Blank Cover Image

Computer study of the ionic mechanisms of organophosphorous-caused long-QT syndrome (LQTS)

フォーマット:
電子ブック
責任表示:
Zoltani, Csaba K.
言語:
英語
出版情報:
Aberdeen Proving Ground, MD
著者名:
Zoltani, Csaba K.  
子書誌情報
Loading
オンライン
ジャーナル/ブックへリンク
所蔵情報
Loading availability information
タイトル・著者・出版者が同じ資料

類似資料:

1
 
2
 
3
 
4
 
5
 
6
 
7
 
8
 
9
 
10
 
11
 
12
 
1 電子ブック Organophosphonate caused cardiac toxicity : action potential dynamics in atrial tissue

Zoltani, Csaba K.
7 その他 Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome

Yamaguchi, Masato, 山口, 正人

金沢大学
2 電子ブック Computational model of soman-induced cardiac toxicity (I) : simulation at the cellular level

Zoltani, Csaba K.
8 論文 Q-T peak dispersion in congenital long QT syndrome: Possible marker of mutation of HERG

Inoue, Masaru, Shimizu, Masami, Ino, Hidekazu, Yamaguchi, Masato, Terai, Hidenobu, Hayashi, Kenshi, Kiyama, Masaru, …

日本循環器学会
3 電子ブック Evaluating performance of OpenMP and MPI on the SGI Origin 2000 with benchmarks of realistic problem sizes

Zoltani, Csaba K.
9 論文 Identical Twins with Long QT Syndrome Associated with a Missense Mutation in the S4 Region of the HERG

Hayashi, Kenshi, Shimizu, Masami, Ino, Hidekazu, Okeie, Kazuyasu, Yamaguchi, Masato, Yasuda, Toshihiko, Fujino, Noboru, …

Japanese Heart Journal Association
4 図書 Acquired long QT syndrome

Camm, A. John, Malik, Marek, Yap, Yee Guan

Blackwell
10 電子ブック Neuroimmune mechanisms and chronic fatigue syndrome : will understanding central mechanisms enhance the search for the causes, consequences, and treatment of …
5 電子ブック Heritable arrhythmias: insight into molecular physiology from the long QT syndrome

Kass, Robert

Henry Stewart Talks Ltd
11 論文 Study on molecular mechanisms of M-cell differentiation and function

Hase, K., Takatsu, H., Koide, Y., Maruyama-Takano, M., Takenouchi, H., Taniura, N., Hashimoto, K., Chihara, R., Ohno, H.

金沢大学がん研究所
6 図書 Ionics

Bockris, J. O'M. (John O'M.), 1923-, Reddy, Amulya K. N.

Plenum Press
12 論文 Second-site mutation in the Wiskott-Aldrich syndrome (WAS) protein gene causes somatic mosaicism in two WAS siblings

Wada, Taizo, Konno, Akihiro, Schurman, Shepherd H., Garabedian, Elizabeth K., Anderson, Stacie M., Kirby, Martha, …

American Society for Clinical Investigation