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OCCULT MACULAR DYSTROPHY
Known as:
OCMD
, OMD
National Institutes of Health
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Related topics
Related topics
1 relation
Autosomal dominant inheritance
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
Clinical spectrum of artery of Percheron infarct: clinical-radiological correlations.
A. Arauz
,
H. M. Patiño-Rodríguez
,
+4 authors
Marco A. Ochoa
Journal of Stroke & Cerebrovascular Diseases
2014
Corpus ID: 24957257
2013
2013
Multimodal imaging of occult macular dystrophy.
Seong Joon Ahn
,
Jeeyun Ahn
,
K. Park
,
S. Woo
JAMA ophthalmology
2013
Corpus ID: 6903376
IMPORTANCE The value of imaging modalities remains unknown in occult macular dystrophy (OMD) because they have not been compared…
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2013
2013
Clinical and genetic characteristics of Korean occult macular dystrophy patients.
Seong Joon Ahn
,
Sung Im Cho
,
Jeeyun Ahn
,
S. Park
,
K. Park
,
S. Woo
Investigative Ophthalmology and Visual Science
2013
Corpus ID: 33356739
PURPOSE We investigated the genetic characteristics of retinitis pigmentosa 1-like 1 (RP1L1) gene in patients with occult macular…
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2012
2012
Autosomal Dominant Occult Macular Dystrophy with an RP1L1 Mutation (R45W)
Takaaki Hayashi
,
T. Gekka
,
+4 authors
H. Tsuneoka
Optometry and Vision Science
2012
Corpus ID: 43568481
Purpose. To characterize clinical features in occult macular dystrophy (OMD) patients with the RP1L1 gene mutation (p.R45W), one…
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Highly Cited
2012
Highly Cited
2012
CLINICAL CHARACTERISTICS OF OCCULT MACULAR DYSTROPHY IN FAMILY WITH MUTATION OF RP1L1 GENE
K. Tsunoda
,
T. Usui
,
+8 authors
Y. Miyake
Retina
2012
Corpus ID: 37969163
Purpose: To report the clinical characteristics of occult macular dystrophy (OMD) in members of one family with a mutation of the…
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2011
2011
Fundus autofluorescence in autosomal dominant occult macular dystrophy.
K. Fujinami
,
K. Tsunoda
,
Gen Hanazono
,
K. Shinoda
,
H. Ohde
,
Y. Miyake
A M A Archives of Ophthalmology
2011
Corpus ID: 26514856
OBJECTIVE To characterize fundus autofluorescence (FAF) images of eyes with autosomal dominant occult macular dystrophy (OMD…
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Highly Cited
2010
Highly Cited
2010
Dominant mutations in RP1L1 are responsible for occult macular dystrophy.
M. Akahori
,
K. Tsunoda
,
+11 authors
T. Iwata
American Journal of Human Genetics
2010
Corpus ID: 32970890
Highly Cited
2010
Highly Cited
2010
Morphologic photoreceptor abnormality in occult macular dystrophy on spectral-domain optical coherence tomography.
S. Park
,
S. Woo
,
K. Park
,
Jeong-Min Hwang
,
Hum Chung
Investigative Ophthalmology and Visual Science
2010
Corpus ID: 9444763
PURPOSE. To investigate morphologic photoreceptor layer abnormalities and their correlation with visual function in occult…
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Highly Cited
2000
Highly Cited
2000
Multifocal electroretinogram in occult macular dystrophy.
C. Piao
,
M. Kondo
,
A. Tanikawa
,
H. Terasaki
,
Y. Miyake
Investigative Ophthalmology and Visual Science
2000
Corpus ID: 8083215
PURPOSE Occult macular dystrophy (OMD) is an unusual macular dystrophy presenting with an essentially normal fundus and…
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Highly Cited
1999
Highly Cited
1999
Immunohistological findings in a patient with unusual late onset manifestation of ligneous conjunctivitis
Sonja Klebe
,
Tony Walkow
,
Christian Hartmann
,
Uwe Pleyer
British Journal of Ophthalmology
1999
Corpus ID: 6268821
Editor,—Ligneous conjunctivitis is a rare chronic membranous conjunctivitis with typical woody induration of the conjunctival…
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