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Developmental Medicine and Child Neurology
|
April 12, 2018
Retinal nerve fibre layer thinning is associated with worse visual outcome after optic neuritis in children with a relapsing demyelinating syndrome
Michael Eyre, Aasim Hameed, Sukhvir Wright, et al.
The Journal of Investigative Dermatology
|
January 8, 2004
Phenotypic diversity and mutation spectrum in hypotrichosis with juvenile macular dystrophy
Margarita Indelman, Christian P Hamel, Reuven Bergman, et al.
Investigative Ophthalmology & Visual Science
|
October 2, 2014
The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotype
Sarah Hull, Gavin Arno, Vincent Plagnol, et al.
American Journal of Ophthalmology
|
August 2, 2008
Ophthalmological aspects of Pierson syndrome
Cecilie Bredrup, Verena Matejas, Margaret Barrow, et al.
The New England Journal of Medicine
|
May 8, 2009
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations
Detlef Bockenhauer, Sally Feather, Horia C Stanescu, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
Developmental Medicine and Child Neurology
|
April 12, 2018
Retinal nerve fibre layer thinning is associated with worse visual outcome after optic neuritis in children with a relapsing demyelinating syndrome
Michael Eyre, Aasim Hameed, Sukhvir Wright, et al.
The Journal of Investigative Dermatology
|
January 8, 2004
Phenotypic diversity and mutation spectrum in hypotrichosis with juvenile macular dystrophy
Margarita Indelman, Christian P Hamel, Reuven Bergman, et al.
Investigative Ophthalmology & Visual Science
|
October 2, 2014
The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotype
Sarah Hull, Gavin Arno, Vincent Plagnol, et al.
American Journal of Ophthalmology
|
August 2, 2008
Ophthalmological aspects of Pierson syndrome
Cecilie Bredrup, Verena Matejas, Margaret Barrow, et al.
The New England Journal of Medicine
|
May 8, 2009
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations
Detlef Bockenhauer, Sally Feather, Horia C Stanescu, et al.
Page
of 2