension space. using this method, the classification accuracy is 100 % to leukemia dataset, and 91. 27 % to clone cancer dataset
把遺傳演算法和lvq神經網路結合進行高維空間的特徵選擇,以解決兩類別的樣本分類問題,並利用白血病和大腸癌基因晶元數據進行了實例計算,分別達到了100和91 . 27的準確度。Molecular and cellular mechanism of parkinson ' s disease ( pd ), drug therapy, surgical therapy, epidemiology of pd, genetics of pd, rehabilitation of pd, psychiatric aspects of pd and alternative medicine of pd
帕金森病的神經生物學、內科藥物治療、外科治療、流行病學、遺傳學、康復治療、精神狀態的處理和老年人帕金森病的治療和康復。Heriditary neuropathies come in many shapes and sizes. charcot - marie - tooth type 2 ( cmt2 ) causes degeneration of peripheral sensory and motor neurons, particularly at the ends of these long axons
遺傳性神經病具有多種特點和方式。 2型腓骨肌萎縮癥( cmt 2 )導致外周特別是長軸突末端的感覺和運動神經元退化。分享友人