Carlos D. De Brasi - Search Results

Year	Number of Results
2002	1
2003	1
2004	2
2005	1
2007	1
2009	1
2010	1
2011	2
2012	2
2013	2
2014	2
2015	1
2016	1
2017	1
2019	1
2020	2
2021	2
2023	2
2024	0

1

Assessment of interleukin-10 promoter variant (-1082A/G) and cytokine production in patients with hemolytic uremic syndrome.

Mongelos MA, Sosa FN, Pineda GE, Fiorentino G, Santiago A, Abelleyro MM, Rossetti LC, Exeni R, De Brasi CD, Palermo MS, Ramos MV. Mongelos MA, et al. Front Pediatr. 2023 Jun 23;11:1210158. doi: 10.3389/fped.2023.1210158. eCollection 2023. Front Pediatr. 2023. PMID: 37425258 Free PMC article.

2

Haemophilia B, severe childhood obesity and other extra-haematological features associated with similar 4Mb-deletions on Xq27: Clinical findings, molecular insights and literature update.

Radic CP, Abelleyro MM, Ziegler B, Marchione VD, Nevado J, Lapunzina P, Sciuccati G, Neme D, Rossetti LC, Bonduel M, De Brasi CD. Radic CP, et al. Among authors: de brasi cd. Haemophilia. 2023 May;29(3):844-854. doi: 10.1111/hae.14779. Epub 2023 Mar 17. Haemophilia. 2023. PMID: 36930806

3

Development of an inverse-PCR approach for characterization of the major BCR-ABL1 breakpoint sequences on genomic DNA: proof of concept.

Gutiérrez LG, Abelleyro MM, Ruiz MS, Anchordoqui MS, Freitas J, Bianchini M, De Brasi CD, Larripa IB. Gutiérrez LG, et al. Among authors: de brasi cd. Clin Chem Lab Med. 2021 Jun 23;59(12):e449-e453. doi: 10.1515/cclm-2020-1482. Print 2021 Nov 25. Clin Chem Lab Med. 2021. PMID: 34162038 No abstract available.

4

Type 2N von Willebrand disease: Is it always a recessive trait?

Woods AI, Rossetti LC, Paiva J, De Brasi CD, Romero ML, Casinelli MM, Blanco AN, Sánchez-Luceros A. Woods AI, et al. Thromb Res. 2021 Feb;198:49-51. doi: 10.1016/j.thromres.2020.11.029. Epub 2020 Nov 28. Thromb Res. 2021. PMID: 33285477 No abstract available.

5

Molecular insights into the mechanism of nonrecurrent F8 structural variants: Full breakpoint characterization and bioinformatics of DNA elements implicated in the upmost severe phenotype in hemophilia A.

Abelleyro MM, Radic CP, Marchione VD, Waisman K, Tetzlaff T, Neme D, Rossetti LC, De Brasi CD. Abelleyro MM, et al. Hum Mutat. 2020 Apr;41(4):825-836. doi: 10.1002/humu.23977. Epub 2020 Jan 16. Hum Mutat. 2020. PMID: 31898853

6

Inverse PCR to perform long-distance haplotyping: main applications to improve preimplantation genetic diagnosis in hemophilia.

Abelleyro MM, Marchione VD, Palmitelli M, Radic CP, Neme D, Larripa IB, Medina-Acosta E, De Brasi CD, Rossetti LC. Abelleyro MM, et al. Eur J Hum Genet. 2019 Apr;27(4):603-611. doi: 10.1038/s41431-018-0334-9. Epub 2019 Jan 9. Eur J Hum Genet. 2019. PMID: 30626931 Free PMC article.

7

Sphingosine kinase 1 participates in the activation, proliferation and survival of chronic lymphocytic leukemia cells.

Almejún MB, Borge M, Colado A, Elías EE, Podaza E, Risnik D, De Brasi CD, Stanganelli C, Slavutsky I, Cabrejo M, Fernández-Grecco H, Bezares RF, Cranco S, Burgos RÁ, Sánchez-Ávalos JC, Oppezzo P, Giordano M, Gamberale R. Almejún MB, et al. Haematologica. 2017 Jul;102(7):e257-e260. doi: 10.3324/haematol.2017.167353. Epub 2017 Mar 30. Haematologica. 2017. PMID: 28360148 Free PMC article. No abstract available.

8

F8 intron 22 inversions and SNP rs73563631 in unrelated families with severe haemophilia A: clinical features and gene testing implications.

Abelleyro MM, Rossetti LC, Curto Mde L, Radic CP, Marchione VD, De Brasi CD. Abelleyro MM, et al. Thromb Haemost. 2016 Mar;115(3):678-81. doi: 10.1160/TH15-08-0643. Epub 2015 Oct 22. Thromb Haemost. 2016. PMID: 26489971 No abstract available.

9

5meCpG epigenetic marks neighboring a primate-conserved core promoter short tandem repeat indicate X-chromosome inactivation.

Machado FB, Machado FB, Faria MA, Lovatel VL, Alves da Silva AF, Radic CP, De Brasi CD, Rios ÁF, de Sousa Lopes SM, da Silveira LS, Ruiz-Miranda CR, Ramos ES, Medina-Acosta E. Machado FB, et al. PLoS One. 2014 Jul 31;9(7):e103714. doi: 10.1371/journal.pone.0103714. eCollection 2014. PLoS One. 2014. PMID: 25078280 Free PMC article.

10

Improved diagnosis of the transition to JAK2 (V⁶¹⁷F) homozygosity: the key feature for predicting the evolution of myeloproliferative neoplasms.

Gonzalez MS, De Brasi CD, Bianchini M, Gargallo P, Stanganelli C, Zalcberg I, Larripa IB. Gonzalez MS, et al. PLoS One. 2014 Jan 27;9(1):e86401. doi: 10.1371/journal.pone.0086401. eCollection 2014. PLoS One. 2014. PMID: 24475114 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

22 results

Results by year

Search Page

Filters

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

Search Results

22 results

Results by year