UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Epidemiological survey of intraocular inflammation in Japan

Japanese journal of ophthalmology, 2007-01, Vol.51 (1), p.41-44

2007

Volltextzugriff (PDF)

Novel GUCY2D Variant (E843Q) at Mutation Hotspot Associated with Macular Dystrophy in a Japanese Patient

Journal of Nippon Medical School = Nippon Ika Daigaku zasshi, 2020-04, Vol.87 (2), p.92-99

2020

Volltextzugriff (PDF)

High-Resolution Retinal Imaging Reveals Preserved Cone Photoreceptor Density and Choroidal Thickness in Female Carriers of Choroideremia

Ophthalmic surgery, lasers & imaging retina, 2019-02, Vol.50 (2), p.76-85

2019

Volltextzugriff (PDF)

Tyrosinase Family Proteins Are Antigens Specific to Vogt-Koyanagi-Harada Disease

The Journal of immunology (1950), 2000-12, Vol.165 (12), p.7323-7329

2000

Volltextzugriff (PDF)

Multimodal imaging of a case of peripheral cone dystrophy

Documenta ophthalmologica, 2015-06, Vol.130 (3), p.241-251

2015

Volltextzugriff (PDF)

Reactive gliosis of astrocytes and Müller glial cells in retina of POMGnT1-deficient mice

Molecular and cellular neuroscience, 2011-06, Vol.47 (2), p.119-130

2011

Volltextzugriff (PDF)

High-Resolution Imaging of Patients with Bietti Crystalline Dystrophy with CYP4V2 Mutation

Journal of Ophthalmology, 2014-01, Vol.2014 (1), p.332-343

2014

Volltextzugriff (PDF)

Application of revised diagnostic criteria for vogt-koyanagi-harada disease in Japanese patients

Japanese journal of ophthalmology, 2005-03, Vol.49 (2), p.143-148

2005

Volltextzugriff (PDF)

Detailed Morphological Changes of Foveoschisis in Patient with X-Linked Retinoschisis Detected by SD-OCT and Adaptive Optics Fundus Camera

Case reports in ophthalmological medicine, 2015-01, Vol.2015 (2015), p.1-8

2015

Volltextzugriff (PDF)

Ocular and Extraocular Inflammation Induced by Immunization of Tyrosinase Related Protein 1 and 2 in Lewis Rats

Experimental eye research, 2000-10, Vol.71 (4), p.361-369

2000

Volltextzugriff (PDF)

CEP250 mutations associated with mild cone-rod dystrophy and sensorineural hearing loss in a Japanese family

Ophthalmic genetics, 2018-08, Vol.39 (4), p.500-507

2018

Volltextzugriff (PDF)

Novel RP1L1 Variants and Genotype-Photoreceptor Microstructural Phenotype Associations in Cohort of Japanese Patients With Occult Macular Dystrophy

Investigative ophthalmology & visual science, 2016-09, Vol.57 (11), p.4837-4846

2016

Volltextzugriff (PDF)

Ultrastructural changes in rat eyes with experimental Vogt-Koyanagi-Harada disease

Japanese journal of ophthalmology, 2004-05, Vol.48 (3), p.222-227

2004

Volltextzugriff (PDF)

Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation

Ophthalmic genetics, 2021-06, Vol.42 (3), p.304-311

2021

Volltextzugriff (PDF)

Wistar Rat Palpebral Conjunctiva Contains More Slow-cycling Stem Cells That Have Larger Proliferative Capacity: Implication for Conjunctival Epithelial Homeostasis

Japanese journal of ophthalmology, 2003-03, Vol.47 (2), p.119-128

2003

Volltextzugriff (PDF)

High-resolution photoreceptor imaging analysis of patients with autosomal dominant retinitis pigmentosa (adRP) caused by HK1 mutation

Ophthalmic genetics, 2020-11, Vol.41 (6), p.629-638

2020

Volltextzugriff (PDF)

High-Resolution En Face Images of Microcystic Macular Edema in Patients with Autosomal Dominant Optic Atrophy

BioMed research international, 2013-01, Vol.2013 (2013), p.1-12

2013

Volltextzugriff (PDF)

Cone Dystrophy in Patient with Homozygous RP1L1 Mutation

BioMed research international, 2015-01, Vol.2015 (2015), p.1-13

2015

Volltextzugriff (PDF)

Novel homozygous in-frame deletion of GNAT1 gene causes golden appearance of fundus and reduced scotopic ERGs similar to that in Oguchi disease in Japanese family

Ophthalmic genetics, 2019-09, Vol.40 (5), p.480-487

2019

Volltextzugriff (PDF)

Identification of the Hexon Region of an Adenovirus Involved in a New Outbreak of Keratoconjunctivitis

Journal of Clinical Microbiology, 2001-08, Vol.39 (8), p.2975-2977

2001

Volltextzugriff (PDF)

Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation

Documenta ophthalmologica, 2016-06, Vol.132 (3), p.233-243

2016

Volltextzugriff (PDF)

Identification of Autoreactive T Cells in Vogt-Koyanagi-Harada Disease

Investigative ophthalmology & visual science, 2001-08, Vol.42 (9), p.2004-2009

2001

Volltextzugriff (PDF)

A new mutation in the RP1L1 gene in a patient with occult macular dystrophy associated with a depolarizing pattern of focal macular electroretinograms

Molecular vision, 2012, Vol.18, p.1031-1039

2012

Volltextzugriff (PDF)

Intraocular Inflammation and Antigen Presentation

Nihon Ika Daigaku Igakkai zasshi, 2008, Vol.4 (1), p.8-14

Yamaki, Kunihiko

2008

Volltextzugriff (PDF)

1 – 25 von 72

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(51)
Mit Volltextzugriff
(46)

Publikationsform

Artikel
(68)
Berichte
(4)

Sprache

Englisch
(66)
Japanisch
(10)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(43)
Science & Technology
(43)
Humans
(34)
Animals
(26)
Female
(26)
Ophthalmology
(26)
Male
(22)
Adult
(18)
Biological And Medical Sciences
(18)
Middle Aged
(18)
Rats
(16)
Rats, Inbred Lew
(13)
Arrestin
(12)
Eye Proteins - Genetics
(12)
Aged
(11)
Amino Acid Sequence
(11)
Peptide Fragments - Immunology
(11)
Fundamental And Applied Biological Sciences. Psychology
(10)
Molecular Sequence Data
(9)
Adaptive Optics
(8)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Epidemiological survey of intraocular inflammation in Japan

Novel GUCY2D Variant (E843Q) at Mutation Hotspot Associated with Macular Dystrophy in a Japanese Patient

High-Resolution Retinal Imaging Reveals Preserved Cone Photoreceptor Density and Choroidal Thickness in Female Carriers of Choroideremia

Tyrosinase Family Proteins Are Antigens Specific to Vogt-Koyanagi-Harada Disease

Multimodal imaging of a case of peripheral cone dystrophy

Reactive gliosis of astrocytes and Müller glial cells in retina of POMGnT1-deficient mice

High-Resolution Imaging of Patients with Bietti Crystalline Dystrophy with CYP4V2 Mutation

Application of revised diagnostic criteria for vogt-koyanagi-harada disease in Japanese patients

Detailed Morphological Changes of Foveoschisis in Patient with X-Linked Retinoschisis Detected by SD-OCT and Adaptive Optics Fundus Camera

Ocular and Extraocular Inflammation Induced by Immunization of Tyrosinase Related Protein 1 and 2 in Lewis Rats

CEP250 mutations associated with mild cone-rod dystrophy and sensorineural hearing loss in a Japanese family

Novel RP1L1 Variants and Genotype-Photoreceptor Microstructural Phenotype Associations in Cohort of Japanese Patients With Occult Macular Dystrophy

A driver role for GABA metabolism in controlling stem and proliferative cell state through GHB production in glioma

Ultrastructural changes in rat eyes with experimental Vogt-Koyanagi-Harada disease

Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation

Wistar Rat Palpebral Conjunctiva Contains More Slow-cycling Stem Cells That Have Larger Proliferative Capacity: Implication for Conjunctival Epithelial Homeostasis

High-resolution photoreceptor imaging analysis of patients with autosomal dominant retinitis pigmentosa (adRP) caused by HK1 mutation

High-Resolution En Face Images of Microcystic Macular Edema in Patients with Autosomal Dominant Optic Atrophy

Cone Dystrophy in Patient with Homozygous RP1L1 Mutation

Novel homozygous in-frame deletion of GNAT1 gene causes golden appearance of fundus and reduced scotopic ERGs similar to that in Oguchi disease in Japanese family

Identification of the Hexon Region of an Adenovirus Involved in a New Outbreak of Keratoconjunctivitis

Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation

Identification of Autoreactive T Cells in Vogt-Koyanagi-Harada Disease

A new mutation in the RP1L1 gene in a patient with occult macular dystrophy associated with a depolarizing pattern of focal macular electroretinograms

Intraocular Inflammation and Antigen Presentation

Suchergebnisse filtern