Results 151 to 160 of about 2,774 (188)

Evolution of antimicrobial resistance and serotype distribution of Streptococcus pneumoniae isolated from children with invasive and noninvasive pneumococcal diseases in Algeria from 2005 to 2012. [PDF]

open access: yesNew Microbes New Infect, 2015
Ramdani-Bouguessa N   +13 more
europepmc   +1 more source

DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study.

open access: yesLancet Neurology, 2016
J. Trinh   +24 more
semanticscholar   +1 more source

Heterozygous Mutations in the ADCK3 Gene in Siblings with Cerebellar Atrophy and Extreme Phenotypic Variability. [PDF]

open access: yesJIMD Rep, 2014
Blumkin L   +5 more
europepmc   +1 more source

Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia. [PDF]

open access: yesBMC Med Genet, 2015
Hamza W   +10 more
europepmc   +1 more source

AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders. [PDF]

open access: yesNat Commun, 2019
Salpietro V   +92 more
europepmc   +1 more source

Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1.

open access: yesJAMA Neurol, 2018
Renaud M   +42 more
europepmc   +1 more source

Role of SHV β-lactamase variants in resistance of clinical Klebsiella pneumoniae strains to β-lactams in an Algerian hospital. [PDF]

open access: yesJ Med Microbiol, 2011
Ramdani-Bouguessa N   +5 more
europepmc   +1 more source

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