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McKenna-Yasek, Diane
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1

Author Correction: The SOD1-mediated ALS phenotype shows a ..:

Opie-Martin, Sarah ; Iacoangeli, Alfredo ; Topp, Simon D....
Nature Communications.  15 (2024)  1 - p. , 2024
Link: https://doi.org/10.1038/..
 
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2

AAV gene therapy for Tay-Sachs disease:

Flotte, Terence R. ; Cataltepe, Oguz ; Puri, Ajit...
Nature Medicine.  28 (2022)  2 - p. 251-259 , 2022
Link: https://doi.org/10.1038/..
 
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3

The SOD1-mediated ALS phenotype shows a decoupling between ..:

Opie-Martin, Sarah ; Iacoangeli, Alfredo ; Topp, Simon D....
Nature Communications.  13 (2022)  1 - p. , 2022
Link: https://doi.org/10.1038/..
 
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4

Suppression of mutant C9orf72 expression by a potent mixed ..:

Tran, Hélène ; Moazami, Michael P. ; Yang, Huiya...
Nature Medicine.  28 (2021)  1 - p. 117-124 , 2021
Link: https://doi.org/10.1038/..
 
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5

Single breath counting is an effective screening tool for f..:

Quinn, Colin ; Mcmillan, Corey T. ; Owegi, Margaret A....
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration.  22 (2021)  sup1 - p. 5-8 , 2021
Link: https://doi.org/10.1080/..
 
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6

A Safe and Reliable Technique for CNS Delivery of AAV Vecto..:

Taghian, Toloo ; Marosfoi, Miklos G. ; Puri, Ajit S....
Molecular Therapy.  28 (2020)  2 - p. 411-421 , 2020
Link: https://doi.org/10.1016/..
 
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7

Randomized trial ofl-serine in patients with hereditary sen..:

Fridman, Vera ; Suriyanarayanan, Saranya ; Novak, Peter...
Neurology.  92 (2019)  4 - p. , 2019
Link: https://doi.org/10.1212/..
 
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8

NurOwn, phase 2, randomized, clinical trial in patients wit..:

Berry, James D. ; Cudkowicz, Merit E. ; Windebank, Anthony J....
Neurology.  93 (2019)  24 - p. , 2019
Link: https://doi.org/10.1212/..
 
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9

Prospective natural history study ofC9orf72ALS clinical cha..:

Cammack, Alexander J. ; Atassi, Nazem ; Hyman, Theodore...
Neurology.  93 (2019)  17 - p. , 2019
Link: https://doi.org/10.1212/..
 
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10

A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, DELAYED-STA..:

Fridman, Vera ; Novak, Peter ; David, William...
Neurology.  88 (2017)  16_supplement - p. , 2017
Link: https://doi.org/10.1212/..
 
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11

Exome sequencing in amyotrophic lateral sclerosis identifie..:

Cirulli, Elizabeth T. ; Lasseigne, Brittany N. ; Petrovski, Slavé...
Science.  347 (2015)  6229 - p. 1436-1441 , 2015
Link: https://doi.org/10.1126/..
 
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12

Exome sequencing in amyotrophic lateral sclerosis identifie..:

Cirulli, Elizabeth T. ; Lasseigne, Brittany N. ; Petrovski, Slavé...
Science.  347 (2015)  6229 - p. 1436-1441 , 2015
Link: http://www.jstor.org/sta..
 
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13

Exome-wide Rare Variant Analysis Identifies TUBA4A Mutation..:

Smith, Bradley N. ; Ticozzi, Nicola ; Fallini, Claudia...
Neuron.  84 (2014)  2 - p. 324-331 , 2014
Link: https://doi.org/10.1016/..
 
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14

Identifying diagnostic DNA methylation profiles for faciosc..:

Jones, Takako I ; Yan, Chi ; Sapp, Peter C...
Clinical Epigenetics.  6 (2014)  1 - p. , 2014
Link: https://doi.org/10.1186/..
 
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15

Mutations in the profilin 1 gene cause familial amyotrophic..:

Wu, Chi-Hong ; Fallini, Claudia ; Ticozzi, Nicola...
Nature.  488 (2012)  7412 - p. 499-503 , 2012
Link: https://doi.org/10.1038/..
 
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