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Internal Medicine Journal
|
August 2, 2001
Prospective study of 424 cases of Staphylococcus aureus bacteraemia: determination of factors affecting incidence and mortality
P C Hill, M Birch, S Chambers, et al.
Nucleic Acid Therapeutics
|
July 20, 2012
Clinical expert panel on monitoring potential lung toxicity of inhaled oligonucleotides: consensus points and recommendations
Eric W Alton, Homer A Boushey, Holger Garn, et al.
Antimicrobial Agents and Chemotherapy
|
August 17, 2016
Antistaphylococcal β-Lactams versus Vancomycin for Treatment of Infective Endocarditis Due to Methicillin-Susceptible Coagulase-Negative Staphylococci: a Prospective Cohort Study from the International Collaboration on Endocarditis
M Carugati, C A Petti, C Arnold, et al.
Molecular Autism
|
May 27, 2014
Rare deleterious mutations of the gene EFR3A in autism spectrum disorders
Abha R Gupta, Michelle Pirruccello, Feng Cheng, et al.
Plos Genetics
|
January 27, 2015
No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins
John D Murdoch, Abha R Gupta, Stephan J Sanders, et al.
High Altitude Medicine & Biology
|
October 30, 2001
Children at high altitude: an international consensus statement by an ad hoc committee of the International Society for Mountain Medicine, March 12, 2001
A J Pollard, S Niermeyer, P Barry, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 30, 2025
Global natural history infrastructure requires international solidarity, support, and investment in local capacity
Bazartseren Boldgiv, Ariuntsetseg Lkhagva, Scott Edwards, et al.
Molecular Psychiatry
|
November 12, 2014
Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons
K Griesi-Oliveira, A Acab, A R Gupta, et al.
Nature
|
April 13, 2012
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
Stephan J Sanders, Michael T Murtha, Abha R Gupta, et al.
Neuron
|
June 11, 2011
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, et al.
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Search research articles
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Showing results (151-160 of 160) with videos related to
Sort By:
Page
of 16
You have reached the last page of results.
This site can display upto 160 results.
Internal Medicine Journal
|
August 2, 2001
Prospective study of 424 cases of Staphylococcus aureus bacteraemia: determination of factors affecting incidence and mortality
P C Hill, M Birch, S Chambers, et al.
Nucleic Acid Therapeutics
|
July 20, 2012
Clinical expert panel on monitoring potential lung toxicity of inhaled oligonucleotides: consensus points and recommendations
Eric W Alton, Homer A Boushey, Holger Garn, et al.
Antimicrobial Agents and Chemotherapy
|
August 17, 2016
Antistaphylococcal β-Lactams versus Vancomycin for Treatment of Infective Endocarditis Due to Methicillin-Susceptible Coagulase-Negative Staphylococci: a Prospective Cohort Study from the International Collaboration on Endocarditis
M Carugati, C A Petti, C Arnold, et al.
Molecular Autism
|
May 27, 2014
Rare deleterious mutations of the gene EFR3A in autism spectrum disorders
Abha R Gupta, Michelle Pirruccello, Feng Cheng, et al.
Plos Genetics
|
January 27, 2015
No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins
John D Murdoch, Abha R Gupta, Stephan J Sanders, et al.
High Altitude Medicine & Biology
|
October 30, 2001
Children at high altitude: an international consensus statement by an ad hoc committee of the International Society for Mountain Medicine, March 12, 2001
A J Pollard, S Niermeyer, P Barry, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 30, 2025
Global natural history infrastructure requires international solidarity, support, and investment in local capacity
Bazartseren Boldgiv, Ariuntsetseg Lkhagva, Scott Edwards, et al.
Molecular Psychiatry
|
November 12, 2014
Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons
K Griesi-Oliveira, A Acab, A R Gupta, et al.
Nature
|
April 13, 2012
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
Stephan J Sanders, Michael T Murtha, Abha R Gupta, et al.
Neuron
|
June 11, 2011
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, et al.
Page
of 16