Platelet Disorders and Thrombosis Mechanisms

Displaying 1 - 17 of 17CSV
Bhutani, D., Chakraborty, R., Wats, K., Hughes, M. S., Dor, L., Sekulic, M., & Lentzsch, S. (2025). Treatment of Refractory Monoclonal Immunoglobulin Deposition Disease With BCMA Bispecific Antibody. European Journal of Haematology. Portico. https://doi.org/10.1111/ejh.14393
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Modi, D., Chowdhury, S. R., Mahamad, S., Modi, H., Cines, D., Neunert, C., Al-Samkari, H., Cooper, N., Moulis, G., Cunningham-Rundles, C., Liebman, H., Bussel, J. B., Breakey, V. R., Nazy, I., & Arnold, D. M. (2024). Primary Versus Secondary Immune Thrombocytopenia (ITP): A Meeting Report from the 2023 McMaster ITP Summit. Thrombosis and Haemostasis. CLOCKSS. https://doi.org/10.1055/a-2508-1112
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Villa, C. H., Biondich, P., Draper, N. L., Dores, G. M., Storch, E., Chada, K., Wong, H., Whitaker, B., Obidi, J., Vossoughi, S., Soares, A., Schilling, L. M., Natarajan, K., Goodman, M., Purkayastha, S., Zucker, R., Falconer, T., Williams, N., Reich, C., … Shoaibi, A. (2024). Patterns of platelet use evaluated in EHR networks of the Biologics Effectiveness and Safety Initiative, 2012–2018. Transfusion. Portico. https://doi.org/10.1111/trf.18114
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Kim, T. O., Geris, J. M., Flanagan, J. M., Grace, R. F., Lambert, M. P., O’Farrell, C., Rose, M. J., Shimano, K. A., Niss, O., Neunert, C., Nakano, T. A., MacMath, D., Dinu, B., Kirk, S. E., Neufeld, E. J., Despotovic, J. M., Scheurer, M. E., & Grimes, A. B. (2024). Genetic variants in canonical Wnt signaling pathway associated with pediatric immune thrombocytopenia. Blood Advances, 8(21), 5529–5538. https://doi.org/10.1182/bloodadvances.2024012776
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Neunert, C. E., & Lambert, M. P. (2024). Lightening the load for paediatric ITP: The importance of health‐related quality of life. British Journal of Haematology. Portico. https://doi.org/10.1111/bjh.19719
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Fakhouri, F., Bomback, A., Kavanagh, D., Remuzzi, G., Sunder-Plassmann, G., Kanellis, J., Daina, E., Walker, P., Wang, Z., & Ahmad, Z. (2024). #1467 Pegcetacoplan for post-transplant recurrent C3 glomerulopathy or immune complex membranoproliferative glomerulonephritis in NOBLE: 12-week evolution. Nephrology Dialysis Transplantation, 39(Supplement_1). https://doi.org/10.1093/ndt/gfae069.442
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Luo, Y., Ferrada, M. A., Sikora, K. A., Rankin, C., Alessi, H. D., Kastner, D. L., Deng, Z., Zhang, M., Merkel, P. A., Kraus, V. B., Allen, A. S., & Grayson, P. C. (2023). Ultra-rare genetic variation in relapsing polychondritis: a whole-exome sequencing study. Annals of the Rheumatic Diseases, 83(2), 253–260. https://doi.org/10.1136/ard-2023-224732
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Stefanucci, L., Collins, J., Sims, M. C., Barrio-Hernandez, I., Sun, L., Burren, O. S., Perfetto, L., Bender, I., Callahan, T. J., Fleming, K., Guerrero, J. A., Hermjakob, H., Martin, M. J., Stephenson, J., Paneerselvam, K., Petrovski, S., Porras, P., Robinson, P. N., Wang, Q., … Vuckovic, D. (2023). The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants. Blood, 142(24), 2055–2068. https://doi.org/10.1182/blood.2023020118
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Rajasekaran, A., Larkina, M., Julian, B. A., Canetta, P. A., Roehm, B. A., Khalid, M., Mariani, L. H., & Rizk, D. V. (2023). Optimal Conservative Therapy Use among Adult Cure Glomerulonephropathy Participants with IgA Nephropathy. Kidney360, 4(12), 1763–1769. https://doi.org/10.34067/kid.0000000000000306
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Vander Haar, E., Abshier Ware, C., Allen, G., Armstrong, R., Black, D., Bombara, M., Dhanraj, D., Lawrence, L., Miller, R., Nanda, S., Paidas, M. J., Patki, K. C., Sitras, V., Skupski, D., Swarup, M., Thorp, J., Tiller, H., Verweij, J., & Bussel, J. B. (2023). Identifying Pregnancies at Higher Risk for HPA-1a Alloimmunization and Fetal/Neonatal Alloimmune Thrombocytopenia (FNAIT): An International, Prospective, Natural History Study. Blood, 142(Supplement 1), 1224–1224. https://doi.org/10.1182/blood-2023-177657
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Kim, T. O., Geris, J. M., Grimes, A. B., Grace, R. F., Lambert, M. P., Rose, M. J., Shimano, K. A., Niss, O., Neunert, C., Nakano, T. A., Macmath, D., Dinu, B., Kirk, S. E., Despotovic, J. M., Flanagan, J. M., & Scheurer, M. E. (2023). Genetic Variants in Canonical Wnt Signaling Pathway Associated with Pediatric ITP. Blood, 142(Supplement 1), 2593–2593. https://doi.org/10.1182/blood-2023-175013
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Kudose, S., Batal, I., Lucia, J., Patel, P., Soni, R. K., Markowitz, G. S., D’Agati, V. D., & Stokes, M. B. (2023). Proliferative Glomerulonephritis With Hidden Monotypic IgG3κ Deposits: A Case Report. American Journal of Kidney Diseases, 81(1), 114–117. https://doi.org/10.1053/j.ajkd.2022.05.018
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Barratt, J., Tumlin, J., Suzuki, Y., Kao, A., Aydemir, A., Pudota, K., Jin, H., Gühring, H., & Appel, G. (2022). Randomized Phase II JANUS Study of Atacicept in Patients With IgA Nephropathy and Persistent Proteinuria. Kidney International Reports, 7(8), 1831–1841. https://doi.org/10.1016/j.ekir.2022.05.017
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Lomax-Browne, H. J., Medjeral-Thomas, N. R., Barbour, S. J., Gisby, J., Han, H., Bomback, A. S., Fervenza, F. C., Cairns, T. H., Szydlo, R., Tan, S.-J., Marks, S. D., Waters, A. M., Appel, G. B., D’Agati, V. D., Sethi, S., Nast, C. C., Bajema, I., Alpers, C. E., Fogo, A. B., … Pickering, M. C. (2022). Association of Histologic Parameters with Outcome in C3 Glomerulopathy and Idiopathic Immunoglobulin-Associated Membranoproliferative Glomerulonephritis. Clinical Journal of the American Society of Nephrology, 17(7), 994–1007. https://doi.org/10.2215/cjn.16801221
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Hillier, K., Rothman, J. A., Klaassen, R. J., Neunert, C., Rose, M. J., Grace, R. F., & Lambert, M. P. (2022). SARS‐CoV‐2 vaccination in pediatric patients with immune thrombocytopenia. Pediatric Blood & Cancer, 69(7). Portico. https://doi.org/10.1002/pbc.29760
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