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Retina (Philadelphia, Pa.)
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December 24, 2005
Inherited and orphan retinal diseases: phenotypes, genotypes, and probable treatment groups
Richard G Weleber
Ophthalmic Genetics
|
August 21, 2002
Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture)
Richard G Weleber
Retina (Philadelphia, Pa.)
|
December 24, 2005
A network of patients with orphan retinal diseases for clinical trials: goals, structure, challenges
Richard G Weleber
Ophthalmology
|
December 29, 2015
Dysregulation of Retinal Transcription Factor PRDM13 and North Carolina Macular Dystrophy
Richard G Weleber
American Journal of Medical Genetics. Part A
|
September 14, 2007
Conorenal dysplasia: a syndrome of cone-shaped epiphysis, renal disease in childhood, retinitis pigmentosa and abnormality of the proximal femur
Rodney K Beals, Richard G Weleber
American Journal of Medical Genetics. Part A
|
September 25, 2004
Distal arthrogryposis 5: a dominant syndrome of peripheral contractures and ophthalmoplegia
Rodney K Beals, Richard G Weleber
Retina (Philadelphia, Pa.)
|
February 9, 2010
High-resolution optical coherence tomography shows new aspects of Bietti crystalline retinopathy
Mark E Pennesi, Richard G Weleber
Experimental Eye Research
|
May 18, 2016
Unique epitopes for carbonic anhydrase II autoantibodies related to autoimmune retinopathy and cancer-associated retinopathy
Grazyna Adamus, Sufang Yang, Richard G Weleber
BMC Ophthalmology
|
June 8, 2004
Autoantibodies against retinal proteins in paraneoplastic and autoimmune retinopathy
Grazyna Adamus, Gaoying Ren, Richard G Weleber
Experimental and Molecular Pathology
|
September 12, 2009
Molecular biomarkers for autoimmune retinopathies: significance of anti-transducin-alpha autoantibodies
Grazyna Adamus, Lori Brown, Richard G Weleber
Page
of 13
Search research articles
Search
Showing results (1-10 of 127) with videos related to
Sort By:
Page
of 13
Retina (Philadelphia, Pa.)
|
December 24, 2005
Inherited and orphan retinal diseases: phenotypes, genotypes, and probable treatment groups
Richard G Weleber
Ophthalmic Genetics
|
August 21, 2002
Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture)
Richard G Weleber
Retina (Philadelphia, Pa.)
|
December 24, 2005
A network of patients with orphan retinal diseases for clinical trials: goals, structure, challenges
Richard G Weleber
Ophthalmology
|
December 29, 2015
Dysregulation of Retinal Transcription Factor PRDM13 and North Carolina Macular Dystrophy
Richard G Weleber
American Journal of Medical Genetics. Part A
|
September 14, 2007
Conorenal dysplasia: a syndrome of cone-shaped epiphysis, renal disease in childhood, retinitis pigmentosa and abnormality of the proximal femur
Rodney K Beals, Richard G Weleber
American Journal of Medical Genetics. Part A
|
September 25, 2004
Distal arthrogryposis 5: a dominant syndrome of peripheral contractures and ophthalmoplegia
Rodney K Beals, Richard G Weleber
Retina (Philadelphia, Pa.)
|
February 9, 2010
High-resolution optical coherence tomography shows new aspects of Bietti crystalline retinopathy
Mark E Pennesi, Richard G Weleber
Experimental Eye Research
|
May 18, 2016
Unique epitopes for carbonic anhydrase II autoantibodies related to autoimmune retinopathy and cancer-associated retinopathy
Grazyna Adamus, Sufang Yang, Richard G Weleber
BMC Ophthalmology
|
June 8, 2004
Autoantibodies against retinal proteins in paraneoplastic and autoimmune retinopathy
Grazyna Adamus, Gaoying Ren, Richard G Weleber
Experimental and Molecular Pathology
|
September 12, 2009
Molecular biomarkers for autoimmune retinopathies: significance of anti-transducin-alpha autoantibodies
Grazyna Adamus, Lori Brown, Richard G Weleber
Page
of 13