Results 111 to 120 of about 706,514 (296)

Multivariate logistic regression analysis to identify factors associated with liver injuries in patients with genotype 1b HCV receiving daclatasvir plus asunaprevir therapy.

open access: yes, 2018
Multivariate logistic regression analysis to identify factors associated with liver injuries in patients with genotype 1b HCV receiving daclatasvir plus asunaprevir therapy.
Kayoko Sugawara (5848991)   +10 more
core   +1 more source

Nationwide Survey of Association Between Fever and Epileptic Seizure in CDKL5 Deficiency Disorder Revealed Therapeutic Implications

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective CDKL5 deficiency disorder (CDD) is a rare, severe developmental and epileptic encephalopathy. There is a pressing need to develop effective and sustainable therapeutic strategies. We aimed to investigate the causal association between febrile episodes and epileptic seizures for therapeutic implications in CDD patients.
Siyi Wang   +13 more
wiley   +1 more source

Best therapy for the easiest to treat hepatitis C virus genotype 1b-infected patients. [PDF]

open access: yesWorld J Gastroenterol, 2022
Zarębska-Michaluk D   +16 more
europepmc   +1 more source

HCV genotype determination in monoinfected and HIV co-infected patients in Cuba.

open access: yes, 2012
With the aim to characterize the HCV genotype distribution in Cuba, sera were collected from two subgroups: HCV-monoinfected and HCV/HIV co-infected patients.
Wonga, Meilin S??nchez   +21 more
core   +1 more source

Autoimmune Comorbidities as Modifiers of Phenotypic Heterogeneity in Facioscapulohumeral Dystrophy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Facioscapulohumeral dystrophy type 1 (FSHD1) shows clinical heterogeneity that is only partly explained by D4Z4 repeat unit (RU) size. Although immune and inflammatory mechanisms may contribute to disease variability, the prevalence and clinical impact of autoimmune diseases in FSHD remain unclear.
Jonathan Pini   +9 more
wiley   +1 more source

Hepatitis C virus (HCV) genotype 1 subtype identification in new HCV drug development and future clinical practice.

open access: yesPLoS ONE, 2009
BackgroundWith the development of new specific inhibitors of hepatitis C virus (HCV) enzymes and functions that may yield different antiviral responses and resistance profiles according to the HCV subtype, correct HCV genotype 1 subtype identification is
Stéphane Chevaliez   +3 more
doaj   +1 more source

Juvenile Huntington Disease With Cerebellar‐Predominant Atrophy Identified by Genome Sequencing

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Juvenile Huntington disease accounts for a small fraction of Huntington disease cases and is driven by the largest trinucleotide repeat expansions. We describe a 6‐year‐old boy with progressive global regression, generalized dystonia, and epilepsy, in whom serial imaging showed striking cerebellar‐predominant atrophy with an initially normal ...
Enrique Gonzalez Saez‐Diez   +5 more
wiley   +1 more source

The ratio of hepatitis C virus genotypes in patients with HCV infection in St. Petersburg in 2024–2025

open access: yesЖурнал инфектологии
The ratio of hepatitis C virus (HCV) genotypes in the Russian Federation and in individual regions is a dynamic process that requires regular research within each region of the country.
D. A. Gusev   +2 more
doaj   +1 more source

Staying Competitive in the High-tech Global Economy: Another Look at the H-1B Visa [PDF]

open access: yes
This paper addresses a specific suggestion for immigration reform—that we must seek skilled immigrants—by examining support for a move to unlimited H-1B visa issuance.
Barry Cynamon
core  

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