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Malka, Samantha
35
results:
Search for persons
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Online (35)
Mediatypes
Articles (Online) (13)
OpenAccess-fulltext (22)
Sorted by: Relevance
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1
Increasing the diagnostic yield of childhood glaucoma cases..:
Al-Saei, Omayma
;
Malka, Samantha
;
Owen, Nicholas
...
BMC Genomics. 25 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1186/..
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2
PHYH c.678+5G>T Leads to In-Frame Exon Skipping and Is Asso..:
Daich Varela, Malena
;
Schiff, Elena
;
Malka, Samantha
...
Investigative Opthalmology & Visual Science. 65 (2024) 2 - p. 38 , 2024
Link:
https://doi.org/10.1167/..
?
3
Spectrum of Genetic Variants in the Most Common Genes Causi..:
Lin, Siying
;
Vermeirsch, Sandra
;
Pontikos, Nikolas
...
Ophthalmology Retina. 8 (2024) 7 - p. 699-709 , 2024
Link:
https://doi.org/10.1016/..
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4
Coats-like Vasculopathy in Inherited Retinal Disease:
Daich Varela, Malena
;
Conti, Giovanni Marco
;
Malka, Samantha
...
Ophthalmology. 130 (2023) 12 - p. 1327-1335 , 2023
Link:
https://doi.org/10.1016/..
?
5
Foveal Hypoplasia in CRB1-Related Retinopathies:
Rodriguez-Martinez, Ana Catalina
;
Higgins, Bethany Elora
;
Tailor-Hamblin, Vijay
...
International Journal of Molecular Sciences. 24 (2023) 18 - p. 13932 , 2023
Link:
https://doi.org/10.3390/..
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6
Prospective study of pediatric patients presenting with idi..:
Aychoua, Nancy
;
Schiff, Elena
;
Malka, Samantha
...
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
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7
Real-world clinical and molecular management of 50 prospect..:
Harding, Philippa
;
Gore, Sri
;
Malka, Samantha
...
British Journal of Ophthalmology. 107 (2022) 12 - p. 1925-1935 , 2022
Link:
https://doi.org/10.1136/..
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8
Prospective Study of the Phenotypic and Mutational Spectrum..:
Chan, Hwei Wuen
;
Schiff, Elena R.
;
Tailor, Vijay K.
...
Genes. 12 (2021) 4 - p. 508 , 2021
Link:
https://doi.org/10.3390/..
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9
Clinical Spectrum and Genetic Diagnosis of 54 Consecutive P..:
Bell, Suzannah
;
Malka, Samantha
;
Lloyd, Ian Christopher
.
Genes. 12 (2021) 2 - p. 131 , 2021
Link:
https://doi.org/10.3390/..
?
10
Practical guide to genetic screening for inherited eye dise..:
Méjécase, Cécile
;
Malka, Samantha
;
Guan, Zeyu
...
Therapeutic Advances in Ophthalmology. 12 (2020) - p. 251584142095459 , 2020
Link:
https://doi.org/10.1177/..
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11
Genetic Basis of Inherited Retinal Disease in a Molecularly..:
Pontikos, Nikolas
;
Arno, Gavin
;
Jurkute, Neringa
...
Ophthalmology. 127 (2020) 10 - p. 1384-1394 , 2020
Link:
https://doi.org/10.1016/..
?
12
Molecular diagnostic challenges for non‐retinal development..:
Jackson, Daniel
;
Malka, Samantha
;
Harding, Philippa
...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 184 (2020) 3 - p. 578-589 , 2020
Link:
https://doi.org/10.1002/..
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13
Spectrum of genetic variants in the commonest genes causing..:
Lin, Siying
;
Vermeirsch, Sandra
;
Pontikos, Nikolas
...
https://discovery.ucl.ac.uk/id/eprint/10185985/1/Pontikos_Functional%20specificity%20of%20recurrent%20inhibition%20in%20visual%20cortex_Pre-proof.pdf. , 2024
Link:
https://discovery.ucl.ac..
?
14
Foveal Hypoplasia in CRB1-Related Retinopathies:
Rodriguez-Martinez, Ana Catalina
;
Higgins, Bethany Elora
;
Tailor-Hamblin, Vijay
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531165/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
15
Real-world clinical and molecular management of 50 prospect..:
Harding, Philippa
;
Gore, Sri
;
Malka, Samantha
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10715525/. , 2023
Link:
http://www.ncbi.nlm.nih...
1-15