Zobrazeno 1 - 8
of 8
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
Autor:
Aghayeva, Fidan A.1,2 (AUTHOR), Schuster, Alexander K.1 (AUTHOR), Diel, Heidi1 (AUTHOR), Chronopoulos, Panagiotis1 (AUTHOR), Wagner, Felix M.1 (AUTHOR), Grehn, Franz1,3 (AUTHOR), Pirlich, Nina4 (AUTHOR), Schweiger, Susann5 (AUTHOR), Pfeiffer, Norbert1 (AUTHOR), Hoffmann, Esther M.1 (AUTHOR) ehoffman@uni-mainz.de
Publikováno v:
BMC Research Notes. 2/10/2022, Vol. 15 Issue 1, p1-10. 10p.
Autor:
Diel, Heidi, Ding, Can, Grehn, Franz, Chronopoulos, Panagiotis, Bartsch, Oliver, Hoffmann, Esther M.
Publikováno v:
BMC Ophthalmology; 1/11/2021, Vol. 21 Issue 1, p1-5, 5p
Autor:
Stingl, Julia V.1 (AUTHOR) julia.stingl@unimedizin-mainz.de, Diederich, Stefan2 (AUTHOR) stefan.diederich@unimedizin-mainz.de, Diel, Heidi1 (AUTHOR) hdiel@students.uni-mainz.de, Schuster, Alexander K.1 (AUTHOR) alexander.schuster@uni-mainz.de, Wagner, Felix M.1 (AUTHOR) felix.wagner@unimedizin-mainz.de, Chronopoulos, Panagiotis1 (AUTHOR) panagiotis.chronopoulos@unimedizin-mainz.de, Aghayeva, Fidan1,3 (AUTHOR) dr.aghayeva@gmail.com, Grehn, Franz1 (AUTHOR) Grehn_F@ukw.de, Winter, Jennifer2 (AUTHOR) jennifer.winter@unimedizin-mainz.de, Schweiger, Susann2 (AUTHOR) susann.schweiger@unimedizin-mainz.de, Hoffmann, Esther M.1 (AUTHOR) ehoffman@uni-mainz.de
Publikováno v:
Journal of Clinical Medicine. Jan2022, Vol. 11 Issue 1, p16. 1p.