M. Ben-ali

发表

Evolutionary Dynamics of Human Toll-Like Receptors and Their Different Contributions to Host Defense

Joseph K. Pickrell, K. Kidd, J. Kidd, 2009, PLoS genetics.

A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients

M. Barbouche, M. Ben-ali, S. Barsaoui, 2016, Journal of Clinical Immunology.

Profound differences in IgE and IgG recognition of micro‐arrayed allergens in hyper‐IgE syndromes

R. Valenta, M. Barbouche, M. Kundi, 2021, Allergy.

A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients

E. Patin, M. Barbouche, M. Bejaoui, 2013, Immunogenetics.

Promoter and neck region length variation of DC-SIGN is not associated with susceptibility to tuberculosis in Tunisian patients.

L. Quintana-Murci, M. Barbouche, L. Barreiro, 2007, Human immunology.

Rare splicing defects of FAS underly severe recessive autoimmune lymphoproliferative syndrome.

M. Barbouche, M. Ben-Ahmed, M. Bejaoui, 2017, Clinical immunology.

Lessons from Genetic Studies of Primary Immunodeficiencies in a Highly Consanguineous Population

M. Barbouche, M. Ben-ali, I. Ben-Mustapha, 2017, Front. Immunol..

Defective glycosylation leads to defective gp130-dependent STAT3 signaling in PGM3-deficient patients.

M. Barbouche, M. Ben-ali, I. Ben-Mustapha, 2019, The Journal of allergy and clinical immunology.

Autoimmune lymphoproliferative syndrome caused by homozygous FAS mutations with normal or residual protein expression.

M. Barbouche, M. Ben-ali, S. Barsaoui, 2017, The Journal of allergy and clinical immunology.

Clinical, Immunological and Genetic Findings of a Large Tunisian Series of Major Histocompatibility Complex Class II Deficiency Patients

M. Barbouche, M. Bejaoui, M. Ben-ali, 2013, Journal of Clinical Immunology.

Inherited IL-12p40 Deficiency: Genetic, Immunologic, and Clinical Features of 49 Patients From 30 Kindreds (vol 92, pg 109, 2013)

Sami Al-Hajjar, C. Picard, L. Abel, 2013 .

X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations

L. Jeddane, F. Ailal, Y. Lau, 2016, Journal of Clinical Immunology.

Clinical, Immunological and Genetic Findings of a Large Tunisian Series of Major Histocompatibility Complex Class II Deficiency Patients

M. Barbouche, M. Bejaoui, M. Ben-ali, 2013, Journal of Clinical Immunology.

A FOUNDER MUTATION IN PGM3 IS RESPONSIBLE FOR A SEVERE FORM OF HYPER-IGE LIKE SYNDROME IN TUNISIAN PATIENTS

M. Ben-ali, 2016 .

Functional characterization of naturally occurring genetic variants in the human TLR1‐2‐6 gene family

L. Quintana-Murci, S. Pellegrini, L. Barreiro, 2011, Human mutation.

Activation induced cytidine deaminase mutant (AID-His130Pro) from Hyper IgM 2 patient retained mutagenic activity on SHM artificial substrate.

T. Jovanic, M. Barbouche, B. Arcangioli, 2016, Molecular immunology.

Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels.

A. Schäffer, U. Kölsch, T. Jakob, 2014, The Journal of allergy and clinical immunology.

A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients

M. Barbouche, M. Ben-ali, S. Barsaoui, 2016, Journal of Clinical Immunology.

Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous Families

A. Bousfiha, Y. Lau, M. Barbouche, 2019, Journal of Clinical Immunology.

Inherited IL-12p40 Deficiency

Sami Al-Hajjar, J. Casanova, C. Picard, 2013, Medicine.

Diagnostic challenge in a series of eleven patients with hyper IgE syndromes

Y. Lau, M. Barbouche, A. Hamzaoui, 2023, Frontiers in Immunology.

A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients

E. Patin, M. Barbouche, M. Bejaoui, 2013, Immunogenetics.

Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients

M. Barbouche, M. Bejaoui, M. Ben-ali, 2015, Immunogenetics.

Study of Human RIG-I Polymorphisms Identifies Two Variants with an Opposite Impact on the Antiviral Immune Response

J. Chiche, A. Heinzmann, P. Vidalain, 2009, PloS one.

Toll-Like Receptor 2 Arg677Trp Polymorphism Is Associated with Susceptibility to Tuberculosis in Tunisian Patients

M. Barbouche, K. Dellagi, M. Ben-ali, 2004, Clinical Diagnostic Laboratory Immunology.

X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations

L. Jeddane, F. Ailal, Y. Lau, 2016, Journal of Clinical Immunology.

Homozygous transcription factor 3 gene (TCF3) mutation is associated with severe hypogammaglobulinemia and B-cell acute lymphoblastic leukemia.

Y. Lau, M. Barbouche, Jing Yang, 2017, The Journal of allergy and clinical immunology.

Antibody response to common human viruses is shaped by genetic factors

M. Ben-ali, N. Mekki, I. Ben‐Mustapha, 2019 .

The Seven STAT3-Related Hyper-IgE Syndromes

L. Jeddane, M. Barbouche, M. Ben-ali, 2021, Journal of Clinical Immunology.

A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients.

M. Barbouche, M. Bejaoui, M. Ben-ali, 2017, Molecular immunology.

Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous Families

A. Bousfiha, Y. Lau, M. Barbouche, 2019, Journal of Clinical Immunology.

Staphylococcal scalded skin syndrome: An uncommon symptomatology revealing an immune deficiency.

M. Barbouche, M. Mokni, M. Ben-ali, 2017, Archives de pédiatrie.

Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients

M. Barbouche, M. Bejaoui, M. Ben-ali, 2015, Immunogenetics.