A. Harper
发表
Bo Wu,
Sapana N. Shah,
Peijuan Lu,
2018,
The American journal of pathology.
T. Crawford,
U. Hellmich,
C. Sumner,
2022,
Annals of clinical and translational neurology.
Yubo Sun,
Bo Wu,
Sapana N. Shah,
2016,
The American journal of pathology.
T. Crawford,
A. Hamosh,
C. Stafstrom,
2016,
Annals of neurology.
S. Petrovski,
V. Shashi,
R. Crimian,
2015,
Clinical genetics.
M. Tarnopolsky,
K. Boycott,
B. Kamien,
2017,
Orphanet Journal of Rare Diseases.
Colleen E. Wahl,
A. Mammen,
C. Toro,
2018,
Neurology: Neuroimmunology & Neuroinflammation.
D. Tchapyjnikov,
M. Mikati,
A. Harper,
2016,
Epileptic disorders : international epilepsy journal with videotape.
A. Harper,
N. Couser,
Graham Pingree,
2021,
International journal of molecular epidemiology and genetics.
E. Hoffman,
C. Zaidman,
A. Connolly,
2020,
JAMA neurology.
A. Harper,
G. Vorona,
Darina Dinov,
2021,
Neurology.
R. Finkel,
A. Pestronk,
E. Mazzone,
2019,
Journal of Pharmacokinetics and Pharmacodynamics.
A. Connolly,
C. Heier,
Yi-Wen Chen,
2020,
Journal of personalized medicine.
A. Cnaan,
A. Connolly,
Yi-Wen Chen,
2018,
Neurology.
Long-Term Functional Efficacy and Safety of Viltolarsen in Patients with Duchenne Muscular Dystrophy
E. Hoffman,
C. Zaidman,
A. Connolly,
2022,
Journal of neuromuscular diseases.
K. Nykamp,
L. Demmer,
A. Deucher,
2016,
American journal of medical genetics. Part A.
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement
Beryl B. Cummings,
Carol J. Saunders,
C. Saunders,
2019,
Acta Neuropathologica.
B. Byrne,
A. Cnaan,
A. Connolly,
2020,
Muscle & nerve.
S. Dougherty,
A. Harper,
G. Vorona,
2018,
Front. Neurol..
R. Finkel,
N. Goemans,
A. Childs,
2022,
JAMA neurology.
K. Campbell,
Q. Lu,
A. Blaeser,
2016
.
C. Zaidman,
A. Connolly,
V. Rao,
2023,
Journal of neuromuscular diseases.
Sapana N. Shah,
Peijuan Lu,
Lauren E. Bollinger,
2018,
American Journal of Pathology.