about
Clinical anatomy of the anterior chamber angle in congenital aniridia - and consequences for trabeculotomy/cyclophotocoagulation.[Morphology of the optic chiasm in albinism][Eye findings in paediatric brain tumour - data basis for a follow-up proposal].Eye movement in amyotrophic lateral sclerosis: a longitudinal study.[PONV after strabismus surgery : Risk adapted prophylaxis?].Can retinoscopy keep up in keratoconus diagnosis?[Unusual course of a chalazion].[Aniridia syndrome: clinical findings, problematic courses and suggestions for optimization of care ("aniridia guide")].[Visual diagnosis: Waardenburg syndrome].[Tapetoretinal dystrophy and unusual facial features in an 8-year-old boy].[Treatment of pediatric cataracts. Part 2: IOL implantation, postoperative complications, aphakia management and postoperative development].[Prevalence of optic atrophy and associated ocular and systemic diseases in a department of paediatric ophthalmology].[Anatomical differences in optic nerve, chiasma and tractus opticus in human albinism as demonstrated by standardised clinical and MRI evaluation].[Choroid-retinal coloboma and unusual facial features in a 16-year-old girl].[Neuroimaging of color and spatial perception].Molecular analysis of patients with aniridia in Russian Federation broadens the spectrum of PAX6 mutations.Diagnostic impact of anterior segment angiography of limbal stem cell insufficiency in PAX6-related aniridia.Configuration of the optic chiasm in humans with albinism as revealed by magnetic resonance imaging.[Introduction to the topic: albinism. Much more than just blue eyes].[Academic teaching at the department of ophthalmology of the University Clinic of Saarland (UKS) : The Homburg "Ophthalmo-Week"].[Bright ocular background with profound cutis laxa and large fontanelles].Incontinentia pigmenti (Bloch-Sulzberger-syndrome): case report and differential diagnosisto related dermato-ocular syndromes.Polymorphisms in the genes for oculocutaneous albinism type 1 and type 4 in the German population.Phänotyp des visuellen Systems bei okulokutanem und okulärem AlbinismusExpression of retinoic acid signaling components ADH7 and ALDH1A1 is reduced in aniridia limbal epithelial cells and a siRNA primary cell based aniridia modelRetrobulbäre Raumforderung bei einem Kleinkind mit akutem ExophthalmusPer aspera ad astra: Einführung einer elektronischen Patientenakte an einer UniversitätsaugenklinikNystagmusAkuter monokularer Visusverlust bei kindlicher akuter lymphatischer LeukämieBilaterale kongenitale Aniridie mit regelrechtem Visus – 2 PatientenTrabekulotomie vor dem errechneten GeburtsterminKongenitale Aniridie oder PAX6-Syndrom?Stadiengerechte Therapie der kongenitalen AniridieGelbe Flecke der MakulaWas hast du für große Augen?Ausgewählte Aspekte der Kinderophthalmologie für Nicht-KinderophthalmologenAusgewählte Aspekte der Kinderophthalmologie für NichtkinderophthalmologenBehandlung der kindlichen Katarakte IAsymmetrische Stauungspapille mit subretinalen Blutungen als Erstmanifestation einer Arnold-Chiari-Malformation vom Typ I im ErwachsenenalterOkihiro-Syndrom
P50
Q30313098-AF1A858A-1312-4084-B252-380748D54169Q31117373-8B26B1D9-651B-42E5-BD9E-4DD8EC25BF43Q32110248-76060F42-B4C5-4B90-916B-E04051240E98Q34391839-CF4B46A5-91C4-48E9-849A-C174E8042059Q40704580-D86F60AB-07E8-4FDB-A6FD-A5E6A1E1316BQ41321977-A6556BC8-E7F0-4B18-8EB6-ACF44E5336F7Q41558350-2F7017EB-0090-472A-AE53-8291E7511B61Q41617732-FC724F50-1D04-4ED1-958A-8ACB2BD238F2Q43213531-C0F2879E-4240-4A0F-ADE1-044A643B397AQ43219627-4E175DB4-C143-4DD1-A5F4-7138D12CE727Q43565156-C4F4748B-BCA0-4F0E-8216-AB616EFE567DQ44397140-316900A9-5856-4BCB-BFB3-D7191B94F70AQ44453801-C5CDD4D8-F174-422A-9D35-2736CA682F18Q44553922-0C311898-D19A-4B4F-93C5-47F55100412BQ46405876-6D2B0273-BEED-400B-8214-353195A35703Q47771262-7C9060BC-9352-4C37-8E49-0D11DEF47D0FQ48347985-BABEC9FF-9C46-40BE-9788-CC2B2CEECD41Q48417409-352F647F-6747-4B8E-BF1C-80F967A9C936Q50466665-DBC05259-4376-495B-92EA-E8EDC81EC619Q50583149-0E5A34B1-8E1C-4301-8E6A-5E53A1ED4407Q50608659-B2B0E3DF-908B-4776-96E3-22B28BD56C7AQ50854793-BF4C0594-4BAB-4689-88C5-311175BC073FQ55043933-43CEB5A7-96BA-44B0-BF51-FA4D084C330EQ56639536-456F225F-47A0-471F-84C7-62969C2A10E1Q57186570-34440AE3-1F92-4DFE-AED7-64C6A45B4759Q57339677-B6985C73-C034-4AC1-8BC2-B876D0013C2EQ59297538-B52A2E8E-154A-4484-85B8-EF5D76576DCBQ59297540-7568427C-1C94-46AA-9710-E6849E96D935Q59297541-21183516-6CF3-4E40-A0CA-744A1B0238BAQ59297542-98F34C1C-1C36-4AA9-BC0B-9F51F52686FEQ59297545-53E9C6A8-684C-44C0-87FE-76D93D9A3D39Q59297547-A0588DC9-B1C3-47C9-9284-1E6717732000Q59297549-15E2CB40-5DA2-46A7-90C9-E2598DC1F0D0Q59297551-135686AB-7F24-4B07-A194-32FA164D6F79Q59297554-19E0B3CE-50A6-4A8A-BFFA-F10F4644666BQ59297560-08B91410-035A-4333-849D-656ABA3B10CDQ59297562-A6F65462-2956-4DFC-BECE-F363AC58CFF7Q59297564-A909984C-58A5-413C-BF00-4A771C5039B5Q59297566-C098BF8F-241E-42ED-8833-4B7AF9AE57C9Q59297570-E1E869C5-1C8A-460B-9C48-34955DEA9A7A
P50
description
researcher, ORCID id # 0000-0002-5137-8658
@en
wetenschapper
@nl
name
Barbara Kasmann-Kellner
@ast
Barbara Kasmann-Kellner
@en
Barbara Kasmann-Kellner
@es
Barbara Kasmann-Kellner
@nl
type
label
Barbara Kasmann-Kellner
@ast
Barbara Kasmann-Kellner
@en
Barbara Kasmann-Kellner
@es
Barbara Kasmann-Kellner
@nl
prefLabel
Barbara Kasmann-Kellner
@ast
Barbara Kasmann-Kellner
@en
Barbara Kasmann-Kellner
@es
Barbara Kasmann-Kellner
@nl
P1053
K-3624-2012
P106
P1153
6701512505
P21
P31
P3829
P496
0000-0002-5137-8658