Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Diel, Heidi"'
Autor:
Aghayeva, Fidan A., Schuster, Alexander K., Diel, Heidi, Chronopoulos, Panagiotis, Wagner, Felix M., Grehn, Franz, Pirlich, Nina, Schweiger, Susann, Pfeiffer, Norbert, Hoffmann, Esther M.
Additional file 3: Figure S3. Extended general anesthesia examination form (extended GAEF). PHPV = Persistent hyperplastic primary vitreous; ROP = Retinopathy of prematurity; FEVR = Familial exudative vitreoretinopathy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::983bbbd70e2bae1e9354461853e219bf
Autor:
Aghayeva, Fidan A., Schuster, Alexander K., Diel, Heidi, Chronopoulos, Panagiotis, Wagner, Felix M., Grehn, Franz, Pirlich, Nina, Schweiger, Susann, Pfeiffer, Norbert, Hoffmann, Esther M.
Additional file 4: Table S1. Causes and genetic data of secondary childhood glaucoma in Germany.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f318b5763ff1d2701147ec03302fd59
Autor:
Aghayeva, Fidan A., Schuster, Alexander K., Diel, Heidi, Chronopoulos, Panagiotis, Wagner, Felix M., Grehn, Franz, Pirlich, Nina, Schweiger, Susann, Pfeiffer, Norbert, Hoffmann, Esther M.
Additional file 2: Figure S2. Patient���s gestational history questionnaire (general information about pregnancy and details of delivery).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ef8971fed925b0707e69bf7d5144f0c
Autor:
Aghayeva, Fidan A., Schuster, Alexander K., Diel, Heidi, Chronopoulos, Panagiotis, Wagner, Felix M., Grehn, Franz, Pirlich, Nina, Schweiger, Susann, Pfeiffer, Norbert, Hoffmann, Esther M.
Additional file 1: Figure S1. Medical history form with medical and social history of the child.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7454458bebc2e70802722e699452d46c
Akademický článek
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Autor:
Diel, Heidi, Ding, Can, Grehn, Franz, Chronopoulos, Panagiotis, Bartsch, Oliver, Hoffmann, Esther M.
Additional file 3. Clinical features of the patient. Image A: Frontal view at the age of 4 months. Note microcephaly, sparse hair, arched eyebrows, abnormal eyes, depressed nasal bridge, short nose, and low-set ears. Image B: Full view aged 1 year an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62abcccdba733bc98a5c81850f0c5906
Autor:
Diel, Heidi, Ding, Can, Grehn, Franz, Chronopoulos, Panagiotis, Bartsch, Oliver, Hoffmann, Esther M.
Publikováno v:
BMC Ophthalmology
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-5 (2021)
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-5 (2021)
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. Recently
Autor:
Diel, Heidi, Ding, Can, Grehn, Franz, Chronopoulos, Panagiotis, Bartsch, Oliver, Hoffmann, Esther M.
Additional file 2. Ocular ultrasound. Exploration of both eyes under general anaesthesia showed fully attached retinae and normal vitreous bodies. Image A: Right eye. Image B: Left eye.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd71e6281acc0c525845df960d829142
Autor:
Diel, Heidi, Ding, Can, Grehn, Franz, Chronopoulos, Panagiotis, Bartsch, Oliver, Hoffmann, Esther M.
Additional file 1. Exploration of the eyes under general anaesthesia at the age of 2 years and 11 months. Image A: Right eye - microcornea, small central corneal opacity (marked with an arrow), and mild conjunctival vasculation of the cornea. Image B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c437bf67398524b24ea58d8b38505d6
Autor:
Aghayeva, Fidan A., Schuster, Alexander K., Diel, Heidi, Chronopoulos, Panagiotis, Wagner, Felix M., Grehn, Franz, Pirlich, Nina, Schweiger, Susann, Pfeiffer, Norbert, Hoffmann, Esther M.
Publikováno v:
BMC Research Notes; 2/10/2022, Vol. 15 Issue 1, p1-10, 10p