Researcher
Daniela Vandresen Pillonetto
Universidade Federal do Paraná Hospital de Clínicas
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5 papers found
All papers authored by Daniela Vandresen Pillonetto
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2017
Daniela V. Pilonetto 
,
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
,
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
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Carmem Bonfim,
Lisandro Ribeiro,
Samantha Nichele,
Gisele Loth,
Marco Bitencourt,
Adriana Koliski,
Cilmara Kuwahara,
Ana Luiza Fabro,
Noemi F. Pereira,
Daniela Pilonetto ,
Monica Thakar,
Hans-Peter Kiem,
Kristin Page,
Ephraim J. Fuchs,
Mary Eapen
and 1 other authors
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,
Monica Thakar,
Hans-Peter Kiem,
Kristin Page,
Ephraim J. Fuchs,
Mary Eapen
and 1 other authors
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2009
Daniela Vandresen Pillonetto
TLR8-dependent TNF-(alpha) overexpression in Fanconi anemia group C cells.
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Vieira,E R.,
D. V. Pilonetto,
Pilonetto,D,
E. R. Vieira,
L. B. A. Veiga,
Veiga,L,
R. C. Ribeiro,
Ribeiro,R C.,
N. F. Pereira,
Pereira,N F.,
M. A. Bitencourt,
N. I. R. Magdalena,
Magdalena,N I. R.,
I. J. Cavalli,
Cavalli,I J.
and 3 other authors
FANCD2 Western blot as a diagnostic tool for Brazilian patients with Fanconi anemia
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2005
N. Magdalena,
D. V. Pilonetto,
R. C. Ribeiro,
M. A. Bitencourt,
Bitencourt Ma,
N. F. Pereira,
M. Jeng,
R. Pasquini,
Daniela Vandresen Pillonetto
Frequency of Fanconi anemia in Brazil and efficacy of screening for the FANCA 3788-3790del mutation
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