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El Shamieh, Said
156  Ergebnisse:
Personensuche X
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1

Genotype-phenotype associations in CRB1 bi-allelic patients..:

Daher, Ahmad ; Banjak, Malak ; Noureldine, Jinane..
BMC Ophthalmology.  24 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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2

ABCA4-related retinopathies in Lebanon:

Ibrahim, Mariam ; Jaffal, Lama ; Assi, Alexandre..
Heliyon.  10 (2024)  9 - p. e30304 , 2024
Link: https://doi.org/10.1016/..
 
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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

The genetic landscape of inherited retinal dystrophies in A..:

Jaffal, Lama ; Joumaa, Hawraa ; Noureldine, Jinane...
BMC Medical Genomics.  16 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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5

Analysis of rod-cone dystrophy genes reveals unique mutatio..:

El Shamieh, Said ; Jaffal, Lama ; Ibrahim, Mariam
doi:10.1136/bmjos-2022-100291.  , 2023
Link: https://zenodo.org/recor..
 
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6

Genotype-phenotype associations in CRB1 bi-allelic patients..:

El Shamieh, Said
https://zenodo.org/communities/dryad.  , 2023
Link: https://zenodo.org/recor..
 
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7

The genetic landscape of inherited retinal dystrophies in A..:

Lama Jaffal ; Hawraa Joumaa ; Jinane Noureldine...
https://doi.org/10.1186/s12920-023-01518-7.  , 2023
Link: https://doi.org/10.1186/..
 
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8

The genetic landscape of inherited retinal dystrophies in A..:

Jaffal, Lama ; Joumaa, Hawraa ; Noureldine, Jinane...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10150479/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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9

Genetics of Inherited Retinal Diseases in Understudied Ethn..:

Maltese, Paolo Enrico ; Colombo, Leonardo ; Martella, Salvatore...
Frontiers in Genetics.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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10

Vitamin D Related Gene Polymorphisms and Cholesterol Levels..:

Fakhoury, Hana M. A. ; El Shamieh, Said ; Rifai, Amru..
Journal of Cardiovascular Development and Disease.  9 (2022)  4 - p. 102 , 2022
Link: https://doi.org/10.3390/..
 
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11

Novel Missense and Splice Site Mutations in USH2A, CDH23, P..:

Jaffal, Lama ; Akhdar, Hanane ; Joumaa, Hawraa...
Frontiers in Genetics.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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12

Editorial: The genetics of inherited retinal diseases in un..:

El Shamieh, Said ; Maltese, Paolo Enrico
Frontiers in Genetics.  13 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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13

Analysis of rod-cone dystrophy genes reveals unique mutatio..:

Jaffal, Lama ; Ibrahim, Mariam ; El Shamieh, Said
BMJ Open Science.  6 (2022)  1 - p. , 2022
Link: https://doi.org/10.1136/..
 
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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

Vitamin D Related Gene Polymorphisms and Cholesterol Levels..:

Hana M. A. Fakhoury ; Said El Shamieh ; Amru Rifai..
https://dx.doi.org/10.3390/jcdd9040102.  , 2022
Link: https://doi.org/10.3390/..
 
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