Moreira-Filho CA - Search Results

1

Persistence of Müllerian remnants in complete androgen insensitivity syndrome.

Damiani D, Mascolli MA, Almeida MJ, Jaubert F, Fellous M, Dichtchekenian V, Tobo PR, Moreira-Filho CA, Setian N. Damiani D, et al. J Pediatr Endocrinol Metab. 2002 Nov-Dec;15(9):1553-6. doi: 10.1515/jpem.2002.15.9.1553. J Pediatr Endocrinol Metab. 2002. PMID: 12503865

2

Blood leukocyte transcriptional modules and differentially expressed genes associated with disease severity and age in COVID-19 patients.

Bando SY, Bertonha FB, Vieira SE, de Oliveira DBL, Chalup VN, Durigon EL, Palmeira P, Curi ACP, Faria CS, Antonangelo L, Lauterbach GDP, Regalio FA, Cesar RM Jr, Moreira-Filho CA. Bando SY, et al. Among authors: moreira filho ca. Sci Rep. 2023 Jan 17;13(1):898. doi: 10.1038/s41598-023-28227-6. Sci Rep. 2023. PMID: 36650374 Free PMC article.

3

Gonadal agenesis in XX and XY sisters: evidence for the involvement of an autosomal gene.

Mendonça BB, Barbosa AS, Arnhold IJ, McElreavey K, Fellous M, Moreira-Filho CA. Mendonça BB, et al. Am J Med Genet. 1994 Aug 1;52(1):39-43. doi: 10.1002/ajmg.1320520108. Am J Med Genet. 1994. PMID: 7977459

4

The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor.

Barbosa AS, Hadjiathanasiou CG, Theodoridis C, Papathanasiou A, Tar A, Merksz M, Györvári B, Sultan C, Dumas R, Jaubert F, Niaudet P, Moreira-Filho CA, Cotinot C, Fellous M. Barbosa AS, et al. Hum Mutat. 1999;13(2):146-53. doi: 10.1002/(SICI)1098-1004(1999)13:2<146::AID-HUMU7>3.0.CO;2-I. Hum Mutat. 1999. PMID: 10094551

5

Ullrich-Turner syndrome: relevance of searching for Y chromosome fragments.

Damiani D, Guedes DR, Fellous M, Barbaux S, McElreavey K, Kalil J, Goldberg AC, Moreira-Filho CA, Barbosa A, Della Manna T, Dichtchekenian V, Setian N. Damiani D, et al. J Pediatr Endocrinol Metab. 1999 Nov-Dec;12(6):827-31. doi: 10.1515/jpem.1999.12.6.827. J Pediatr Endocrinol Metab. 1999. PMID: 10614539

6

Absence of mutations involving the LIM homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis.

Ottolenghi C, Moreira-Filho C, Mendonça BB, Barbieri M, Fellous M, Berkovitz GD, McElreavey K. Ottolenghi C, et al. J Clin Endocrinol Metab. 2001 Jun;86(6):2465-9. doi: 10.1210/jcem.86.6.7539. J Clin Endocrinol Metab. 2001. PMID: 11397841

7

Mutation analysis of CACNA1A and ATP1A2 genes in Brazilian FHM families.

Lopes LR, Peres MF, Vanmolkot KR, Tobo PR, Zukerman E, Frants RR, van den Maagdenberg AM, Moreira-Filho CA. Lopes LR, et al. Arq Neuropsiquiatr. 2006 Sep;64(3A):549-52. doi: 10.1590/s0004-282x2006000400001. Arq Neuropsiquiatr. 2006. PMID: 17119788 Free article.

8

Characterization of bovine transcripts preferentially expressed in testis and with a putative role in spermatogenesis.

Alves BC, Tobo PR, Rodrigues R, Ruiz JC, de Lima VF, Moreira-Filho CA. Alves BC, et al. Theriogenology. 2011 Oct 1;76(6):991-8. doi: 10.1016/j.theriogenology.2011.04.027. Epub 2011 Jun 12. Theriogenology. 2011. PMID: 21664671 Free article.

9

Mesenchymal stem cells from umbilical cord blood: parameters for isolation, characterization and adipogenic differentiation.

Sibov TT, Severino P, Marti LC, Pavon LF, Oliveira DM, Tobo PR, Campos AH, Paes AT, Amaro E Jr, F Gamarra L, Moreira-Filho CA. Sibov TT, et al. Cytotechnology. 2012 Oct;64(5):511-21. doi: 10.1007/s10616-012-9428-3. Epub 2012 Feb 12. Cytotechnology. 2012. PMID: 22328147 Free PMC article.

10

Normal expression of the serologically defined H-Y antigen in Leydig cell hypoplasia.

Arnhold IJ, Mendonça BB, Bisi H, Russo FO, Nicolau W, Bloise W, Moreira-Filho CA. Arnhold IJ, et al. J Urol. 1988 Dec;140(6):1549-52. doi: 10.1016/s0022-5347(17)42104-5. J Urol. 1988. PMID: 3193536

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