Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Heidi Diel"'
Autor:
Fidan A. Aghayeva, Alexander K. Schuster, Heidi Diel, Panagiotis Chronopoulos, Felix M. Wagner, Franz Grehn, Nina Pirlich, Susann Schweiger, Norbert Pfeiffer, Esther M. Hoffmann
Publikováno v:
BMC Research Notes, Vol 15, Iss 1, Pp 1-10 (2022)
Abstract Objective The aim of this prospective pilot study is to establish an initial database to register patients diagnosed with different types of childhood glaucoma and the set-up of a national registry for childhood glaucoma (ReCG) in Germany. 2
Externí odkaz:
https://doaj.org/article/836cfc6dbb7948f5b75ce3aa8ffeb8e3
Autor:
Heidi Diel, Can Ding, Franz Grehn, Panagiotis Chronopoulos, Oliver Bartsch, Esther M. Hoffmann
Publikováno v:
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-5 (2021)
Abstract Background Severe congenital ophthalmological malformations and glaucoma might be an important occasional feature in patients with Coffin-Siris syndrome (CSS), especially Coffin-Siris syndrome 9 (CSS9, OMIM #615866) caused by SOX11 mutation.
Externí odkaz:
https://doaj.org/article/a78cb162550747a784acebe72e1d319c
Autor:
Heidi Diel, Can Ding, Franz Grehn, Panagiotis Chronopoulos, Oliver Bartsch, Esther M. Hoffmann
Publikováno v:
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-1 (2021)
An amendment to this paper has been published and can be accessed via the original article.
Externí odkaz:
https://doaj.org/article/d4c451f303ae4abf93d050a2ff5cdff5
Autor:
Julia V. Stingl, Stefan Diederich, Heidi Diel, Alexander K. Schuster, Felix M. Wagner, Panagiotis Chronopoulos, Fidan Aghayeva, Franz Grehn, Jennifer Winter, Susann Schweiger, Esther M. Hoffmann
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine; Volume 11; Issue 1; Pages: 16
Journal of Clinical Medicine, Vol 11, Iss 16, p 16 (2022)
Journal of Clinical Medicine; Volume 11; Issue 1; Pages: 16
Journal of Clinical Medicine, Vol 11, Iss 16, p 16 (2022)
Childhood glaucoma is a heterogeneous disease and can be associated with various genetic alterations. The aim of this study was to report first results of the phenotype–genotype relationship in a German childhood glaucoma cohort. Forty-nine eyes of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e6efd67c756bcd8b48b99d2ea341196
http://europepmc.org/articles/PMC8745723
http://europepmc.org/articles/PMC8745723
Autor:
Panagiotis Chronopoulos, Esther M. Hoffmann, Franz Grehn, Heidi Diel, Can Ding, Oliver Bartsch
Publikováno v:
BMC Ophthalmology
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-1 (2021)
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-1 (2021)
Severe congenital ophthalmological malformations and glaucoma might be an important occasional feature in patients with Coffin-Siris syndrome (CSS), especially Coffin-Siris syndrome 9 (CSS9, OMIM #615866) caused by SOX11 mutation. Recently, primary (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a36ccaeb6e667b0a74b009aee74f0e75
https://doi.org/10.1186/s12886-021-01821-w
https://doi.org/10.1186/s12886-021-01821-w