All papers authored by Lucie Heurtier
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2019
Amine Bouafia,
Sébastien Lofek,
Julie Bruneau 
,
Loïc Chentout,
Hicham Lamrini,
Amélie Trinquand,
Marie-Céline Deau ,
Lucie Heurtier ,
Véronique Meignin,
Capucine Picard ,
Elizabeth Macintyre ,
Olivier Alibeu ,
Marc Bras,
Thierry Jo Molina,
Marina Cavazzana
and 5 other authors
,
Loïc Chentout,
Hicham Lamrini,
Amélie Trinquand,
Marie-Céline Deau ,
Lucie Heurtier ,
Véronique Meignin,
Capucine Picard ,
Elizabeth Macintyre ,
Olivier Alibeu ,
Marc Bras,
Thierry Jo Molina,
Marina Cavazzana
and 5 other authors
Loss of ARHGEF1 causes a human primary antibody deficiency
Download from doi.org
2016
Elodie Elkaim,
Benedicte Neven,
Julie Bruneau ,
Kanako Mitsui-Sekinaka,
Aurelie Stanislas,
Lucie Heurtier ,
Carrie L. Lucas,
Helen Matthews,
Marie-Céline Deau,
Svetlana Sharapova,
James Curtis,
Janine Reichenbach,
Catherine Glastre,
David A. Parry,
Gururaj Arumugakani
and 28 other authors
Upload
,
Kanako Mitsui-Sekinaka,
Aurelie Stanislas,
Lucie Heurtier ,
Carrie L. Lucas,
Helen Matthews,
Marie-Céline Deau,
Svetlana Sharapova,
James Curtis,
Janine Reichenbach,
Catherine Glastre,
David A. Parry,
Gururaj Arumugakani
and 28 other authors
Upload
2015
David Buchbinder,
Jeffrey R. Stinson,
Diane J. Nugent,
Lucie Heurtier ,
Felipe Suarez,
Gauthaman Sukumar ,
Clifton L. Dalgard ,
Cécile Masson,
Mélanie Parisot ,
Yu Zhang,
Helen F. Matthews,
Helen C. Su,
Anne Durandy,
Alain Fischer,
Sven Kracker
and 1 other authors
,
Felipe Suarez,
Gauthaman Sukumar ,
Clifton L. Dalgard ,
Cécile Masson,
Mélanie Parisot ,
Yu Zhang,
Helen F. Matthews,
Helen C. Su,
Anne Durandy,
Alain Fischer,
Sven Kracker
and 1 other authors
Mild B-cell lymphocytosis in patients with a CARD11 C49Y mutation
Download from europepmc.org
2014
Marie-Céline Deau,
Pierre Frange,
Felipe Suarez,
Lucie Heurtier ,
Patrick Nitschke,
Christine Bole-Feysot,
Marina Cavazzana,
Capucine Picard ,
Anne Durandy,
Sven Kracker,
Alain Fischer
,
Patrick Nitschke,
Christine Bole-Feysot,
Marina Cavazzana,
Capucine Picard ,
Anne Durandy,
Sven Kracker,
Alain Fischer
A human immunodeficiency caused by mutations in the PIK3R1 gene
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