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Retinal morphology in patients with BBS1 and BBS10 related Bardet-Biedl Syndrome evaluated by Fourier-domain optical coherence tomographyOptical Coherence Tomography and Magnetic Resonance Imaging in Multiple Sclerosis and Neuromyelitis Optica Spectrum DisorderDental phenotype in Jalili syndrome due to a c.1312 dupC homozygous mutation in the CNNM4 geneMaculopathy following exposure to visible and infrared radiation from a laser pointer: a clinical case study.Characterization of two novel intronic OPA1 mutations resulting in aberrant pre-mRNA splicingA secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant coloboma.Multifocal electroretinogram: age-related changes for different luminance levels.Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies.Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single center.Senescent Changes and Topography of the Dark-Adapted Multifocal Electroretinogram.Boucher-Neuhäuser syndrome: cerebellar degeneration, chorioretinal dystrophy and hypogonadotropic hypogonadism: two novel cases and a review of 40 cases from the literature.[Yellow stains and what now?].Intra-familial phenotype variability in patients with Jalili syndromeOptic disc doubling or pseudo-optic disc in colobomatous retinal abnormality?Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches.Infantile hemangiomas with conjunctival involvement: An underreported occurrence.Biallelic Mutations in CRB1 Underlie Autosomal Recessive Familial Foveal Retinoschisis.Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population.Long-Term Follow-Up in Children with Anisocoria: Cocaine Test Results and Patient Outcome.Retinal Ganglion Cell Topography in Patients With Visual Pathway Pathology.Bilateral vitreous hemorrhage in a newborn with Stickler syndrome associated with a novel COL2A1 mutation.Horizontal Gaze Palsy in Two Brothers with Compound Heterozygous ROBO3 Gene Mutations.Alternating IV nerve palsy and ptosis as a first sign of childhood ocular myasthenia gravis.Spontaneous Nystagmus in the Dark in an Infantile Nystagmus Patient May Represent Negative Optokinetic Afternystagmus.Outcome of Pediatric Cataract Surgeries in a Tertiary Center in Switzerland.Iris cyst in a child with Aicardi syndrome: a novel associationTeaching NeuroImages: Recurrent oculomotor palsies caused by neurosarcoidosisCongenital Lamellar CataractDie Neuritis nervi opticiThe impulse response of the aging visual system: Comparison of psychophysical and electrophysiological data[Ciliopathies][Unusual congenital iris finding][Ocular Phenotype and Complications in Patients with Tuberous Sclerosis Complex (TSC)]Higher incidence of retinopathy of prematurity in extremely preterm infants associated with improved survival rates
P50
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P50
description
hulumtuese
@sq
onderzoeker
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researcher
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հետազոտող
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name
Christina Gerth-kahlert
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Christina Gerth-kahlert
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Christina Gerth-kahlert
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Christina Gerth-kahlert
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Christina Gerth-kahlert
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type
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Christina Gerth-kahlert
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Christina Gerth-kahlert
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Christina Gerth-kahlert
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Christina Gerth-kahlert
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Christina Gerth-kahlert
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Christina Gerth
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prefLabel
Christina Gerth-kahlert
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Christina Gerth-kahlert
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Christina Gerth-kahlert
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Christina Gerth-kahlert
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Christina Gerth-kahlert
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P108
P106
P1153
35580592700
37010873800
P21
P31
P496
0000-0001-6298-615X