✦ LIBER ✦

Muscle coenzyme Q10 in mitochondrial encephalomyopathies

✍ Scribed by Matsuoka, Taro; Maeda, Hiroko; Goto, Yu-ichi; Nonaka, Ikuya

Book ID: 122670867
Publisher: Elsevier Science
Year: 1991
Tongue: English
Weight: 345 KB
Volume: 1
Category: Article
ISSN: 0960-8966
DOI: 10.1016/0960-8966(91)90007-F

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Muscle Coenzyme Q Deficiency in Familial

Muscle Coenzyme Q Deficiency in Familial Mitochondrial Encephalomyopathy

✍ Saburo Ogasahara, Andrew G. Engel, David Frens and Diane Mack 📂 Article 📅 1989 🏛 National Academy of Sciences 🌐 English ⚖ 679 KB

Mitochondrial encephalomyopathy with coe

Mitochondrial encephalomyopathy with coenzyme Q10 deficiency

✍ Sobreira, C.; Hirano, M.; Shanske, S.; Keller, R. K.; Haller, R. G.; Davidson, E 📂 Article 📅 1997 🏛 Lippincott Williams and Wilkins 🌐 English ⚖ 677 KB

A case of mitochondrial encephalomyopath

A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiency

✍ Eric Boitier; Françoise Degoul; Isabelle Desguerre; Christiane Charpentier; Domi 📂 Article 📅 1998 🏛 Elsevier Science 🌐 English ⚖ 66 KB

Clinical improvement after administratio

Clinical improvement after administration of coenzyme Q10in a patient with mitochondrial encephalomyopathy

✍ S. Goda; T. Hamada; S. Ishimoto; T. Kobayashi; I. Goto; Y. Kuroiwa 📂 Article 📅 1987 🏛 Springer 🌐 English ⚖ 218 KB

Coenzyme Q10 is frequently reduced in mu

Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy

✍ Sabrina Sacconi; Eva Trevisson; Leonardo Salviati; Ségolène Aymé; Odile Rigal; A 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 203 KB

Superoxide dismutases of muscle in mitoc

Superoxide dismutases of muscle in mitochondrial encephalomyopathies

✍ Norio Ohkoshi; Hldehlro Mizusawa; Nobuko Shiraiwa; Shin'Ichi Shoji; Katsutoshi H 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 734 KB

lmmunohistochemical analyses were made of the superoxide dismutases (Mn-SOD and Cu/Zn-SOD) in biopsied muscles from 7 patients with mitochondrial encephalomyopathies that included mitochondrial encephalomyopathy, lactic acidosis and strokelike episodes (MELAS), and chronic progressive external ophth