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Translational research in muscular d...

Mori-Yoshimura, Madoka.

Translational research in muscular dystrophy

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	Translational research in muscular dystrophy/ edited by Shin'ichi Takeda, Yuko Miyagoe-Suzuki, Madoka Mori-Yoshimura.
其他作者:	Takeda, Shin'ichi.
出版者:	Tokyo :Springer Japan : : 2016.,
面頁冊數:	viii, 199 p. :ill., digital ; : 24 cm.;
Contained By:	Springer eBooks
標題:	Muscular dystrophy - Research. -
電子資源:	http://dx.doi.org/10.1007/978-4-431-55678-7
ISBN:	9784431556787

Translational research in muscular dystrophy
Translational research in muscular dystrophy[electronic resource] /edited by Shin'ichi Takeda, Yuko Miyagoe-Suzuki, Madoka Mori-Yoshimura. - Tokyo :Springer Japan :2016. - viii, 199 p. :ill., digital ;24 cm.

This book presents recent advances in translational research on muscular dystrophy (MD) to physicians and researchers, including cutting-edge research on the disease such as regenerative medicine, next-generation DNA sequencing, and nucleic acid therapies. It also describes the current systems for clinical trials and MD patient databases, resources, which will support the early realization of clinical application and improve patients' quality of life. MD is the one of the most widely known inherited neuromuscular diseases and is classified into diverse types by symptoms, age of onset, mode of inheritance, and clinical progression. With the development of molecular biology, the occurrence mechanisms of each type of MD are gradually being elucidated. Although there is no known permanent cure yet, the stage of treatment research has now advanced to clinical trials.

ISBN: 9784431556787

Standard No.: 10.1007/978-4-431-55678-7doiSubjects--Topical Terms:

1106245
Muscular dystrophy
--Research.

LC Class. No.: RC935.M7

Dewey Class. No.: 616.748

Translational research in muscular dystrophy
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245 0 0 $a Translational research in muscular dystrophy $h [electronic resource] / $c edited by Shin'ichi Takeda, Yuko Miyagoe-Suzuki, Madoka Mori-Yoshimura.
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520 $a This book presents recent advances in translational research on muscular dystrophy (MD) to physicians and researchers, including cutting-edge research on the disease such as regenerative medicine, next-generation DNA sequencing, and nucleic acid therapies. It also describes the current systems for clinical trials and MD patient databases, resources, which will support the early realization of clinical application and improve patients' quality of life. MD is the one of the most widely known inherited neuromuscular diseases and is classified into diverse types by symptoms, age of onset, mode of inheritance, and clinical progression. With the development of molecular biology, the occurrence mechanisms of each type of MD are gradually being elucidated. Although there is no known permanent cure yet, the stage of treatment research has now advanced to clinical trials.
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