Incidence of Leber hereditary optic neuropathy in 2019 in Japan: a second nationwide questionnaire survey
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1750-1172
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Incidence of Leber hereditary optic neuropathy in 2019 in Japan: a second nationwide questionnaire survey ; volume:17 ; number:1 ; day:20 ; month:8 ; year:2022 ; pages:1-6 ; date:12.2022
Orphanet journal of rare diseases ; 17, Heft 1 (20.8.2022), 1-6, 12.2022
- Creator
-
Takano, Fumio
Ueda, Kaori
Godefrooij, Daniel A.
Yamagami, Akiko
Ishikawa, Hiroto
Chuman, Hideki
Ishikawa, Hitoshi
Ikeda, Yasuhiro
Sakamoto, Taiji
Nakamura, Makoto
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13023-022-02478-4
- URN
-
urn:nbn:de:101:1-2022110921002877355981
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:31 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Takano, Fumio
- Ueda, Kaori
- Godefrooij, Daniel A.
- Yamagami, Akiko
- Ishikawa, Hiroto
- Chuman, Hideki
- Ishikawa, Hitoshi
- Ikeda, Yasuhiro
- Sakamoto, Taiji
- Nakamura, Makoto
- SpringerLink (Online service)
Other Objects (12)
Electroretinographic oscillatory potentials in Leber hereditary optic neuropathy
Developments in the Treatment of Leber Hereditary Optic Neuropathy
Leber’s hereditary optic neuropathy following unilateral painful optic neuritis: a case report
Propagation and Selectivity of Axonal Loss in Leber Hereditary Optic Neuropathy
A Rare ND5 Mutation Causing Leber’s Hereditary Optic Neuropathy
Ischemic optic neuropathy
Mitochondrial DNA mutations in Korean patients with Leber’s hereditary optic neuropathy
Macular thickness changes in a patient with Leber’s hereditary optic neuropathy
Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort study
Hereditary sensory neuropathy type I
Anterior ischemic optic neuropathy
Leber’s Hereditary Optic Neuropathy as a Promising Disease for Gene Therapy Development
Electroretinographic oscillatory potentials in Leber hereditary optic neuropathy
Developments in the Treatment of Leber Hereditary Optic Neuropathy
Leber’s hereditary optic neuropathy following unilateral painful optic neuritis: a case report
Propagation and Selectivity of Axonal Loss in Leber Hereditary Optic Neuropathy
A Rare ND5 Mutation Causing Leber’s Hereditary Optic Neuropathy
Ischemic optic neuropathy
Mitochondrial DNA mutations in Korean patients with Leber’s hereditary optic neuropathy
Macular thickness changes in a patient with Leber’s hereditary optic neuropathy
Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort study
Hereditary sensory neuropathy type I
Anterior ischemic optic neuropathy
Leber’s Hereditary Optic Neuropathy as a Promising Disease for Gene Therapy Development
Electroretinographic oscillatory potentials in Leber hereditary optic neuropathy
Developments in the Treatment of Leber Hereditary Optic Neuropathy
Leber’s hereditary optic neuropathy following unilateral painful optic neuritis: a case report
Propagation and Selectivity of Axonal Loss in Leber Hereditary Optic Neuropathy
A Rare ND5 Mutation Causing Leber’s Hereditary Optic Neuropathy
Ischemic optic neuropathy
Mitochondrial DNA mutations in Korean patients with Leber’s hereditary optic neuropathy
Macular thickness changes in a patient with Leber’s hereditary optic neuropathy
Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort study
Hereditary sensory neuropathy type I
Anterior ischemic optic neuropathy