๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Cell membrane abnormalities and muscular dystrophy

โœ Scribed by Wulter G. Bradby

Publisher
John Wiley and Sons
Year
1980
Tongue
English
Weight
122 KB
Volume
3
Category
Article
ISSN
0148-639X

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Mitochondrial abnormalities in oculophar
Mitochondrial abnormalities in oculopharyngeal muscular dystrophy
โœ Dr.; MD Rachel Pauzner; MD Ilan Blatt; MD Meir Mouallem; Eitan Ben-David; MD Zvi ๐Ÿ“‚ Article ๐Ÿ“… 1991 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 815 KB

A family with oculopharyngeal muscular dystrophy (OPMD) is described. Histological and histochemical studies of muscle biopsy showed nonspecific myopathic changes; no "ragged-red'' fibers were seen. Electron microscopy demonstrated bizarre large mitochondria with abnormal cristae, but no intranuclea

Abnormalities of erythrocytes in duchenn
Abnormalities of erythrocytes in duchenne muscular dystrophy
โœ Dr Mizuko Yoshida; Kazuya Ando; Eijiro Satoyoshi ๐Ÿ“‚ Article ๐Ÿ“… 1983 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 585 KB

Erythrocytes from patients with Duchenne muscular dystrophy (DMD) were studied in relation to the extracellular calcium ion concentration. The shape of fresh erythrocytes in DMD was normal and not affected by Ca++. When DMD erythrocytes were stored in buffer solution with Ca++, however, the rate of

A new congenital muscular dystrophy with
A new congenital muscular dystrophy with mitochondrial structural abnormalities
โœ Ichizo Nishino; Osamu Kobayashi; Yu-ichi Goto; Mana Kurihara; Komei Kumagai; Tak ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 625 KB

We report a new form of congenital muscular dystrophy (CMD) in 4 patients from three unrelated families with probable autosomalrecessive inheritance. All patients had the clinical characteristics of merosinpositive congenital muscular dystrophy, but had marked mental retardation. The disease was slo