Home

persuasivo necessità Irrequieto lancet booster St Esercizi mattutini mano

Heterologous mRNA vaccine boosters induce a stronger and longer-lasting  antibody response against Omicron XBB variant - The Lancet Regional Health  – Western Pacific
Heterologous mRNA vaccine boosters induce a stronger and longer-lasting antibody response against Omicron XBB variant - The Lancet Regional Health – Western Pacific

Immunogenicity and reactogenicity of BNT162b2 booster in ChAdOx1-S-primed  participants (CombiVacS): a multicentre, open-label, randomised,  controlled, phase 2 trial - The Lancet
Immunogenicity and reactogenicity of BNT162b2 booster in ChAdOx1-S-primed participants (CombiVacS): a multicentre, open-label, randomised, controlled, phase 2 trial - The Lancet

Number needed to vaccinate with a COVID-19 booster to prevent a  COVID-19-associated hospitalization during SARS-CoV-2 Omicron BA.1 variant  predominance, December 2021–February 2022, VISION Network: a retrospective  cohort study - The Lancet Regional
Number needed to vaccinate with a COVID-19 booster to prevent a COVID-19-associated hospitalization during SARS-CoV-2 Omicron BA.1 variant predominance, December 2021–February 2022, VISION Network: a retrospective cohort study - The Lancet Regional

Safety of the fourth COVID-19 BNT162b2 mRNA (second booster) vaccine: a  prospective and retrospective cohort study - The Lancet Respiratory Medicine
Safety of the fourth COVID-19 BNT162b2 mRNA (second booster) vaccine: a prospective and retrospective cohort study - The Lancet Respiratory Medicine

Effect of prophylactic paracetamol administration at time of vaccination on  febrile reactions and antibody responses in children: two open-label,  randomised controlled trials - The Lancet
Effect of prophylactic paracetamol administration at time of vaccination on febrile reactions and antibody responses in children: two open-label, randomised controlled trials - The Lancet

Safety and immunogenicity of ChAdOx1 nCoV-19 vaccine administered in a  prime-boost regimen in young and old adults (COV002): a single-blind,  randomised, controlled, phase 2/3 trial - The Lancet
Safety and immunogenicity of ChAdOx1 nCoV-19 vaccine administered in a prime-boost regimen in young and old adults (COV002): a single-blind, randomised, controlled, phase 2/3 trial - The Lancet

Spike-antibody waning after second dose of BNT162b2 or ChAdOx1 - The Lancet
Spike-antibody waning after second dose of BNT162b2 or ChAdOx1 - The Lancet

Severity of omicron variant of concern and effectiveness of vaccine boosters  against symptomatic disease in Scotland (EAVE II): a national cohort study  with nested test-negative design - The Lancet Infectious Diseases
Severity of omicron variant of concern and effectiveness of vaccine boosters against symptomatic disease in Scotland (EAVE II): a national cohort study with nested test-negative design - The Lancet Infectious Diseases

Immunogenicity, otitis media, hearing impairment, and nasopharyngeal  carriage 6-months after 13-valent or ten-valent booster pneumococcal  conjugate vaccines, stratified by mixed priming schedules: PREVIX_COMBO and  PREVIX_BOOST randomised controlled ...
Immunogenicity, otitis media, hearing impairment, and nasopharyngeal carriage 6-months after 13-valent or ten-valent booster pneumococcal conjugate vaccines, stratified by mixed priming schedules: PREVIX_COMBO and PREVIX_BOOST randomised controlled ...

Pregnancy outcomes and vaccine effectiveness during the period of omicron  as the variant of concern, INTERCOVID-2022: a multinational, observational  study - The Lancet
Pregnancy outcomes and vaccine effectiveness during the period of omicron as the variant of concern, INTERCOVID-2022: a multinational, observational study - The Lancet

Safety and immunogenicity of seven COVID-19 vaccines as a third dose ( booster) following two doses of ChAdOx1 nCov-19 or BNT162b2 in the UK (COV- BOOST): a blinded, multicentre, randomised, controlled, phase 2 trial -
Safety and immunogenicity of seven COVID-19 vaccines as a third dose ( booster) following two doses of ChAdOx1 nCov-19 or BNT162b2 in the UK (COV- BOOST): a blinded, multicentre, randomised, controlled, phase 2 trial -

Immunogenicity and safety of homologous and heterologous booster  vaccination of ChAdOx1 nCoV-19 (COVISHIELD™) and BBV152 (COVAXIN®): a  non-inferiority phase 4, participant and observer-blinded, randomised study  - The Lancet Regional Health - Southeast
Immunogenicity and safety of homologous and heterologous booster vaccination of ChAdOx1 nCoV-19 (COVISHIELD™) and BBV152 (COVAXIN®): a non-inferiority phase 4, participant and observer-blinded, randomised study - The Lancet Regional Health - Southeast

Long-term COVID-19 booster effectiveness by infection history and clinical  vulnerability and immune imprinting: a retrospective population-based  cohort study - The Lancet Infectious Diseases
Long-term COVID-19 booster effectiveness by infection history and clinical vulnerability and immune imprinting: a retrospective population-based cohort study - The Lancet Infectious Diseases

Dose-escalated simultaneous integrated boost radiotherapy in early breast  cancer (IMPORT HIGH): a multicentre, phase 3, non-inferiority, open-label,  randomised controlled trial - The Lancet
Dose-escalated simultaneous integrated boost radiotherapy in early breast cancer (IMPORT HIGH): a multicentre, phase 3, non-inferiority, open-label, randomised controlled trial - The Lancet

Severe COVID-19 outcomes after full vaccination of primary schedule and  initial boosters: pooled analysis of national prospective cohort studies of  30 million individuals in England, Northern Ireland, Scotland, and Wales -  The Lancet
Severe COVID-19 outcomes after full vaccination of primary schedule and initial boosters: pooled analysis of national prospective cohort studies of 30 million individuals in England, Northern Ireland, Scotland, and Wales - The Lancet

Antibody and cellular immune responses following dual COVID-19 vaccination  within infection-naive residents of long-term care facilities: an  observational cohort study - The Lancet Healthy Longevity
Antibody and cellular immune responses following dual COVID-19 vaccination within infection-naive residents of long-term care facilities: an observational cohort study - The Lancet Healthy Longevity

Effectiveness of a bivalent mRNA vaccine booster dose to prevent severe  COVID-19 outcomes: a retrospective cohort study - The Lancet Infectious  Diseases
Effectiveness of a bivalent mRNA vaccine booster dose to prevent severe COVID-19 outcomes: a retrospective cohort study - The Lancet Infectious Diseases

Omicron BA.1-containing mRNA-1273 boosters compared with the original  COVID-19 vaccine in the UK: a randomised, observer-blind, active-controlled  trial - The Lancet Infectious Diseases
Omicron BA.1-containing mRNA-1273 boosters compared with the original COVID-19 vaccine in the UK: a randomised, observer-blind, active-controlled trial - The Lancet Infectious Diseases

COVID-19 vaccine booster dose needed to achieve Omicron-specific  neutralisation in nursing home residents - eBioMedicine
COVID-19 vaccine booster dose needed to achieve Omicron-specific neutralisation in nursing home residents - eBioMedicine

Effectiveness of a third dose of the BNT162b2 mRNA COVID-19 vaccine for  preventing severe outcomes in Israel: an observational study - The Lancet
Effectiveness of a third dose of the BNT162b2 mRNA COVID-19 vaccine for preventing severe outcomes in Israel: an observational study - The Lancet

Considerations in boosting COVID-19 vaccine immune responses - The Lancet
Considerations in boosting COVID-19 vaccine immune responses - The Lancet

Single-dose administration and the influence of the timing of the booster  dose on immunogenicity and efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine: a  pooled analysis of four randomised trials - The Lancet
Single-dose administration and the influence of the timing of the booster dose on immunogenicity and efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine: a pooled analysis of four randomised trials - The Lancet

Two-dose ChAdOx1 nCoV-19 vaccine protection against COVID-19 hospital  admissions and deaths over time: a retrospective, population-based cohort  study in Scotland and Brazil - The Lancet
Two-dose ChAdOx1 nCoV-19 vaccine protection against COVID-19 hospital admissions and deaths over time: a retrospective, population-based cohort study in Scotland and Brazil - The Lancet

Hepatitis B immune memory in children primed with hexavalent vaccines and  given monovalent booster vaccines: an open-label, randomised, controlled,  multicentre study - The Lancet Infectious Diseases
Hepatitis B immune memory in children primed with hexavalent vaccines and given monovalent booster vaccines: an open-label, randomised, controlled, multicentre study - The Lancet Infectious Diseases

Risk of infection, hospitalisation, and death up to 9 months after a second  dose of COVID-19 vaccine: a retrospective, total population cohort study in  Sweden - The Lancet
Risk of infection, hospitalisation, and death up to 9 months after a second dose of COVID-19 vaccine: a retrospective, total population cohort study in Sweden - The Lancet

The effectiveness of COVID-19 vaccines against severe cases and deaths in  Brazil from 2021 to 2022: a registry-based study - The Lancet Regional  Health – Americas
The effectiveness of COVID-19 vaccines against severe cases and deaths in Brazil from 2021 to 2022: a registry-based study - The Lancet Regional Health – Americas

Safety and efficacy of the ChAdOx1 nCoV-19 vaccine (AZD1222) against  SARS-CoV-2: an interim analysis of four randomised controlled trials in  Brazil, South Africa, and the UK - The Lancet
Safety and efficacy of the ChAdOx1 nCoV-19 vaccine (AZD1222) against SARS-CoV-2: an interim analysis of four randomised controlled trials in Brazil, South Africa, and the UK - The Lancet

Safety and immunogenicity of the ChAdOx1 nCoV-19 vaccine against  SARS-CoV-2: a preliminary report of a phase 1/2, single-blind, randomised  controlled trial - The Lancet
Safety and immunogenicity of the ChAdOx1 nCoV-19 vaccine against SARS-CoV-2: a preliminary report of a phase 1/2, single-blind, randomised controlled trial - The Lancet