scholarly journals Novel Mutation chrX:110644366 C>A of the DCX Gene in 4-year-old Girl with Sporadic Double Cortex Syndrome

2017 ◽  
Vol 7 (1) ◽  
pp. 67-70
Author(s):  
Natalia Shnayder ◽  
◽  
Ivan Artyukhov ◽  
Ekaterina Egorova ◽  
Diana Dmitrienko ◽  
...  
2016 ◽  
Vol 03 (02) ◽  
pp. 101
Author(s):  
Saurabh Bansal ◽  
Manoj Goyal ◽  
Manish Modi ◽  
Chirag Ahuja

2006 ◽  
Vol 27 (6) ◽  
pp. 535-543 ◽  
Author(s):  
Jeffrey D. Jirsch ◽  
Neda Bernasconi ◽  
Flavio Villani ◽  
Paolo Vitali ◽  
Giuliano Avanzini ◽  
...  

1999 ◽  
Vol 45 (2) ◽  
pp. 146-153 ◽  
Author(s):  
Joseph G. Gleeson ◽  
Sharon R. Minnerath ◽  
Jeremy W. Fox ◽  
Kristina M. Allen ◽  
Robert F. Luo ◽  
...  

2017 ◽  
Vol 117 (9) ◽  
pp. 75
Author(s):  
A. M. Teplyshova ◽  
V. V. Gaskin ◽  
G. V. Kustov ◽  
A. A. Gudkova ◽  
R. V. Luzin ◽  
...  

1994 ◽  
Vol 15 (1) ◽  
pp. 15-23 ◽  
Author(s):  
T. Granata ◽  
G. Battaglia ◽  
L. D'Incerti ◽  
S. Franceschetti ◽  
C. Zucca ◽  
...  

2013 ◽  
Vol 44 (02) ◽  
Author(s):  
C Cag ◽  
A Olze ◽  
J Neef ◽  
JAK Ohlmann ◽  
K Strobl ◽  
...  

Epilepsia ◽  
2004 ◽  
Vol 45 (5) ◽  
pp. 562-563 ◽  
Author(s):  
P.C. Tai ◽  
J.D.S. McKean ◽  
B.M. Wheatley ◽  
D.W. Gross

2016 ◽  
Vol 15 (1) ◽  
pp. 129-130
Author(s):  
Ankush Sharma ◽  
Tajinder Talwar ◽  
Nitin Gupta ◽  
Munish Gupta ◽  
Bahar Ramzan ◽  
...  

Subcortical band heterotopia (SBH) is a disorder of neural migration. Also called as double cortex syndrome due to its appearance. Patient presents with mental retardation and epilepsy. Usually seizures start in first decade of life and may vary between focal seizures to generalized seizures. MRI is the diagnostic investigation of choice that reveals the characteristic findings. It is a rare disorder with only a few hundred cases reported till date.Bangladesh Journal of Medical Science Vol.15(1) 2016 p.129-130


1997 ◽  
Vol 150 ◽  
pp. S193
Author(s):  
A. Federico ◽  
P. Tommasetti ◽  
M. Zollino ◽  
M. Diomedi ◽  
M.T. Dotti ◽  
...  

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