Detalhe da pesquisa
1.
The clinical presentation and genotype of protein C deficiency with double mutations of the protein C gene.
Pediatr Blood Cancer;
64(7)2017 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28111891
2.
Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism.
Pediatr Res;
79(1-1): 81-6, 2016 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26372516
3.
[Analysis of the Neuraminidase Amino Acid Sequences of Influenza A/H1N1pdm09, A/H3N2, and B Viruses Isolated from Influenza Patients in the 2013/14 Japanese Influenza Season].
Fukuoka Igaku Zasshi;
106(8): 231-9, 2015 Aug.
Artigo
em Japonês
| MEDLINE
| ID: mdl-26630841
4.
[Analysis of influenza A/H3N2 neuraminidase genes obtained from influenza patients in the 2011/12 and 2012/13 seasons in Japan].
Fukuoka Igaku Zasshi;
106(1): 16-22, 2015 Jan.
Artigo
em Japonês
| MEDLINE
| ID: mdl-25942938
5.
Staphylococcal endocarditis as the first manifestation of heritable protein S deficiency in childhood.
J Infect Chemother;
20(2): 128-30, 2014 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24462440
6.
Involvement of protein kinase D in uridine diphosphate-induced microglial macropinocytosis and phagocytosis.
Glia;
60(7): 1094-105, 2012 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22488958
7.
Involvement of vasodilator-stimulated phosphoprotein in UDP-induced microglial actin aggregation via PKC- and Rho-dependent pathways.
Purinergic Signal;
7(4): 403-11, 2011 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21567128
8.
Activation of P2X7 receptors induces CCL3 production in microglial cells through transcription factor NFAT.
J Neurochem;
108(1): 115-25, 2009 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19014371