Optical Coherence Tomography Evolution in a Case of X-Linked Juvenile Retinoschisis: 15 Years of Follow-Up
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
Optical Coherence Tomography Evolution in a Case of X-Linked Juvenile Retinoschisis: 15 Years of Follow-Up ; volume:8 ; number:3 ; year:2017 ; pages:459-464
Case reports in ophthalmology ; 8, Heft 3 (2017), 459-464
- Urheber
-
Chatziralli, Irini
Theodossiadis, George
Brouzas, Dimitrios
Emfietzoglou, Ioannis
Theodossiadis, Panagiotis
- DOI
-
10.1159/000480069
- URN
-
urn:nbn:de:101:1-2018053114330601206732
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:31 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Chatziralli, Irini
- Theodossiadis, George
- Brouzas, Dimitrios
- Emfietzoglou, Ioannis
- Theodossiadis, Panagiotis
Ähnliche Objekte (12)
Easily misdiagnosed X-linked adrenoleukodystrophy
X-linked disorders with cerebellar dysgenesis
Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study
X-linked SCID with a rare mutation
X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management
X-Linked Retinitis Pigmentosa Gene Therapy: Preclinical Aspects
X-linked Hyper-IgM Syndrome with Bronchiectasis
Molecular genetic mechanisms surrounding x-linked Dystonia-Parkinsonism
Germline mosaicism in X-linked periventricular nodular heterotopia
Sporadic Case of Heterozygous X-Linked Alport Syndrome
X-linked congenital adrenal hypoplasia: a case presentation
Optimising Gene Therapy for X-linked Retinitis Pigmentosa
Easily misdiagnosed X-linked adrenoleukodystrophy
X-linked disorders with cerebellar dysgenesis
Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study
X-linked SCID with a rare mutation
X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management
X-Linked Retinitis Pigmentosa Gene Therapy: Preclinical Aspects
X-linked Hyper-IgM Syndrome with Bronchiectasis
Molecular genetic mechanisms surrounding x-linked Dystonia-Parkinsonism
Germline mosaicism in X-linked periventricular nodular heterotopia
Sporadic Case of Heterozygous X-Linked Alport Syndrome
X-linked congenital adrenal hypoplasia: a case presentation
Optimising Gene Therapy for X-linked Retinitis Pigmentosa
Easily misdiagnosed X-linked adrenoleukodystrophy
X-linked disorders with cerebellar dysgenesis
Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study
X-linked SCID with a rare mutation
X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management
X-Linked Retinitis Pigmentosa Gene Therapy: Preclinical Aspects
X-linked Hyper-IgM Syndrome with Bronchiectasis
Molecular genetic mechanisms surrounding x-linked Dystonia-Parkinsonism
Germline mosaicism in X-linked periventricular nodular heterotopia
Sporadic Case of Heterozygous X-Linked Alport Syndrome
X-linked congenital adrenal hypoplasia: a case presentation