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Condroyer, Christel
187
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Online (187)
Mediatypes
Articles (Online) (35)
OpenAccess-fulltext (152)
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1
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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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/..
?
3
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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4
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/..
?
5
Retrospective Natural History Study of RPGR-Related Cone- a..:
Nassisi, Marco
;
De Bartolo, Giuseppe
;
Mohand-Said, Saddek
...
International Journal of Molecular Sciences. 23 (2022) 13 - p. 7189 , 2022
Link:
https://doi.org/10.3390/..
?
6
Large Benefit from Simple Things: High-Dose Vitamin A Impro..:
Smirnov, Vasily M.
;
Wilmet, Baptiste
;
Nassisi, Marco
...
International Journal of Molecular Sciences. 23 (2022) 12 - p. 6590 , 2022
Link:
https://doi.org/10.3390/..
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7
A New Mouse Model for Complete Congenital Stationary Night ..:
Orhan, Elise
;
Neuillé, Marion
;
de Sousa Dias, Miguel
...
International Journal of Molecular Sciences. 22 (2021) 9 - p. 4424 , 2021
Link:
https://doi.org/10.3390/..
?
8
Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is..:
Zeitz, Christina
;
Méjécase, Cécile
;
Michiels, Christelle
...
International Journal of Molecular Sciences. 22 (2021) 15 - p. 7875 , 2021
Link:
https://doi.org/10.3390/..
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9
Near-infrared fundus autofluorescence alterations correlate..:
Nassisi, Marco
;
Lavia, Carlo
;
Mohand-Said, Saddek
...
Scientific Reports. 11 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1038/..
?
10
CNGB1‐related rod‐cone dystrophy: A mutation review and upd..:
Nassisi, Marco
;
Smirnov, Vasily M.
;
Solis Hernandez, Cyntia
...
Human Mutation. 42 (2021) 6 - p. 641-666 , 2021
Link:
https://doi.org/10.1002/..
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11
WDR34, a candidate gene for non‐syndromic rod‐cone dystroph:
Solaguren‐Beascoa, Maria
;
Bujakowska, Kinga M.
;
Méjécase, Cécile
...
Clinical Genetics. 99 (2020) 2 - p. 298-302 , 2020
Link:
https://doi.org/10.1111/..
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12
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
The American Journal of Human Genetics. 107 (2020) 3 - p. 580 , 2020
Link:
https://doi.org/10.1016/..
?
13
Loss of Function of RIMS2 Causes a Syndromic Congenital Con..:
Mechaussier, Sabrina
;
Almoallem, Basamat
;
Zeitz, Christina
...
The American Journal of Human Genetics. 106 (2020) 6 - p. 859-871 , 2020
Link:
https://doi.org/10.1016/..
?
14
Spectrum of Disease Severity in Patients With X-Linked Reti..:
Di Iorio, Valentina
;
Karali, Marianthi
;
Melillo, Paolo
...
Investigative Opthalmology & Visual Science. 61 (2020) 14 - p. 36 , 2020
Link:
https://doi.org/10.1167/..
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15
Peripapillary Sparing With Near Infrared Autofluorescence C..:
Nassisi, Marco
;
Mohand-Saïd, Saddek
;
Andrieu, Camille
...
Investigative Opthalmology & Visual Science. 60 (2019) 15 - p. 4951 , 2019
Link:
https://doi.org/10.1167/..
1-15