24 Aug 2026Open access
Major histocompatibility complex class II deficiency in Morocco: a 26-year retrospective cohort studyPublisher siteFrontiers in Immunology, Immunodeficiency and Autoimmune Disorders
UniversitiesNoufissa Benajiba
Active, last published 2026
In immunodeficiency and autoimmune disorders
Noufissa
Benajiba
Scholar“Research focused on Immunodeficiency and Autoimmune Disorders and adjacent fields.”
Mother Hospital
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01 · About the work
What I study
oufissa Benajiba is a researcher working on Immunodeficiency and Autoimmune Disorders. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Noufissa's work has been cited 285 times across 4 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
03 · Research focus
Topics
Immunodeficiency and Autoimmune Disorders×9Acute Lymphoblastic Leukemia research×9Autoimmune and Inflammatory Disorders Research×8Blood disorders and treatments×5Sarcoma Diagnosis and Treatment×5
04 · Where I am
Affiliations
Affiliation on published researchMother HospitalDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
23 works1 Nov 2025Open access
A Survival Analysis of Pediatric Acute Lymphoblastic Leukemia in MoroccoPublisher siteAsian Pacific Journal of Cancer Prevention, Acute Lymphoblastic Leukemia research
12 Jun 2025Open access
Identification of the Genetic Causes of Inherited Diseases in a North African Biobank: Implications for Genetic DiagnosisPublisher siteMolecular Syndromology, Genomics and Rare Diseases
11 Jun 2024Open access
Albinism and Primary Immunodeficiency in Infants: A Case Study of Griscelli SyndromePublisher siteCureus, Autoimmune and Inflammatory Disorders Research
3 Jun 2024Open access1cites
Exceptional case of a hemangioma-like rabdomyosarcoma in the hand's palmPublisher siteRadiology Case Reports, Sarcoma Diagnosis and Treatment
10 May 2024Open access
Christ-Siemens-Touraine Syndrome: A Report of a Rare Pediatric CasePublisher siteCureus, dental development and anomalies
1 May 2024Open access1cites
A rare case of steroid 11 beta-hydroxylase deficiency in a child revealed by acute pulmonary edemaPublisher siteOxford Medical Case Reports, Sexual Differentiation and Disorders
22 Jan 2024Open access3cites
First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism arrayPublisher siteArchives de Pédiatrie, Genomic variations and chromosomal abnormalities
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