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X
Sallum, Juliana M. F.
~ 100  Ergebnisse:
Personensuche X
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1

The cost of genetic diagnosis of suspected hereditary pedia..:

Neves, Luiza M. ; Pinto, Márcia ; Zin, Olivia A....
Journal of Community Genetics.  , 2024
Link: https://doi.org/10.1007/..
 
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2

Genotypic–Phenotypic Correlations of Hereditary Hyperferrit..:

Zin, Olivia A. ; Neves, Luiza M. ; Cunha, Daniela P....
International Journal of Molecular Sciences.  24 (2023)  15 - p. 11876 , 2023
Link: https://doi.org/10.3390/..
 
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3

Molecular and Clinical Characterization of CNGA3 and CNGB3 ..:

Amaral, Rebeca A. S. ; Motta, Fabiana L. ; Zin, Olivia A....
Genes.  14 (2023)  6 - p. 1296 , 2023
Link: https://doi.org/10.3390/..
 
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4

Epidemiology of Mutations in the 65-kDa Retinal Pigment Epi..:

Sallum, Juliana M. F. ; Kaur, Vinay Preet ; Shaikh, Javed...
Advances in Therapy.  39 (2022)  3 - p. 1179-1198 , 2022
Link: https://doi.org/10.1007/..
 
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5

RNA-based therapies in inherited retinal diseases:

Girach, Aniz ; Audo, Isabelle ; Birch, David G....
Therapeutic Advances in Ophthalmology.  14 (2022)  - p. 251584142211346 , 2022
Link: https://doi.org/10.1177/..
 
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6

Novel Mutation in CRYBB3 Causing Pediatric Cataract and Mic..:

Zin, Olivia A. ; Neves, Luiza M. ; Motta, Fabiana L....
Genes.  12 (2021)  7 - p. 1069 , 2021
Link: https://doi.org/10.3390/..
 
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7

Retinal Architecture in Autosomal Recessive Spastic Ataxia ..:

Rezende Filho, Flávio Moura ; Bremner, Fion ; Pedroso, José Luiz...
Movement Disorders.  36 (2021)  9 - p. 2027-2035 , 2021
Link: https://doi.org/10.1002/..
 
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8

Ophthalmological changes in hereditary spastic paraplegia a..:

de Freitas, Júlian Letícia ; Rezende Filho, Flávio Moura ; Sallum, Juliana M.F....
Journal of the Neurological Sciences.  409 (2020)  - p. 116620 , 2020
Link: https://doi.org/10.1016/..
 
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9

Genotype-Phenotype Correlations in CYP1B1-Associated Primar..:

de Melo, Mônica Barbosa ; Mandal, Anil K. ; Tavares, Ivan M....
PLOS ONE.  10 (2015)  5 - p. e0127147 , 2015
Link: https://doi.org/10.1371/..
 
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10

Familial Behr syndrome-like phenotype with autosomal domina..:

Felicio, Andre C. ; Godeiro-Junior, Clecio ; Alberto, Lucianna G....
Parkinsonism & Related Disorders.  14 (2008)  4 - p. 370-372 , 2008
Link: https://doi.org/10.1016/..
 
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11

Molecular and Clinical Characterization of CNGA3 and CNGB3 ..:

Amaral, Rebeca A. S ; Motta, Fabiana L ; Zin, Olivia A...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298554/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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12

Epidemiology of Mutations in the 65-kDa Retinal Pigment Epi..:

Sallum, Juliana M. F ; Kaur, Vinay Preet ; Shaikh, Javed...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918161/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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13

RNA-based therapies in inherited retinal diseases:

Girach, Aniz ; Audo, Isabelle ; Birch, David G...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643766/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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14

Novel Mutation in CRYBB3 Causing Pediatric Cataract and Mic..:

Zin, Olivia A ; Neves, Luiza M ; Motta, Fabiana L...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308043/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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15

HYPERAUTOFLUORESCENT RING IN AUTOIMMUNE RETINOPATHY:

LIMA, LUIZ H ; GREENBERG, JONATHAN P ; GREENSTEIN, VIVIENNE C...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC.  , 2012
Link: http://www.ncbi.nlm.nih...
 
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