Non-invasive assessment of retinal alterations in mouse models of infantile and juvenile neuronal ceroid lipofuscinosis by spectral domain optical coherence tomography
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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In: Acta Neuropathologica Communications 2014, 2:54. doi:10.1186/2051-5960-2-54
- Keyword
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Augenheilkunde
Augenkrankheit
- Event
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Veröffentlichung
- (where)
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Würzburg
- (who)
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Universität Würzburg
- (when)
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2015
- Creator
- URN
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urn:nbn:de:bvb:20-opus-110566
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:47 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
- Groh, Janos
- Stadler, David
- Buttmann, Mathias
- Martini, Rudolf
- Universität Würzburg
Time of origin
- 2015
Other Objects (12)
Non-invasive assessment of retinal alterations in mouse models of infantile and juvenile neuronal ceroid lipofuscinosis by spectral domain optical coherence tomography
Infantile und juvenile Geräusche
Juvenile neuronal ceroid lipofuscinosis : toponomics approach to identifying new drug targets
Identification of disease modulating compounds in juvenile neuronal ceroid lipofuscinosis (JNCL)
Retinal degeneration and immunomodulation in juvenile Neuronal Ceroid Lipofuscinosis (jNCL) mice
Presymptomatic treatment of classic late-infantile neuronal ceroid lipofuscinosis with cerliponase alfa
Compromised astrocyte function and survival negatively impact neurons in infantile neuronal ceroid lipofuscinosis
Glial cells are functionally impaired in juvenile neuronal ceroid lipofuscinosis and detrimental to neurons
Immune modulation attenuates infantile neuronal ceroid lipofuscinosis in mice before and after disease onset
Defective synaptic transmission causes disease signs in a mouse model of juvenile neuronal ceroid lipofuscinosis
Defective synaptic transmission causes disease signs in a mouse model of Juvenile Neuronal Ceroid Lipofuscinosis
CRISPR/Cas9 mediated generation of an ovine model for infantile neuronal ceroid lipofuscinosis (CLN1 disease)
Non-invasive assessment of retinal alterations in mouse models of infantile and juvenile neuronal ceroid lipofuscinosis by spectral domain optical coherence tomography
Infantile und juvenile Geräusche
Juvenile neuronal ceroid lipofuscinosis : toponomics approach to identifying new drug targets
Identification of disease modulating compounds in juvenile neuronal ceroid lipofuscinosis (JNCL)
Retinal degeneration and immunomodulation in juvenile Neuronal Ceroid Lipofuscinosis (jNCL) mice
Presymptomatic treatment of classic late-infantile neuronal ceroid lipofuscinosis with cerliponase alfa
Compromised astrocyte function and survival negatively impact neurons in infantile neuronal ceroid lipofuscinosis
Glial cells are functionally impaired in juvenile neuronal ceroid lipofuscinosis and detrimental to neurons
Immune modulation attenuates infantile neuronal ceroid lipofuscinosis in mice before and after disease onset
Defective synaptic transmission causes disease signs in a mouse model of juvenile neuronal ceroid lipofuscinosis
Defective synaptic transmission causes disease signs in a mouse model of Juvenile Neuronal Ceroid Lipofuscinosis
CRISPR/Cas9 mediated generation of an ovine model for infantile neuronal ceroid lipofuscinosis (CLN1 disease)
Non-invasive assessment of retinal alterations in mouse models of infantile and juvenile neuronal ceroid lipofuscinosis by spectral domain optical coherence tomography
Infantile und juvenile Geräusche
Juvenile neuronal ceroid lipofuscinosis : toponomics approach to identifying new drug targets
Identification of disease modulating compounds in juvenile neuronal ceroid lipofuscinosis (JNCL)
Retinal degeneration and immunomodulation in juvenile Neuronal Ceroid Lipofuscinosis (jNCL) mice
Presymptomatic treatment of classic late-infantile neuronal ceroid lipofuscinosis with cerliponase alfa
Compromised astrocyte function and survival negatively impact neurons in infantile neuronal ceroid lipofuscinosis
Glial cells are functionally impaired in juvenile neuronal ceroid lipofuscinosis and detrimental to neurons
Immune modulation attenuates infantile neuronal ceroid lipofuscinosis in mice before and after disease onset
Defective synaptic transmission causes disease signs in a mouse model of juvenile neuronal ceroid lipofuscinosis
Defective synaptic transmission causes disease signs in a mouse model of Juvenile Neuronal Ceroid Lipofuscinosis