Search details
1.
Mendelian Susceptibility to Mycobacterial Disease (MSMD): Clinical, Immunological, and Genetic Features of 22 Patients from 15 Moroccan Kindreds.
J Clin Immunol
; 43(4): 728-740, 2023 05.
Article
in English
| MEDLINE | ID: mdl-36630059
2.
Genetic Diagnosis of Inborn Errors of Immunity in an Emerging Country: a Retrospective Study of 216 Moroccan Patients.
J Clin Immunol
; 43(2): 485-494, 2023 02.
Article
in English
| MEDLINE | ID: mdl-36367635
3.
The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity.
J Clin Immunol
; 42(7): 1508-1520, 2022 10.
Article
in English
| MEDLINE | ID: mdl-36198931
4.
Clinical and Immunological Features of 96 Moroccan Children with SCID Phenotype: Two Decades' Experience.
J Clin Immunol
; 41(3): 631-638, 2021 04.
Article
in English
| MEDLINE | ID: mdl-33411152
5.
Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification.
J Clin Immunol
; 40(1): 66-81, 2020 01.
Article
in English
| MEDLINE | ID: mdl-32048120
6.
The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
J Clin Immunol
; 38(1): 129-143, 2018 01.
Article
in English
| MEDLINE | ID: mdl-29226301
7.
Primary Immunodeficiencies: Epidemiology in the Maghreb.
Tunis Med
; 96(10-11): 672-677, 2018.
Article
in English
| MEDLINE | ID: mdl-30746660
8.
The Seven STAT3-Related Hyper-IgE Syndromes.
J Clin Immunol
; 41(6): 1384-1389, 2021 08.
Article
in English
| MEDLINE | ID: mdl-33903995
9.
Correction to: The Seven STAT3Related HyperIgE Syndromes.
J Clin Immunol
; 41(6): 1390, 2021 Aug.
Article
in English
| MEDLINE | ID: mdl-33970386
10.
X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations.
J Clin Immunol
; 36(3): 187-94, 2016 Apr.
Article
in English
| MEDLINE | ID: mdl-26931785
11.
The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies.
J Clin Immunol
; 35(8): 727-38, 2015 Nov.
Article
in English
| MEDLINE | ID: mdl-26445875
12.
Chronic granulomatous disease in Morocco: genetic, immunological, and clinical features of 12 patients from 10 kindreds.
J Clin Immunol
; 34(4): 452-8, 2014 May.
Article
in English
| MEDLINE | ID: mdl-24596025
13.
Primary immunodeficiency diseases worldwide: more common than generally thought.
J Clin Immunol
; 33(1): 1-7, 2013 Jan.
Article
in English
| MEDLINE | ID: mdl-22847546
14.
A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedside.
J Clin Immunol
; 33(6): 1078-87, 2013 Aug.
Article
in English
| MEDLINE | ID: mdl-23657403
15.
Clinical and serological correlation of systemic sclerosis in Moroccan patients.
Rheumatol Adv Pract
; 7(2): rkad036, 2023.
Article
in English
| MEDLINE | ID: mdl-37091295
16.
Primary Immunodeficiency Classification on Smartphone.
J Clin Immunol
; 37(1): 1-2, 2017 01.
Article
in English
| MEDLINE | ID: mdl-27888368
17.
When to suspect an immune deficiency in adults?
Tunis Med
; 100(8-9): 585-591, 2022.
Article
in English
| MEDLINE | ID: mdl-36571726
18.
[Genetic basis of common variable immunodeficiency: from common to variable]. / Les bases génétiques du déficit immunitaire commun variable : du commun au variable.
Ann Biol Clin (Paris)
; 79(5): 407-413, 2021 Oct 01.
Article
in French
| MEDLINE | ID: mdl-34704938
19.
A-Project : a Training Program from ASID.
J Clin Immunol
; 35(6): 517-8, 2015 Aug.
Article
in English
| MEDLINE | ID: mdl-26376911
20.
[Clinical and immunological profile of 15 Moroccan patients with Hyper IgM syndrome]. / Le profil clinique et immunologique de 15 patients Marocains atteints de syndrome hyper IgM.
Pan Afr Med J
; 26: 212, 2017.
Article
in French
| MEDLINE | ID: mdl-28690727