Innovations in genomics for undiagnosed diseases: vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome

por Stubbins, Ryan J., Cherniawsky, Hannah, Chen, Luke Y.C., Nevill, Thomas J.
Publicado 2022

Innovations en génomique pour les maladies non diagnostiquées: le syndrome VEXAS (vacuoles intracytoplasmiques dans les progéniteurs médullaires, E1 ubiquitine ligase, liée à l’X,...

por Stubbins, Ryan J., Cherniawsky, Hannah, Chen, Luke Y. C., Nevill, Thomas J.
Publicado 2022

VEXAS syndrome in a female patient with constitutional 45,X (Turner syndrome)

por Stubbins, Ryan J., McGinnis, Eric, Johal, Bhupinder, Chen, Luke YC, Wilson, Lorena, Cardona, Daniela Ospina, Nevill, Thomas J.
Publicado 2021

High-dose chemotherapy and autologous bone marrow transplantation for patients with poor prognosis nonseminomatous germ cell tumours.

por Barnett, M. J., Coppin, C. M., Murray, N., Nevill, T. J., Reece, D. E., Klingemann, H. G., Shepherd, J. D., Nantel, S. H., Sutherland, H. J., Phillips, G. L.
Publicado 1993

High transferrin saturation predicts inferior clinical outcomes in patients with myelodysplastic syndromes

por Teichman, Jennifer, Geddes, Michelle, Zhu, Nancy, Keating, Mary-Margaret, Sabloff, Mitchell, Christou, Grace, Leber, Brian, Khalaf, Dina, St-Hilaire, Eve, Finn, Nicholas, Shamy, April, Yee, Karen W.L., Storring, John M., Nevill, Thomas J., Delage, Robert, Elemary, Mohamed, Banerji, Versha, Houston, Brett, Mozessohn, Lee, Chodirker, Lisa, Zhang, Liying, Siddiqui, Mohammed, Parmentier, Anne, Leitch, Heather A., Buckstein, Rena J.
Publicado 2022

The relationship of TP53 R72P polymorphism to disease outcome and TP53 mutation in myelodysplastic syndromes

por McGraw, K L, Zhang, L M, Rollison, D E, Basiorka, A A, Fulp, W, Rawal, B, Jerez, A, Billingsley, D L, Lin, H-Y, Kurtin, S E, Yoder, S, Zhang, Y, Guinta, K, Mallo, M, Solé, F, Calasanz, M J, Cervera, J, Such, E, González, T, Nevill, T J, Haferlach, T, Smith, A E, Kulasekararaj, A, Mufti, G, Karsan, A, Maciejewski, J P, Sokol, L, Epling-Burnette, P K, Wei, S, List, A F
Publicado 2015