Antonia Howaldt
Kerpener Str. 62, Deutschland
Koeln, NW 50937, Germany
Koeln, NW 50937, Germany
Last Updated: 09/26/2026
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Found 13 publications
Innovative surgical treatment approaches for endothelial dysfunction : Descemet stripping only (DSO) and endothelial cell injection
Journal: Die Ophthalmologie
Published: August 07, 2024
Pathogenesis of Fuchs endothelial corneal dystrophy, the fibrillar layer and individualized treatment
Journal: Die Ophthalmologie
Published: July 08, 2024
Leadership from the perspective of next generation ophthalmologists
Journal: Die Ophthalmologie
Published: July 31, 2023
Corneal Infantile Myofibromatosis Caused by Novel Activating Imatinib-Responsive Variants in PDGFRB.
Corneal Infantile Myofibromatosis Caused by Novel Activating Imatinib-Responsive Variants in PDGFRB.
Journal: Ophthalmology science
Published: June 16, 2023
Blood-Aqueous Barrier Disruption in Penetrating and Posterior Lamellar Keratoplasty: Implications for Clinical Outcome.
Journal: Klinische Monatsblatter fur Augenheilkunde
Published: May 19, 2023
The novel role of lymphatic vessels in the pathogenesis of ocular diseases.
Journal: Progress in retinal and eye research
Published: September 22, 2022
Correlation of Clinical Fibrillar Layer Detection and Corneal Thickness in Advanced Fuchs Endothelial Corneal Dystrophy.
Journal: Journal of clinical medicine
Published: March 31, 2022
Diagnostics, clinical aspects and genetics of congenital corneal opacities
Journal: Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft
Published: January 24, 2022
Scheimpflug Backscatter Imaging of the Fibrillar Layer in Fuchs Endothelial Corneal Dystrophy.
Journal: American journal of ophthalmology
Published: April 28, 2021
Adult Osteosclerotic Metaphyseal Dysplasia With Progressive Osteonecrosis of the Jaws and Abnormal Bone Resorption Pattern Due to a LRRK1 Splice Site Mutation.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: October 16, 2019
Four novel mutations in EFNB1 in Indian patients with craniofrontonasal syndrome.
Journal: Journal of human genetics
Published: February 18, 2019
Last Updated: 09/26/2026