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Modern Pathology(3)
Human Pathology(2)
American Journal of Hematology(1)
Bone Marrow Transplantation(1)
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Cirugía y especialidades médicas afines(1)
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scopus(9)
Chronic lymphocytic leukemia with proliferation centers in bone marrow is associated with younger age at initial presentation, complex karyotype, and TP53 disruption
ArticleAbstract: The presence of expanded proliferation centers (PCs) in lymph nodes involved by chronic lymphocyticPalabras claves:Bone marrow, Chronic lymphocytic leukemia/small lymphocytic lymphoma, Complex karyotype, Proliferation centers, TP53Autores:Bueso-Ramos C., Hu S., Kanagal-Shamanna R., Khoury J.D., Loghavi S., Luthra R., Medeiros L.J., Ok C.Y., Patel K.P., Routbort M.J., Salem A., Schlette E., Sofía A. Garcés, Tang G., Wang S.A.Fuentes:scopusClassic Hodgkin lymphoma with marked granulomatous reaction: A clinicopathologic study of 20 cases
ArticleAbstract: Granulomatous reactions can be associated with various types of lymphoma, most commonly classic HodgPalabras claves:chronic granulomatous inflammation, Classic Hodgkin lymphoma, Epstein-Barr virus, JAK/STAT, Mixed cellularity, PD-L1Autores:Li S., Lin P., Medeiros L.J., Miranda R.N., Patel K.P., Sofía A. Garcés, Tang G., Tang Z., Wang W., Xu J., Yin C.C.Fuentes:scopusClinical, histopathologic, and immunoarchitectural features of dermatopathic lymphadenopathy: an update
ArticleAbstract: Dermatopathic lymphadenopathy is a distinctive form of paracortical lymph node hyperplasia that usuaPalabras claves:Autores:Castellano-Sánchez A., Garces J.C., Khoury J.D., Li S., Medeiros L.J., Medina A.M., Miranda R.N., Patel K.P., Poppiti R.J., Sofía A. Garcés, Sriganeshan V., Thakral B., Xu J., Yin C.C.Fuentes:scopusAcquired WT1 mutations contribute to relapse of NPM1-mutated acute myeloid leukemia following allogeneic hematopoietic stem cell transplant
ArticleAbstract: The role of WT1 protein in hematopoiesis and leukemogenesisis incompletely elucidated. WT1 overexprePalabras claves:Autores:DiNardo C.D., El Hussein S., Fang H., Furudate K., Kanagal-Shamanna R., Khoury J.D., Loghavi S., Lyapichev K.A., Medeiros L.J., Ok C.Y., Patel K.P., Ravandi F., Routbort M.J., Sofía A. Garcés, Takahashi K., Wang S.A.Fuentes:scopusFocal Rosai–Dorfman disease coexisting with lymphoma in the same anatomic site: a localized histiocytic proliferation associated with MAPK/ERK pathway activation
ArticleAbstract: Rosai–Dorfman disease is a rare histiocytic disorder shown to have gene mutations that activate thePalabras claves:Autores:González S., Johnson M.R., Khoury J.D., Li S., Manning J.T., Medeiros L.J., Molgó M., Patel K.P., Pina-Oviedo S., Ruiz-Cordero R., Sofía A. Garcés, Xu J., Yin C.C.Fuentes:scopusETNK1 mutation occurs in a wide spectrum of myeloid neoplasms and is not specific for atypical chronic myeloid leukemia
ArticleAbstract: Background: ETNK1 mutation has been suggested as a useful tool to support the diagnosis of atypicalPalabras claves:acute myeloid leukemia (AML), ethanolamine kinase 1 (ETNK1), myelodysplastic syndrome (MDS), myelodysplastic/myeloproliferative neoplasm (MDS/MPN), myeloproliferative neoplasm (MPN)Autores:Jabbour E.J., Jelloul F.Z., Li N., Li S., Medeiros L.J., Ok C.Y., Patel K.P., Rehder C., Shuai W., Sofía A. Garcés, Wang W., Xu J., Yin C.C., You M.J., Zuo Z.Fuentes:scopusMutually exclusive recurrent KRAS and MAP2K1 mutations in Rosai-Dorfman disease
ArticleAbstract: Rosai-Dorfman disease is a histiocytic disorder with a poorly defined pathogenesis. Recent molecularPalabras claves:Autores:Garces J.C., Khoury J.D., Li J., Li S., Medeiros L.J., Patel K.P., Pina-Oviedo S., Sofía A. Garcés, Yin C.C.Fuentes:scopusNon-coding NOTCH1 mutations in chronic lymphocytic leukemia negatively impact prognosis
OtherAbstract:Palabras claves:Autores:Bassett R.L., Floyd K., Jain N., Jelloul F.Z., Kanagal-Shamanna R., Loghavi S., Luthra R., Medeiros L.J., Ok C.Y., Patel K.P., Routbort M.J., Sofía A. Garcés, Thompson P.A., Wang P., Wierda W.G., Yang R.K., Yin C.C., Zuo Z.Fuentes:scopusLandscape of NOTCH1 mutations and co-occurring biomarker alterations in chronic lymphocytic leukemia
ArticleAbstract: NOTCH1 is one of the most frequently mutated genes in chronic lymphocytic leukemia and has emerged aPalabras claves:Chronic lymphocytic leukemia, Coding, Non-coding, NOTCH1 mutationsAutores:Bassett R.L., Floyd K., Jain N., Jelloul F.Z., Kanagal-Shamanna R., Loghavi S., Luthra R., Medeiros L.J., Ok C.Y., Patel K.P., Routbort M.J., Sofía A. Garcés, Thompson P.A., Wierda W.G., Yang R.K., Yin C.C., Zuo Z.Fuentes:scopus