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Proceedings of the National Academy of Sciences of the United States of America
|
September 4, 2025
Complementary biomolecular coassemblies direct energy transport for cardiac photostimulators
Ze-Fan Yao, Sujeung Lim, Yuyao Kuang, et al.
Human Molecular Genetics
|
November 10, 2012
iPS cell modeling of Best disease: insights into the pathophysiology of an inherited macular degeneration
Ruchira Singh, Wei Shen, David Kuai, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
August 3, 2016
Executive Summary: Practice Guidelines for the Diagnosis and Management of Aspergillosis: 2016 Update by the Infectious Diseases Society of America
Thomas F Patterson, George R Thompson, David W Denning, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
July 2, 2016
Practice Guidelines for the Diagnosis and Management of Aspergillosis: 2016 Update by the Infectious Diseases Society of America
Thomas F Patterson, George R Thompson, David W Denning, et al.
Translational Vision Science & Technology
|
June 10, 2021
Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone Structure
Katie M Litts, Erica N Woertz, Niamh Wynne, et al.
American Journal of Human Genetics
|
May 7, 2002
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa
Debra K Breuer, Beverly M Yashar, Elena Filippova, et al.
Investigative Ophthalmology & Visual Science
|
December 7, 2007
Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarrays
Anneke I den Hollander, Irma Lopez, Suzanne Yzer, et al.
The New England Journal of Medicine
|
January 25, 2008
HLA-mismatched renal transplantation without maintenance immunosuppression
Tatsuo Kawai, A Benedict Cosimi, Thomas R Spitzer, et al.
Human Molecular Genetics
|
August 2, 2014
Analysis of the ABCA4 genomic locus in Stargardt disease
Jana Zernant, Yajing Angela Xie, Carmen Ayuso, et al.
Retina (Philadelphia, Pa.)
|
February 2, 2017
REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA
Christopher S Langlo, Laura R Erker, Maria Parker, et al.
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of 101
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Showing results (971-980 of 1,001) with videos related to
Sort By:
Page
of 101
Proceedings of the National Academy of Sciences of the United States of America
|
September 4, 2025
Complementary biomolecular coassemblies direct energy transport for cardiac photostimulators
Ze-Fan Yao, Sujeung Lim, Yuyao Kuang, et al.
Human Molecular Genetics
|
November 10, 2012
iPS cell modeling of Best disease: insights into the pathophysiology of an inherited macular degeneration
Ruchira Singh, Wei Shen, David Kuai, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
August 3, 2016
Executive Summary: Practice Guidelines for the Diagnosis and Management of Aspergillosis: 2016 Update by the Infectious Diseases Society of America
Thomas F Patterson, George R Thompson, David W Denning, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
July 2, 2016
Practice Guidelines for the Diagnosis and Management of Aspergillosis: 2016 Update by the Infectious Diseases Society of America
Thomas F Patterson, George R Thompson, David W Denning, et al.
Translational Vision Science & Technology
|
June 10, 2021
Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone Structure
Katie M Litts, Erica N Woertz, Niamh Wynne, et al.
American Journal of Human Genetics
|
May 7, 2002
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa
Debra K Breuer, Beverly M Yashar, Elena Filippova, et al.
Investigative Ophthalmology & Visual Science
|
December 7, 2007
Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarrays
Anneke I den Hollander, Irma Lopez, Suzanne Yzer, et al.
The New England Journal of Medicine
|
January 25, 2008
HLA-mismatched renal transplantation without maintenance immunosuppression
Tatsuo Kawai, A Benedict Cosimi, Thomas R Spitzer, et al.
Human Molecular Genetics
|
August 2, 2014
Analysis of the ABCA4 genomic locus in Stargardt disease
Jana Zernant, Yajing Angela Xie, Carmen Ayuso, et al.
Retina (Philadelphia, Pa.)
|
February 2, 2017
REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA
Christopher S Langlo, Laura R Erker, Maria Parker, et al.
Page
of 101