myotonic muscular dystrophy中文的意思、翻譯及用法：n.a severe form of muscular ... myotonia) 先天性副肌強直(Paramyotonia Congenita) 軟骨 . ... <看更多>
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myotonic muscular dystrophy中文的意思、翻譯及用法：n.a severe form of muscular ... myotonia) 先天性副肌強直(Paramyotonia Congenita) 軟骨 . ... <看更多>
#1. 肌強直症與肌強直型進行性肌肉萎縮症Myotonia and Myotonic ...
先天性副肌強直(Paramyotonia Congenita) 軟骨萎縮性肌強直(Chondrodystrophic myotonia, Schwartz-Jampel syndrome) 後天性的： 由一些藥物及毒素引起的肌強直。
#2. Airiti Library華藝線上圖書館_肌肉強直症之分子診斷
肌強直症(Myotonic disorders)是一種肌肉收縮後不易放鬆的現象，患者的骨骼肌會出現自發性收縮現象，也常常在自主性收縮或是電刺激之後無法正常地馬上放鬆。
#3. 強直性肌肉失養症 - 维基百科
其症狀包括逐漸惡化的肌肉損失（英语：Muscle atrophy）和虛弱，肌肉經常收縮而且無法放鬆（英语：Myotonia）。其他症狀可能包括白內障，智能障礙和心律不整問題。而男性 ...
#4. 天性副肌强直症_百度百科
肌强直(Myotonia)是一种肌肉收缩后不易放松的现象，在临床上敲打肌肉后可发现收缩后很缓慢的才放松。有肌强直现象得肌肉疾病通称为肌强直症( Myotonic disorders )。
#5. 先天性肌強直(myotonia congenita) - 漫談神經醫學
先天性肌強直是一種遺傳性的肌肉離子通道疾病， 該疾病的特徵是肌肉收縮後會延遲放鬆，又稱肌強直。 先天性肌強直有…
#6. paramyotonia congenita 中文 - 查查綫上辭典
paramyotonia congenita中文 :[網絡] 先天性副肌強直；先天性副肌強直癥；先天性肌強直病…，點擊查查權威綫上辭典詳細解釋paramyotonia congenita的中文翻譯 ...
語文別: 中文 ... A1737T) with variable clinical features such as potassi-um-aggravated myotonia, paramyotonia congenita, or hyperkalemic-periodic paralysis.
#8. Paramyotonia Congenita 先天性肌张力障碍
如何用「Paramyotonia Congenita」写出专业的英文句子? 参考「Paramyotonia Congenita」学术论文例句，一次搞懂!
#9. 0906 肌肉強直症Myotonic Dystrophy 有 - 罕見疾病基金會
診斷： 醫師從病人外觀及臨床症狀即可診斷，但是一些實驗室的檢驗仍是必須的，例如肌電圖、血清中肌酐酸磷酸酶濃度(CPK)、基因分析，肌肉病理切片、眼睛檢查等。另產前診斷 ...
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#11. paramyotonia congenita — 中文翻译- TechDico辞書
包含许多翻译示例按活动分类“paramyotonia congenita” – 英语-中文字典和智能翻译助手。
#12. Computational modeling of the muscle disorder paramyotonia ... - Gale
Paramyotonia congenita (PC) is a muscular disorder characterized by myotonia, or muscular stiffness, at cold temperatures. Myotonia is a burst of excess ...
#13. definition of paramyotonia by Medical dictionary
paramyotonia conge´nita a condition similar to myotonia congenita, except that the precipitating factor is exposure to cold, the myotonia is aggravated by ...
#14. 美国ACCDON公司旗下品牌 - LetPub编辑-SCI论文润色
the paramyotonia congenita NaV 1.4 gain-of-function mutations, R1448C, R1448H, and ... All 5 versions · Severe phenotypes of paralysis periodica paramyotonia ...
#15. 先天性肌强直 - 中文版GeneReviews
Shapiro B, Ruff R. Disorders of skeletal muscle membrane excitability: myotonia congenita, paramyotonia congenita, periodic paralysis, and ...
#16. 什么是先天性副肌强直？(paramyotonia congenita?) - tl80互动问答网
先天性副肌强直，又称欧伦堡病或欧伦堡先天性副肌强直，是一种罕见的先天性神经肌肉疾病，肌肉收缩后松弛缓慢。与其他神经肌肉疾病不同，先天性副肌强直患者放松肌肉的 ...
#17. 林明宏助理教授Ming-Hong Lin Ph.D
中文. 高雄醫學大學/醫學院/醫學系/微生物暨免疫學科 ... resurgent sodium currents of mutant Nav1.4 channel in two patients affected by paramyotonia congenita; ...
#18. Induce symptoms 释义| 柯林斯英语词典
Some patients also indicate that specific foods are able to induce symptoms of paramyotonia congenita. Retrieved from Wikipedia CC BY-SA 3.0 ...
#19. Differential diagnosis of myotonic disorders
Paramyotonia congenita and hyperkalemic periodic paralysis are associated with clinical paramyotonia and electrical myotonia. Acid maltase deficiency often ...
#20. Myotonia Congenita - Children's Health Issues - MSD Manuals
Myotonia congenita is an inherited disorder that causes muscle stiffness and muscle enlargement. It affects what most people think of as muscle, ...
#21. 期刊界All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息 ...
Paramyotonia congenita (PMC), a dominant disorder featuring cold-induced myotonia (muscle stiffness), has recently been genetically linked to a candidate ...
#22. 【佳学基因】需要多长时间可以拿先天强直性肌痉挛基因解码
先天强直性肌痉挛是英文paramyotonia congenita的中文翻译。该病是一种基因病、遗传病。佳学基因通过基因解码找到了导致这一疾病发生的基因。
#23. 一个骨骼肌钠离子通道病家系的临床特点和SCN4A基因变异分析
... 英文关键词：Channelopathy;SCN4A gene;Normokalemic periodic paralysis;Paramyotonia congenita; 中文刊名：中华医学遗传学杂志 ...
#24. 認識疾病- 社團法人中華民國肌萎縮症病友協會
先天性副肌強直(Paramyotonia Congenita) ... 三、先天性副肌強直(Paramyotonia cogenita) ... 以下資料蒙澳州肌萎縮症協會授權譯成中文謹此致謝 ...
#25. Pmc 中文
Paramyotonia congenita, a genetic disorder; PhysMath Central, a defunct journal imprint; Pontine micturition center, part of the brainstem; Premotor cortex, ...
#26. Types of Muscular Dystrophy and Neuromuscular Diseases
Central core disease · Hyperthyroid myopathy · Myotonia congenita · Myotubular myopathy · Nemaline myopathy · Paramyotonia congenita · Periodic paralysis-hypokalemic- ...
#27. 在"英语"词典里myotonic}的意思
Myotonia is present in Myotonia congenita, Paramyotonia Congenita and myotonic dystrophy. Generally, repeated contraction of ... 翻译者英语- 中文. 强直性肌.
#28. Types of Muscular Dystrophy and Neuromuscular Diseases
Myotonia congenita. Myotubular myopathy. Nemaline myopathy. Paramyotonia congenita ... English |; العربية |; 中文 |; Italiano |; 日本語 |; 한국어 |; فارسی ...
#29. 先天性肌强直- 维基百科，自由的百科全书
先天性肌强直（Myotonia congenita）是一种先天性神经肌肉离子通道病，会影响骨骼肌。这是一种遗传性疾病。该疾病的特点是肌肉无法终止收缩，延迟松弛， ...
#30. 冯字英文怎么缩写- 头条搜索
VHL-- 冯Hippel Lindau 英文缩写:VHL 中文全称:冯Hippel Lindau 英文全称:Von Hippel Lindau 英文缩写VHL ... PMC-- Congenita Paramyotonia的Eulenburg冯-搜英文缩写.
#31. myotonic dystrophy中文2022-精選在臉書/Facebook/Dcard上的 ...
myotonic muscular dystrophy中文的意思、翻譯及用法：n.a severe form of muscular ... myotonia) 先天性副肌強直(Paramyotonia Congenita) 軟骨 .
#32. ▷ Is Paramyotonia congenita hereditary? - Diseasemaps
Here you can see if Paramyotonia congenita can be hereditary. Do you have any genetic components? Does any member of your family have Paramyotonia congenita ...
#33. 三好氏远端肌肉无力症 - 万维百科
Myotonia congenita · Thomsen disease（英语：Thomsen disease） · Neuromyotonia/Isaacs syndrome（英语：Isaacs syndrome） · Paramyotonia congenita（ ...
#34. Myotonic dystrophy - VisualDx
Differential Diagnosis & Pitfalls · Myotonia congenita · Paramyotonia congenita · Duchenne muscular dystrophy · Becker muscular dystrophy · Emery- ...
#35. SCN4A基因详情-基因数据库-基因云馆
[中文简述(自动翻译):] 电压门控钠通道是一个大的α亚基具有24个跨膜结构域和一个或多个 ... Sodium channel mutations in paramyotonia congenita exhibit similar ...
#36. 肌肉营养不良和神经肌肉疾病的类型
核心的疾病; 甲状腺亢进肌病; 肌强直congenita; Myotubular肌病; Nemaline肌病; Paramyotonia congenita; 周期性paralysis-hypokalemic-hyperkalemic. 找一个医生.
#37. 什么是先天性副肌强直？ - Netinbag
先天性副肌强直，也称为Eulenberg病或Eulenberg的先天性肌强直，是一种罕见的先天性神经肌肉疾病，其中肌肉在收缩后缓慢放松。 在先天性肌强直中，与其他神经肌肉疾病不同 ...
#38. contracture musculaire - Translation into English
The primary symptom of paramyotonia congenita is muscle contracture which develops during exercise or activity. Elle se manifeste par une contracture ...
#39. "pc"是什么意思|"pc"的中文翻译- 医学词典
[=paramyotonia congenita](拉)先天性肌强直病 [=paratyphoid c]丙型副伤寒 [=parent cell(s)]母细胞,母代细胞,亲本细胞 [=parietal cell]胃壁细胞
#40. SCN4A抗体(ab65165)| Abcam中文官网
Defects in SCN4A are the cause of paramyotonia congenita of von Eulenburg (PMC) [MIM:168300]. PMC is an autosomal dominant channelopathy characterized by ...
#41. 科技部補助專題研究計畫報告 - 國立成功大學機構典藏
中文 摘要：研究背景：隨著高通量次世代定序的成本降低，此技術也逐漸應用 ... 一） 計畫中文摘要。 ... Paramyotonia Congenita p.R1448C.
#42. Central core disease - Wikipedia - Index of /
External links[edit] · Myotonia congenita · Thomsen disease · Neuromyotonia/Isaacs syndrome · Paramyotonia congenita.
#43. Matthew Larsen DO - Owner - Ascend Mental Health Center
I studied a disease called Paramyotonia Congenita and the effect of temperature on sodium channel function in mutated channels specific to the disease.
#44. Causes and Treatment for Temporary and Permanent Paralysis
The weakness in the muscles may be mild and only occur in certain muscle groups, or be may severe and impair the arms and legs. Paramyotonia congenita: a ...
#45. dyskeratosis congenita clinical: Topics by Science.gov
Genetics Home Reference: paramyotonia congenita ... Traditional (Cantonese dialect) (繁體中文) Expand Section Clinical Trials - English PDF Clinical Trials ...
#46. Muscle Velocity Recovery Cycles to Examine Muscle ... - JoVE
... sodium channel myotonia, paramyotonia congenita 16, myotonic dystrophy 17, Andersen-Tawil syndrome 18, and myotonia congenita 19, 20 ).
#47. myotonia congenita - 先天性肌強直病 - 國家教育研究院雙語詞彙
審譯日期: 103.1.21. 以myotonia congenita 進行詞彙精確檢索結果. 出處/學術領域, 英文詞彙, 中文 ...
#48. Thomsen and Becker disease - Orphanet
Myotonia congenita may be inherited as an autosomal dominant (Thomsen disease) or ... the so-called ''paradoxical myotonia'' (paramyotonia congenita).
#49. Que Veut Dire MYOTONIA en Français - Traduction En Français
muscles like paramyotonia congenita and myotonia congenita; whether it is a disorder of the nervous system;. [...] or whether it is a combination of both.
#50. Chapter 14 Flashcards - Quizlet
Explain how impaired inactivation of muscle voltage-gated Na+ channels can cause myotonia (paramyotonia congenita) and/or periodic paralysis.
#51. Structural study of skeletal muscle fibres in healthy and ...
Background: Paramyotonia congenita and Brody disease are well-described conditions in ... 中文摘要 Ⅰ 英文摘要 Ⅱ 目錄 Ⅲ 圖表目錄 Ⅴ 壹、文獻序論 1 一、 ...
#52. 先天性肌强直的临床特点是什么？ 爱问知识人
答： 先天性副肌强直（paramyotonia congenita)是由Eulenbei (1866 年）及Rich (1894 年）首先 ... NFP22-471中文-焊接作业 · 小型工厂员工规章制度 ...
#53. Dichlorphenamide (Diclofenamide，二氯苯二磺胺) - 仅供科研
... Hyperkalemic Periodic|Hypokalemic Periodic Paralysis|Paramyotonia Congenita ... 中文名称. 二氯苯二磺胺. 运输条件. Room temperature in continental US; ...
#54. 熱性痙攣
原始內容存檔於2015-03-06） （中文（繁體））. ... 癱瘓（英語：Hyperkalemic periodic paralysis）(HYPP, HyperKPP); 先天性肌強直（英語：Paramyotonia congenita） ...
#55. Adenosine nucleobase editors and uses thereof
Paramyotonia congenita of von Eulenburg; Parathyroid carcinoma; ... CN106893739A 2015-11-17 2017-06-27 香港中文大学 For the new method and system of target ...
#56. periodic paralysis sentence in Hindi (11-20) - Hindlish
11. Mutations in the gene are associated with hypokalemic periodic paralysis, hyperkalemic periodic paralysis, paramyotonia congenita, and potassium-aggravated ...
#57. "pc"是什么意思 | pc醫學中文 - 訂房優惠
[=capillarypressure]毛细血管[1]压[=packedcells]浓集细胞[2],积层电池,组式电池,细胞叠集,压榨细胞[=palmitoylcarnitine]软脂基肉毒碱[=pancuronium]双哌[3]雄双 ...
#58. 2022 ICD-10-CM Diagnosis Code G71.12: Myotonia congenita
Free, official coding info for 2022 ICD-10-CM G71.12 - includes detailed rules, notes, synonyms, ICD-9-CM conversion, index and annotation crosswalks, ...
#59. 肌肉強直症
肌⾁強直症(Myotonic Dystrophy )是⼀種遺傳性的肌肉萎縮症，為成年人發病中最常見的⼀類。超過九成的病⼈為一型，病因是因為肌強直營養不良蛋⽩質磷酸根轉移 ...
#60. Paramyotonia congenita - sl.wiki-3arabi.com
Paramyotonia congenita (PC), je redka prirojena avtosomno dominantna živčno-mišična motnja, za katero je značilna "paradoksalna" miotonija.
#61. First two Case Reports of Becker's type Myotonia Congenita
Becker's type Myotonia Congenita is an autosomal recessive nondystrophic skeletal muscle disorder characterized by muscle stiffness.
paramyotonia congenita 中文 在 myotonic dystrophy中文2022-精選在臉書/Facebook/Dcard上的 ... 的推薦與評價
myotonic muscular dystrophy中文的意思、翻譯及用法：n.a severe form of muscular ... myotonia) 先天性副肌強直(Paramyotonia Congenita) 軟骨 . ... <看更多>