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Siddique, Nailah
32  results:
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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