Cohen, J. L., Burfield, J., Valdez-Gonzalez, K., Samuels, A., Stefanatos, A. K., Yudkoff, M., … Ficicioglu, C. (2019). Early diagnosis of infantile-onset lysosomal acid lipase deficiency in the advent of available enzyme replacement therapy. Orphanet Journal of Rare Diseases, 14(1). https://doi.org/10.1186/s13023-019-1129-y

Cohen, Jennifer L., Jessica Burfield, Karen Valdez-Gonzalez, Angela Samuels, Arianna K. Stefanatos, Marc Yudkoff, Helio Pedro, and Can Ficicioglu. “Early diagnosis of infantile-onset lysosomal acid lipase deficiency in the advent of available enzyme replacement therapy.” Orphanet Journal of Rare Diseases 14, no. 1 (December 2019). https://doi.org/10.1186/s13023-019-1129-y.

Cohen JL, Burfield J, Valdez-Gonzalez K, Samuels A, Stefanatos AK, Yudkoff M, et al. Early diagnosis of infantile-onset lysosomal acid lipase deficiency in the advent of available enzyme replacement therapy. Orphanet Journal of Rare Diseases. 2019 Dec;14(1).

Cohen, Jennifer L., et al. “Early diagnosis of infantile-onset lysosomal acid lipase deficiency in the advent of available enzyme replacement therapy.” Orphanet Journal of Rare Diseases, vol. 14, no. 1, Springer Science and Business Media LLC, Dec. 2019. Crossref, doi:10.1186/s13023-019-1129-y.

Cohen JL, Burfield J, Valdez-Gonzalez K, Samuels A, Stefanatos AK, Yudkoff M, Pedro H, Ficicioglu C. Early diagnosis of infantile-onset lysosomal acid lipase deficiency in the advent of available enzyme replacement therapy. Orphanet Journal of Rare Diseases. Springer Science and Business Media LLC; 2019 Dec;14(1).