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Search Results - Mansour, Lamia Sfaihi Ben
Search Results - Mansour, Lamia Sfaihi Ben
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Clinical, Functional and Genetic Analysis of Twenty-Four Patients with Chronic Granulomatous Disease – Identification of Eight Novel Mutations in CYBB and NCF2 Genes
by
Martel, Cécile
,
Mollin, Michelle
,
Beaumel, Sylvain
,
Brion, Jean Paul
,
Coutton, Charles
,
Satre, Véronique
,
Vieville, Gaëlle
,
Callanan, Mary
,
Lefebvre, Christine
,
Salmon, Alexandra
,
Pagnier, Anne
,
Plantaz, Dominique
,
Bost-Bru, Cécile
,
Eitenschenck, Laurence
,
Durieu, Isabelle
,
Floret, Daniel
,
Galambrun, Claire
,
Chambost, Hervé
,
Michel, Gérard
,
Stephan, Jean-Louis
,
Hermine, Olivier
,
Blanche, Stéphane
,
Blot, Nathalie
,
Rubié, Hervé
,
Pouessel, Guillaume
,
Drillon-Haus, Stephanie
,
Conrad, Bernard
,
Posfay-Barbe, Klara M.
,
Havlicekova, Zuzana
,
Voskresenky-Baricic, Tamara
,
Jadranka, Kelecic
,
Arriazu, Maria Cristina
,
Garcia, Luis Alberto
,
Mansour, Lamia Sfaihi Ben
,
Bordigoni, Pierre
,
Stasia, Marie José
Published in
Journal of clinical immunology
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Autoimmune lymphoproliferative syndrome caused by homozygous FAS mutations with normal or residual protein expression
by
Agrebi, Nourhen, PhD
,
Sfaihi Ben-Mansour, Lamia, MD
,
Medhaffar, Moez, MD
,
Hadiji, Sondes, MD
,
Fedhila, Faten, MD
,
Ben-Ali, Meriem, MD
,
Mekki, Najla, MD
,
Hachicha, Mongia, MD
,
Barsaoui, Sihem, MD
,
Barbouche, Mohamed-Ridha, MD, PhD
,
Ben-Mustapha, Imen, MD
Published in
Journal of allergy and clinical immunology
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Molecular and clinical heterogeneity in CLCN7-dependent osteopetrosis: report of 20 novel mutations
by
Pangrazio, Alessandra
,
Pusch, Michael
,
Caldana, Elena
,
Frattini, Annalisa
,
Lanino, Edoardo
,
Tamhankar, Parag M
,
Phadke, Shubha
,
Lopez, Antonio Gonzalez Meneses
,
Orchard, Paul
,
Mihci, Ercan
,
Abinun, Mario
,
Wright, Michael
,
Vettenranta, Kim
,
Bariæ, Ivo
,
Melis, Daniela
,
Tezcan, Ilhan
,
Baumann, Clarisse
,
Locatelli, Franco
,
Zecca, Marco
,
Horwitz, Edwin
,
Mansour, Lamia Sfaihi Ben
,
Van Roij, Mirjam
,
Vezzoni, Paolo
,
Villa, Anna
,
Sobacchi, Cristina
Published in
Human mutation
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Mutational analysis in patients with neuromuscular disorders: Detection of mitochondrial deletion and double mutations in the MT-ATP6 gene
by
Felhi, Rahma
,
Mkaouar-Rebai, Emna
,
Sfaihi-Ben Mansour, Lamia
,
Alila-Fersi, Olfa
,
Tabebi, Mouna
,
Ben Rhouma, Bochra
,
Ammar, Marwa
,
Keskes, Leila
,
Hachicha, Mongia
,
Fakhfakh, Faiza
Published in
Biochemical and biophysical research communications
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Erratum to: Clinical, Functional and Genetic Analysis of Twenty-Four Patients with Chronic Granulomatous Disease—Identification of Eight Novel Mutations in CYBB and NCF2 Genes
by
Martel, Cécile
,
Mollin, Michelle
,
Beaumel, Sylvain
,
Brion, Jean Paul
,
Coutton, Charles
,
Satre, Véronique
,
Vieville, Gaëlle
,
Callanan, Mary
,
Lefebvre, Christine
,
Salmon, Alexandra
,
Pagnier, Anne
,
Plantaz, Dominique
,
Bost-Bru, Cécile
,
Eitenschenck, Laurence
,
Durieu, Isabelle
,
Floret, Daniel
,
Galambrun, Claire
,
Chambost, Hervé
,
Michel, Gérard
,
Stephan, Jean-Louis
,
Hermine, Olivier
,
Blanche, Stéphane
,
Blot, Nathalie
,
Rubié, Hervé
,
Pouessel, Guillaume
,
Drillon-Haus, Stephanie
,
Conrad, Bernard
,
Posfay-Barbe, Klara M.
,
Havlicekova, Zuzana
,
Voskresenky-Baricic, Tamara
,
Jadranka, Kelecic
,
Arriazu, Maria Cristina
,
Garcia, Luis Alberto
,
Sfaihi, Lamia Ben Mansour
,
Bordigoni, Pierre
,
Stasia, Marie José
Published in
Journal of clinical immunology
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