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Najla Mekki
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1

Diagnostic challenge in a series of eleven patients with hy..:

Yaakoubi, Roukaya ; Mekki, Najla ; Ben-Mustapha, Imen...
Frontiers in Immunology.  13 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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2

Clinical, immunological, molecular and therapeutic findings..:

Jamee, Mahnaz ; Azizi, Gholamreza ; Baris, Safa...
Clinical Immunology.  244 (2022)  - p. 109131 , 2022
Link: https://doi.org/10.1016/..
 
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3

A Novel Point-of-Care Rapid Diagnostic Test for Screening I..:

Israeli, Shirli ; Golden, Allison ; Atalig, Melissa...
Journal of Clinical Immunology.  42 (2021)  2 - p. 394-403 , 2021
Link: https://doi.org/10.1007/..
 
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4

Case Report: FOXP3 Mutation in a Patient Presenting With AL..:

Rais, Afef ; Mekki, Najla ; Fedhila, Faten...
Frontiers in Immunology.  12 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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5

Profound differences in IgE and IgG recognition of micro‐ar..:

Garib, Victoria ; Ben‐Ali, Meriem ; Kundi, Michael...
Allergy.  77 (2021)  6 - p. 1761-1771 , 2021
Link: https://doi.org/10.1111/..
 
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6

Genetic Approaches for Definitive Diagnosis of Agammaglobul..:

Ben-Ali, Meriem ; Kechout, Nadia ; Mekki, Najla...
Journal of Clinical Immunology.  40 (2019)  1 - p. 96-104 , 2019
Link: https://doi.org/10.1007/..
 
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7

Defective glycosylation leads to defective gp130-dependent ..:

Ben-Ali, Meriem ; Ben-Khemis, Leila ; Mekki, Najla...
Journal of Allergy and Clinical Immunology.  143 (2019)  4 - p. 1638-1640.e2 , 2019
Link: https://doi.org/10.1016/..
 
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8

Homozygous transcription factor 3 gene(TCF3)mutation is ass..:

Ben-Ali, Meriem ; Yang, Jing ; Chan, Koon Wing...
Journal of Allergy and Clinical Immunology.  140 (2017)  4 - p. 1191-1194.e4 , 2017
Link: https://doi.org/10.1016/..
 
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9

Lessons from Genetic Studies of Primary Immunodeficiencies ..:

Barbouche, Mohamed-Ridha ; Mekki, Najla ; Ben-Ali, Meriem.
Frontiers in Immunology.  8 (2017)  - p. , 2017
Link: https://doi.org/10.3389/..
 
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10

A founder mutation underlies a severe form of phosphoglutam..:

Ben-Khemis, Leila ; Mekki, Najla ; Ben-Mustapha, Imen...
Molecular Immunology.  90 (2017)  - p. 57-63 , 2017
Link: https://doi.org/10.1016/..
 
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11

Autoimmune lymphoproliferative syndrome caused by homozygou..:

Agrebi, Nourhen ; Sfaihi Ben-Mansour, Lamia ; Medhaffar, Moez...
Journal of Allergy and Clinical Immunology.  140 (2017)  1 - p. 298-301.e3 , 2017
Link: https://doi.org/10.1016/..
 
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12

A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Un..:

Ben-Farhat, Khaoula ; Ben-Mustapha, Imen ; Ben-Ali, Meriem...
Journal of Clinical Immunology.  36 (2016)  6 - p. 547-554 , 2016
Link: https://doi.org/10.1007/..
 
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13

Report of the Tunisian Registry of Primary Immunodeficienci..:

Mellouli, Fethi ; Mustapha, Imen Ben ; Khaled, Monia Ben...
Journal of Clinical Immunology.  35 (2015)  8 - p. 745-753 , 2015
Link: https://doi.org/10.1007/..
 
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14

A 1,100-year-old founder effect mutation in IL12B gene is r..:

Ben-Mustapha, Imen ; Ben-Ali, Meriem ; Mekki, Najla...
Immunogenetics.  66 (2013)  1 - p. 67-71 , 2013
Link: https://doi.org/10.1007/..
 
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15

DataSheet_1_Diagnostic challenge in a series of eleven pati..:

Roukaya Yaakoubi ; Najla Mekki ; Imen Ben-Mustapha...
doi:10.3389/fimmu.2022.1057679.s001.  , 2023
Link: https://doi.org/10.3389/..
 
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