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Author response for "Complete resolution of epileptic spasms with vigabatrin in a patient with 3‐methylglutaconic aciduria caused by TIMM50 gene mutation"
Mapping Intimacies
◽
10.1111/cge.13763/v2/response1
◽
2020
◽
Author(s):
Ali Mir
◽
Safeya Hadab
◽
Mohammed Sammak
◽
Rami Alhazmi
◽
Yousef Housawi
◽
...
Keyword(s):
Gene Mutation
◽
Complete Resolution
◽
Author Response
◽
Epileptic Spasms
◽
Methylglutaconic Aciduria
Download Full-text
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Cited By
References
Review for "Complete resolution of epileptic spasms with vigabatrin in a patient with 3‐methylglutaconic aciduria caused by TIMM50 gene mutation"
10.1111/cge.13763/v1/review1
◽
2020
◽
Author(s):
Simon Edvardson
Keyword(s):
Gene Mutation
◽
Complete Resolution
◽
Epileptic Spasms
◽
Methylglutaconic Aciduria
Download Full-text
Complete resolution of epileptic spasms with vigabatrin in a patient with 3‐methylglutaconic aciduria caused by TIMM50 gene mutation
Clinical Genetics
◽
10.1111/cge.13763
◽
2020
◽
Vol 98
(1)
◽
pp. 102-103
Author(s):
Ali Mir
◽
Safeya Hadab
◽
Mohammed Sammak
◽
Rami Alhazmi
◽
Yousef Housawi
◽
...
Keyword(s):
Gene Mutation
◽
Complete Resolution
◽
Epileptic Spasms
◽
Methylglutaconic Aciduria
Download Full-text
Review for "Complete resolution of epileptic spasms with vigabatrin in a patient with 3‐methylglutaconic aciduria caused by TIMM50 gene mutation"
10.1111/cge.13763/v1/review2
◽
2020
◽
Author(s):
Deeba Baig
Keyword(s):
Gene Mutation
◽
Complete Resolution
◽
Epileptic Spasms
◽
Methylglutaconic Aciduria
Download Full-text
Decision letter for "Complete resolution of epileptic spasms with vigabatrin in a patient with 3‐methylglutaconic aciduria caused by TIMM50 gene mutation"
10.1111/cge.13763/v1/decision1
◽
2020
◽
Keyword(s):
Gene Mutation
◽
Complete Resolution
◽
Epileptic Spasms
◽
Methylglutaconic Aciduria
Download Full-text
Decision letter for "Complete resolution of epileptic spasms with vigabatrin in a patient with 3‐methylglutaconic aciduria caused by TIMM50 gene mutation"
10.1111/cge.13763/v2/decision1
◽
2020
◽
Keyword(s):
Gene Mutation
◽
Complete Resolution
◽
Epileptic Spasms
◽
Methylglutaconic Aciduria
Download Full-text
Author response for "Encephalopathy due to defective mitochondrial and peroxisomal fission 2 caused by a novel MFF gene mutation in a young child"
10.1111/cge.13740/v2/response1
◽
2020
◽
Author(s):
Isha Panda
◽
Istaq Ahmad
◽
Shakti Sagar
◽
Sana Zahra
◽
Uzma Shamim
◽
...
Keyword(s):
Young Child
◽
Gene Mutation
◽
Author Response
◽
I Gene
Download Full-text
Author response: Skd3 (human ClpB) is a potent mitochondrial protein disaggregase that is inactivated by 3-methylglutaconic aciduria-linked mutations
10.7554/elife.55279.sa2
◽
2020
◽
Author(s):
Ryan R Cupo
◽
James Shorter
Keyword(s):
Mitochondrial Protein
◽
Author Response
◽
Methylglutaconic Aciduria
Download Full-text
Epileptic spasms: a previously unreported manifestation of WDR45 gene mutation
Epileptic Disorders
◽
10.1684/epd.2015.0784
◽
2015
◽
Vol 17
(4)
◽
pp. 467-472
◽
Cited By ~ 4
Author(s):
Kathryn I Xixis
◽
Mohamad A Mikati
Keyword(s):
Gene Mutation
◽
Epileptic Spasms
Download Full-text
Author response for "How can methylprednisolone work on epileptic spasms with malformation of cortical development?"
10.1111/ejn.14539/v2/response1
◽
2019
◽
Author(s):
Minyoung Lee
◽
Min‐Jee Kim
◽
Eun‐Jin Kim
◽
Dong‐Cheol Woo
◽
Mi‐Sun Yum
◽
...
Keyword(s):
Cortical Development
◽
Author Response
◽
Epileptic Spasms
◽
Malformation Of Cortical Development
Download Full-text
Epileptic spasms: a previously unreported manifestation of WDR45 gene mutation
Epileptic Disorders
◽
10.1684/epd.2016.0840
◽
2016
◽
Vol 18
(3)
◽
pp. 336-336
◽
Cited By ~ 2
Author(s):
Kathryn I Xixis
◽
Mohamad A Mikati
Keyword(s):
Gene Mutation
◽
Epileptic Spasms
Download Full-text
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