Marcia T. Schramm

Rio De Janeiro, RJ, Brazil

Last Updated: 09/26/2026

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Found 9 publications

Comments on "Mode of delivery and the risk of lymphoblastic leukemia during childhood-A Swedish population-based cohort study".

Comments on "Mode of delivery and the risk of lymphoblastic leukemia during childhood-A Swedish population-based cohort study".

Journal: International journal of cancer

Published: September 01, 2025

Long-Term Outcomes of Childhood Acute Lymphocytic Leukemia Treated with Adapted Berlin-Frankfurt-Münster (BFM) Protocols: A Multicentric Analysis from a Developing Country.

Long-Term Outcomes of Childhood Acute Lymphocytic Leukemia Treated with Adapted Berlin-Frankfurt-Münster (BFM) Protocols: A Multicentric Analysis from a Developing Country.

Journal: Cancers

Published: July 09, 2024

Characterisation of cells markers associated with IKZF1plus in BCP-ALL.

Characterisation of cells markers associated with IKZF1plus in BCP-ALL.

Journal: Translational oncology

Published: June 22, 2024

The recombinome of IKZF1 deletions in B-cell precursor ALL.

The recombinome of IKZF1 deletions in B-cell precursor ALL.

Journal: Leukemia

Published: March 15, 2023

Pharmacogenetic testing for thiopurine drugs in Brazilian acute lymphoblastic leukemia patients.

Pharmacogenetic testing for thiopurine drugs in Brazilian acute lymphoblastic leukemia patients.

Journal: Clinics (Sao Paulo, Brazil)

Published: January 13, 2023

IKZF1 deletions associate with CRLF2 overexpression leading to a poor prognosis in B-cell precursor acute lymphoblastic leukaemia.

IKZF1 deletions associate with CRLF2 overexpression leading to a poor prognosis in B-cell precursor acute lymphoblastic leukaemia.

Journal: Translational oncology

Published: August 09, 2021

Myelodysplastic syndrome with clonal karyotype evolution associated with trisomy 8 and ASXL1 mutation in well-controlled HIV patient: Case report and literature review.

Myelodysplastic syndrome with clonal karyotype evolution associated with trisomy 8 and ASXL1 mutation in well-controlled HIV patient: Case report and literature review.

Journal: EJHaem

Published: April 23, 2020

IKZF1 deletion and co-occurrence with other aberrations in a child with chronic myeloid leukemia progressing to acute lymphoblastic leukemia.

IKZF1 deletion and co-occurrence with other aberrations in a child with chronic myeloid leukemia progressing to acute lymphoblastic leukemia.

Journal: Pediatric blood & cancer

Published: August 02, 2018

An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia.

An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia.

Journal: Molecular cytogenetics

Published: May 11, 2018

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Last Updated: 09/26/2026