De L. Chauffaille

Sao Paulo, SP, Brazil

Last Updated: 09/26/2026

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Found 24 publications

Familial acute myeloid leukemia due to a novel germline CEBPA pathogenic variant - a case report.

Familial acute myeloid leukemia due to a novel germline CEBPA pathogenic variant - a case report.

Journal: Hematology, transfusion and cell therapy

Published: November 20, 2023

Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseases.

Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseases.

Journal: American journal of medical genetics. Part C, Seminars in medical genetics

Published: October 09, 2020

Reduced SLIT2 is Associated with Increased Cell Proliferation and Arsenic Trioxide Resistance in Acute Promyelocytic Leukemia.

Reduced SLIT2 is Associated with Increased Cell Proliferation and Arsenic Trioxide Resistance in Acute Promyelocytic Leukemia.

Journal: Cancers

Published: September 29, 2020

New reference values for the old erythrocyte sedimentation rate.

New reference values for the old erythrocyte sedimentation rate.

Journal: International journal of laboratory hematology

Published: September 22, 2020

NTAL is associated with treatment outcome, cell proliferation and differentiation in acute promyelocytic leukemia.

NTAL is associated with treatment outcome, cell proliferation and differentiation in acute promyelocytic leukemia.

Journal: Scientific reports

Published: January 07, 2020

Detection of somatic TP53 mutations and 17p deletions in patients with chronic lymphocytic leukemia: a review of the current methods.

Detection of somatic TP53 mutations and 17p deletions in patients with chronic lymphocytic leukemia: a review of the current methods.

Journal: Hematology, transfusion and cell therapy

Published: December 13, 2019

JAK2-mutated acute myeloid leukemia: comparison of next-generation sequencing (NGS) and single nucleotide polymorphism array (SNPa) findings between two cases.

JAK2-mutated acute myeloid leukemia: comparison of next-generation sequencing (NGS) and single nucleotide polymorphism array (SNPa) findings between two cases.

Journal: Autopsy & case reports

Published: November 23, 2018

Additional information offered by single nucleotide polymorphism array advantages in two myelodysplastic syndromes with excess blasts cases and future perspectives.

Additional information offered by single nucleotide polymorphism array advantages in two myelodysplastic syndromes with excess blasts cases and future perspectives.

Journal: Hematology, transfusion and cell therapy

Published: March 22, 2018

Mutational profiling of acute myeloid leukemia with normal cytogenetics in Brazilian patients: the value of next-generation sequencing for genomic classification.

Mutational profiling of acute myeloid leukemia with normal cytogenetics in Brazilian patients: the value of next-generation sequencing for genomic classification.

Journal: Journal of investigative medicine : the official publication of the American Federation for Clinical Research

Published: September 04, 2017

Clinical impact of BAALC expression in high-risk acute promyelocytic leukemia.

Clinical impact of BAALC expression in high-risk acute promyelocytic leukemia.

Journal: Blood advances

Published: February 16, 2017

Frequency of polycythemia in individuals with normal complete blood cell counts according to the new 2016 WHO classification of myeloid neoplasms.

Frequency of polycythemia in individuals with normal complete blood cell counts according to the new 2016 WHO classification of myeloid neoplasms.

Journal: International journal of laboratory hematology

Published: February 15, 2017

FMS-related tyrosine kinase 3 internal tandem duplication (FLT3-ITD): a villain among others.

FMS-related tyrosine kinase 3 internal tandem duplication (FLT3-ITD): a villain among others.

Journal: Revista brasileira de hematologia e hemoterapia

Published: November 23, 2016

Showing 1-12 of 24

Last Updated: 09/26/2026