Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Animesh D Pardanani"'
Autor:
Evandro D. Bezerra, Terra L. Lasho, Christy M. Finke, Antoine N. Saliba, Michelle A. Elliott, Animesh D. Pardanani, Naseema Gangat, Abhishek A. Mangaonkar, Rhett P. Ketterling, Ayalew Tefferi, Eric Solary, Mrinal M. Patnaik
Publikováno v:
Blood Cancer Journal, Vol 11, Iss 3, Pp 1-4 (2021)
Externí odkaz:
https://doaj.org/article/d7ea425dc65a4e80a9ec782fcb1e2ec2
Autor:
Ayalew Tefferi, Maura Nicolosi, Domenico Penna, Mythri Mudireddy, Natasha Szuber, Terra L. Lasho, Curtis A. Hanson, Rhett P. Ketterling, Naseema Gangat, Animesh D. Pardanani
Publikováno v:
Blood Advances, Vol 2, Iss 15, Pp 1980-1984 (2018)
Externí odkaz:
https://doaj.org/article/227de734e2e349a6acb62355f32868fa
Autor:
Naseema Gangat, Andrew T Kuykendall, Najla H Al Ali, Swati Goel, Maymona Abdelmagid, Aref Al-Kali, Hassan B Alkhateeb, Kebede Begna, Abhishek A. Mangaonkar, Mark R Litzow, William J Hogan, Mithun Vinod Shah, Mrinal M. Patnaik, Animesh D Pardanani, Rami S. Komrokji, Ayalew Tefferi
Publikováno v:
Blood Advances.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0466a4a1f98f95c3bab1ad31d180701
https://doi.org/10.1182/bloodadvances.2022009611
https://doi.org/10.1182/bloodadvances.2022009611
Autor:
Naseema Gangat, Natasha Szuber, Yamna Jadoon, Faiqa Farrukh, Kebede Begna, Michelle A. Elliott, Alexandra P. Wolanskyj-Spinner, Curtis A. Hanson, Animesh D. Pardanani, Valerio De Stefano, Tiziano Barbui, Alessandro Maria Vannucchi, Ayalew Tefferi
Publikováno v:
Blood advances. 6(13)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5763e1d0ba2f5845dd3795e4032c009
https://pubmed.ncbi.nlm.nih.gov/35271689
https://pubmed.ncbi.nlm.nih.gov/35271689
Autor:
Naseema, Gangat, Mrinal M, Patnaik, Kebede, Begna, Taxiarchis, Kourelis, Aref, Al-Kali, Michelle A, Elliott, William J, Hogan, Louis, Letendre, Mark R, Litzow, Ryan A, Knudson, Rhett P, Ketterling, Janice M, Hodnefield, Curtis A, Hanson, Animesh D, Pardanani, Ayalew, Tefferi
Publikováno v:
Mayo Clinic proceedings. 90(12)
To share our 25 years of experience with patients with primary myelodysplastic syndromes (MDS) and to describe the natural history of the disease including presenting clinical and laboratory characteristics and long-term disease outcomes.One thousand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::deb6f95e51ef7d11e13486b652cd9b22
https://pubmed.ncbi.nlm.nih.gov/26546107
https://pubmed.ncbi.nlm.nih.gov/26546107
Publikováno v:
European journal of haematology. 71(1)
We sought to better define a group of rare and poorly understood myeloproliferative disorders that are characterized by prominent chronic basophilia in the absence of the Philadelphia chromosome (Ph) or its molecular equivalent.We screened our instit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a71e891743755c3d52ae75cfdf9a62e8
https://pubmed.ncbi.nlm.nih.gov/12801294
https://pubmed.ncbi.nlm.nih.gov/12801294
Publikováno v:
Journal of Thrombosis and Haemostasis. 5:1784-1785
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a96c8e3bce9cb1fa054a2df2516b566
https://doi.org/10.1111/j.1538-7836.2007.02616.x
https://doi.org/10.1111/j.1538-7836.2007.02616.x
Autor:
Ruben A. Mesa, Srdan Verstovsek, Kris Vaddi, Animesh D. Pardanani, Hagop M. Kantarjian, Sue Erickson-Viitanen, Jorge E. Cortes, Ayalew Tefferi, John R. Redman, William J. Hogan, Jordan Fridman, Deborah A. Thomas, Edward Bradley, Richard Levy
Publikováno v:
Blood. 112:1762-1762
Background : Myelofibrosis (MF) is characterized by progressive bone marrow dysfunction, extramedullary hematopoiesis, massive splenomegaly, elevated levels of inflammatory cytokines, severe constitutional symptoms, cachexia and premature death. INCB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a2001082f9b501c04f53c0ab940d92f
https://doi.org/10.1182/blood.v112.11.1762.1762
https://doi.org/10.1182/blood.v112.11.1762.1762
Autor:
Ayalew Tefferi, Srdan Verstovsek, Pat Ault, Francis J. Giles, Farhad Ravandi-Kashani, Animesh D. Pardanani, Alfonso Quintás-Cardama, Hagop M. Kantarjian, Jorge E. Cortes
Publikováno v:
Blood. 108:4902-4902
Idiopathic HES is a myeloproliferative disorder (MPD) characterized by persistent overproduction of eosinophils resulting in organ damage. In a small subset of patients (pts), the disease is caused by the FIP1L1-PDGFR-α fusion tyrosine kinase. Its e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb9dfdaffbd472efa6b00315b34d1b88
https://doi.org/10.1182/blood.v108.11.4902.4902
https://doi.org/10.1182/blood.v108.11.4902.4902