Výsledky vyhledávání - "Viprakasit V"

Akademický článek

Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with nontransfusion-dependent thalassemia syndromes

Autor: Taher AT, Porter JB, Kattamis A, Viprakasit V, Cappellini MD

Publikováno v: Drug Design, Development and Therapy, Vol Volume 10, Pp 4073-4078 (2016)

Ali T Taher,1 John B Porter,2 Antonis Kattamis,3 Vip Viprakasit,4 M Domenica Cappellini51Department of Internal Medicine, American University of Beirut, Beirut, Lebanon; 2Department of Haematology, University College London, London, UK; 3First Depart

Externí odkaz: https://doaj.org/article/f794bf6e4b5442aaac6de0e426b2972d

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Akademický článek

IMPROVEMENTS IN FATIGUE AND 6-MINUTE WALK TEST IN ADULTS WITH ALPHA- OR BETA-NON–TRANSFUSION-DEPENDENT THALASSEMIA: THE PHASE 3 ENERGIZE TRIAL OF MITAPIVAT

Autor: Kuo, KH, Al-Samkari, H, Aydinok, Y, Besser, M, Gheuens, S, Luna, G, Glenthj, A, Goh, AS, Kattamis, A, Loggetto, SR, Musallam, KM, Ricchi, P, Salido-Fiérrez, E, Sheth, S, Viprakasit, V, Cappellini, MD, Taher, AT

Publikováno v: In Hematology, Transfusion and Cell Therapy October 2024 46 Supplement 4:S34-S35

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Akademický článek

ENERGIZE: A GLOBAL PHASE 3 STUDY OF MITAPIVAT DEMONSTRATING EFFICACY AND SAFETY IN ADULTS WITH ALPHA- OR BETA-NON–TRANSFUSION-DEPENDENT THALASSEMIA

Autor: Taher, AT, Al-Samkari, H, Aydinok, Y, Besser, M, Luna, G, Gheuens, S, Glenthj, A, Goh, AS, Kattamis, A, Loggetto, SR, Musallam, KM, Ricchi, P, Salido-Fiérrez, E, Sheth, S, Viprakasit, V, Cappellini, MD, Kuo, KH

Publikováno v: In Hematology, Transfusion and Cell Therapy October 2024 46 Supplement 4:S32-S33

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Luspatercept in pediatric patients (pts) with transfusion-dependent beta-thalassemia (TDT): design, inclusion and exclusion criteria of a phase 2a study evaluating the safety and pharmacokinetics (PK) of luspatercept in children

Autor: Cario, H., Viprakasit, V., Coates, T. D., Musallam, K. M., Vienne, Buerki J., Patturajan, M., Holot, N.

[No Abstract Available]

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______9436::03f6f09ae629d6a0197443c32e41cc6c
https://hdl.handle.net/11454/79351

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Akademický článek

What is the evidence of a role for host genetics in susceptibility to influenza A/H5N1?

Autor: HORBY, P., SUDOYO, H., VIPRAKASIT, V., FOX, A., THAI, P. Q., YU, H., DAVILA, S., HIBBERD, M., DUNSTAN, S. J., MONTEERARAT, Y., FARRAR, J. J., MARZUKI, S., HIEN, N. T.

Publikováno v: Epidemiology and Infection, 2010 Nov 01. 138(11), 1550-1558.

Externí odkaz: https://www.jstor.org/stable/40928488

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Akademický článek

Evaluation of potassium peroxymonosulfate (MPS) efficacy against SARS-CoV-2 virus using RT-qPCR-based method

Autor: Tulalamba, W., Assawamakin, A., Thayananuphat, A., Viprakasit, V.

Publikováno v: In International Journal of Infectious Diseases September 2021 110:162-164

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Akademický článek

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Revisiting the non-transfusion-dependent (NTDT) vs. transfusion-dependent (TDT) thalassemia classification 10 years later

Autor: Musallam, K.M. Cappellini, M.D. Viprakasit, V. Kattamis, A. Rivella, S. Taher, A.T.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::8540cc25b871d0a317d34d3b9cc0f79e
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3102861

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A phase 3 trial of luspatercept in patients with transfusion-dependent β-thalassemia

Autor: Domenica Cappellini, M. Viprakasit, V. Taher, A.T. Georgiev, P. Kuo, K.H.M. Coates, T. Voskaridou, E. Liew, H.-K. Pazgal-Kobrowski, I. Forni, G.L. Perrotta, S. Khelif, A. Lal, A. Kattamis, A. Vlachaki, E. Origa, R. Aydinok, Y. Bejaoui, M. Joy Ho, P. Chew, L.-P. Bee, P.-C. Lim, S.-M. Lu, M.-Y. Tantiworawit, A. Ganeva, P. Gercheva, L. Shah, F. Neufeld, E.J. Thompson, A. Laadem, A. Shetty, J.K. Zou, J. Zhang, J. Miteva, D. Zinger, T. Linde, P.G. Sherman, M.L. Hermine, O. Porter, J. Piga, A. BELIEVE Investigators

BACKGROUND Patients with transfusion-dependent β-thalassemia need regular red-cell transfusions. Luspatercept, a recombinant fusion protein that binds to select transforming growth factor β superfamily ligands, may enhance erythroid maturation and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::d65fb3b1b840e3960ecd85e22afd780e
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3104621

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Changing patterns in the epidemiology of β-thalassemia

Autor: Kattamis, A. Forni, G.L. Aydinok, Y. Viprakasit, V.

β-thalassemia major is an inherited hemoglobinopathy that requires lifelong red blood cell transfusions and iron chelation therapy to prevent complications due to iron overload. Traditionally, β-thalassemia has been more common in certain regions o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::05a7095188caa8a4acd1013d80dbb3b5
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3103520

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