THE CENTRAL NERVOUS SYSTEM IN DUCHENNE MUSCULAR DYSTROPHY

Brain ◽  
1969 ◽  
Vol 92 (4) ◽  
pp. 805-808 ◽  
Author(s):  
VICTOR DUBOWITZ ◽  
LEONARD CROME
1994 ◽  
Vol 87 (2) ◽  
pp. 129-134 ◽  
Author(s):  
Makoto Uchino ◽  
Hitoo Teramoto ◽  
Hiroaki Naoe ◽  
Teruhisa Miike ◽  
Kowashi Yoshioka ◽  
...  

2015 ◽  
Vol 24 (4) ◽  
pp. 562-568 ◽  
Author(s):  
Valeria Ricotti ◽  
Herbert Jägle ◽  
Maria Theodorou ◽  
Anthony T Moore ◽  
Francesco Muntoni ◽  
...  

1994 ◽  
Vol 87 (2) ◽  
pp. 129-134 ◽  
Author(s):  
Makoto Uchino ◽  
Hitoo Teramoto ◽  
Hiroaki Naoe ◽  
Teruhisa Miike ◽  
Kowashi Yoshioka ◽  
...  

1997 ◽  
Vol 21 (4) ◽  
pp. 355-360 ◽  
Author(s):  
Tomoko Yamamoto ◽  
Noriyuki Shibata ◽  
Miho Kanazawa ◽  
Makio Kobayashi ◽  
Takashi Komori ◽  
...  

2011 ◽  
Vol 39 (1) ◽  
pp. 336-339 ◽  
Author(s):  
Jane E. Hewitt

During the last 10 years it has become apparent that a significant subset of inherited muscular dystrophy is caused by errors in the glycosylation of α-dystroglycan. Many of these dystrophies are also associated with abnormalities of the central nervous system. Dystroglycan has to be fully glycosylated in order bind to its ligands. To date, six genes have been shown to be essential for functional dystroglycan glycosylation and most, if not all, of these genes act in the formation of O-mannosyl glycans. Genetic heterogeneity indicates that other genes are involved in this pathway. Identification of these additional genes would increase our understanding of this specific and essential glycosylation pathway.


2000 ◽  
Vol 15 (3) ◽  
pp. 172-178 ◽  
Author(s):  
Umbertina C. Reed ◽  
Suely K. Nagahashi Marie ◽  
Mariz Vainzof ◽  
Lucio F. Gobbo ◽  
Juliana E.P. Gurgel ◽  
...  

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