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Najla Mekki
50
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Search for persons
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Online (50)
Mediatypes
Articles (Online) (17)
Bookchapter (Online) (2)
OpenAccess-fulltext (31)
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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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
1-15