Research output per year
Research output per year
Personal profile
Research interests
Neuromuscular Disorders
Clinical interests
Clinical neurology, neuromuscular disease, neuroimmunology, glycolipids, proteoglycans, aging and the nervous system, history of neurology, myopathy, neuropathy, weakness, myasthenia, muscle, nerve, numbness, sensory loss, pain, fatigue, muscular dystrophy, neuro muscular.
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Dive into the research topics where Alan Pestronk is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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Ophthalmoparesis as an unusual manifestation of anti-3‑hydroxy-3-methyl-glutaryl-coenzyme A reductase antibody-associated myopathies
Putko, B., Pestronk, A., Van Stavern, G. P., Phan, C. L., Beecher, G. & Liewluck, T., Sep 2024, In: Neuromuscular Disorders. 42, p. 1-4 4 p.Research output: Contribution to journal › Article › peer-review
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Safety and efficacy of losmapimod in facioscapulohumeral muscular dystrophy (ReDUX4): a randomised, double-blind, placebo-controlled phase 2b trial
Tawil, R., Wagner, K. R., Hamel, J. I., Leung, D. G., Statland, J. M., Wang, L. H., Genge, A., Sacconi, S., Lochmüller, H., Reyes-Leiva, D., Diaz-Manera, J., Alonso-Perez, J., Muelas, N., Vilchez, J. J., Pestronk, A., Gibson, S., Goyal, N. A., Hayward, L. J., Johnson, N. & LoRusso, S. & 19 others, , May 2024, In: The Lancet Neurology. 23, 5, p. 477-486 10 p.Research output: Contribution to journal › Article › peer-review
2 Scopus citations -
Biallelic variants in COQ7 cause distal hereditary motor neuropathy with upper motor neuron signs
Rebelo, A. P., Tomaselli, P. J., Medina, J., Wang, Y., Dohrn, M. F., Nyvltova, E., Danzi, M. C., Garrett, M., Smith, S. E., Pestronk, A., Li, C., Ruiz, A., Jacobs, E., Feely, S. M. E., França, M. C., Gomes, M. V., Santos, D. F., Kumar, S., Lombard, D. B. & Saporta, M. & 6 others, , Oct 1 2023, In: Brain. 146, 10, p. 4191-4199 9 p.Research output: Contribution to journal › Article › peer-review
Open Access10 Scopus citations -
Expanding the muscle imaging spectrum in dysferlinopathy: description of an outlier population from the classical MRI pattern
Llansó, L., Moore, U., Bolano-Diaz, C., James, M., Blamire, A. M., Carlier, P. G., Rufibach, L., Gordish-Dressman, H., Boyle, G., Hilsden, H., Day, J. W., Jones, K. J., Bharucha-Goebel, D. X., Salort-Campana, E., Pestronk, A., Walter, M. C., Paradas, C., Stojkovic, T., Mori-Yoshimura, M. & Bravver, E. & 4 others, , Apr 2023, In: Neuromuscular Disorders. 33, 4, p. 349-357 9 p.Research output: Contribution to journal › Article › peer-review
Open Access4 Scopus citations -
Myostatin and follistatin as monitoring and prognostic biomarkers in dysferlinopathy
The Jain COS Consortium, Feb 2023, In: Neuromuscular Disorders. 33, 2, p. 199-207 9 p.Research output: Contribution to journal › Article › peer-review
Open Access4 Scopus citations