Markus N. Preising - Klinik und Poliklinik für Augenheilkunde, Justus Liebig-Universität Gießen

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Single Center Experience with Voretigene Neparvovec Gene Augmentation Therapy in RPE65 Mutation–Associated Inherited Retinal Degeneration in a Clinical Setting

Birgit Lorenz,Sandrine H. Kuenzel,Markus N. Preising,Johanna P. Scholz,Petrus Chang,Frank G. Holz,Philipp Herrmann

OPHTHALMOLOGY（2024）

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Characterising the Refractive Error in Paediatric Patients with Congenital Stationary Night Blindness: a Multicentre Study

Austin D. Igelman, Elizabeth White,Alaa Tayyib,Lesley Everett,Ajoy Vincent,Elise Heon,Christina Zeitz,Michel Michaelides,Omar A. Mahroo,Mohamed Katta,Andrew Webster,Markus Preising,Birgit Lorenz,Samer Khateb,Eyal Banin, Dror Sharon, Shahar Luski,Filip Van Den Broeck,Bart Peter Leroy,Elfride De Baere,Sophie Walraedt,Katarina Stingl,Laura Kuehlewein,Susanne Kohl,Milda Reith,Anne Fulton,Aparna Raghuram,Isabelle Meunier,Helene Dollfus,Tomas S. Aleman,Emma C. Bedoukian,Erin C. O'Neil,Emily Krauss,Andrea Vincent,Charlotte Jordan,Alessandro Iannaccone,Parveen Sen,Srilekha Sundaramurthy,Soumittra Nagasamy,Irina Balikova,Ingele Casteels,Shyamanga Borooah,Shaden Yassin,Aaron Nagiel,Hillary Schwartz,Xavier Zanlonghi,Irene Gottlob,Rebecca J. Mclean,Francis L. Munier, Andrew Stephenson,Robert Sisk,Robert Koenekoop,Lorri B. Wilson,Douglas Fredrick,Dongseok Choi,Paul Yang,Mark Edward Pennesi

BRITISH JOURNAL OF OPHTHALMOLOGY (2024)

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Longitudinal characterization of chorioretinal atrophies after subretinal gene augmentation therapy with Voretigene Neparvovec in RPE65-mediated retinal degeneration

Sandrine Kuenzel,Marlene Sassmannshausen,Josua Sassen,Markus Preising,Frank Holz,Birgit Lorenz,Philipp Herrmann

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCEno. 8 (2023)

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Taurin supplementation in two brothers with a homozygous mutation in SLC6A6

Markus N. Preising,Kerstin Holve, Sandra Schuetz,Borros Arneth,Christian Jux,Andreas Hahn,Christoph Friedburg

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCEno. 8 (2023)

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Functional benefits of subretinal gene augmentation therapy with Voretigene Neparvovec for inherited retinal disease associated with biallelic mutations in RPE65

Birgit Lorenz,Markus N. Preising,Johanna Pauline Scholz,Sandrine H. Kuenzel,Philipp Herrmann,Frank G. Holz

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCEno. 8 (2023)

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Multimodal widefield imaging for postoperative monitoring in patients treated with voretigene neparvovec

Philipp Herrmann,Birgit Lorenz,Johanna Pauline Scholz,Ralf Brinken,Markus N. Preising, Kristina Kupper, Naike Cavriani,Laura Wirtz,Frank G. Holz

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE（2022）

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Biallelic Mutations in L-dopachrome Tautomerase (DCT) Cause Infantile Nystagmus and Oculocutaneous Albinism

Volk Alexander E.,Hedergott Andrea,Preising Markus,Rading Sebastian,Fricke Julia,Herkenrath Peter,Nürnberg Peter,Altmüller Janine,von Ameln Simon, University Hospital of Bonn,Neugebauer Antje,Karsak Meliha,Kubisch Christian

Human Genetics（2021）

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Inherited Retinal Degenerations in the Pediatric Population

B. Lorenz,M. Preising

semanticscholar（2021）

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Inherited Retinal Degenerations in the Pediatric Population

Birgit Lorenz,Markus N. Preising

A Quick Guide to Pediatric Retinapp.183-209, (2021)

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