E-LIB Suche - Ergebnisse für: Grider, Tiffany

1

P004: Urine polyols for diagnosis of sorbitol dehydrogenase..:

White, Amy ; Bontrager, Jordan ; Laxen, William...
Genetics in Medicine Open. 2 (2024) - p. 100881 , 2024

Link: https://doi.org/10.1016/..

2

Combined clinical, structural, and cellular studies discrim..:

Berth, Sarah H ; Vo, Linh ; Kwon, Do Hoon...
Brain. , 2024

Link: https://doi.org/10.1093/..

3

Quantitative Foot Muscle Magnetic Resonance Imaging Reliabl..:

Doherty, Carolynne M. ; Howard, Paige ; O'Donnell, Luke F....
Annals of Neurology. 96 (2024) 1 - p. 170-174 , 2024

Link: https://doi.org/10.1002/..

4

Lower limb muscle MRI fat fraction is a responsive outcome ..:

Doherty, Carolynne M. ; Morrow, Jasper M. ; Zuccarino, Riccardo...
Annals of Clinical and Translational Neurology. 11 (2024) 3 - p. 607-617 , 2024

Link: https://doi.org/10.1002/..

5

A Rare MED13 Variant as the Potential Cause of Early Onset ..:

Deniz, Kaancan ; Grider, Tiffany ; Grueter, Chad.
Neurology. 98 (2022) 18_supplement - p. , 2022

Link: https://doi.org/10.1212/..

6

Disease Progression in Charcot–Marie–Tooth Disease Related ..:

Fridman, Vera ; Sillau, Stefan ; Bockhorst, Jacob...
Annals of Neurology. 93 (2022) 3 - p. 563-576 , 2022

Link: https://doi.org/10.1002/..

7

Loss of function MPZ mutation causes milder CMT1B neuropath:

Howard, Paige ; Feely, Shawna M. E. ; Grider, Tiffany...
Journal of the Peripheral Nervous System. 26 (2021) 2 - p. 177-183 , 2021

Link: https://doi.org/10.1111/..

8

A Unique Phenotype of a Novel AIFM1 Gene Mutation: Case Rep..:

Halhouli, Oday ; Kamholz, John ; Drack, Arlene..
Neurology. 96 (2021) 15_supplement - p. , 2021

Link: https://doi.org/10.1212/..

9

MicroRNAs as Biomarkers of Charcot-Marie-Tooth Disease Type..:

Wang, Hongge ; Davison, Matthew ; Wang, Kathryn...
Neurology. 97 (2021) 5 - p. , 2021

Link: https://doi.org/10.1212/..

10

A longitudinal study of CMT1A using Rasch analysis based CM..:

Fridman, Vera ; Sillau, Stefan ; Acsadi, Gyula...
Neurology. 94 (2020) 9 - p. , 2020

Link: https://doi.org/10.1212/..

11

Transmembrane protease serine 5: a novel Schwann cell plasm..:

Wang, Hongge ; Davison, Matthew ; Wang, Kathryn...
Annals of Clinical and Translational Neurology. 7 (2019) 1 - p. 69-82 , 2019

Link: https://doi.org/10.1002/..

12

Validation of MRC Centre MRI calf muscle fat fraction proto..:

Morrow, Jasper M. ; Evans, Matthew R.B. ; Grider, Tiffany...
Neurology. 91 (2018) 12 - p. , 2018

Link: https://doi.org/10.1212/..

13

PMP22 exon 4 deletion causes ER retention of PMP22 and a ga..:

Wang, David S. ; Wu, Xingyao ; Bai, Yunhong...
Annals of Clinical and Translational Neurology. 4 (2017) 4 - p. 236-245 , 2017

Link: https://doi.org/10.1002/..

14

Genotype–phenotype characteristics and baseline natural his..:

Sanmaneechai, Oranee ; Feely, Shawna ; Scherer, Steven S....
Brain. 138 (2015) 11 - p. 3180-3192 , 2015

Link: https://doi.org/10.1093/..

15

Coexistence of a T118M PMP22 missense mutation and chromoso..:

Jerath, Nivedita U. ; Kamholz, John ; Grider, Tiffany...
Muscle & Nerve. 52 (2015) 5 - p. 905-908 , 2015

Link: https://doi.org/10.1002/..