E-LIB Suche - Ergebnisse für: Findlay, Andrew R

1

DNAJB6 isoform specific knockdown: Therapeutic potential fo..:

Findlay, Andrew R. ; Paing, May M. ; Daw, Jil A....
Molecular Therapy - Nucleic Acids. 32 (2023) - p. 937-948 , 2023

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

2

Natural History and Phenotypic Spectrum of LGMD-D1: Implica..:

Findlay, Andrew R. ; Robinson, Sarah ; Seiffert, Michelle..
Neurology. 98 (2022) 18_supplement - p. , 2022

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

3

Loss of function variants in DNAJB4 cause a myopathy with e..:

Weihl, Conrad C. ; Töpf, Ana ; Bengoechea, Rocio...
Acta Neuropathologica. 145 (2022) 1 - p. 127-143 , 2022

Link: https://doi.org/10.1007/..

4

LGMDD1 natural history and phenotypic spectrum: Implication..:

Findlay, Andrew R. ; Robinson, Sarah E. ; Poelker, Stephanie...
Annals of Clinical and Translational Neurology. 10 (2022) 2 - p. 181-194 , 2022

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

5

Clinical utility of anti‐cytosolic 5'‐nucleotidase 1A antib..:

Ikenaga, Chiseko ; Findlay, Andrew R. ; Goyal, Namita A....
Annals of Clinical and Translational Neurology. 8 (2021) 3 - p. 571-578 , 2021

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

6

Immune and Inflammatory Myopathies:

, In: Neuroimmunology,

Findlay, Andrew R. ; Bucelli, Robert C. - p. 321-345 , 2021

Link: https://doi.org/10.1007/..

7

Phenotypic diversity in an international Cure VCP Disease r..:

Ikenaga, Chiseko ; Findlay, Andrew R. ; Seiffert, Michelle...
Orphanet Journal of Rare Diseases. 15 (2020) 1 - p. , 2020

Link: https://doi.org/10.1186/..

8

Homozygous recessive MYH2 mutation mimicking dominant MYH2 ..:

Findlay, Andrew R. ; Harms, Matthew B. ; Pestronk, Alan.
Neuromuscular Disorders. 28 (2018) 8 - p. 675-679 , 2018

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

9

The first exon duplication mouse model of Duchenne muscular..:

Vulin, Adeline ; Wein, Nicolas ; Simmons, Tabatha R....
Neuromuscular Disorders. 25 (2015) 11 - p. 827-834 , 2015

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

10

An overview of polymyositis and dermatomyositis:

Findlay, Andrew R. ; Goyal, Namita A. ; Mozaffar, Tahseen
Muscle & Nerve. 51 (2015) 5 - p. 638-656 , 2015

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

11

Clinical phenotypes as predictors of the outcome of skippin..:

Findlay, Andrew R. ; Wein, Nicolas ; Kaminoh, Yuuki...
Annals of Neurology. 77 (2015) 4 - p. 668-674 , 2015

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

12

Exome sequencing identifies a DNAJB6 mutation in a family w..:

Couthouis, Julien ; Raphael, Alya R. ; Siskind, Carly...
Neuromuscular Disorders. 24 (2014) 5 - p. 431-435 , 2014

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

13

Camptocormia as a late presentation in a manifesting carrie..:

Findlay, Andrew R. ; Lewis, Sarah ; Sahenk, Zarife.
Muscle & Nerve. 47 (2012) 1 - p. 124-127 , 2012

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

14

DNAJB6 Isoform Specific Knockdown: Therapeutic Potential fo..:

Findlay, Andrew R ; Paing, May M ; Daw, Jil A...
https://doi.org/10.1101/2022.11.17.516920. , 2023

Link: https://doi.org/10.1101/..

15

DNAJB6 isoform specific knockdown: Therapeutic potential fo..:

Findlay, Andrew R ; Paing, May M ; Daw, Jil A...
https://doi.org/10.1016/j.omtn.2023.05.017. , 2023

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