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http://hub.abes.fr/oup/periodical/cid/1993/volume_16/issue_1/101093clinids16182/authorship/6
http://hub.abes.fr/oup/periodical/jid/1998/volume_177/issue_3/101086514217/authorship/6
http://hub.abes.fr/oup/periodical/jid/1992/volume_165/issue_3/101093infdis1653569/authorship/7
http://hub.abes.fr/edp/periodical/medsci/2016/volume_32/issue_5/medsci20163205p523/authorship/1
http://hub.abes.fr/oup/periodical/jid/1992/volume_165/issue_1/101093infdis1651147/authorship/8
http://hub.abes.fr/edp/periodical/medsci/2014/volume_30/issue_11/medsci20143011p946/authorship/2
http://hub.abes.fr/oup/periodical/jid/1996/volume_174/issue_3/101093infdis1743520/authorship/5
http://hub.abes.fr/oup/periodical/cid/1996/volume_22/issue_1/101093clinids221152/authorship/4
http://hub.abes.fr/oup/periodical/cid/1992/volume_15/issue_1/101093clinids15130/authorship/7
http://hub.abes.fr/oup/periodical/ndt/2003/volume_18/issue_4/101093ndtgfg041/authorship/7
http://hub.abes.fr/bmj/periodical/jmedgenet/2003/volume_40/issue_4/B3598D6B5FFA7CBEE053120B220A90C5/authorship/5
http://hub.abes.fr/acs/periodical/bichaw/1980/volume_19/issue_15/101021bi00556a005/authorship/3
http://hub.abes.fr/springer/periodical/125/1990/volume_33/issue_3/B9267F13686C5090E053120B220A1D5D/authorship/7
http://hub.abes.fr/springer/periodical/439/1992/volume_89/issue_3/B927678D92815706E053120B220AC130/authorship/9
http://hub.abes.fr/springer/periodical/239/1995/volume_41/issue_4/B937B7D0A2695EAFE053120B220A9FCB/authorship/4
http://hub.abes.fr/springer/periodical/439/1992/volume_89/issue_3/B927678D92945706E053120B220AC130/authorship/6
http://hub.abes.fr/springer/periodical/439/1991/volume_87/issue_5/B9280FB2F1055EE6E053120B220A60AA/authorship/2
http://hub.abes.fr/springer/periodical/439/1994/volume_93/issue_3/B927DD9E86255D90E053120B220A1EA8/authorship/4
http://hub.abes.fr/springer/periodical/439/1993/volume_91/issue_5/B927DD9E8A745D90E053120B220A1EA8/authorship/8
http://hub.abes.fr/springer/periodical/10096/1992/volume_11/issue_5/B901D968E6593B97E053120B220AAC03/authorship/8
http://hub.abes.fr/springer/periodical/125/1984/volume_27/issue_6/B9267F1368DB5090E053120B220A1D5D/authorship/4
http://hub.abes.fr/springer/periodical/439/1992/volume_90/issue_1_2/B927DD9E88EA5D90E053120B220A1EA8/authorship/6
http://hub.abes.fr/springer/periodical/439/1992/volume_89/issue_6/B927678D92725706E053120B220AC130/authorship/5
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Molecular Analysis Provides Evidence for the Endogenous Origin of Bacteremia and Meningitis Due to Enterobacter cloacae in an Infant
Phylogenetic Analysis of Escherichia coli Strains Causing Neonatal Meningitis Suggests Horizontal Gene Transfer from a Predominant Pool of Highly Virulent B2 Group Strains
http://hub.abes.fr/edp/periodical/medsci/2016/volume_32/issue_5/medsci20163205p523/w
Analysis of DNA Restriction Fragment Length Polymorphism Extends the Evidence for Breast Milk Transmission in Streptococcus agalactiae Late-Onset Neonatal Infection
Mechanisms of the Spread of Penicillin Resistance in Streptococcus pneumoniae Strains Causing Meningitis in Children in France
Genotyping May Provide Rapid Identification of Escherichia coli K1 Organisms That Cause Neonatal Meningitis
Molecular Analysis of Multiply Recurrent Meningitis Due to Escherichia coli K1 in an Infant
Mother-to-Infant Vertical Transmission and Cross-Colonization of Streptococcus pyogenes Confirmed by DNA Restriction Fragment Length Polymorphism Analysis
http://hub.abes.fr/edp/periodical/medsci/2014/volume_30/issue_11/medsci20143011p946/w
WT1 splice site mutation in a 46,XX female with minimal-change nephrotic syndrome and Wilms' tumour
A novel sickle cell mutation of yet another origin in Africa: the Cameroon type
Molecular epidemiological analysis ofPseudomonas aeruginosa strains causing failure of antibiotic therapy in cystic fibrosis patients
Haemoglobinopathies: a pitfall in the assessment of glycosylated haemoglobin by ion-exchange chromatography
A haplotype-linked four base pair deletion upstream of the Aγ globin gene coincides with decreased gene expression
An additional HpaII polymorphism in exon 2 of the human platelet membrane glycoprotein IIIa gene
Interaction of prothrombin and its fragments with monolayers containing phosphatidylserine. 1. Binding of prothrombin and its fragment I to phosphatidylserine-containing monolayers
Sex in Escherichia coli does not disrupt the clonal structure of the population: evidence from random amplified polymorphic DNA and restriction-fragment-length polymorphism
HLA-DQB 1 codon 57 and genetic susceptibility to Type 1 (insulin-dependent) diabetes mellitus in French children
A rare FokI RFLP in the human dopamine D2 receptor gene (DRD2)
Inter-ethnic polymorphism of the β-globin gene locus control region (LCR) in sickle-cell anemia patients
Nucleotide sequence evidence of the unicentric origin of the βC mutation in Africa
Analysis of the 5′ flanking sequence of the Gγ globin gene by denaturing gradient gel electrophoresis confirms the heterogeneity of the Bantu βs haplotype
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