Lista de obras - Barbara Kasmann-Kellner - Dominio Público Uruguay

Academic teaching at the department of ophthalmology of the University Clinic of Saarland (UKS) : The Homburg "Ophthalmo-Week"

artículo científico publicado en 2015

Akuter monokularer Visusverlust bei kindlicher akuter lymphatischer Leukämie

artículo científico publicado en 2016

Analysis of genotype-phenotype correlations in PAX6-associated aniridia

artículo científico publicado en 2020

Anatomical differences in optic nerve, chiasma and tractus opticus in human albinism as demonstrated by standardised clinical and MRI evaluation

artículo científico publicado en 2003

Aniridia syndrome: clinical findings, problematic courses and suggestions for optimization of care ("aniridia guide")

artículo científico publicado en 2014

Anisomyopie und markhaltige Nervenfasern -ein Syndrom*

artículo científico publicado en 1999

Asymmetrische Stauungspapille mit subretinalen Blutungen als Erstmanifestation einer Arnold-Chiari-Malformation vom Typ I im Erwachsenenalter

scientific article published on 24 November 2010

Ausgewählte Aspekte der Kinderophthalmologie für Nicht-Kinderophthalmologen

artículo científico publicado en 2012

Ausgewählte Aspekte der Kinderophthalmologie für Nichtkinderophthalmologen

scientific article published on 01 February 2012

Behandlung der kindlichen Katarakte I

artículo científico publicado en 2012

Bilaterale kongenitale Aniridie mit regelrechtem Visus – 2 Patienten

artículo científico publicado en 2015

Bright ocular background with profound cutis laxa and large fontanelles

artículo científico publicado en 2015

Can retinoscopy keep up in keratoconus diagnosis?

artículo científico publicado en 2015

Choroid-retinal coloboma and unusual facial features in a 16-year-old girl

artículo científico publicado en 2013

Clinical anatomy of the anterior chamber angle in congenital aniridia - and consequences for trabeculotomy/cyclophotocoagulation

artículo científico publicado en 2017

Configuration of the optic chiasm in humans with albinism as revealed by magnetic resonance imaging.

artículo científico publicado en 2003

Correspondence

Detection of 53 novel DNA variations within the tyrosinase gene and accumulation of mutations in 17 patients with albinism

article

Developments in eye and general diseases in the Landesschule für Blinde und Sehbehinderte des Saarlandes in the last 20 years

scientific article published on 01 January 1998

Diagnostic impact of anterior segment angiography of limbal stem cell insufficiency in PAX6-related aniridia

artículo científico publicado en 2017

Eclamptogenic Gerstmann's syndrome in combination with cortical agnosia and cortical diplopia

artículo científico publicado en 1995

Ein- oder beidseitige Abduzensparese als Erstsymptom einer Sinusvenenthrombose

artículo científico publicado en 2002

Expression of retinoic acid signaling components ADH7 and ALDH1A1 is reduced in aniridia limbal epithelial cells and a siRNA primary cell based aniridia model

article

Eye movement in amyotrophic lateral sclerosis: a longitudinal study.

artículo científico publicado en 1995

Gelbe Flecke der Makula

artículo científico publicado en 2014

Genetik bei okulokutanem Albinismus

artículo científico publicado en 2007

Incontinentia pigmenti (Bloch-Sulzberger-syndrome): case report and differential diagnosisto related dermato-ocular syndromes.

artículo científico publicado en 1999

Introduction to the topic: albinism. Much more than just blue eyes

artículo científico publicado en 2007

Kongenitale Aniridie oder PAX6-Syndrom?

scientific article published on 01 December 2014

Might the refractive state in oculocutaneous albino patients be a clue for distinguishing between tyrosinase-positive and tyrosinase-negative forms of oculocutaneous albinism?

scientific article published on 01 November 1996

Molecular analysis of patients with aniridia in Russian Federation broadens the spectrum of PAX6 mutations

artículo científico publicado en 2017

Monocular visual activation patterns in albinism as revealed by functional magnetic resonance imaging

scientific article published on 01 September 2004

Morphology of the optic chiasm in albinism

artículo científico publicado en 2007

Multifocal Visual Evoked Potentials Reveal Normal Optic Nerve Projections in Human Carriers of Oculocutaneous Albinism Type 1a

scientific article published on 22 February 2008

Neuroimaging of color and spatial perception

artículo científico publicado en 2013

Nystagmus

scientific article published on 01 March 2016

Ocular Changes in Mucopolysaccharidosis IV A (Morquio A Syndrome) and Long-Term Results of Perforating Keratoplasty

artículo científico publicado en 1999

Ocular manifestations in a father and son with EEC syndrome ⬇️

artículo científico publicado el 1 de agosto de 1997

Okihiro-Syndrom

artículo científico publicado en 2008

Okulomandibul�re Dyskranie

scientific article published on 01 September 2004

PONV after strabismus surgery : Risk adapted prophylaxis?

artículo científico publicado en 2016

Per aspera ad astra: Einführung einer elektronischen Patientenakte an einer Universitätsaugenklinik

scientific article published on 01 October 2018

Phänotyp des visuellen Systems bei okulokutanem und okulärem Albinismus

scientific article published on 01 August 2007

Polymorphisms in the genes for oculocutaneous albinism type 1 and type 4 in the German population.

artículo científico publicado en 2007

Prevalence of optic atrophy and associated ocular and systemic diseases in a department of paediatric ophthalmology

artículo científico publicado en 2003

Results of occlusion therapy in anisomyopic amblyopia with myelinated nerve fibers

artículo científico publicado en 1996

Retrobulbäre Raumforderung bei einem Kleinkind mit akutem Exophthalmus

artículo científico publicado en 2006

Screening-Untersuchung auf Amblyopie, Strabismus und Refraktionsanomalie bei 1030 Kindergartenkindern

artículo científico publicado en 1998

Stadiengerechte Therapie der kongenitalen Aniridie

artículo científico publicado en 2014

Tapetoretinal dystrophy and unusual facial features in an 8-year-old boy

artículo científico publicado en 2010

Trabekulotomie vor dem errechneten Geburtstermin

artículo científico publicado en 2015

Treatment of pediatric cataracts. Part 2: IOL implantation, postoperative complications, aphakia management and postoperative development

artículo científico publicado en 2013

Unusual course of a chalazion

artículo científico publicado en 2015

Visual diagnosis: Waardenburg syndrome

artículo científico publicado en 2010

Was hast du für große Augen?

scientific article published on 01 December 2013

Zunehmendes Blendungs- und Verschwommensehen

scientific article published on 01 December 2000

[Amblyopia. 6th Meeting of the Bielschowsky Society for Amblyopia Research, 29-31 August 1997 in Giessen]

artículo científico publicado en 1998

[Central areolar pigment epithelium dystrophy. Its differentiation from other dominant macular dystrophies]

scientific article published on 01 February 1992

[Clinical and Genetic Characteristics of Ocular Developmental Disorders: MAC-Spectrum, Anterior Segment Dysgenesis]

artículo científico publicado en 2019

[Establishment of a PJ Faculty at the Medical Faculty of Saarland University UdS : "Docendo discimus", "Transparency and communication"]

artículo científico publicado en 2019

[Eye findings in paediatric brain tumour - data basis for a follow-up proposal].

artículo científico publicado en 2002

[Familial drusen of the macula]

artículo científico publicado en 1990

[Follow-up of retinoblastoma during homeopathic therapy]

artículo científico publicado en 1999

[Ocular and neuro-ophthalmologic involvement in borreliosis]

artículo científico publicado en 1998

[Types of albinism and their ocular and cutaneous manifestations]

scientific article published on 01 June 1999

[Work in progress: adaptation of electronic medical records to the requirements of a university eye clinic : Individual extensions of the software "FIDUS" at the Department of Ophthalmology of the Saarland University Medical Center UKS]

scientific article published on 01 November 2019

Lista de obras de Barbara Kasmann-Kellner

Academic teaching at the department of ophthalmology of the University Clinic of Saarland (UKS) : The Homburg "Ophthalmo-Week"

Akuter monokularer Visusverlust bei kindlicher akuter lymphatischer Leukämie

Analysis of genotype-phenotype correlations in PAX6-associated aniridia

Anatomical differences in optic nerve, chiasma and tractus opticus in human albinism as demonstrated by standardised clinical and MRI evaluation

Aniridia syndrome: clinical findings, problematic courses and suggestions for optimization of care ("aniridia guide")

Anisomyopie und markhaltige Nervenfasern -ein Syndrom*

Asymmetrische Stauungspapille mit subretinalen Blutungen als Erstmanifestation einer Arnold-Chiari-Malformation vom Typ I im Erwachsenenalter

Ausgewählte Aspekte der Kinderophthalmologie für Nicht-Kinderophthalmologen

Ausgewählte Aspekte der Kinderophthalmologie für Nichtkinderophthalmologen

Behandlung der kindlichen Katarakte I

Bilaterale kongenitale Aniridie mit regelrechtem Visus – 2 Patienten

Bright ocular background with profound cutis laxa and large fontanelles

Can retinoscopy keep up in keratoconus diagnosis?

Choroid-retinal coloboma and unusual facial features in a 16-year-old girl

Clinical anatomy of the anterior chamber angle in congenital aniridia - and consequences for trabeculotomy/cyclophotocoagulation

Configuration of the optic chiasm in humans with albinism as revealed by magnetic resonance imaging.

Correspondence

Detection of 53 novel DNA variations within the tyrosinase gene and accumulation of mutations in 17 patients with albinism

Developments in eye and general diseases in the Landesschule für Blinde und Sehbehinderte des Saarlandes in the last 20 years

Diagnostic impact of anterior segment angiography of limbal stem cell insufficiency in PAX6-related aniridia

Eclamptogenic Gerstmann's syndrome in combination with cortical agnosia and cortical diplopia

Ein- oder beidseitige Abduzensparese als Erstsymptom einer Sinusvenenthrombose

Expression of retinoic acid signaling components ADH7 and ALDH1A1 is reduced in aniridia limbal epithelial cells and a siRNA primary cell based aniridia model

Eye movement in amyotrophic lateral sclerosis: a longitudinal study.

Gelbe Flecke der Makula

Genetik bei okulokutanem Albinismus

Incontinentia pigmenti (Bloch-Sulzberger-syndrome): case report and differential diagnosisto related dermato-ocular syndromes.

Introduction to the topic: albinism. Much more than just blue eyes

Kongenitale Aniridie oder PAX6-Syndrom?

Might the refractive state in oculocutaneous albino patients be a clue for distinguishing between tyrosinase-positive and tyrosinase-negative forms of oculocutaneous albinism?

Molecular analysis of patients with aniridia in Russian Federation broadens the spectrum of PAX6 mutations

Monocular visual activation patterns in albinism as revealed by functional magnetic resonance imaging

Morphology of the optic chiasm in albinism

Multifocal Visual Evoked Potentials Reveal Normal Optic Nerve Projections in Human Carriers of Oculocutaneous Albinism Type 1a

Neuroimaging of color and spatial perception

Nystagmus

Ocular Changes in Mucopolysaccharidosis IV A (Morquio A Syndrome) and Long-Term Results of Perforating Keratoplasty

Ocular manifestations in a father and son with EEC syndrome ⬇️

Okihiro-Syndrom

Okulomandibul�re Dyskranie

PONV after strabismus surgery : Risk adapted prophylaxis?

Per aspera ad astra: Einführung einer elektronischen Patientenakte an einer Universitätsaugenklinik

Phänotyp des visuellen Systems bei okulokutanem und okulärem Albinismus

Polymorphisms in the genes for oculocutaneous albinism type 1 and type 4 in the German population.

Prevalence of optic atrophy and associated ocular and systemic diseases in a department of paediatric ophthalmology

Results of occlusion therapy in anisomyopic amblyopia with myelinated nerve fibers

Retrobulbäre Raumforderung bei einem Kleinkind mit akutem Exophthalmus

Screening-Untersuchung auf Amblyopie, Strabismus und Refraktionsanomalie bei 1030 Kindergartenkindern

Stadiengerechte Therapie der kongenitalen Aniridie

Tapetoretinal dystrophy and unusual facial features in an 8-year-old boy

Trabekulotomie vor dem errechneten Geburtstermin

Treatment of pediatric cataracts. Part 2: IOL implantation, postoperative complications, aphakia management and postoperative development

Unusual course of a chalazion

Visual diagnosis: Waardenburg syndrome

Was hast du für große Augen?

Zunehmendes Blendungs- und Verschwommensehen

[Amblyopia. 6th Meeting of the Bielschowsky Society for Amblyopia Research, 29-31 August 1997 in Giessen]

[Central areolar pigment epithelium dystrophy. Its differentiation from other dominant macular dystrophies]

[Clinical and Genetic Characteristics of Ocular Developmental Disorders: MAC-Spectrum, Anterior Segment Dysgenesis]

[Establishment of a PJ Faculty at the Medical Faculty of Saarland University UdS : "Docendo discimus", "Transparency and communication"]

[Eye findings in paediatric brain tumour - data basis for a follow-up proposal].

[Familial drusen of the macula]

[Follow-up of retinoblastoma during homeopathic therapy]

[Ocular and neuro-ophthalmologic involvement in borreliosis]

[Types of albinism and their ocular and cutaneous manifestations]

[Work in progress: adaptation of electronic medical records to the requirements of a university eye clinic : Individual extensions of the software "FIDUS" at the Department of Ophthalmology of the Saarland University Medical Center UKS]