Rigatti B - Search Results

1

Nivolumab in Patients with Metastatic Castration-Resistant Prostate Cancer with and without DNA Repair Defects.

Isaacsson Velho P, Bastos DA, Saint'ana PT, Rigatti B, da Costa ET, Muniz DQB, Andreis F, Ferreira RDP, Giongo Pedrotti L, Maistro S, Katayama MLH, Folgueira MAAK, Morelle A, Leal A, de Castro G Jr. Isaacsson Velho P, et al. Among authors: rigatti b. Clin Cancer Res. 2024 Dec 2;30(23):5342-5352. doi: 10.1158/1078-0432.CCR-24-1595. Clin Cancer Res. 2024. PMID: 39330991 Clinical Trial.

2

Prospective monitoring of patients undergoing radiotherapy during COVID-19.

Alves DFS, Rosa DD, Finatto LB, Rigatti B, Anna PTS. Alves DFS, et al. Among authors: rigatti b. Rev Assoc Med Bras (1992). 2024 Jul 19;70(6):e20231421. doi: 10.1590/1806-9282.20231421. eCollection 2024. Rev Assoc Med Bras (1992). 2024. PMID: 39045950 Free PMC article.

3

Pulmonary embolism in patients with COVID-19 and D-dimer diagnostic value: A retrospective study.

Vivan MA, Rigatti B, da Cunha SV, Frison GC, Antoniazzi LQ, de Oliveira PHK, Oliveira JPS, Fontanari C, Seligman BGS, Seligman R. Vivan MA, et al. Among authors: rigatti b. Braz J Infect Dis. 2022 Nov-Dec;26(6):102702. doi: 10.1016/j.bjid.2022.102702. Epub 2022 Sep 2. Braz J Infect Dis. 2022. PMID: 36096159 Free PMC article.

4

A novel RPGR exon ORF15 mutation in a family with X-linked retinitis pigmentosa and Coats'-like exudative vasculopathy.

Demirci FY, Rigatti BW, Mah TS, Gorin MB. Demirci FY, et al. Among authors: rigatti bw. Am J Ophthalmol. 2006 Jan;141(1):208-10. doi: 10.1016/j.ajo.2005.07.077. Am J Ophthalmol. 2006. PMID: 16387007

5

Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15.

Demirci FY, Gupta N, Radak AL, Rigatti BW, Mah TS, Milam AH, Gorin MB. Demirci FY, et al. Among authors: rigatti bw. Am J Ophthalmol. 2005 Feb;139(2):386-8. doi: 10.1016/j.ajo.2004.08.041. Am J Ophthalmol. 2005. PMID: 15734019

6

A presumed missense mutation of RPGR causes abnormal RNA splicing with exon skipping.

Demirci FY, Radak AL, Rigatti BW, Mah TS, Gorin MB. Demirci FY, et al. Among authors: rigatti bw. Am J Ophthalmol. 2004 Sep;138(3):504-5. doi: 10.1016/j.ajo.2004.04.019. Am J Ophthalmol. 2004. PMID: 15364249

7

A novel compound heterozygous mutation in the cellular retinaldehyde-binding protein gene (RLBP1) in a patient with retinitis punctata albescens.

Demirci FY, Rigatti BW, Mah TS, Gorin MB. Demirci FY, et al. Among authors: rigatti bw. Am J Ophthalmol. 2004 Jul;138(1):171-3. doi: 10.1016/j.ajo.2004.02.060. Am J Ophthalmol. 2004. PMID: 15234312

8

Detection and assignment of mutations and minihaplotypes in human DNA using peptide mass signature genotyping (PMSG): application to the human RDS/peripherin gene.

Telmer CA, Retchless AC, Kinsey AD, Conley Y, Rigatti B, Gorin MB, Jarvik JW. Telmer CA, et al. Among authors: rigatti b. Genome Res. 2003 Aug;13(8):1944-51. doi: 10.1101/gr.995103. Genome Res. 2003. PMID: 12902384 Free PMC article.

9

Refinement of the physical location and the genomic characterization of the CRSP2 (EXLM1) gene on Xp11.4.

Demirci FY, Ramser J, White NJ, Rigatti BW, Meindl A, Lewis KF, Wen G, Gorin MB. Demirci FY, et al. Among authors: rigatti bw. DNA Seq. 2003 Apr;14(2):123-7. doi: 10.1080/1042517021000056952. DNA Seq. 2003. PMID: 12825353

10

X-linked cone-rod dystrophy (locus COD1): identification of mutations in RPGR exon ORF15.

Demirci FY, Rigatti BW, Wen G, Radak AL, Mah TS, Baic CL, Traboulsi EI, Alitalo T, Ramser J, Gorin MB. Demirci FY, et al. Among authors: rigatti bw. Am J Hum Genet. 2002 Apr;70(4):1049-53. doi: 10.1086/339620. Epub 2002 Feb 20. Am J Hum Genet. 2002. PMID: 11857109 Free PMC article.

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