𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Congenital muscular dystrophy

✍ Scribed by Korinthenberg, R.; Palm, D.


Book ID
121770497
Publisher
Elsevier Science
Year
1983
Tongue
English
Weight
93 KB
Volume
5
Category
Article
ISSN
0387-7604

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Congenital muscular dystrophy
✍ Q. H. Leyten; H. J. Laak; F. J. M. GabreΓ«ls; W. O. Renier; K. Renkawek; R. C. A. πŸ“‚ Article πŸ“… 1993 πŸ› Springer-Verlag 🌐 English βš– 708 KB

Histomorphological and histochemical variability was studied in muscle specimens from 30 patients with congenital muscular dystrophy (CMD). We found involvement of the central nervous system in 8 patients (Fukuyama CMD, F-CMD), involvement of the brain and the eyes in 5 patients (muscle, eye and bra

CONGENITAL MUSCULAR DYSTROPHY
✍ Bradley, W.G.; Jenkison, Margaret πŸ“‚ Article πŸ“… 1972 πŸ› The Lancet 🌐 English βš– 147 KB
CONGENITAL MUSCULAR DYSTROPHY
✍ Joseph, BarryS.; Netsky, MartinG.; Bischel, MargaretD.; Gans, DavidS.; Barbour, πŸ“‚ Article πŸ“… 1972 πŸ› The Lancet 🌐 English βš– 163 KB
Congenital muscular dystrophy
✍ Leyten, Q.H.; GabreΓ«ls, F.J.M.; Renier, W.O.; Joosten, E.M.G.; ter Laak, H.J.; R πŸ“‚ Article πŸ“… 1990 πŸ› Elsevier Science 🌐 English βš– 63 KB
Merosin and congenital muscular dystroph
✍ Miyagoe-Suzuki, Yuko; Nakagawa, Masahiro; Takeda, Shin'Ichi πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 181 KB

Merosin (also called as Laminin-2) is an isoform of laminin comprised of the ␣2, ␀1 and β₯1 chains. In European populations, half of the patients with classical congenital muscular dystrophy have mutations of the LAMA2 gene (6q22-23) and present reduced or absence of laminin ␣2 chain. This form is ge