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European Journal of Human Genetics : EJHG
|
August 14, 2020
Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications
Christina Lissewski, Valérie Chune, Francesca Pantaleoni, et al.
The Journal of Antimicrobial Chemotherapy
|
October 23, 2014
Low-frequency drug-resistant HIV-1 and risk of virological failure to first-line NNRTI-based ART: a multicohort European case-control study using centralized ultrasensitive 454 pyrosequencing
Alessandro Cozzi-Lepri, Marc Noguera-Julian, Francesca Di Giallonardo, et al.
Antiviral Therapy
|
April 13, 2019
Very high pre-therapy viral load is a predictor of virological rebound in HIV-1-infected patients starting a modern first-line regimen
Daniele Armenia, Domenico Di Carlo, Alessandro Cozzi-Lepri, et al.
Diagnostics (Basel, Switzerland)
|
February 10, 2024
The Performance of Pulmonary Function Tests in Predicting Systemic Sclerosis-Interstitial Lung Disease in the European Scleroderma Trial and Research Database
Gemma Lepri, Cosimo Bruni, Lorenzo Tofani, et al.
The Journal of Antimicrobial Chemotherapy
|
January 31, 2016
Improved darunavir genotypic mutation score predicting treatment response for patients infected with HIV-1 subtype B and non-subtype B receiving a salvage regimen
Andrea De Luca, Philippe Flandre, David Dunn, et al.
Human Mutation
|
January 12, 2017
Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome
Luca Pannone, Gianfranco Bocchinfuso, Elisabetta Flex, et al.
Human Mutation
|
February 12, 2009
Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum
Anna Sarkozy, Claudio Carta, Sonia Moretti, et al.
Frontiers in Medicine
|
March 26, 2024
Development and validation of a prediction score for failure to casirivimab/imdevimab in hospitalized patients with COVID-19 pneumonia
Alessandro Cozzi-Lepri, Vanni Borghi, Salvatore Rotundo, et al.
American Journal of Human Genetics
|
July 13, 2010
Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype
Simone Martinelli, Alessandro De Luca, Emilia Stellacci, et al.
Science (New York, N.Y.)
|
July 21, 2007
A whole-genome association study of major determinants for host control of HIV-1
Jacques Fellay, Kevin V Shianna, Dongliang Ge, et al.
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of 96
Search research articles
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Showing results (901-910 of 959) with videos related to
Sort By:
Page
of 96
European Journal of Human Genetics : EJHG
|
August 14, 2020
Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications
Christina Lissewski, Valérie Chune, Francesca Pantaleoni, et al.
The Journal of Antimicrobial Chemotherapy
|
October 23, 2014
Low-frequency drug-resistant HIV-1 and risk of virological failure to first-line NNRTI-based ART: a multicohort European case-control study using centralized ultrasensitive 454 pyrosequencing
Alessandro Cozzi-Lepri, Marc Noguera-Julian, Francesca Di Giallonardo, et al.
Antiviral Therapy
|
April 13, 2019
Very high pre-therapy viral load is a predictor of virological rebound in HIV-1-infected patients starting a modern first-line regimen
Daniele Armenia, Domenico Di Carlo, Alessandro Cozzi-Lepri, et al.
Diagnostics (Basel, Switzerland)
|
February 10, 2024
The Performance of Pulmonary Function Tests in Predicting Systemic Sclerosis-Interstitial Lung Disease in the European Scleroderma Trial and Research Database
Gemma Lepri, Cosimo Bruni, Lorenzo Tofani, et al.
The Journal of Antimicrobial Chemotherapy
|
January 31, 2016
Improved darunavir genotypic mutation score predicting treatment response for patients infected with HIV-1 subtype B and non-subtype B receiving a salvage regimen
Andrea De Luca, Philippe Flandre, David Dunn, et al.
Human Mutation
|
January 12, 2017
Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome
Luca Pannone, Gianfranco Bocchinfuso, Elisabetta Flex, et al.
Human Mutation
|
February 12, 2009
Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum
Anna Sarkozy, Claudio Carta, Sonia Moretti, et al.
Frontiers in Medicine
|
March 26, 2024
Development and validation of a prediction score for failure to casirivimab/imdevimab in hospitalized patients with COVID-19 pneumonia
Alessandro Cozzi-Lepri, Vanni Borghi, Salvatore Rotundo, et al.
American Journal of Human Genetics
|
July 13, 2010
Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype
Simone Martinelli, Alessandro De Luca, Emilia Stellacci, et al.
Science (New York, N.Y.)
|
July 21, 2007
A whole-genome association study of major determinants for host control of HIV-1
Jacques Fellay, Kevin V Shianna, Dongliang Ge, et al.
Page
of 96