✦ LIBER ✦

Tissue distribution of mutant mitochondrial DNA in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)

✍ Scribed by Y. Shoji; W. Sato; K. Hayasaka; G. Takada

Publisher: Springer
Year: 1993
Tongue: English
Weight: 328 KB
Volume: 16
Category: Article
ISSN: 0141-8955
DOI: 10.1007/bf00711311

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Single muscle fiber analysis of mitochon

Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)

✍ Makoto Tokunaga; Dr. Shuji Mita; Tatsufumi Murakami; Toshihide Kumamoto; Makoto 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 698 KB

The 3260 mutation in mitochondrial DNA c

The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)

✍ Ichizo Nishino; Mikio Komatsu; Soichi Kodama; Satoshi Horai; Ikuya Nonaka; Yu-Ic 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 248 KB

Maternally inherited myopathy and cardiomyopathy (MIMyCa) is one of the phenotypic subgroups of mitochondrial diseases. There are two reports of European families with MyMICa associated with an Ato-G transition at nucleotide (nt) 3260 in the mitochondrial tRNAkU(UUR) We have identified the 3260 mut

Mitochondrial myopathy, encephalopathy,

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) decrease in diastolic left ventricular function assessed by echocardiography

✍ Yukiko Suzuki; Kenji Harada; Yasunori Miura; Wataru Sato; Kiyoshi Hayasaka; Koic 📂 Article 📅 1993 🏛 Springer 🌐 English ⚖ 880 KB

Mitochondrial DNA mutation and muscle pa

Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

✍ Dr. Shuji Mita; Dr. Makoto Tokunaga; Dr. Toshihide Kumamoto; Dr. Makoto Uchino; 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 618 KB

Strongly succinate dehydrogenase–reactiv

Strongly succinate dehydrogenase–reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes

✍ Dr Hitomi Hasegawa; Taro Matsuoka; Yu-ichi Goto; Ikuya Nonaka 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 543 KB

Myo-leukoencephalopathy in twins: Study

Myo-leukoencephalopathy in twins: Study of 3243-myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutation

✍ Dr. F. Degoul; M. Diry; A. Pou-Serradell; J. Lloreta; C. Marsac 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 677 KB