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Magalhães Tarantino, Roberta
79
results:
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Online (79)
Mediatypes
Articles (Online) (68)
Bookchapter (Online) (1)
OpenAccess-fulltext (10)
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?
1
Identification of the First PAX4-MODY Family Reported in Br..:
de Medeiros Abreu, Gabriella
;
de Almeida Pereira Dias Soares, Camila
;
Magalhães Tarantino, Roberta
...
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy. 13 (2020) - p. 2623-2631 , 2020
Link:
https://doi.org/10.2147/..
?
2
Identification of Variants Responsible for Monogenic Forms ..:
Abreu, Gabriella de Medeiros
;
Tarantino, Roberta Magalhães
;
da Fonseca, Ana Carolina Proença
...
Frontiers in Endocrinology. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
3
MODY probability calculator for GCK and HNF1A screening in ..:
Tarantino, Roberta Magalhães
;
Abreu, Gabriella de Medeiros
;
Fonseca, Ana Carolina Proença de
...
Archives of Endocrinology and Metabolism. , 2019
Link:
https://doi.org/10.20945..
?
4
The first case of NEUROD1‐MODY reported in Latin America:
Abreu, Gabriella de Medeiros
;
Tarantino, Roberta Magalhães
;
Cabello, Pedro Hernan
...
Molecular Genetics & Genomic Medicine. 7 (2019) 12 - p. , 2019
Link:
https://doi.org/10.1002/..
?
5
Identification of the First PAX4-MODY Family Reported in Br..:
de Medeiros Abreu, Gabriella
;
de Almeida Pereira Dias Soares, Camila
;
Magalhães Tarantino, Roberta
...
info:eu-repo/semantics/altIdentifier/doi/10.2147/DMSO.S256858. , 2020
Link:
https://www.dovepress.co..
?
6
DataSheet_1_Identification of Variants Responsible for Mono..:
Gabriella de Medeiros Abreu
;
Roberta Magalhães Tarantino
;
Ana Carolina Proença da Fonseca
...
doi:10.3389/fendo.2022.827325.s001. , 2022
Link:
https://doi.org/10.3389/..
?
7
Identification of Variants Responsible for Monogenic Forms ..:
Abreu, Gabriella de Medeiros
;
Tarantino, Roberta Magalhães
;
da Fonseca, Ana Carolina Proença
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110842/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
8
DataSheet_2_Identification of Variants Responsible for Mono..:
Gabriella de Medeiros Abreu
;
Roberta Magalhães Tarantino
;
Ana Carolina Proença da Fonseca
...
doi:10.3389/fendo.2022.827325.s002. , 2022
Link:
https://doi.org/10.3389/..
?
9
Image_1_Identification of Variants Responsible for Monogeni..:
Gabriella de Medeiros Abreu
;
Roberta Magalhães Tarantino
;
Ana Carolina Proença da Fonseca
...
doi:10.3389/fendo.2022.827325.s003. , 2022
Link:
https://doi.org/10.3389/..
?
10
Identification of Variants Responsible for Monogenic Forms ..:
Gabriella de Medeiros Abreu
;
Roberta Magalhães Tarantino
;
Ana Carolina Proença da Fonseca
...
https://www.frontiersin.org/articles/10.3389/fendo.2022.827325/full. , 2022
Link:
https://doi.org/10.3389/..
?
11
MODY probability calculator for GCK and HNF1A screening in ..:
Tarantino, Roberta Magalhães
;
Abreu, Gabriella de Medeiros
;
Fonseca, Ana Carolina Proença de
...
10.20945/2359-3997000000173. , 2020
Link:
http://www.scielo.br/sci..
?
12
MODY probability calculator for GCK and HNF1A screening in ..:
Tarantino, Roberta Magalhães
;
Abreu, Gabriella de Medeiros
;
Fonseca, Ana Carolina Proença de
...
10.20945/2359-3997000000173. , 2019
Link:
http://www.scielo.br/sci..
?
13
The first case of NEUROD1‐MODY reported in Latin America:
Gabriella de Medeiros Abreu
;
Roberta Magalhães Tarantino
;
Pedro Hernan Cabello
...
https://doi.org/10.1002/mgg3.989. , 2019
Link:
https://doi.org/10.1002/..
?
14
MODY probability calculator for GCK and HNF1A screening in ..:
Roberta Magalhães Tarantino
;
Gabriella de Medeiros Abreu
;
Ana Carolina Proença de Fonseca
...
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972019005008101&lng=en&tlng=en. ,
Link:
https://doi.org/10.20945..
?
15
PDX1-MODY: A rare missense mutation as a cause of monogenic..:
Abreu Miss, Gabriella de M.
;
Tarantino, Roberta M.
;
da Fonseca, Ana Carolina P.
...
European Journal of Medical Genetics. 64 (2021) 5 - p. 104194 , 2021
Link:
https://doi.org/10.1016/..
1-15