Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mihaela, Tevet"'
Autor:
Oana Patrinoiu, Claudia Bănescu, Marius Lucian Aurel Balea, Elena Coleș, Delia Dima, Ljubomir Petrov, Meilin Murat, Mihaela Tevet, Anca Vasilache, Mihnea Zdrenghea, Carmen Șaguna, Daniela Georgescu, Laura Urian, Roxana M. Costache, Mihaela Popescu, Adrian P. Trifa, Viola Maria Popov, Nicoleta Berbec, Andrei Cucuianu, Romeo G. Mihăilă, Radu A. Popp, Anca Bojan, Horia Bumbea, Ana-Maria Vladareanu, Tünde Török-Vistai
Publikováno v:
British Journal of Haematology. 174:218-226
Polycythaemia vera (PV), essential thrombocythaemia (ET) and primary myelofibrosis (PMF) represent typical myeloproliferative neoplasms (MPN), usually characterized by specific somatic driver mutations (JAK2 V617F, CALR and MPL). JAK2 46/1 haplotype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8a70b64d134e7bce2a7ab900206ecfd
https://doi.org/10.1111/bjh.14041
https://doi.org/10.1111/bjh.14041
Autor:
Jan Jacques, Michiels, Mihaela, Tevet, Adrian, Trifa, Emilia, Niculescu-Mizil, Anca, Lupu, Ana Maria, Vladareanu, Horia, Bumbea, Anca, Ilea, Camelia, Dobrea, Daniela, Georgescu, Oana, Patrinoiu, Mihaela, Popescu, Meilin, Murat, Cornel, Dragan, Felicia, Mihai, Sabina, Zurac, Silvana, Angelescu, Anamaria, Iova, Alina, Popa, Rodica, Gogulescu, Violeta, Popov
Publikováno v:
Maedica. 11(1)
The 2016 WHO-CMP classification proposal defines a broad spectrum of JAK2 V617F mutated MPN phenotypes: normocellular ET, hypercellular ET due to increased erythropoiesis (prodromal PV), hypercellular ET with megakaryocytic-granulocytic myeloprolifer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2376f9ceea64c3e07f72ac1f4369c67e
https://pubmed.ncbi.nlm.nih.gov/28465746
https://pubmed.ncbi.nlm.nih.gov/28465746
Autor:
Mihaela Tevet, Radu A. Popp, Claudia Bănescu, Adrian P. Trifa, Ștefan Cristian Vesa, Cristina Skrypnyk, Meilin Murat, Anca Bojan, Ioan Victor Pop, Delia Dima, Valeriu Moldovan
Publikováno v:
Hematology (Amsterdam, Netherlands). 21(9)
Objectives: To analyze the relationship between six polymorphisms in genes related to oxidative stress, namely CAT-262 C>T, MnSOD Ala16Val, GPX1 Pro198Leu, GSTM1 and GSTT1 null genotypes, and GSTP1 Ile105Val, and the occurrence of BCR-ABL negative my
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b0ca116c2c6eea8a3f17ac31d0d5b8d
https://pubmed.ncbi.nlm.nih.gov/27077777
https://pubmed.ncbi.nlm.nih.gov/27077777
Autor:
Mihaela Popescu, Violeta Popov, Adrian P. Trifa, Cornel Dragan, Felicia Mihai, Meilin Murat, Mihaela Tevet, Horia Bumbea, Anamaria Iova, Anca Ilea, Ana-Maria Vladareanu, Alina Popa, Daniela Georgescu, Sabina Zurac, Oana Patrinoiu, Anca Roxana Lupu, Camelia Dobrea, Silvana Angelescu, Jan Jacques Michiels, Rodica Gogulescu, Emilia Niculescu-Mizil
Publikováno v:
Journal of Blood Disorders & Transfusion.
The 2016 WHO-CMP classification proposal defines a broad spectrum of JAK2 V617F mutated MPN phenotypes: normocellular ET, hypercellular ET due to increased erythropoiesis (prodromal PV), hypercellular ET with megakaryocytic-granulocytic myeloprolifer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bb0a7e20d7f681c9d3cac64e7bbb146
https://doi.org/10.4172/2155-9864.c1.015
https://doi.org/10.4172/2155-9864.c1.015
Autor:
Ioan Victor Pop, Andrei Cucuianu, Adrian P. Trifa, Bianca Martin, Claudia Bănescu, Mihaela Tevet, Stefan Cristian Vesa, Delia Dima, Mariela S. Militaru, Marcela Cândea, Meilin Murat, Radu A. Popp
Publikováno v:
British Journal of Haematology. 168:151-153
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fd7a47abea0153c4b19cb9f4a72934a
https://doi.org/10.1111/bjh.13076
https://doi.org/10.1111/bjh.13076
Autor:
B, Mastalier, Violeta, Deaconescu, W, Elaiah, C, Drăghici, Cristiana, Popp, Sabina, Zurac, M, Balea, Mihaela, Tevet, C, Botezatu
Publikováno v:
Romanian journal of internal medicine = Revue roumaine de medecine interne. 53(1)
Gastrointestinal tract is the most common location for extralymphonodular lymphomas. The small intestine is affected only in 9% of the cases. Intestinal lymphoma may have single or multiple location. This paper describes a case of multiple location i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a572b83d2d24eedd44dfa5177cc212ec
https://pubmed.ncbi.nlm.nih.gov/26076564
https://pubmed.ncbi.nlm.nih.gov/26076564
Publikováno v:
Maedica. 10(1)
A number of studies showed that the JAK2 V617F mutation increases the thrombotic risk in patients with myeloproliferative disorders (MPN) while others did not reveal this correlation, and it is unknown whether inherited thrombophilia is an additive r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3313aa581e8f390925eb6b0113c1b1f4
https://pubmed.ncbi.nlm.nih.gov/26225146
https://pubmed.ncbi.nlm.nih.gov/26225146
Autor:
Daniela, Georgescu G.1, Mihaela, Popescu1, Mihaela, Tevet1, Meilin, Murat1, Rahnea, Nita Gabriela2, Natalia, Ciuhu Anda2 andadum@yahoo.com
Publikováno v:
Therapeutics, Pharmacology & Clinical Toxicology. Sep2014, Vol. 18 Issue 3, p109-115. 7p. 2 Charts.
Autor:
C., Drăgan1 dragan_cornel@yahoo.com, Murat, Meilin1, A., Trifa2, Mihaela, Tevet1, Roxana, Lupu Anca3
Publikováno v:
Therapeutics, Pharmacology & Clinical Toxicology. Dec2015, Vol. 19 Issue 4, p149-151. 3p. 1 Black and White Photograph.