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Robert Ritter

Showing results (11-20 of 17) with videos related to

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Optometry and Vision Science : Official Publication of the American Academy of Optometry|December 18, 2013
Quantification of conjunctival TNF-α in aqueous-deficient dry eyeBarbara E Caffery, Elizabeth Joyce, Miriam L Heynen, et al.
Journal of Clinical Apheresis|December 15, 2007
Performance of a new separator system for routine autologous hematopoietic progenitor cell collection in small childrenVolker Witt, Elisabeth Beiglböck, Robert Ritter, et al.
Molecular Vision|January 6, 2009
MUC16 expression in Sjogren's syndrome, KCS, and control subjectsBarbara Caffery, Elizabeth Joyce, Miriam L Heynen, et al.
American Journal of Ophthalmology|November 14, 2002
Identification of a stop codon mutation in exon 2 of the collagen 2A1 gene in a large stickler syndrome familyLarry A Donoso, Albert O Edwards, Arcilee T Frost, et al.
Survey of Ophthalmology|April 11, 2003
Clinical variability of Stickler syndrome: role of exon 2 of the collagen COL2A1 geneLarry A Donoso, Albert O Edwards, Arcilee T Frost, et al.
Molecular Vision|March 16, 2007
Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4Anne McMahon, Igor A Butovich, Nathan L Mata, et al.
Stem Cell Research & Therapy|September 24, 2025
Allogeneic bone marrow-derived mesenchymal stem cells in the aging kidney: secondary results of a Parkinson's disease clinical trialJuan D Martinez-Lemus, Donald A Molony, Jessika Suescun, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Optometry and Vision Science : Official Publication of the American Academy of Optometry|December 18, 2013
Quantification of conjunctival TNF-α in aqueous-deficient dry eyeBarbara E Caffery, Elizabeth Joyce, Miriam L Heynen, et al.
Journal of Clinical Apheresis|December 15, 2007
Performance of a new separator system for routine autologous hematopoietic progenitor cell collection in small childrenVolker Witt, Elisabeth Beiglböck, Robert Ritter, et al.
Molecular Vision|January 6, 2009
MUC16 expression in Sjogren's syndrome, KCS, and control subjectsBarbara Caffery, Elizabeth Joyce, Miriam L Heynen, et al.
American Journal of Ophthalmology|November 14, 2002
Identification of a stop codon mutation in exon 2 of the collagen 2A1 gene in a large stickler syndrome familyLarry A Donoso, Albert O Edwards, Arcilee T Frost, et al.
Survey of Ophthalmology|April 11, 2003
Clinical variability of Stickler syndrome: role of exon 2 of the collagen COL2A1 geneLarry A Donoso, Albert O Edwards, Arcilee T Frost, et al.
Molecular Vision|March 16, 2007
Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4Anne McMahon, Igor A Butovich, Nathan L Mata, et al.
Stem Cell Research & Therapy|September 24, 2025
Allogeneic bone marrow-derived mesenchymal stem cells in the aging kidney: secondary results of a Parkinson's disease clinical trialJuan D Martinez-Lemus, Donald A Molony, Jessika Suescun, et al.
Pageof 2