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Matthew Wicklund
Matthew Wicklund
University of Colorado
Verified email at CUAnschutz.edu
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Cited by
Cited by
Year
Evidence-based guideline summary: diagnosis and treatment of limb-girdle and distal dystrophies: report of the guideline development subcommittee of the American Academy of …
P Narayanaswami, M Weiss, D Selcen, W David, E Raynor, G Carter, ...
Neurology 83 (16), 1453-1463, 2014
2182014
Limb-girdle muscular dystrophy in the United States
SA Moore, CJ Shilling, S Westra, C Wall, MP Wicklund, C Stolle, ...
Journal of Neuropathology & Experimental Neurology 65 (10), 995-1003, 2006
2012006
Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients
BRR Nallamilli, S Chakravorty, A Kesari, A Tanner, A Ankala, T Schneider, ...
Annals of clinical and translational neurology 5 (12), 1574-1587, 2018
1502018
A randomized controlled trial of methotrexate for patients with generalized myasthenia gravis
M Pasnoor, J He, L Herbelin, TM Burns, S Nations, V Bril, AK Wang, ...
Neurology 87 (1), 57-64, 2016
1292016
The limb-girdle muscular dystrophies
MP Wicklund, JT Kissel
Neurologic clinics 32 (3), 729-749, 2014
1002014
The muscular dystrophies
MP Wicklund
CONTINUUM: Lifelong Learning in Neurology 19 (6), 1535-1570, 2013
792013
Developing standardized corticosteroid treatment for Duchenne muscular dystrophy
M Guglieri, K Bushby, MP McDermott, KA Hart, R Tawil, WB Martens, ...
Contemporary clinical trials 58, 34-39, 2017
722017
Effect of different corticosteroid dosing regimens on clinical outcomes in boys with Duchenne muscular dystrophy: a randomized clinical trial
M Guglieri, K Bushby, MP McDermott, KA Hart, R Tawil, WB Martens, ...
Jama 327 (15), 1456-1468, 2022
712022
Amyotrophic lateral sclerosis: what role does environment play?
A Ahmed, MP Wicklund
Neurologic clinics 29 (3), 689-711, 2011
612011
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
Q Gang, C Bettencourt, PM Machado, S Brady, JL Holton, AM Pittman, ...
Neurobiology of aging 47, 218. e1-218. e9, 2016
542016
SCN4A mutation as modifying factor of myotonic dystrophy type 2 phenotype
E Bugiardini, I Rivolta, A Binda, AS Caminero, F Cirillo, A Cinti, ...
Neuromuscular disorders 25 (4), 301-307, 2015
522015
Novel clinical features of glycine receptor antibody syndrome: a series of 17 cases
AL Piquet, M Khan, JEA Warner, MP Wicklund, JL Bennett, MA Leehey, ...
Neurology: Neuroimmunology & Neuroinflammation 6 (5), e592, 2019
502019
Spinal angiography and epidural venography in juvenile muscular atrophy of the distal arm “Hirayama disease”
B Elsheikh, JT Kissel, G Christoforidis, M Wicklund, DT Kehagias, ...
Muscle & Nerve: Official Journal of the American Association of …, 2009
492009
The limb-girdle muscular dystrophies
MP Wicklund
CONTINUUM: Lifelong Learning in Neurology 25 (6), 1599-1618, 2019
482019
Paraproteinemic neuropathy
MP Wicklund, JT Kissel
Current Treatment Options in Neurology 3, 147-156, 2001
442001
A checklist for clinical trials in rare disease: obstacles and anticipatory actions—lessons learned from the FOR-DMD trial
RA Crow, KA Hart, MP McDermott, R Tawil, WB Martens, BE Herr, ...
Trials 19, 1-9, 2018
362018
Amyotrophic lateral sclerosis: possible role of environmental influences
MP Wicklund
Neurologic clinics 23 (2), 461-484, 2005
352005
KIF1Bβ mutations detected in hereditary neuropathy impair IGF1R transport and axon growth
F Xu, H Takahashi, Y Tanaka, S Ichinose, S Niwa, MP Wicklund, ...
Journal of Cell Biology 217 (10), 3480-3496, 2018
302018
Patient assisted intervention for neuropathy: comparison of treatment in real life situations (PAIN-CONTRoLS): Bayesian adaptive comparative effectiveness randomized trial
RJ Barohn, B Gajewski, M Pasnoor, A Brown, LL Herbelin, KS Kimminau, ...
JAMA neurology 78 (1), 68-76, 2021
292021
Guideline Development Subcommittee of the American Academy of Neurology
P Narayanaswami, M Weiss, D Selcen, W David, E Raynor, G Carter, ...
272014
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