Publications by authors named "Chadia Mekki"

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Multiple thrombosis in a patient with Gardos channelopathy and a new KCNN4 mutation.
Lamisse Mansour-Hendili, Stéphane Egée, David Monedero-Alonso, Guillaume Bouyer, Bertrand Godeau, Chadia Mekki

Am J Hematol· September 2021

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Prenatal Ultrasound Suspicion of Cystic Fibrosis in a Multiethnic Population: Is Extensive Genotyping Needed?
Chadia Mekki, Abdel Aissat, Véronique Mirlesse, Sophie Mayer Lacrosniere, Elsa Eche

Genes (Basel)· April 2021

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Unsolved severe chronic rhinosinusitis elucidated by extensive genotyping.
Fanny Degrugillier, Stéphanie Simon, Abdel Aissat, Natascha Remus, Chadia Mekki

Clin Case Rep· November 2019

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Cis variants identified in F508del complex alleles modulate CFTR channel rescue by small molecules.
Nesrine Baatallah, Sara Bitam, Natacha Martin, Nathalie Servel, Bruno Costes, Chadia Mekki

Hum Mutat· April 2018

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CFTR-France, a national relational patient database for sharing genetic and phenotypic data associated with rare CFTR variants.
Mireille Claustres, Corinne Thèze, Marie des Georges, David Baux, Emmanuelle Girodon, Chadia Mekki

Hum Mutat· October 2017

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Amyl nitrite inhalation, a "volatile" anemia.
Lauriane Filliatre, Julien Broséus, Serge Pissard, Chadia Mekki, Pierre Feugier

Am J Hematol· June 2016

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Practical approach for characterization of glucose 6-phosphate dehydrogenase (G6PD) deficiency in countries with population ethnically heterogeneous: description of seven new G6PD mutants.
Kamran Moradkhani, Chadia Mekki, Michel Bahuau, Valerie Li Thiao Te, Muriel Holder

Am J Hematol· February 2012

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