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Siddique, Nailah
32
results:
Search for persons
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Online (32)
Mediatypes
Articles (Online) (20)
Bookchapter (Online) (2)
OpenAccess-fulltext (10)
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?
1
Intricacies of aetiology in intrafamilial degenerative dise..:
Lowry, Jessica L
;
Ryan, Éanna B
;
Esengul, Y Taylan
..
Brain Communications. 2 (2020) 2 - p. , 2020
Link:
https://doi.org/10.1093/..
?
2
Evaluation of Mitochondrial Function in CHCHD10 Mutation (P..:
Yan, Jianhua
;
Ahmeti, Kreshnik
;
Siddique, Nailah
...
Neurology. 86 (2016) 16_supplement - p. , 2016
Link:
https://doi.org/10.1212/..
?
3
Macular sub-layer thinning and association with pulmonary f..:
Simonett, Joseph M.
;
Huang, Russell
;
Siddique, Nailah
...
Scientific Reports. 6 (2016) 1 - p. , 2016
Link:
https://doi.org/10.1038/..
?
4
Atypical Electropherogram Patterns are Observed Among C9orf..:
Lowry, Jessica
;
Yan, Jianhua
;
Feiz, Farnoosh
...
Neurology. 86 (2016) 16_supplement - p. , 2016
Link:
https://doi.org/10.1212/..
?
5
Whole Exome Sequencing of Familial ALS and Trios of Sporadi..:
Ahmeti, Kushtrim
;
Ahmeti, Kreshnik
;
Yan, Jianhua
...
Neurology. 86 (2016) 16_supplement - p. , 2016
Link:
https://doi.org/10.1212/..
?
6
Identification of TMEM230 mutations in familial Parkinson's..:
Deng, Han-Xiang
;
Shi, Yong
;
Yang, Yi
...
Nature Genetics. 48 (2016) 7 - p. 733-739 , 2016
Link:
https://doi.org/10.1038/..
?
7
Study of Intermediate-Length polyQ Repeats in Sporadic and ..:
Nunez-Santana, Felix
;
Yan, Jianhua
;
Ryan, Eanna
...
Neurology. 86 (2016) 16_supplement - p. , 2016
Link:
https://doi.org/10.1212/..
?
8
Mutation in the novel nuclear-encoded mitochondrial protein..:
Ajroud-Driss, Senda
;
Fecto, Faisal
;
Ajroud, Kaouther
...
neurogenetics. 16 (2014) 1 - p. 1-9 , 2014
Link:
https://doi.org/10.1007/..
?
9
A New Mutation in Ubiquilin Gene Family and Its Effect on P..:
Yan, Jianhua
;
Ajroud, Kaouther
;
Fecto, Faisal
...
Neurology. 80 (2013) 7_supplement - p. , 2013
Link:
https://doi.org/10.1212/..
?
10
Inclusions in frontotemporal lobar degeneration with TDP-43..:
Bigio, Eileen H.
;
Wu, Jane Y.
;
Deng, Han-Xiang
...
Acta Neuropathologica. 125 (2013) 3 - p. 463-465 , 2013
Link:
https://doi.org/10.1007/..
?
11
Ubiquilin2 Mutations in Parkinson's Disease Extend the Spec..:
Shi, Yong
;
Chen, Wenjie
;
Fecto, Faisal
...
Neurology. 80 (2013) 7_supplement - p. , 2013
Link:
https://doi.org/10.1212/..
?
12
Ubiquilin2 Mutations in Parkinson's Disease Extend the Spec..:
Shi, Yong
;
Chen, Wenjie
;
Fecto, Faisal
...
Neurology. 80 (2013) 7_supplement - p. , 2013
Link:
https://doi.org/10.1212/..
?
13
Mutations in UBQLN2 cause dominant X-linked juvenile and ad..:
Deng, Han-Xiang
;
Chen, Wenjie
;
Hong, Seong-Tshool
...
Nature. 477 (2011) 7363 - p. 211-215 , 2011
Link:
https://doi.org/10.1038/..
?
14
Marked accumulation of 27-hydroxycholesterol in SPG5 patien..:
Schüle, Rebecca
;
Siddique, Teepu
;
Deng, Han-Xiang
...
Journal of Lipid Research. 51 (2010) 4 - p. 819-823 , 2010
Link:
https://doi.org/10.1194/..
?
15
FUS‐immunoreactive inclusions are a common feature in spora..:
Deng, Han‐Xiang
;
Zhai, Hong
;
Bigio, Eileen H.
...
Annals of Neurology. 67 (2010) 6 - p. 739-748 , 2010
Link:
https://doi.org/10.1002/..
1-15