Arginase 1 Deficiency in Patients Initially Diagnosed with Hereditary Spastic Paraplegia

por McNutt, Markey C., Foreman, Nathan, Gotway, Garrett
Publicado 2022

Partial N‐acetyl glutamate synthase deficiency presenting as postpartum hyperammonemia: Diagnosis and subsequent pregnancy management

por Abou Haidar, Lea, Pachnis, Panayotis, Gotway, Garrett K., Ni, Min, DeBerardinis, Ralph J., McNutt, Markey C.
Publicado 2023

Human promoter genomic composition demonstrates non-random groupings that reflect general cellular function

por McNutt, Markey C, Tongbai, Ron, Cui, Wenwu, Collins, Irene, Freebern, Wendy J, Montano, Idalia, Haggerty, Cynthia M, Chandramouli, GVR, Gardner, Kevin
Publicado 2005

Clinical effect and safety profile of pegzilarginase in patients with arginase 1 deficiency

por Diaz, George A., Schulze, Andreas, McNutt, Markey C., Leão‐Teles, Elisa, Merritt, J. Lawrence, Enns, Gregory M., Batzios, Spyros, Bannick, Allison, Zori, Roberto T., Sloan, Leslie S., Potts, Susan L., Bubb, Gillian, Quinn, Anthony G.
Publicado 2021

Functional Assessment of Lipoyltransferase-1 Deficiency in Cells, Mice, and Humans

por Ni, Min, Solmonson, Ashley, Pan, Chunxiao, Yang, Chendong, Li, Dan, Notzon, Ashley, Cai, Ling, Guevara, Gerardo, Zacharias, Lauren G., Faubert, Brandon, Vu, Hieu S., Jiang, Lei, Ko, Bookyung, Morales, Noriko Merida, Pei, Jimin, Vale, Gonçalo, Rakheja, Dinesh, Grishin, Nick V., McDonald, Jeffrey G., Gotway, Garrett K., McNutt, Markey C., Pascual, Juan M., DeBerardinis, Ralph J.
Publicado 2019