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A Fishman

Showing results (961-970 of 1,001) with videos related to

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Human Molecular Genetics|August 7, 2013
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt diseaseTerry A Braun, Robert F Mullins, Alex H Wagner, et al.
The Journal of Physical Chemistry Letters|August 20, 2015
Two-Photon Absorption Spectrum of a Single Crystal Cyanine-like DyeHonghua Hu, Dmitry A Fishman, Andrey O Gerasov, et al.
Neuromodulation : Journal of the International Neuromodulation Society|December 9, 2020
Long-Term Efficacy of a Novel Spinal Cord Stimulation Clinical Workflow Using Kilohertz Stimulation: Twelve-Month Results From the Vectors StudyJohn A Hatheway, Vipul Mangal, Michael A Fishman, et al.
Nature Genetics|February 2, 2000
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fateN B Haider, S G Jacobson, A V Cideciyan, et al.
American Journal of Ophthalmology|September 11, 2012
Assessing retinal structure in complete congenital stationary night blindness and Oguchi diseasePooja Godara, Robert F Cooper, Panagiotis I Sergouniotis, et al.
Annals of Internal Medicine|November 4, 2009
National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving HealthAlfred O Berg, Macaran A Baird, Jeffrey R Botkin, et al.
The European Respiratory Journal|April 13, 2012
The risk of tuberculosis in transplant candidates and recipients: a TBNET consensus statementDragos Bumbacea, Sandra M Arend, Fusun Eyuboglu, et al.
Blood|June 2, 2019
Haploidentical hematopoietic cell and kidney transplantation for hematological malignancies and end-stage renal failureYi-Bin Chen, Nahel Elias, Eliot Heher, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 24, 2008
Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kineticsArtur V Cideciyan, Tomas S Aleman, Sanford L Boye, et al.
Human Mutation|February 24, 2011
BBS genotype-phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definitionCatherine Deveault, Gail Billingsley, Jacque L Duncan, et al.
Pageof 101

Showing results (961-970 of 1,001) with videos related to

Sort By:
Pageof 101
Human Molecular Genetics|August 7, 2013
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt diseaseTerry A Braun, Robert F Mullins, Alex H Wagner, et al.
The Journal of Physical Chemistry Letters|August 20, 2015
Two-Photon Absorption Spectrum of a Single Crystal Cyanine-like DyeHonghua Hu, Dmitry A Fishman, Andrey O Gerasov, et al.
Neuromodulation : Journal of the International Neuromodulation Society|December 9, 2020
Long-Term Efficacy of a Novel Spinal Cord Stimulation Clinical Workflow Using Kilohertz Stimulation: Twelve-Month Results From the Vectors StudyJohn A Hatheway, Vipul Mangal, Michael A Fishman, et al.
Nature Genetics|February 2, 2000
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fateN B Haider, S G Jacobson, A V Cideciyan, et al.
American Journal of Ophthalmology|September 11, 2012
Assessing retinal structure in complete congenital stationary night blindness and Oguchi diseasePooja Godara, Robert F Cooper, Panagiotis I Sergouniotis, et al.
Annals of Internal Medicine|November 4, 2009
National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving HealthAlfred O Berg, Macaran A Baird, Jeffrey R Botkin, et al.
The European Respiratory Journal|April 13, 2012
The risk of tuberculosis in transplant candidates and recipients: a TBNET consensus statementDragos Bumbacea, Sandra M Arend, Fusun Eyuboglu, et al.
Blood|June 2, 2019
Haploidentical hematopoietic cell and kidney transplantation for hematological malignancies and end-stage renal failureYi-Bin Chen, Nahel Elias, Eliot Heher, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 24, 2008
Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kineticsArtur V Cideciyan, Tomas S Aleman, Sanford L Boye, et al.
Human Mutation|February 24, 2011
BBS genotype-phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definitionCatherine Deveault, Gail Billingsley, Jacque L Duncan, et al.
Pageof 101