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Zeitz, Christina
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1

Genetic findings of inherited retinal diseases in France:

Zeitz, Christina ; Audo, Isabelle
Acta Ophthalmologica.  102 (2024)  S279 - p. , 2024
Link: https://doi.org/10.1111/..
 
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2

RDH5 and RLBP1-Associated Inherited Retinal Diseases: Refin..:

Bianco, Lorenzo ; Antropoli, Alessio ; Benadji, Amine...
American Journal of Ophthalmology.  267 (2024)  - p. 160-171 , 2024
Link: https://doi.org/10.1016/..
 
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3

Extensive Macular Atrophy with Pseudodrusen-like appearance:

Antropoli, Alessio ; Bianco, Lorenzo ; Condroyer, Christel...
Ophthalmology.  , 2024
Link: https://doi.org/10.1016/..
 
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4

Do differentially expressed genes explain high myopia in co..:

Zeitz, Christina ; Roger, Jerome E. ; Michiels, Christelle...
Acta Ophthalmologica.  102 (2024)  S279 - p. , 2024
Link: https://doi.org/10.1111/..
 
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5

DRD2 activation inhibits choroidal neovascularization in pa..:

Mathis, Thibaud ; Baudin, Florian ; Mariet, Anne-Sophie...
Journal of Clinical Investigation.  , 2024
Link: https://doi.org/10.1172/..
 
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6

Validation of Nanopore long-read sequencing to resolve RPGR..:

Vaché, Christel ; Faugère, Valérie ; Baux, David...
European Journal of Human Genetics.  , 2024
Link: https://doi.org/10.1038/..
 
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7

Variants in UBAP1L lead to autosomal recessive rod-cone and..:

Zeitz, Christina ; Navarro, Julien ; Azizzadeh Pormehr, Leila...
Genetics in Medicine.  26 (2024)  6 - p. 101081 , 2024
Link: https://doi.org/10.1016/..
 
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8

The importance of precisely phenotyping patients with high ..:

Audo, Isabelle ; Zeitz, Christina
Acta Ophthalmologica.  102 (2024)  S279 - p. , 2024
Link: https://doi.org/10.1111/..
 
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9

Genetic Testing of Patients with Inherited Retinal Diseases..:

Calzetti, Giacomo ; Schwarzwälder, Kerstin ; Ottonelli, Giorgia...
Ophthalmic Research.  , 2024
Link: https://doi.org/10.1159/..
 
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10

Shedding light on myopia by studying complete congenital st..:

Zeitz, Christina ; Roger, Jérome E. ; Audo, Isabelle...
Progress in Retinal and Eye Research.  93 (2023)  - p. 101155 , 2023
Link: https://doi.org/10.1016/..
 
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11

Generation of gene corrected human isogenic iPSC lines (IDV..:

Ben yacoub, Tasnim ; Letellier, Camille ; Wohlschlegel, Juliette...
Stem Cell Research.  71 (2023)  - p. 103166 , 2023
Link: https://doi.org/10.1016/..
 
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12

Retinal Phenotype of Patients withCLRN1-Associated Usher 3A..:

Smirnov, Vasily M. ; Nassisi, Marco ; Mohand-Saïd, Saddek...
Investigative Opthalmology & Visual Science.  63 (2022)  4 - p. 25 , 2022
Link: https://doi.org/10.1167/..
 
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13

Shedding light on myopia by studying complete congenital st..:

Zeitz, Christina ; Roger, Jerome E. ; Michiels, Christelle...
Acta Ophthalmologica.  100 (2022)  S275 - p. , 2022
Link: https://doi.org/10.1111/..
 
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14

The research output of rod-cone dystrophy genetics:

Jaffal, Lama ; Mrad, Zamzam ; Ibrahim, Mariam...
Orphanet Journal of Rare Diseases.  17 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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15

Establishment and measurement of myopia in mice with ON‐bip..:

Baptiste, Wilmet ; Robert, Duvoisin ; Jacques, Callebert...
Acta Ophthalmologica.  100 (2022)  S275 - p. , 2022
Link: https://doi.org/10.1111/..
 
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