Daniela Vandresen Pillonetto (Daniela V Pilonetto)

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 3

Top Topics

Patient Reported Outcomes

Autism Spectrum Disorder

Ejection Fraction

Top Venues

International journal of laboratory hematology

Molecular genetics & genomic medicine

Universidade Federal do Paraná Hospital de Clínicas

Universidade Federal do Paraná (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Universidade Federal do Paraná Hospital de Clínicas

Brazil

Bioquímica :: Laboratório de Imunogenética

Education History

Universidade Federal do Paraná

Brazil

PHD :: Clinica Médica

Universidade Federal do Paraná

Brazil

MSC :: Clinica Médica

Publications

Camila Oliveira Pereira, Daniela Vandresen Pillonetto, Tamara Borgonovo, Carmen Lúcia Kuniyoshi Rebelatto, Miriam Lacerda Barbosa, Maria Cristina Finger, Samantha Nichele, Joanna Trennepohl, Gisele Loth, Carmem Maria Sales Bonfim
Somatic mosaicism in patients with Fanconi anaemia: Proposal of alternative tissue for inconclusive diagnoses. International journal of laboratory hematology 44 (5) (2022)
Daniela Vandresen Pillonetto, Bruno Zagonel Piovezan, Samantha Nichele, Alberto Cardoso Martins Lima, Ricardo Pasquini, Noemi Farah Pereira, Carmem Maria Sales Bonfim
Investigation of mutations in Fanconi anemia genes and malignancy predisposition in Brazilian patients. International journal of laboratory hematology (2022)
Daniela Vandresen Pillonetto, Noemi F Pereira, Carmem M S Bonfim, Lisandro L Ribeiro, Marco A Bitencourt, Lianne Kerkhoven, Karijn Floor, Najim Ameziane, Hans Joenje, Johan J P Gille, Ricardo Pasquini
A strategy for molecular diagnostics of Fanconi anemia in Brazilian patients. Molecular genetics & genomic medicine 5 (4) (2017)