All papers authored by Lamisse Mansour-Hendili
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2022
Lamisse Mansour‐Hendili 
,
Edouard Flamarion,
Marc Michel,
Caroline Morbieu,
Christine Gameiro,
Ivan Sloma ,
Bouchra Badaoui,
Luc Darnige,
Marion Camard,
Ariane Lunati‐Rozie ,
Abdelrazak Aissat,
Sihem Tarfi,
Chloé Friedrich,
Véronique Picard,
Loïc Garçon
and 9 other authors
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,
Edouard Flamarion,
Marc Michel,
Caroline Morbieu,
Christine Gameiro,
Ivan Sloma ,
Bouchra Badaoui,
Luc Darnige,
Marion Camard,
Ariane Lunati‐Rozie ,
Abdelrazak Aissat,
Sihem Tarfi,
Chloé Friedrich,
Véronique Picard,
Loïc Garçon
and 9 other authors
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2021
Lamisse Mansour‐Hendili ,
Stéphane Egée,
David Monedero‐Alonso,
Guillaume Bouyer ,
Bertrand Godeau,
Bouchra Badaoui,
Ariane Lunati ,
Clara Noizat,
Abdelrazak Aissat,
Laurent Kiger,
Chadia Mekki,
Véronique Picard,
Stéphane Moutereau,
Pascale Fanen,
Pablo Bartolucci
and 3 other authors
,
Stéphane Egée,
David Monedero‐Alonso,
Guillaume Bouyer ,
Bertrand Godeau,
Bouchra Badaoui,
Ariane Lunati ,
Clara Noizat,
Abdelrazak Aissat,
Laurent Kiger,
Chadia Mekki,
Véronique Picard,
Stéphane Moutereau,
Pascale Fanen,
Pablo Bartolucci
and 3 other authors
Multiple thrombosis in a patient with Gardos channelopathy and a new KCNN4 mutation
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Ariane Lunati ,
Arnaud Petit ,
Hélène Lapillonne,
Christine Gameiro,
Virginie Saillour,
Catherine Garel,
Diane Doummar,
Leila Qebibo,
Abdelrazak Aissat,
Pascale Fanen,
Pablo Bartolucci,
Fréderic Galactéros,
Benoit Funalot,
Lydie Burglen,
Lamisse Mansour‐Hendili
,
Arnaud Petit ,
Hélène Lapillonne,
Christine Gameiro,
Virginie Saillour,
Catherine Garel,
Diane Doummar,
Leila Qebibo,
Abdelrazak Aissat,
Pascale Fanen,
Pablo Bartolucci,
Fréderic Galactéros,
Benoit Funalot,
Lydie Burglen,
Lamisse Mansour‐Hendili
VPS4A mutation in syndromic congenital hemolytic anemia without obvious signs of dyserythropoiesis
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2020
Lamisse Mansour-Hendili ,
Abdelrazak Aissat,
Bouchra Badaoui,
Mehdi Sakka,
Christine Gameiro,
Valérie Ortonne,
Orianne Wagner-Ballon,
Serge Pissard,
Véronique Picard,
Khaldoun Ghazal,
Michel Bahuau,
Corinne Guitton,
Ziad Mansour,
Mylène Duplan,
Arnaud Petit
and 6 other authors
,
Abdelrazak Aissat,
Bouchra Badaoui,
Mehdi Sakka,
Christine Gameiro,
Valérie Ortonne,
Orianne Wagner-Ballon,
Serge Pissard,
Véronique Picard,
Khaldoun Ghazal,
Michel Bahuau,
Corinne Guitton,
Ziad Mansour,
Mylène Duplan,
Arnaud Petit
and 6 other authors
Exome sequencing for diagnosis of congenital hemolytic anemia
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