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Curiati, Marco Antônio
46
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Online (46)
Mediatypes
Articles (Online) (35)
OpenAccess-fulltext (11)
Sorted by: Relevance
Sorted by: Year
?
1
General overview of urea cycle disorders (UCDs) in Brazil:
Schwartz, Ida Vanessa Doederlein
;
dos Santos, Mariana Lopes
;
Fink, Isabela Alicia
...
Molecular Genetics and Metabolism. 141 (2024) 4 - p. 108217 , 2024
Link:
https://doi.org/10.1016/..
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2
Impact of ERT and follow-up of 17 patients from the same fa..:
Stephan, Bruno de Oliveira
;
Quaio, Caio Robledo
;
Spolador, Gustavo Marquezani
...
Clinics. 77 (2022) - p. 100082 , 2022
Link:
https://doi.org/10.1016/..
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3
Leigh syndrome in a patient with a novel C12orf65 pathogeni..:
Perrone, Eduardo
;
Cavole, Thiago R.
;
Oliveira, Manuella G.
...
Genetics and Molecular Biology. 43 (2020) 2 - p. , 2020
Link:
https://doi.org/10.1590/..
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4
A New Mutation in IDS Gene Causing Hunter Syndrome: A Case ..:
Gomes, Caio Perez
;
Marins, Maryana Mara
;
Motta, Fabiana Louise
...
Frontiers in Genetics. 10 (2020) - p. , 2020
Link:
https://doi.org/10.3389/..
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5
Brain MRI findings in patients with mucopolysaccharidosis t..:
Mendes, Carmen Silvia Curiati
;
Campos, Ana Eduarda Saraiva
;
Bacon, Milagros Natahly Gutarra
...
Molecular Genetics and Metabolism. 129 (2020) 2 - p. S44-S45 , 2020
Link:
https://doi.org/10.1016/..
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6
Clinical profile of mucopolysaccharidosis type I patients f..:
Sobreira, Joselito
;
Curiati, Marco Antônio
;
Mendes, Carmen Silvia Curiati
..
Molecular Genetics and Metabolism. 126 (2019) 2 - p. S136 , 2019
Link:
https://doi.org/10.1016/..
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7
Lysosomal Acid Lipase Deficiency: Report of Five Cases acro..:
Curiati, Marco Antonio
;
Kyosen, Sandra Obikawa
;
Pereira, Vanessa Gonçalves
..
Case Reports in Pediatrics. 2018 (2018) - p. 1-5 , 2018
Link:
https://doi.org/10.1155/..
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8
The impact of the disease burden on the quality of life of ..:
Curiati, Marco Antonio
;
Kyosen, Sandra Obikawa
;
Coelho, Erika Mitie Yamashiro
...
Molecular Genetics and Metabolism. 120 (2017) 1-2 - p. S38-S39 , 2017
Link:
https://doi.org/10.1016/..
?
9
Impact of ERT and follow-up of 17 patients from the same fa..:
Stephan, Bruno de Oliveira
;
Quaio, Caio Robledo
;
Spolador, Gustavo Marquezani
...
https://www.revistas.usp.br/clinics/article/view/213520/195617. , 2022
Link:
https://www.revistas.usp..
?
10
Leigh syndrome in a patient with a novel C12orf65 pathogeni..:
Perrone, Eduardo
;
Cavole, Thiago R
;
Oliveira, Manuella G
...
10.1590/1678-4685-gmb-2018-0271. , 2020
Link:
http://www.scielo.br/sci..
?
11
A New Mutation in IDS Gene Causing Hunter Syndrome: A Case ..:
Gomes, Caio Perez
;
Marins, Maryana Mara
;
Motta, Fabiana Louise
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093562/. , 2020
Link:
http://www.ncbi.nlm.nih...
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12
Presentation_1_A New Mutation in IDS Gene Causing Hunter Sy..:
Caio Perez Gomes
;
Maryana Mara Marins
;
Fabiana Louise Motta
...
doi:10.3389/fgene.2019.01383.s001. , 2020
Link:
https://doi.org/10.3389/..
?
13
A New Mutation in IDS Gene Causing Hunter Syndrome: A Case ..:
Caio Perez Gomes
;
Maryana Mara Marins
;
Fabiana Louise Motta
...
https://www.frontiersin.org/article/10.3389/fgene.2019.01383/full. , 2020
Link:
https://doi.org/10.3389/..
?
14
Table_1_A New Mutation in IDS Gene Causing Hunter Syndrome:..:
Caio Perez Gomes
;
Maryana Mara Marins
;
Fabiana Louise Motta
...
doi:10.3389/fgene.2019.01383.s002. , 2020
Link:
https://doi.org/10.3389/..
?
15
Lysosomal Acid Lipase Deficiency: Report of Five Cases acro..:
Marco Antonio Curiati
;
Sandra Obikawa Kyosen
;
Vanessa Gonçalves Pereira
..
http://dx.doi.org/10.1155/2018/4375434. , 2018
Link:
https://doi.org/10.1155/..
1-15