Sökresultat - Burrow, Thomas A

Velaglucerase alfa in the treatment of Gaucher disease type 1 av Burrow, Thomas A, Grabowski, Gregory A

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CNS, Lung, and Lymph Node involvement in Gaucher disease type 3 after 11 years of therapy: Clinical, Histopathologic, and Biochemical Findings av Burrow, Thomas A, Sun, Ying, Prada, Carlos E, Bailey, Laurie, Zhang, Wujuan, Brewer, Amanda, Wu, Steve W., Setchell, Kenneth D R, Witte, David, Cohen, Mitchell B, Grabowski, Gregory A

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De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy av Esmaeeli Nieh, Sahar, Madou, Maura R Z, Sirajuddin, Minhajuddin, Fregeau, Brieana, McKnight, Dianalee, Lexa, Katrina, Strober, Jonathan, Spaeth, Christine, Hallinan, Barbara E, Smaoui, Nizar, Pappas, John G, Burrow, Thomas A, McDonald, Marie T, Latibashvili, Mariam, Leshinsky-Silver, Esther, Lev, Dorit, Blumkin, Luba, Vale, Ronald D, Barkovich, Anthony James, Sherr, Elliott H

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KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defect av Metz, Kyle A, Teng, Xinchen, Coppens, Isabelle, Lamb, Heather M., Wagner, Bart E., Rosenfeld, Jill A., Chen, Xianghui, Zhang, Yu, Kim, Hee Jong, Meadow, Michael E., Wang, Tim Sen, Haberlandt, Edda D., Anderson, Glenn W., Leshinsky-Silver, Esther, Bi, Weimin, Markello, Thomas C., Pratt, Marsha, Makhseed, Nawal, Garnica, Adolfo, Danylchuk, Noelle R., Burrow, Thomas A., Jayakar, Parul, McKnight, Dianalee, Agadi, Satish, Gbedawo, Hatha, Stanley, Christine, Alber, Michael, Prehl, Isabelle, Peariso, Katrina, Ong, Min Tsui, Mordekar, Santosh R, Parker, Michael J, Crooks, Daniel, Agrawal, Pankaj B., Berry, Gerard T., Loddenkemper, Tobias, Yang, Yaping, Maegawa, Gustavo H.B., Aouacheria, Abdel, Markle, Janet G., Wohlschlegel, James A., Hartman, Adam L., Hardwick, J. Marie

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