[HTML][HTML] Impaired retinal function and vitamin A availability in mice lacking retinol-binding protein

L Quadro, WS Blaner, DJ Salchow, S Vogel… - The EMBO …, 1999 - embopress.org
Retinol-binding protein (RBP) is the sole specific transport protein for retinol (vitamin A) in
the circulation, and its single known function is to deliver retinol to tissues. Within tissues, …

Retinal nerve fiber layer thickness in normal children measured with optical coherence tomography

DJ Salchow, YS Oleynikov, MF Chiang… - Ophthalmology, 2006 - Elsevier
PURPOSE: To measure the peripapillary retinal nerve fiber layer (RNFL) thickness in normal
children. DESIGN: Observational cross-sectional study. PARTICIPANTS: Ninety-two eyes of …

De novo mutation in ELOVL1 causes ichthyosis, acanthosis nigricans, hypomyelination, spastic paraplegia, high frequency deafness and optic atrophy

…, J Schneider, DJ Salchow… - Journal of medical …, 2019 - jmg.bmj.com
Background Very long-chain fatty acids (VLCFAs) are essential for functioning of biological
membranes. ELOVL fatty acid elongase 1 catalyses elongation of saturated and …

[HTML][HTML] Biometric and structural ocular manifestations of Marfan syndrome

…, D Pilger, P Ruokonen, PN Robinson, DJ Salchow - PloS one, 2017 - journals.plos.org
Background To study biometric and structural ocular manifestations of Marfan syndrome (MFS).
Methods Observational, retrospective, comparative cohort study in a tertiary referral …

Ocular manifestations of Marfan syndrome in children and adolescents

DJ Salchow, P Gehle - European journal of ophthalmology, 2019 - journals.sagepub.com
Ocular manifestations of Marfan syndrome in children and adolescents - Daniel J Salchow,
Petra Gehle, 2019 … Daniel J SalchowDaniel J Salchow

[HTML][HTML] Gene therapy with voretigene neparvovec improves vision and partially restores electrophysiological function in pre-school children with Leber congenital …

…, K Hufendiek, C Framme, H Jägle, DJ Salchow… - Biomedicines, 2022 - mdpi.com
Leber congenital amaurosis caused by mutations in the RPE65 gene belongs to the most
severe early-onset hereditary childhood retinopathies naturally progressing to legal blindness. …

Identifying barriers to follow-up eye care for children after failed vision screening in a primary care setting

…, T van Zyl, MD Elia, EN Garza, DJ Salchow… - Journal of American …, 2013 - Elsevier
Purpose To identify barriers to follow-up eye care in children who failed a visual acuity
screening conducted by their primary care provider. Methods Children aged 3-14 years who …

[HTML][HTML] Epithelial-mesenchymal transdifferentiation in pediatric lens epithelial cells

…, N Reichhart, O Strauß, DJ Salchow - … & visual science, 2018 - iovs.arvojournals.org
Purpose: Posterior capsule opacification (PCO) is a complication after cataract surgery,
particularly in children. Epithelial-mesenchymal transition (EMT) of lens epithelial cells, mediated …

Laser in situ keratomileusis after automated lamellar keratoplasty and penetrating keratoplasty

A Parisi, DJ Salchow, ME Zirm, C Stieldorf - Journal of Cataract & …, 1997 - Elsevier
We present three patients who had laser in situ keratomileusis (LASIK) after corneal surgery
as follows: 15 months after automated lamellar keratoplasty (ALK) for hyperopia, 6 months …

Laser in situ keratomileusis for myopia and myopic astigmatism

DJ Salchow, ME Zirm, C Stieldorf, A Parisi - Journal of Cataract & …, 1998 - Elsevier
Purpose: To evaluate the precision and safety of myopia and astigmatism correction using
laser in situ keratomileusis (LASIK). Setting: Augenchirurgie and Laserzentrum Hoch-Rum (…