Selected Publications
Benatar M, Hansen T, Rom D, Geist MA, Blaettler T, Camu W, Kuzma-Kozakiewicz M, van den Berg LH, Morales RJ, Chio A, Andersen PM, Pradat PF, Lange D, Van Damme P, Mora G, Grudniak M, Elliott M, Petri S, Olney N, Ladha S, Goyal NA, Meyer T, Hanna MG, Quinn C, Genge A, Zinman L, Jabari D, Shoesmith C, Ludolph AC, Neuwirth C, Nations S, Shefner JM, Turner MR, Wuu J, Bennett R, Dang H, Sundgreen C; ORARIALS-01 trial team.: Safety and efficacy of arimoclomol in patients with early amyotrophic lateral sclerosis (ORARIALS-01): a randomised, double-blind, placebo-controlled, multicentre, phase 3 trial Lancet Neurol : 2024.
Quinn C, Baer M, Amado DA, Kelley M, Elman L.: A single ALS center experience with clinical use of sodium phenylbutyrate-taurursodiol Muscle Nerve : 2024.
Baldwin A, Copeland J, Azage M, Dratch L, Johnson K, Paul RA, Amado DA, Baer M, Deik A, Elman LB, Guo M, Hamedani AG, Irwin DJ, Lasker A, Orthmann-Murphy J, Quinn CC, Tropea TF, Scherer SS, Shinohara RT, Hamilton RH, Ellis CA.: Disparities in Genetic Testing for Neurologic Disorders Neurology 102 : e209161,2024.
Dratch L, Azage M, Baldwin A, Johnson K, Paul RA, Bardakjian TM, Michon SC, Amado DA, Baer M, Deik AF, Elman LB, Gonzalez-Alegre P, Guo MH, Hamedani AG, Irwin DJ, Lasker A, Orthmann-Murphy J, Quinn C, Tropea TF, Scherer SS, Ellis CA.: Genetic testing in adults with neurologic disorders: indications, approach, and clinical impacts J Neurol : 2024.
Singer M, Khella S, Bird S, McIntosh P, Paudyal B, Wadhwani A, Quinn C, Karam C.: Single institution experience with efgartigimod in patients with myasthenia gravis: Patient selection, dosing schedules, treatment response, and adverse events Muscle Nerve : 2024.
Morganroth J, Bardakjian TM, Dratch L, Quinn CC, Elman LB.: Enhancing Clinical Infrastructure for the Delivery of Intrathecal and Genetic Therapies: A Qalsody (Tofersen) Model for Patients With SOD1-ALS Neurol Clin Pract : 2024.
Shellikeri S, Cho S, Ash S, Gonzalez-Recober C, Mcmillan CT, Elman L, Quinn C, Amado DA, Baer M, Irwin DJ, Massimo L, Olm CA, Liberman MY, Grossman M, Nevler N.: Digital markers of motor speech impairments in spontaneous speech of patients with ALS-FTD spectrum disorders Amyotroph Lateral Scler Frontotemporal Degener : 2023.
Quinn C, Moulton K, Farwell M, Le W, Wilson I, Goel N, McConathy J, Greenberg SA.: Imaging With PET/CT of Diffuse CD8 T-Cell Infiltration of Skeletal Muscle in Patients With Inclusion Body Myositis Neurology 101 : e1158-e1166,2023.
Morganroth J, Ljungberg L, Goldstein A, Kallish S, Asher SB, Quinn C, Price RS, Karam C.: Pearls and Oy-sters: Case Report of a Patient With Adult-Onset Thymidine Kinase Gene (TK2) Deficiency Neurology : 2023.
Columbres RCA, Chin Y, Pratti S, Quinn C, Gonzalez-Cuyar LF, Weiss M, Quintero-Rivera F, Kimonis V.: Novel Variants in the VCP Gene Causing Multisystem Proteinopathy 1 Genes (Basel) 14 : 676,2023.
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