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European Journal of Human Genetics : EJHG
|
July 11, 2013
Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations
Solaf M Elsayed, Raoul Heller, Michaela Thoenes, et al.
Journal of Cataract and Refractive Surgery
|
November 16, 2020
Prospective comparison of apex-centered vs standard pupil-centered femtosecond laser-assisted capsulotomy in cataract surgery
Anna Sophie Mursch-Edlmayr, Leon Julian Pomberger, Philipp Hermann, et al.
Journal of Bacteriology
|
May 17, 2011
Identification of an African Bacillus anthracis lineage that lacks expression of the spore surface-associated anthrose-containing oligosaccharide
Marco Tamborrini, Mark Bauer, Miriam Bolz, et al.
American Journal of Ophthalmology
|
December 17, 2023
Exploring Patient Demographics and Presence of Retinal Vascular Disease in Paracentral Acute Middle Maculopathy
Celeste Limoli, Laxmi Deepa Raja, Siegfried Karl Wagner, et al.
Investigative Ophthalmology & Visual Science
|
August 7, 2019
A Specific Macula-Predominant Retinal Phenotype Is Associated With the CDHR1 Variant c.783G>A, a Silent Mutation Leading to In-Frame Exon Skipping
Peter Charbel Issa, Martin Gliem, Imran H Yusuf, et al.
Current Eye Research
|
June 2, 2026
Difference in Ocular Perfusion Drop After Intravitreal Aflibercept in Patients with Neovascular AMD and Diabetic Macular Edema
Nina Anna Maria Karl, Anna Cornelia Schuhmayer, Leon Pomberger, et al.
Plos Neglected Tropical Diseases
|
February 11, 2015
Identification of the Mycobacterium ulcerans protein MUL_3720 as a promising target for the development of a diagnostic test for Buruli ulcer
Anita Dreyer, Katharina Röltgen, Jean Pierre Dangy, et al.
European Journal of Medical Genetics
|
July 6, 2016
MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosum
Ingrid Bader, E Decker, J A Mayr, et al.
Circulation
|
April 27, 2012
Tumor necrosis factor-α-mediated downregulation of the cystic fibrosis transmembrane conductance regulator drives pathological sphingosine-1-phosphate signaling in a mouse model of heart failure
Anja Meissner, Jingli Yang, Jeffrey T Kroetsch, et al.
American Journal of Ophthalmology
|
November 12, 2022
The CRW1 Index: Identification of Eyes with Previous Myopic Laser Vision Correction Using Only a Swept-Source OCT Biometer
David L Cooke, Kamran M Riaz, David A Murphy, et al.
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of 87
Search research articles
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Showing results (651-660 of 866) with videos related to
Sort By:
Page
of 87
European Journal of Human Genetics : EJHG
|
July 11, 2013
Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations
Solaf M Elsayed, Raoul Heller, Michaela Thoenes, et al.
Journal of Cataract and Refractive Surgery
|
November 16, 2020
Prospective comparison of apex-centered vs standard pupil-centered femtosecond laser-assisted capsulotomy in cataract surgery
Anna Sophie Mursch-Edlmayr, Leon Julian Pomberger, Philipp Hermann, et al.
Journal of Bacteriology
|
May 17, 2011
Identification of an African Bacillus anthracis lineage that lacks expression of the spore surface-associated anthrose-containing oligosaccharide
Marco Tamborrini, Mark Bauer, Miriam Bolz, et al.
American Journal of Ophthalmology
|
December 17, 2023
Exploring Patient Demographics and Presence of Retinal Vascular Disease in Paracentral Acute Middle Maculopathy
Celeste Limoli, Laxmi Deepa Raja, Siegfried Karl Wagner, et al.
Investigative Ophthalmology & Visual Science
|
August 7, 2019
A Specific Macula-Predominant Retinal Phenotype Is Associated With the CDHR1 Variant c.783G>A, a Silent Mutation Leading to In-Frame Exon Skipping
Peter Charbel Issa, Martin Gliem, Imran H Yusuf, et al.
Current Eye Research
|
June 2, 2026
Difference in Ocular Perfusion Drop After Intravitreal Aflibercept in Patients with Neovascular AMD and Diabetic Macular Edema
Nina Anna Maria Karl, Anna Cornelia Schuhmayer, Leon Pomberger, et al.
Plos Neglected Tropical Diseases
|
February 11, 2015
Identification of the Mycobacterium ulcerans protein MUL_3720 as a promising target for the development of a diagnostic test for Buruli ulcer
Anita Dreyer, Katharina Röltgen, Jean Pierre Dangy, et al.
European Journal of Medical Genetics
|
July 6, 2016
MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosum
Ingrid Bader, E Decker, J A Mayr, et al.
Circulation
|
April 27, 2012
Tumor necrosis factor-α-mediated downregulation of the cystic fibrosis transmembrane conductance regulator drives pathological sphingosine-1-phosphate signaling in a mouse model of heart failure
Anja Meissner, Jingli Yang, Jeffrey T Kroetsch, et al.
American Journal of Ophthalmology
|
November 12, 2022
The CRW1 Index: Identification of Eyes with Previous Myopic Laser Vision Correction Using Only a Swept-Source OCT Biometer
David L Cooke, Kamran M Riaz, David A Murphy, et al.
Page
of 87