Selected Publications
Morganroth J, Karam C.: Anti-Myelin-Associated Glycoprotein Neuropathy: Recent Developments Neurol Clin Pract. : 2025.
Qarni TN, Jones FJS, Drachman B, Khella S, Pieretti J, Bustamante NS, Karam C.: Treatment characteristics of patients with hereditary transthyretin amyloidosis: a cohort study Orphanet J Rare Dis. : 2024 .
Karam C, Moffit C, Summers C, Merkel MP, Kochman FM, Weijers L, Puls M, Schurer M, Jones E, Mason N, Finkel M, Schmitt P, Hanna M.: The journey to diagnosis of wild-type transthyretin-mediated (ATTRwt) amyloidosis: a path with multisystem involvement. Orphanet J Rare Dis. : 2024.
Jones FJS, Zager E, Karam C.: Clinical Reasoning: A 61-Year-Old Man With Progressive Right Leg Numbness and Weakness. Neurology. 2024 Oct 22;103(8):e209900 : 2024.
Qarni T, Moshe-Lilie O, Kaku MC, Karam C.: Hereditary Transthyretin Amyloidosis Polyneuropathy Semin Neurol. : 2024.
Suhr, O. B., Grogan, M., Silva, A. M. da, Karam, C., Garcia-Pavia, P., Drachman, B., … Kinney, G. G.: PRX004 in variant amyloid transthyretin (ATTRv) amyloidosis: results of a phase 1, open-label, dose-escalation study. Amyloid. 2024 Oct 29:1-8.
: 2024.
Jones FJS, Cohen AD, Karam C.: Clinical Reasoning: A 49-Year-Old Man With Progressive Numbness, Gait Instability, and Tremors Neurology. 2024 Oct 8;103(7):e209879. : 2024.
Berth SH, Vo L, Kwon DH, Grider T, Damayanti YS, Kosmanopoulos G, Fox A, Lau AR, Carr P, Donohue JK, Hoke M, Thomas S, Karam C, Fay AJ, Meltzer E, Crawford TO, Gaudet R, Shy ME, Hellmich UA, Lee SY, Sumner CJ, McCray BA.: Combined clinical, structural, and cellular studies discriminate pathogenic and benign TRPV4 variants. Brain. : 2024.
Jones FJS, Singer M, Zager E, Karam C.: Mononeuropathy Due to Inflammatory Pseudotumor of Nerve Neurology. : 2024.
Pottinger TD, Motelow JE, Povysil G, Moreno CAM, Ren Z, Phatnani H; New York Genome Center ALS Sequencing Consortium; Aitman TJ, Santoyo-Lopez J; Scottish Genomes Partnership; Mitsumoto H; ALS COSMOS Study Group; PLS COSMOS Study Group; GTAC Investigators; Goldstein DB, Harms MB. Rare: Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLS.
BMC Genomics. : 2024.
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