Experienced in X-Linked Juvenile Retinoschisis

Birgit Lorenz

Giessen, HE, DE 
Experienced in X-Linked Juvenile Retinoschisis
Giessen, HE, DE 
OverviewLocationsClinical Research

Overview

Birgit Lorenz practices in Giessen, Germany. Ms. Lorenz is rated as an Experienced expert by MediFind in the treatment of X-Linked Juvenile Retinoschisis. Her top areas of expertise are Late-Onset Retinal Degeneration, X-Linked Infantile Nystagmus, Retinopathy Pigmentary Mental Retardation, Vitrectomy, and Cataract Removal.

Her clinical research consists of co-authoring 170 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years.

Gender
Female

Locations

Giessen, HE, Germany
Other Locations
Bonn, NW, Germany
Darmstadt, HE 64291, Germany
Hamburg, HH, Germany
Juelich, NW 52425, Germany

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.

2 Clinical Trials

Natural History Study of CEP290-Related Retinal Degeneration
Natural History Study of CEP290-Related Retinal Degeneration
Enrollment Status: Completed
Publish Date: May 19, 2022
Double-masked, Randomized, Controlled, Multiple-dose Study to Evaluate Efficacy, Safety, Tolerability and Syst. Exposure of QR-110 in Leber's Congenital Amaurosis (LCA) Due to c.2991+1655A>G Mutation (p.Cys998X) in the CEP290 Gene
Double-masked, Randomized, Controlled, Multiple-dose Study to Evaluate Efficacy, Safety, Tolerability and Syst. Exposure of QR-110 in Leber's Congenital Amaurosis (LCA) Due to c.2991+1655A>G Mutation (p.Cys998X) in the CEP290 Gene
Enrollment Status: Active_not_recruiting
Publish Date: March 17, 2022
Intervention Type: Other, Drug
Study Phase: Phase 2/Phase 3
View 1 Less Clinical Trial

170 Total Publications

Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations.
Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations.
Journal: medRxiv : the preprint server for health sciences
Published: July 09, 2025

Areas of Expertise

MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.

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