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Sean M. Healey & AMG Center for ALS

At the Healey & AMG Center for ALS, we are on a quest to discover life-saving therapies for approximately 500,000 people worldwide who are affected by amyotrophic lateral sclerosis (ALS).

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Email: HealeyAMGCenterforALS@mgh.harvard.edu
HealeyAMGCenterforALS@mgh.harvard.edu
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https://www.mgbgiving.org/healey

Overview

The Healey & AMG Center for ALS leads one of the world’s most active and comprehensive ALS research programs, with hundreds of research studies underway at any given time. Under the leadership of Merit Cudkowicz, MD, MSc, and guided by a Science Advisory Council (SAC) of international experts, the Center is tireless in its pursuit of a cure.

Since 1993—when a research team at Massachusetts General Hospital identified the first ALS‑associated gene—the Center has remained at the forefront of ALS discovery. Its teams continue to advance new treatments, develop better biomarkers, and improve clinical trial designs to move promising therapies forward faster.

The Healey & AMG Center specializes in translating scientific discoveries into real clinical progress. Research efforts span cell and gene therapies, targeted antibodies, machine learning, and small‑molecule therapeutics — all aimed at slowing or stopping the drivers of ALS. Because ALS affects each person differently, The Center uses precision‑medicine approaches to match therapies to an individual’s unique biology.

What makes the Healey & AMG Center unique is its fully integrated model that brings together scientists, clinicians, engineers, and people living with ALS to accelerate breakthroughs from the laboratory to clinical trials. The Center also invests deeply in the next generation of ALS leaders through global fellowships, innovation prizes, and training programs.

The mission of the Healey & AMG Center is bold and simple: to speed the development of treatments that slow, halt, repair, and ultimately prevent ALS.

Research focus areas

Clinical Research

The driving force behind the Healey & AMG Center for ALS is to disrupt the standard pace of ALS therapy development. The Center offers both clinical trials and observational studies for people living with ALS, including the HEALEY ALS Platform Trial, Healey ALS MyMatch, and Access for ALL in ALS.

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Expanded Access Protocols (EAPs)

Expanded Access Protocol programs provide valuable research options for those who are not eligible for clinical trials.

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Preclinical & Translational Research

By integrating cutting-edge molecular biology, human patient data, and advanced model systems, Healey & AMG Center researchers are developing next-generation therapeutic strategies that directly target the biological drivers of ALS. The Center’s translational pipeline includes cell and gene therapies, targeted antibody approaches, and small molecule therapeutics.

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Supporting Innovation & Education

The Center is committed to fostering and recognizing scientific breakthroughs and clinical transformations that are altering ALS therapy development and solving clinical care challenges for people living with ALS.

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Patient Care

Advancing clinical care through innovation

Our top priority is delivering care that truly makes a difference for people living with ALS. We focus on innovations that enhance comfort, independence, and access to vital programs – ensuring every patient and family receive the support they need throughout their journey.
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View patient care services
https://www.massgeneralbrigham.org/en/services/als

One of the ideas behind the Healey & AMG Center is to really revolutionize how we treat people with ALS. To accelerate how drugs are treated and brought to patients, to personalize treatments, and to increase access to experimental treatments for people with ALS.

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Merit Cudkowicz

  • Director, Healey & AMG Center
  • Executive Director, MGB Neuroscience Institute

Publications

Sharing the results of our work with the ALS and scientific community is central to our mission. Highlighted below are key publications, with more exciting findings to be shared in the future.
2026
  1. Approaching Serious Illness Conversations in Amyotrophic Lateral Sclerosis Using Telehealth| Neurology: Clinical Practice
  2. Bridging the gap: understanding participation barriers in ALS clinical trials through on-the-ground insights| Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration | Taylor & Francis
  3. The Amyotrophic Lateral Sclerosis House Call Program: A Single-Center Experience in the United States| Neurology Research International | Wiley Online
  4. Impaired nucleocytoplasmic transport in SOD1-mediated ALS | Molecular Neurodegeneration | Springer Nature
  5. Blocking RAN translation without altering repeat RNAs rescues C9ORF72-related ALS and FTD phenotypes| Science
2025
  1. Amyotrophic Lateral Sclerosis Clinical Research Site Operations: Emerging Challenges and Potential Solutions From Multiple Sites in the US | Muscle & Nerve | Wiley Online
  2. Real-World Clinical Experience With Sodium Phenylbutyrate and Taurursodiol at a Single Amyotrophic Lateral Sclerosis Center in the United States | European Journal of Neurology | Wiley Online
  3. Multicenter Expanded Access Protocol for Research Through Access to Trehalose in People With Amyotrophic Lateral Sclerosis | Muscle & Nerve | Wiley Online
  4. Research access barriers in amyotrophic lateral sclerosis | Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration | Taylor & Francis
  5. Toward therapeutic trials in primary lateral sclerosis | Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration | Taylor & Francis
  6. Cervical spinal cord MRI in ALS individuals: a systematic review and meta-analysis | NeuroImage: Clinical | ScienceDirect
  7. Financing drug development via adaptive platform trials | PLOS One
  8. Operational Development and Launch of an Adaptive Platform Trial in Amyotrophic Lateral Sclerosis: Processes and Learnings from the First Four Regimens of the HEALEY ALS Platform Trial | Muscle & Nerve | Wiley Online
  9. Safety and Efficacy of Trehalose in Amyotrophic Lateral Sclerosis (HEALEY ALS Platform Trial): An Adaptive, Phase 2/3, Double-blind, Randomised, Placebo-controlled Trial | The Lancet Neurology | ScienceDirect
  10. An Expanded Access Protocol of RNS60 in Amyotrophic Lateral Sclerosis | Muscle & Nerve | Wiley Online
  11. Akt Activation With IPL344 Treatment for Amyotrophic Lateral Sclerosis: First in Human, Open-Label Study | Muscle & Nerve | Wiley Online
  12. Efficacy and Safety of Zilucoplan in Amyotrophic Lateral Sclerosis: A Randomized Clinical Trial | Neurology | JAMA Network Open | JAMA Network
  13. Verdiperstat in Amyotrophic Lateral Sclerosis: Results From the Randomized HEALEY ALS Platform Trial | Amyotrophic Lateral Sclerosis | JAMA Neurology | JAMA Network
  14. CNM-Au8 in Amyotrophic Lateral Sclerosis: The HEALEY ALS Platform Trial | Amyotrophic Lateral Sclerosis | JAMA | JAMA Network
  15. Pridopidine in Amyotrophic Lateral Sclerosis: The HEALEY ALS Platform Trial | Amyotrophic Lateral Sclerosis | JAMA | JAMA Network
2024
  1. Allogeneic B Cell Immunomodulatory Therapy in Amyotrophic Lateral Sclerosis.
    Sîrbulescu RF, Nicholson K, Kawai K, Hilton OM, Sobell D, Jin G, Verrill DE, Dwyer LJ, Xiong Y, Bachanová P, Kim SE, Gallup S, Gelevski D, Daley H, Hernandez Rodriguez DE, Negre H, Sturtevant O, Nikiforow S, Ritz J, Chen YB, Reeves PM, Sluder AE, Berry JD, Sadri-Vakili G, Cudkowicz M, Poznansky MC.FASEB J. 2024 Jul 15;38(13):e23796. doi: 10.1096/fj.202302659R.PMID: 38967302
  2. Characterization of Cortico-Meningeal Translocator Protein Expression in Multiple Sclerosis.
    Herranz E, Treaba CA, Barletta VT, Mehndiratta A, Ouellette R, Sloane JA, Ionete C, Babu S, Mastantuono M, Magon S, Loggia ML, Makary MM, Hooker JM, Catana C, Kinkel RP, Nicholas R, Klawiter EC, Magliozzi R, Mainero C.Brain. 2024 Jul 5;147(7):2566-2578. doi: 10.1093/brain/awae030.PMID: 38289855
  3. Failures to Replicate: What Recent Negative Phase 3 Trials Have Taught Us about Amyotrophic Lateral Sclerosis Clinical Research.
    Shefner JM, Cudkowicz ME.Ann Neurol.
    2024 Jun 18. doi: 10.1002/ana.26999.
  4. Multicenter Expanded Access Program for Access to Investigational Products for Amyotrophic Lateral Sclerosis
    Neel D, Baselga-Garriga C, Benson M, Keegan M, Chase M, D'Agostino D, Drake K, Hagar J, Hasenoehrl M, Kulesa-Kelley J, Leite A, Mohapatra S, Portaro S, Pothier L, Rosenthal J, Sherman A, Yu H, McCaffrey A, Ho D, Luppino S, Bedlack R, Heitzman D, Ajroud-Driss S, Katz J, Felice K, Whitaker C, Ladha S, Alameda G, Locatelli E, Qureshi I, Hotchkin M, Hayden M, Cudkowicz M, Babu S, Berry J, Paganoni S. Multicenter expanded access program for access to investigational products for amyotrophic lateral sclerosis. Muscle & Nerve. 2024 June 6. doi: 10.1002/mus.28169.
  5. Apilimod Dimesylate in C9orf72 Amyotrophic Lateral Sclerosis: A Randomized Phase 2a Clinical Trial
    Babu S, Nicholson KA, Rothstein JD, Swenson A, Sampognaro PJ, Pant P, Macklin EA, Spruill S, Paganoni S, Gendron TF, Prudencio M, Petrucelli L, Nix D, Landrette S, Nkrumah E, Fandrick K, Edwards J, Young PR. Apilimod dimesylate in C9orf72 amyotrophic lateral sclerosis: a randomized phase 2a clinical trial. Brain. 2024 Apr 12:awae109. doi: 10.1093/brain/awae109. Epub ahead of print. PMID: 38606777.
  6. Debamestrocel Multimodal Effects on Biomarker Pathways in Amyotrophic Lateral Sclerosis are Linked to Clinical Outcomes
    Lindborg SR, Goyal NA, Katz J, Burford M, Li J, Kaspi H, Abramov N, Boulanger B, Berry JD, Nicholson K, Mozaffar T, Miller R, Jenkins L, Baloh RH, Lewis R, Staff NP, Owegi MA, Dagher B, Blondheim-Shraga NR, Gothelf Y, Levy YS, Kern R, Aricha R, Windebank AJ, Bowser R, Brown RH Jr, Cudkowicz ME. Debamestrocel multimodal effects on biomarker pathways in amyotrophic lateral sclerosis are linked to clinical outcomes. Muscle Nerve. 2024 Apr 9. doi: 10.1002/mus.28093. Epub ahead of print. PMID: 38593477.
  7. Longitudinal Comparison of the Self-Administered ALSFRS-RSE and ALS-SFRS-R as Functional Outcome Measures in ALS
    Erb MK, Calcagno N, Brown R, Burke KM, Scheier ZA, Iyer AS, Clark A, Higgins MP, Keegan M, Gupta AS, Johnson SA, Chew S, Berry JD. Longitudinal comparison of the self-administered ALSFRS-RSE and ALSFRS-R as functional outcome measures in ALS. Amyotroph Lateral Scler Frontotemporal Degener. 2024 Mar 19:1-11. doi: 10.1080/21678421.2024.2322549. Epub ahead of print. PMID: 38501453.
  8. Medication Use and Risk of Amyotrophic Lateral Sclerosis: Using Machine Learning For an Exposome-Wide Screen of a Large Clinical Database
    Rotem RS, Bellavia A, Paganoni S, Weisskopf MG. Medication use and risk of amyotrophic lateral sclerosis: using machine learning for an exposome-wide screen of a large clinical database. Amyotroph Lateral Scler Frontotemporal Degener. 2024 Mar 1:1-9. doi: 10.1080/21678421.2024.2320878. Epub ahead of print. PMID: 38426489.
  9. Artificial Intelligence in Neurology: Opportunities, Challenges, and Policy Implications
    Voigtlaender S, Pawelczyk J, Geiger M, Vaios EJ, Karschnia P, Cudkowicz M, Dietrich J, Haraldsen IRJH, Feigin V, Owolabi M, White TL, Świeboda P, Farahany N, Natarajan V, Winter SF. Artificial intelligence in neurology: opportunities, challenges, and policy implications. J Neurol. 2024 Feb 17. doi: 10.1007/s00415-024-12220-8. Epub ahead of print. PMID: 38367046.
2023
  1. Design and Statistical Innovations in a Platform Trial for Amyotrophic Lateral Sclerosis
    Melanie Quintana PhD, Benjamin R. Saville PhD, Matteo Vestrucci PhD, Michelle A. Detry PhD, Lori Chibnik PhD, MPH, Jeremy Shefner MD, PhD, James D. Berry MD, MPH, Marianne Chase BA, Jinsy Andrews MD, Alexander V. Sherman MSc, Hong Yu MS, Kristin Drake MBA, Merit Cudkowicz MD, MSc, Sabrina Paganoni MD, PhD, Eric A. Macklin PhD, for the HEALEY ALS Platform Trial Study Group. Annals of Neurology. 28 May 2023 https://doi.org/10.1002/ana.26714
  2. Expanded access protocol (EAP) program for access to investigational products for amyotrophic lateral sclerosis (ALS).
    Yerton M, Winter A, Gelevski D, Addy G, Kostov A, Lieberman C, Weber H, Doyle M, Kane G, Cohen C, Parikh N, Burke KM, Rohrer M, Stirrat T, Bruno M, Hochman A, Luppino S, Scalia J, D'Agostino D, Sinani E, Yu H, Drake K, Hagar J, Sherman AV, Babu S, Berry JD, Cudkowicz ME, Paganoni S. Muscle Nerve. 2023 Jun;67(6):456-463. doi: 10.1002/mus.27819. Epub 2023 Apr 5.PMID: 36929648
  3. Safety and activity of anti-CD14 antibody IC14 (atibuclimab) in ALS: Experience with expanded access protocol.
    Gelevski D, Addy G, Rohrer M, Cohen C, Roderick A, Winter A, Carey J, Scalia J, Yerton M, Weber H, Doyle M, Parikh N, Kane G, Ellrodt A, Burke K, D'Agostino D, Sinani E, Yu H, Sherman A, Agosti J, Redlich G, Charmley P, Crowe D, Appleby M, Ziegelaar B, Hanus K, Li Z, Babu S, Nicholson K, Luppino S, Berry J, Baecher-Allan C, Paganoni S, Cudkowicz M. Muscle Nerve. 2023 May;67(5):354-362. doi: 10.1002/mus.27775. Epub 2022 Dec 30.PMID: 36533976
  4. Combination of ciprofloxacin/celecoxib as a novel therapeutic strategy for ALS.
    Salomon-Zimri S, Pushett A, Russek-Blum N, Van Eijk RPA, Birman N, Abramovich B, Eitan E, Elgrart K, Beaulieu D, Ennist DL, Berry JD, Paganoni S, Shefner JM, Drory VE. Amyotroph Lateral Scler Frontotemporal Degener. 2023 May;24(3-4):263-271. doi: 10.1080/21678421.2022.2119868. Epub 2022 Sep 15.PMID: 36106817 Clinical Trial.
  5. Randomized trial of inosine for urate elevation in amyotrophic lateral sclerosis.
    Walk, D., Nicholson, K., Locatelli, E., Chan, J., Macklin, E. A., Ferment, V., Manousakis, G., Chase, M., Connolly, M., Dagostino, D., Hall, M., Ostrow, J., Pothier, L., Lieberman, C., Gelevski, D., Randall, R., Sherman, A. V., Steinhart, E., Walker, D. G., Walker, J., Paganoni, S. (2023). Muscle & nerve 67(5), 378–386.
  6. Wearable device and smartphone data quantify ALS progression and may provide novel outcome measures.
    Johnson, S. A., Karas, M., Burke, K. M., Straczkiewicz, M., Scheier, Z. A., Clark, A. P., Iwasaki, S., Lahav, A., Iyer, A. S., Onnela, J. P., & Berry, J. D. (2023). NPJ digital medicine 6(1), 34.
  7. Development and Evaluation of a Simulation-Based Algorithm to Optimize the Planning of Interim Analyses for Clinical Trials in ALS.
    an Unnik, J. W. J., Nikolakopoulos, S., Eijkemans, M. J. C., Gonzalez-Bermejo, J., Bruneteau, G., Morelot-Panzini, C., van den Berg, L. H., Cudkowicz, M. E., McDermott, C. J., Similowski, T., & van Eijk, R. P. A. (2023). Neurology, 10.1212/WNL.0000000000207306.
  8. CDISC Implementation in an Academic Research Organization, Jentoft, K. & Tustison, E. & Yu, H., (2023) “Journal of the Society for Clinical Data Management 2(3). doi
2022
  1. Safety and activity of anti-CD14 antibody IC14 (atibuclimab) in ALS: Experience with expanded access protocol.
    Gelevski D, Addy G, Rohrer M, Cohen C, Roderick A, Winter A, Carey J, Scalia J, Yerton M, Weber H, Doyle M, Parikh N, Kane G, Ellrodt A, Burke K, D'Agostino D, Sinani E, Yu H, Sherman A, Agosti J, Redlich G, Charmley P, Crowe D, Appleby M, Ziegelaar B, Hanus K, Li Z, Babu S, Nicholson K, Luppino S, Berry J, Baecher-Allan C, Paganoni S, Cudkowicz M. Muscle Nerve. 2022 Dec 19. doi: 10.1002/mus.27775.
  2. Restoring arm function with a soft robotic wearable for individuals with amyotrophic lateral sclerosis.
    Proietti T, O'Neill C, Gerez L, Cole T, Mendelowitz S, Nuckols K, Hohimer C, Lin D, Paganoni S, Walsh C.
    Sci Transl Med. 2023 Feb;15(681):eadd1504. doi: 10.1126/scitranslmed.add1504. Epub 2023 Feb 1.PMID: 36724237
  3. Causal inference in medical records and complementary systems pharmacology for metformin drug repurposing towards dementia.Charpignon, M.-L., B. Vakulenko-Lagun, B. Zheng, C. Magdamo, B. Su, K. Evans, S. Rodriguez, A. Sokolov, S. Boswell, Y.-H. Sheu, M. Somai, L. Middleton, B. T. Hyman, R. A. Betensky, S. N. Finkelstein, R. E. Welsch, I. Tzoulaki, D. Blacker, S. Das and M. W. Albers (2022). Nature Communications 13(1).
  4. Amyotrophic Lateral Sclerosis Clinical Trials and Interpretation of Functional End Points and Fluid Biomarkers: A Review
    Shefner JM, Bedlack R, Andrews JA, Berry JD, Bowser R, Brown R, Glass JD, Maragakis NJ, Miller TM, Rothstein JD, Cudkowicz ME. Amyotrophic Lateral Sclerosis Clinical Trials and Interpretation of Functional End Points and Fluid Biomarkers: A Review.
  5. Selective atrophy of the cervical enlargement in whole spinal cord MRI of amyotrophic lateral sclerosis
    Barry, R. L., Torrado-Carvajal, A., Kirsch, J. E., Arabasz, G. E., Albrecht, D. S., Alshelh, Z., Pijanowski, O., Lewis, A. J., Keegan, M., Reynolds, B., Knight, P. C., Morrissey, E. J., Loggia, M. L., Atassi, N., Hooker, J. M., & Babu, S. (2022). Selective atrophy of the cervical enlargement in whole spinal cord MRI of amyotrophic lateral sclerosis. NeuroImage: Clinical, 36, 103199.
  6. Pharmacotherapy for Amyotrophic Lateral Sclerosis: A Review of Approved and Upcoming Agents
    Johnson SA, Fang T, De Marchi F, Neel D, Van Weehaeghe D, Berry JD, Paganoni S. Pharmacotherapy for Amyotrophic Lateral Sclerosis: A Review of Approved and Upcoming Agents. Drugs. 2022 Sep 19. doi: 10.1007/s40265-022-01769-1. Epub ahead of print. PMID: 36121612.
  7. Evidence-Based Medicine Training in United States-Based Physiatry Residency Programs.
    Annaswamy TM, Rizzo JR, Schnappinger A, Morgenroth DC, Engkasan JP, Ilieva E, Arnold WD, Boninger ML, Bean AC, Cirstea CM, Dicianno BE, Fredericson M, Jayabalan P, Raghavan P, Sawaki L, Suri P, Suskauer SJ, Wang QM, Hosseini M, Case CM, Whyte J, Paganoni S. Am J Phys Med Rehabil. 2022 Jul 1;101(7 Suppl 1):S40-S44. doi: 10.1097/PHM.0000000000001752.
  8. Identification of Therapeutic Targets for Amyotrophic Lateral Sclerosis Using PandaOmics – An AI-Enabled Biological Target Discovery Platform
    Pun FW, Liu1 BHM, Long X, Leung HW, Leung GHD, Mewborne QT, Gao J, Shneyderman A, Ozerov IV, Wang J, Ren F, Aliper A, Bischof E, Izumchenko E, Guan X, Zhang K, Lu B, Rothstein JD, Cudkowicz ME, Zhavoronkov A. Front. Aging Neurosci., 28 June 2022. doi: fnagi.2022.914017
  9. An Expanded Access Protocol of RT001 in Amyotrophic Lateral Sclerosis-Initial Experience with a Lipid Peroxidation Inhibitor.
    Yerton M, Winter A, Kostov A, Lieberman C, Gelevski D, Weber H, Doyle M, Kane G, Parikh N, Burke K, Rohrer M, Stirrat T, Bruno M, Hochman A, Luppino S, Scalia J, Skoniecki D, D'Agostino D, Sinani E, Yu H, Sherman AV, Babu S, Berry JD, Midei MG, Milner PG, Cudkowicz ME, Paganoni S. Muscle Nerve. 2022 Jun 28. doi: 10.1002/mus.27672.
  10. Effect of sodium phenylbutyrate/taurursodiol on tracheostomy/ventilation-free survival and hospitalisation in amyotrophic lateral sclerosis: long-term results from the CENTAUR trial.
    Paganoni S, Hendrix S, Dickson SP, Knowlton N, Berry JD, Elliott MA, Maiser S, Karam C, Caress JB, Owegi MA, Quick A, Wymer J, Goutman SA, Heitzman D, Heiman-Patterson TD, Jackson C, Quinn C, Rothstein JD, Kasarskis EJ, Katz J, Jenkins L, Ladha SS, Miller TM, Scelsa SN, Vu TH, Fournier C, Johnson KM, Swenson A, Goyal N, Pattee GL, Babu S, Chase M, Dagostino D, Hall M, Kittle G, Eydinov M, Ostrow J, Pothier L, Randall R, Shefner JM, Sherman AV, Tustison E, Vigneswaran P, Yu H, Cohen J, Klee J, Tanzi R, Gilbert W, Yeramian P, Cudkowicz M. J Neurol Neurosurg Psychiatry. 2022 May 16:jnnp-2022-329024. doi: 10.1136/jnnp-2022-329024.
  11. Survival Analyses From the CENTAUR Trial in Amyotrophic Lateral Sclerosis: Evaluating the Impact of Treatment Crossover on Outcomes.
    Paganoni S, Watkins C, Cawson M, Hendrix S, Dickson SP, Knowlton N, Timmons J, Manuel M, Cudkowicz M. Muscle Nerve. 2022 May 4. doi: 10.1002/mus.27569.
  12. Regulatory Approval in ALS; When Is a Single Study Enough?
    Cudkowicz ME, Shefner JM. Ann Neurol. 2022 Apr 28. doi: 10.1002/ana.26371.
2021
  1. Adaptive Platform Trials to Transform ALS Therapy Development.
    Paganoni S, Berry JD, Quintana M, Macklin E, Saville BR, Detry MA, Chase M, Sherman A, Yu H, Drake K, Andrews J, Shefner J, Chibnik L, Vestrucci M, Cudkowicz ME; HEALEY ALS Platform Trial Study Group. Ann Neurol. 2021 Dec 21. doi: 10.1002/ana.26285
  2. A Randomized Placebo-Controlled Phase 3 Study of Mesenchymal stem cells induced to secrete high levels of neurotrophic factors in Amyotrophic Lateral Sclerosis.
    Cudkowicz ME, Lindborg SR, Goyal NA, Miller RG, Burford MJ, Berry JD, Nicholson KA, Mozaffar T, Katz JS, Jenkins LJ, Baloh RH, Lewis RA, Staff N, Owegi MA, Berry DA, Gothelf Y, Levy YS, Aricha R, Kern RZ, Windebank AJ, Brown RH Jr. Muscle Nerve. 2021 Dec 10. doi: 10.1002/mus.27472.
  3. Novel genetic variants in MAPT and alterations in tau phosphorylation in amyotrophic lateral sclerosis post-mortem motor cortex and cerebrospinal fluid.
    Petrozziello T, Amaral AC, Dujardin S, Farhan SMK, Chan J, Trombetta BA, Kivisäkk P, Mills AN, Bordt EA, Kim SE, Dooley PM, Commins C, Connors TR, Oakley DH, Ghosal A, Gomez-Isla T, Hyman BT, Arnold SE, Spires-Jones T, Cudkowicz ME, Berry JD, Sadri-Vakili G. Brain Pathol. 2021 Nov 14:e13035. doi: 10.1111/bpa.13035.
  4. Targeting Tau Mitigates Mitochondrial Fragmentation and Oxidative Stress in Amyotrophic Lateral Sclerosis.
    Petrozziello T, Bordt EA, Mills AN, Kim SE, Sapp E, Devlin BA, Obeng-Marnu AA, Farhan SMK, Amaral AC, Dujardin S, Dooley PM, Henstridge C, Oakley DH, Neueder A, Hyman BT, Spires-Jones TL, Bilbo SD, Vakili K, Cudkowicz ME, Berry JD, DiFiglia M, Silva MC, Haggarty SJ, Sadri-Vakili G. Mol Neurobiol. 2021 Nov 10. doi: 10.1007/s12035-021-02557-w.
  5. Safety and efficacy of oral levosimendan in people with amyotrophic lateral sclerosis (the REFALS study): a randomised, double-blind, placebo-controlled phase 3 trial.
    Cudkowicz M, Genge A, Maragakis N, Petri S, van den Berg L, Aho VV, Sarapohja T, Kuoppamäki M, Garratt C, Al-Chalabi A; REFALS investigators. Lancet Neurol. 2021 Oct;20(10):821-831. doi: 10.1016/S1474-4422(21)00242-8.
  6. Human sensorimotor organoids derived from healthy and amyotrophic lateral sclerosis stem cells form neuromuscular junctions.
    Pereira JD, DuBreuil DM, Devlin AC, Held A, Sapir Y, Berezovski E, Hawrot J, Dorfman K, Chander V, Wainger BJ. Nat Commun. 2021 Aug 6;12(1):4744. doi: 10.1038/s41467-021-24776-4.
  7. Radicava/Edaravone Findings in Biomarkers From Amyotrophic Lateral Sclerosis (REFINE-ALS): Protocol and Study Design.
    Berry J, Brooks B, Genge A, Heiman-Patterson T, Appel S, Benatar M, Bowser R, Cudkowicz M, Gooch C, Shefner J, Westra J, Agnese W, Merrill C, Nelson S, Apple S. Neurol Clin Pract. 2021 Aug;11(4):e472-e479. doi: 10.1212/CPJ.0000000000000968.
  8. Genome-encoded cytoplasmic double-stranded RNAs, found in C9ORF72 ALS-FTD brain, propagate neuronal loss.
    Rodriguez S, Sahin A, Schrank BR, Al-Lawati H, Costantino I, Benz E, Fard D, Albers AD, Cao L, Gomez AC, Evans K, Ratti E, Cudkowicz M, Frosch MP, Talkowski M, Sorger PK, Hyman BT, Albers MW. Sci Transl Med. 2021 Jul 7;13(601):eaaz4699. doi: 10.1126/scitranslmed.aaz4699.
  9. A high-content platform for physiological profiling and unbiased classification of individual neurons.
    DuBreuil DM, Chiang BM, Zhu K, Lai X, Flynn P, Sapir Y, Wainger BJ. Cell Rep Methods. 2021 May 24;1(1):100004. doi: 10.1016/j.crmeth.2021.100004.
  10. Ibudilast (MN-166) In Amyotrophic Lateral Sclerosis - an Open Label, Safety and Pharmacodynamic Trial
    Babu S, Hightower BG, Chan J,  Zürcher NR,  Kivisäkk P, Tseng CJ, Sanders DL, Robichaud A,  Banno H, Evora A,  Ashokkumar A,  Pothier L,  Paganoni S,  Chew S,  Dojillo J,  Matsuda K, Gudesblatt M, Berry JD,  Cudkowicz ME,  Hooker JM, Atassi N. NeuroImage: Clinical. 2021 April 15. doi: 10.1016/j.nicl.2021.102672
  11. Ultra-high field (7T) functional magnetic resonance imaging in amyotrophic lateral sclerosis: a pilot study.
    Barry RL, Babu S, Anteraper SA, Triantafyllou C, Keil B, Rowe OE, Rangaprakash D, Paganoni S, Lawson R, Dheel C, Cernasov PM, Rosen BR, Ratai EM, Atassi N. Neuroimage Clin. 2021 Mar 30;30:102648. doi: 10.1016/j.nicl.2021.102648.
  12. Patient reported outcomes in ALS: characteristics of the self-entry ALS Functional Rating Scale-revised and the Activities-specific Balance Confidence Scale.
    Chew S, Burke KM, Collins E, Church R, Paganoni S, Nicholson K, Babu S, Scalia JB, De Marchi F, Ellrodt AL, Moura LMVR, Chan J, Berry JD. Amyotroph Lateral Scler Frontotemporal Degener. 2021 Mar 26:1-11. doi: 10.1080/21678421.2021.1900259.
  13. Regional prefrontal cortical atrophy predicts specific cognitive-behavioral symptoms in ALS-FTD.
    Ratti E, Domoto-Reilly K, Caso C, Murphy A, Brickhouse M, Hochberg D, Makris N, Cudkowicz ME, Dickerson BC. Brain Imaging Behav. 2021 Feb 15. doi: 10.1007/s11682-021-00456-1.
  14. Comparison of Two Clinical Upper Motor Neuron Burden Rating Scales in ALS Using Quantitative Brain Imaging.
    Makary MM, Weerasekara A, Rodham H, Hightower BG, Tseng CJ, Chan J, Chew S, Paganoni S, Ratai EM, Zürcher NR, Hooker JM, Atassi N, Babu S. ACS Chem Neurosci. 2021 Feb 12. doi: 10.1021/acschemneuro.0c00772.
2020
  1. Effects of Mexiletine on Hyperexcitability in Sporadic ALS: Preliminary Findings from A Small Phase II Randomized Controlled Trial.
    Weiss MD, Macklin EA, McIlduff CE, Vucic S, Wainger BJ, Kiernan MC, Goutman SA, Goyal NA, Rutkove SB, Ladha SS, Amy Chen IH, Harms MB, Brannagan TH, Lacomis D, Zivkovic S, Ma M, Wang LH, Simmons Z, Rivner MH, Shefner JM, Cudkowicz ME, Atassi N; Mexiletine-2 ALS Study Group. Muscle Nerve. 2020 Dec 19. doi: 10.1002/mus.27146.
  2. Sodium Phenylbutyrate-Taurursodiol for ALS. Reply.
    Paganoni S, Cudkowicz ME. N Engl J Med. 2020 Dec 3;383(23):2294. doi: 10.1056/NEJMc2030710.
  3. Effect of Ezogabine on Cortical and Spinal Motor Neuron Excitability in Amyotrophic Lateral Sclerosis: A Randomized Clinical Trial.
    Wainger BJ, Macklin EA, Vucic S, McIlduff CE, Paganoni S, Maragakis NJ, Bedlack R, Goyal NA, Rutkove SB, Lange DJ, Rivner MH, Goutman SA, Ladha SS, Mauricio EA, Baloh RH, Simmons Z, Pothier L, Kassis SB, La T, Hall M, Evora A, Klements D, Hurtado A, Pereira JD, Koh J, Celnik PA, Chaudhry V, Gable K, Juel VC, Phielipp N, Marei A, Rosenquist P, Meehan S, Oskarsson B, Lewis RA, Kaur D, Kiskinis E, Woolf CJ, Eggan K, Weiss MD, Berry JD, David WS, Davila-Perez P, Camprodon JA, Pascual-Leone A, Kiernan MC, Shefner JM, Atassi N, Cudkowicz ME. JAMA Neurol. 2020 Nov 23. doi: 10.1001/jamaneurol.2020.4300.
  4. The human gut microbiota in people with amyotrophic lateral sclerosis.
    Nicholson K, Bjornevik K, Abu-Ali G, Chan J, Cortese M, Dedi B, Jeon M, Xavier R, Huttenhower C, Ascherio A, Berry JD. Amyotroph Lateral Scler Frontotemporal Degener. 2020 Nov 2:1-9. doi: 10.1080/21678421.2020.1828475.
  5. Smartphone data during the COVID-19 pandemic can quantify behavioral changes in people with ALS.
    Beukenhorst AL, Collins E, Burke KM, Rahman SM, Clapp M, Konanki SC, Paganoni S, Miller TM, Chan J, Onnela JP, Berry JD. Muscle Nerve. 2020 Oct 29. doi: 10.1002/mus.27110.
  6. Long-Term Survival of Participants in the CENTAUR Trial of Sodium Phenylbutyrate-Taurursodiol in ALS.
    Paganoni S, Hendrix S, Dickson SP, Knowlton N, Macklin EA, Berry JD, Elliott MA, Maiser S, Karam C, Caress JB, Owegi MA, Quick A, Wymer J, Goutman SA, Heitzman D, Heiman-Patterson TD, Jackson CE, Quinn C, Rothstein JD, Kasarskis EJ, Katz J, Jenkins L, Ladha S, Miller TM, Scelsa SN, Vu TH, Fournier CN, Glass JD, Johnson KM, Swenson A, Goyal NA, Pattee GL, Andres PL, Babu S, Chase M, Dagostino D, Hall M, Kittle G, Eydinov M, McGovern M, Ostrow J, Pothier L, Randall R, Shefner JM, Sherman AV, St Pierre ME, Tustison E, Vigneswaran P, Walker J, Yu H, Chan J, Wittes J, Yu ZF, Cohen J, Klee J, Leslie K, Tanzi RE, Gilbert W, Yeramian PD, Schoenfeld D, Cudkowicz ME. Muscle Nerve. 2020 Oct 16. doi: 10.1002/mus.27091.
  7. The NEALS primary lateral sclerosis registry.
    Paganoni S, De Marchi F, Chan J, Thrower SK, Staff NP, Datta N, Kisanuki YY, Drory V, Fournier C, Pioro EP, Goutman SA, Atassi N; NEALS PLS Registry Study Group. Amyotroph Lateral Scler Frontotemporal Degener. 2020 Sep 11:1-8. doi: 10.1080/21678421.2020.1804591.
  8. Engaging ALS patients and caregivers (the ALS research ambassadors) to help design the REFINE-ALS biomarker study.
    Berry JD, Bedlack R, Mathews D, Agnese W, Apple S. Amyotroph Lateral Scler Frontotemporal Degener. 2020 Aug 24:1-4. doi: 10.1080/21678421.2020.1804939.
  9. Exploring the use of educational materials for increasing participation in a stretching program: a quality improvement project in people with motor neuron disease.
    Burke K, De Marchi F, Ellrodt AS, Doyle M, Koul M, Comeau O, Adelson E, Walter R, Kusy M, Amaya F, Anderson C, Honda J, Chan J, Berry J, Paganoni S. Eur J Phys Rehabil Med. 2020 Aug 3. doi: 10.23736/S1973-9087.20.06245-0.
  10. Amyotrophic Lateral Sclerosis: Fuel for the Corticofugal Feud.
    Wainger BJ, Brown RH Jr. Ann Neurol. 2020 Aug 2. doi: 10.1002/ana.25861.
  11. Longitudinal biomarkers in amyotrophic lateral sclerosis.
    Huang F, Zhu Y, Hsiao-Nakamoto J, Tang X, Dugas JC, Moscovitch-Lopatin M, Glass JD, Brown RH Jr, Ladha SS, Lacomis D, Harris JM, Scearce-Levie K, Ho C, Bowser R, Berry JD. Ann Clin Transl Neurol. 2020 Jun 9. doi: 10.1002/acn3.51078.
  12. Lipocalin-2 is increased in amyotrophic lateral sclerosis.
    Petrozziello T, Mills AN, Farhan SMK, Mueller KA, Granucci EJ, Glajch KE, Chan J, Chew S, Berry JD, Sadri-Vakili G. Muscle Nerve. 2020 May 5. doi: 10.1002/mus.26911.
  13. Understanding the needs of people with ALS: a national survey of patients and caregivers.
    Brizzi KT, Bridges JFP, Yersak J, Balas C, Thakur N, Galvin M, Hardiman O, Heatwole C, Ravits J, Simmons Z, Bruijn L, Chan J, Bedlack R, Berry JD. Amyotroph Lateral Scler Frontotemporal Degener. 2020 May 12:1-9. doi: 10.1080/21678421.2020.1760889.
  14. Upper motor neuron burden measurement in motor neuron diseases: Does one scale fit all?
    Babu S. Muscle Nerve. 2020 Apr;61(4):431-432. doi: 10.1002/mus.26836.
  15. Moving towards multicenter therapeutic trials in ALS: feasibility of data pooling using different TSPO positron emission tomography (PET) radioligands.
    Van Weehaeghe D, Babu S, De Vocht J, Zurcher NR, Chew S, Tseng CJ, Loggia M, Koole M, Rezaei A, Schramm G, Van Damme P, Hooker JM, Van Laere K, Atassi N. J Nucl Med. 2020 Mar 13. pii: jnumed.119.241059. doi: 10.2967/jnumed.119.241059.
  16. Patient reported outcome measures (PROMs) in amyotrophic lateral sclerosis.
    De Marchi F, Berry JD, Chan J, Caldwell S, Ellrodt A, Scalia J, Burke K, Fang T, Clark Sisodia R, Schwamm LH, Moura LMVR, Paganoni S. J Neurol. 2020 Mar 3. doi: 10.1007/s00415-020-09774-8.
  17. Upper Motor Neuron Burden Measurement in motor neuron diseases- Does one scale fit all?
    Babu, S. Muscle Nerve. 2020 Feb 18. doi: 10.1002/mus.26836. [Epub ahead of print]
  18. Addressing Heterogeneity in ALS Clinical Trials.
    Goyal NA, Berry JD, Windebank A, Nathan P, Maragakis NJ, van den Berg LH, Genge A, Miller R, Baloh RH, Kern R, Gothelf Y, Lebovits C, Cudkowicz M. Muscle & Nerve. 2020 Jan 3. doi: 10.1002/mus.26801.
2019
  1. Cromolyn sodium delays disease onset and is neuroprotective in the SOD1G93A Mouse Model of amyotrophic lateral sclerosis.
    Granucci EJ, Griciuc A, Mueller KA, Mills AN, Le H, Dios AM, McGinty D, Pereira J, Elmaleh D, Berry JD, Paganoni S, Cudkowicz ME, Tanzi RE, Sadri-Vakili G. Sci Rep. 2019 Nov 27;9(1):17728. doi: 10.1038/s41598-019-53982-w.
  2. NurOwn, phase 2, randomized, clinical trial in patients with ALS: Safety, clinical, and biomarker results.
    Berry JD, Cudkowicz ME, Windebank AJ, Staff NP, Owegi M, Nicholson K, McKenna-Yasek D, Levy YS, Abramov N, Kaspi H, Mehra M, Aricha R, Gothelf Y, Brown RH. Neurology. 2019 Nov 18. pii: 10.1212/WNL.0000000000008620. doi: 10.1212/WNL.0000000000008620.
  3. Selection design phase II trial of high dosages of tamoxifen and creatine in amyotrophic lateral sclerosis.
    Babu S, Macklin EA, Jackson KE, Simpson E, Mahoney K, Yu H, Walker J, Simmons Z, David WS, Barkhaus PE, Simionescu L, Dimachkie MM, Pestronk A, Salameh JS, Weiss MD, Brooks BR, Schoenfeld D, Shefner J, Aggarwal S, Cudkowicz ME, Atassi N. Amyotroph Lateral Scler Frontotemporal Degener. 2019 Oct 14:1-9. doi: 10.1080/21678421.2019.1672750.
  4. Adjusted cost analysis of video televisits for the care of people with amyotrophic lateral sclerosis.
    Paganoni S, van de Rijn M, Drake K, Burke K, Doyle M, Ellrodt AS, Nicholson K, Atassi N, de Marchi F, Babu S, Estrada J, Schwamm LH, Berry JD. Muscle Nerve. 2019 Aug;60(2):147-154. doi: 10.1002/mus.26606. Epub 2019 Jun 27.
  5. Integration of a palliative care specialist in an amyotrophic lateral sclerosis clinic: Observations from one center.
    Brizzi K, Paganoni S, Zehm A, De Marchi F, Berry JD. Muscle & Nerve. 2019 Aug;60(2):137-140. doi: 10.1002/mus.26607.
  6. Pharmacological Profiling of Purified Human Stem Cell-Derived and Primary Mouse Motor Neurons.
    Moakley D, Koh J, Pereira JD, DuBreuil DM, Devlin AC, Berezovski E, Zhu K, Wainger BJ. Sci Rep. 2019 Jul 25;9(1):10835. doi: 10.1038/s41598-019-47203-7.
  7. Design and analysis of a clinical trial using previous trials as historical control.
    Schoenfeld DA, Finkelstein DM, Macklin E, Zach N, Ennist DL, Taylor AA, Atassi N. Pooled Resource Open-Access ALS Clinical Trials Consortium. Clin Trials. 2019 Jul 1:1740774519858914. doi: 10.1177/1740774519858914.
  8. ALS/SURV: a modification of the CAFS statistic.
    Goutman SA, Brown MB, Cudkowicz M, Atassi N, Feldman EL. Amyotroph Lateral Scler Frontotemporal Degener. 2019 Jul 23:1-8. doi: 10.1080/21678421.2019.1643375.
  9. All-Cause and Cause-Specific Mortality Among Major League Baseball Players.
    Nguyen VT, Zafonte RD, Kponee-Shovein KZ, Paganoni S, Weisskopf MG. JAMA Intern Med. 2019 Jul 22. doi: 10.1001/jamainternmed.2019.1218.
  10. Class I and II histone deacetylase expression is not altered in human amyotrophic lateral sclerosis: Neuropathological and positron emission tomography molecular neuroimaging evidence.
    Dios AM, Babu S, Granucci EJ, Mueller KA, Mills AN, Alshikho MJ, Zürcher NR,Cernasov P, Gilbert TM, Glass JD, Berry JD, Atassi N, Hooker JM, Sadri-Vakili G.  Muscle & Nerve. 2019 Jun 26. doi: 10.1002/mus.26620.
  11. When a negative trial in ALS has a positive effect on research.
    Atassi N. Lancet Neurol. 2018 Aug;17(8):653-655. doi: 10.1016/S1474-4422(18)30210-2. Epub 2018 Jun 19.
  12. Nutritional counseling with or without mobile health technology: a randomized open-label standard-of-care-controlled trial in ALS.
    Wills AM, Garry J, Hubbard J, Mezoian T, Breen CT, Ortiz-Miller C, Nalipinski P, Sullivan S, Berry JD, Cudkowicz M, Paganoni S, Chan J, Macklin EA. BMC Neurol. 2019 May 29;19(1):104. doi: 10.1186/s12883-019-1330-6.
  13. VITALITY-ALS STUDY GROUP. A phase III trial of tirasemtiv as a potential treatment for amyotrophic lateral sclerosis.
    Shefner JM, Cudkowicz ME, Hardiman O, Cockroft BM, Lee JH, Malik FI, Meng L, Rudnicki SA, Wolff AA, Andrews JA. Amyotroph Lateral Scler Frontotemporal Degener. 2019 May 13:1-11. doi:10.1080/21678421.2019.1612922. [Epub ahead of print] Erratum in: Amyotroph Lateral Scler Frontotemporal Degener. 2019 Jul 14;:1.
  14. Provisional best practices guidelines for the evaluation of bulbar dysfunction in amyotrophic lateral sclerosis.
    Contributing Members of the NEALS Bulbar Subcommittee.  Pattee GL, Plowman EK, Focht Garand KL, Costello J, Brooks BR, Berry JD, Smith RA, Atassi N, Chapin JL, Yunusova Y, McIlduff CE, Young E, Macklin EA, Locatelli ER, Silani V, Heitzman D, Wymer J, Goutman SA, Gelinas DF, Perry B, Nalipinski P, Stipancic K, O'Brien M, Sullivan SL, Pioro EP, Gargiulo G, Green JR. Muscle & Nerve. 2019 May;59(5):531-536. doi: 10.1002/mus.26408. Epub 2019 Jan 22.
  15. Design and results of a smartphone-based digital phenotyping study to quantify ALS progression.
    Berry JD, Paganoni S, Carlson K, Burke K, Weber H, Staples P, Salinas J, Chan J, Green JR, Connaghan K, Barback J, Onnela JP. Ann Clin Transl Neurol. 2019 Apr 3;6(5):873-881. doi: 10.1002/acn3.770. eCollection 2019 May.
  16. Disruption of RNA Metabolism in Neurological Diseases and Emerging Therapeutic Interventions.
    Nussbacher JK, Tabet R, Yeo GW, Lagier-Tourenne C. Neuron. 2019 Apr 17;102(2):294-320. doi: 10.1016/j.neuron.2019.03.014. Review.
  17. Positron Emission Tomography Molecular Imaging Biomarkers for Amyotrophic Lateral Sclerosis.
    Chew S, Atassi N.   Front Neurol. 2019 Mar 1;10:135. doi: 10.3389/fneur.2019.00135. eCollection 2019. Review.
  18. Lunasin does not slow ALS progression: results of an open-label, single-center, hybrid-virtual 12-month trial.
    Bedlack RS, Wicks P, Vaughan T, Opie A, Blum R, Dios A, Sadri-Vakili G. Amyotroph Lateral Scler Frontotemporal Degener. 2019 Jan 21:1-9. doi: 10.1080/21678421.2018.1556698. [Epub ahead of print]
  19. Heterogeneity, urgency, generalizability, and enrollment: The HUGE balance in ALS trials.
    Karam C, Berry JD.  Neurology. 2019 Jan 9. pii: 10.1212/WNL.0000000000006837. doi: 10.1212/WNL.0000000000006837. [Epub ahead of print]
2018
  1. A pilot trial of RNS60 in amyotrophic lateral sclerosis.
    Paganoni S, Alshikho MJ, Luppino S, Chan J, Pothier L, Schoenfeld D, Andres PL, Babu S, Zürcher NR, Loggia ML, Barry RL, Luotti S, Nardo G, Trolese MC, Pantalone S, Bendotti C, Bonetto V, De Marchi F, Rosen B, Hooker J, Cudkowicz M, Atassi N. Muscle & Nerve. 2019 Mar;59(3):303-308. doi: 10.1002/mus.26385. Epub 2018 Dec 26.
  2. Telemedicine to innovate amyotrophic lateral sclerosis multidisciplinary care: The time has come.
    Paganoni S, Simmons Z. Muscle & Nerve. 2019 Jan;59(1):3-5. doi: 10.1002/mus.26311. Epub 2018 Dec 18.
  3. Taking on the Elephant in the Tissue Culture Room: iPSC Modeling for Sporadic ALS.
    Wainger BJ, Lagier-Tourenne C. Cell Stem Cell. 2018 Oct 4;23(4):466-467. doi: 10.1016/j.stem.2018.09.015.
  4. Animal models of neurodegenerative diseases.
    Dawson TM, Golde TE, Lagier-Tourenne C. Nat Neurosci. 2018 Oct;21(10):1370-1379. doi: 10.1038/s41593-018-0236-8. Epub 2018 Sep 24. Review.
  5. Integrated imaging of [11C]-PBR28 PET, MR diffusion and magnetic resonance spectroscopy 1H-MRS in amyotrophic lateral sclerosis.
    Ratai EM, Alshikho MJ, Zürcher NR, Loggia ML, Cebulla CL, Cernasov P, Reynolds B, Fish J, Seth R, Babu S, Paganoni S, Hooker JM, Atassi N. Neuroimage Clin. 2018 Aug 9;20:357-364. doi: 10.1016/j.nicl.2018.08.007. eCollection 2018.
  6. Integrated magnetic resonance imaging and [11 C]-PBR28 positron emission tomographic imaging in amyotrophic lateral sclerosis.
    Alshikho MJ, Zürcher NR, Loggia ML, Cernasov P, Reynolds B, Pijanowski O, Chonde DB, Izquierdo Garcia D, Mainero C, Catana C, Chan J, Babu S, Paganoni S, Hooker JM, Atassi N.  Ann Neurol. 2018 Jun;83(6):1186-1197. doi: 10.1002/ana.25251.
  7. Nonmotor manifestations in ALS patients with tracheostomy and invasive ventilation.
    Atassi N.  Muscle & Nerve. 2018 May;57(5):699-700. doi: 10.1002/mus.26068. Epub 2018 Feb 19. No abstract available.
  8. Exploring the Use of Educational Material About Shoulder Dysfunction: A Quality Improvement Project in People With Amyotrophic Lateral Sclerosis.
    Burke K, Ellrodt AS, Levine J, Adams T, Allis R, Macmurdie I, Paganoni S.Am J Phys Med Rehabil. 2018 May;97(5):379-382. doi: 10.1097/PHM.0000000000000885.
  9. Urate levels predict survival in amyotrophic lateral sclerosis: Analysis of the expanded Pooled Resource Open-Access ALS clinical trials database.
    Paganoni S, Nicholson K, Chan J, Shui A, Schoenfeld D, Sherman A, Berry J, Cudkowicz M, Atassi N. Pooled Resource Open-Access ALS Clinical Trials Consortium. Muscle & Nerve. 2018 Mar;57(3):430-434. doi: 10.1002/mus.25950. Epub 2017 Sep 21.

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