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4 research outputs found
Histiocitose de células de Langerhans com envolvimento ungueal em criança: relato de caso
Author
Alanna Mara Bezerra
Alsina MM
+14Â more
Beatriz de Camargo
Bender B
Chu T
Claudia Zavaloni Melotti
Diestelmeier MR
Ellis JP
Fernando Augusto Soares
Harper JI
Holzberg M
Jain S
Kahn G
Lahey ME
Timpatanapong P
Wellington Luiz Mendes
Publication venue
'FapUNIFESP (SciELO)'
Publication date
Field of study
No full text
Crossref
Whole exome sequencing of philadelphia-negative (Ph-negative) myeloproliferative neoplasms (MPNs) and myelodysplastic/myeloproliferative disorders (MDS/MPD)
Author
Bacal Nydia
Bello Isabel C.
+34Â more
Bezerra Alanna Mara P. S.
Bollman Patricia W.
Campregher Paulo Vidal
Cordeiro De Farias Danielle Leao
Costa Erika M. M.
Datoguia Tarcila S.
Diniz Michelli Silva
Fadel Adriana Valente
Guerra Joao Carlos
Hamerschlak Nelson
Helman Ricardo
Higashi Marcia
Kassab Carolina
Lima Marinus M.
Lisboa Bianca
Mata Evelyn H. A. da
Mattos Vinicius R. P.
Miyagi Mariana
Musacchio Juliane
Nakashima Sandra S.
Padua Leandro
Pasqualin Denise Da Cunha
Pereira Welbert Oliveira
Perini Guilherme F.
Perobelli Leila Martins
Puga Renato D.
Salvino Marco Aurelio
Santos Fabio P. S.
Santucci Rodrigo
Schriefer Ana Fernandes
Silveira Paulo A. A.
Soares Rodolfo
Souto Eizabeth Xisto
Velloso Elvira
Publication venue
Amer Soc Hematology
Publication date
Field of study
No full text
Incidence and impact of activating mutations of the RAS-RAF- MEK-ERK pathway in patients with philadelphia-negative (Ph-negative) myeloproliferative neoplasms (MPNs) and myelodysplastic/myeloproliferative disorders-unclassified (MDS/MPD-U)
Author
Bacal Nydia
Bello Isabel C.
+34Â more
Bezerra Alanna Mara P. S.
Bollman Patricia W.
Campregher Paulo Vidal
Cordeiro De Farias Danielle Leao
Costa Erika M. M.
Datoguia Tarcila S.
Diniz Michelli Silva
Fadel Adriana Valente
Guerra Joao Carlos
Hamerschlak Nelson
Helman Ricardo
Higashi Marcia
Kassab Carolina
Lima Marinus M.
Lisboa Bianca
Mata Evelyn H. A. da
Mattos Vinicius R. P.
Miyagi Mariana
Musacchio Juliane
Nakashima Sandra S.
Padua Leandro
Pasqualin Denise da Cunha
Pereira Welbert Oliveira
Perini Guilherme F.
Perobelli Leila Martins
Puga Renato D.
Salvino Marco Aurelio
Santos Fabio P. S.
Santucci Rodrigo
Schriefer Ana Fernandes
Silveira Paulo A. A.
Soares Rodolfo
Souto Eizabeth Xisto
Velloso Elvira
Publication venue
Amer Soc Hematology
Publication date
Field of study
No full text
The presence of ASXL1 mutations as well as a total number of myeloid driver mutations higher than two is strongly associated with the diagnosis of primary myelofibrosis as opposed to essential thrombocythemia
Author
Ascendino Evelyn Helena
Bacal Nydia
+37Â more
Bello Isabel C.
Bezerra Alanna Mara P. S.
Bollman Patricia W.
Campregher Paulo Vidal
Cordeiro De Farias Danielle Leao
Costa Erika M. M.
Costa Fernando Ferreira
Datoguia Tarcila S.
De Souza Santos Fabio Pires
Diniz Michelli Silva
Fadel Adriana Valente
Guerra Joao Carlos
Hamerschlak Nelson
Helman Ricardo
Higashi Marcia
Kassab Carolina
Lima Marinus de Moraes
Lisboa Bianca
Mattos Vinicius R. P.
Miyagi Mariana
Musacchio Juliane
Padua Leandro
Pasqualin Denise da Cunha
Pereira Welbert Oliveira
Perini Guilherme Fleury
Perobelli Leila Martins
Petroni Roberta Cardoso
Puga Renato D.
Salvino Marco A.
Santucci Rodrigo
Schriefer Ana Fernandes
Silveira Paulo A. A.
Soares Rodolfo
Souto Eizabeth Xisto
Tiburcio Manuela Pinto
Velloso Elvira
Yoshida Sandra Nakashima
Publication venue
Amer Soc Hematology
Publication date
Field of study
No full text