الرئيسية › دليل الباحثين › Fatima Ailal
Fatima Ailal
الانتماء : Centre Hospitalier Universitaire Ibn Rochd · University of Hassan II Casablanca
- 124منشورات (انتماء مغربي)
- 150مجموع المنشورات
- 4288الاستشهادات
- 24مؤشر h
الملف البحثي
لدى Fatima Ailal 124 منشور(ات) مفهرسة (2014–2026). تُنشر أعماله أساسًا في «Journal of Human Immunity»، «Journal of Clinical Immunology» و«Frontiers in Immunology». أكثر مقالاته استشهادًا هو «Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification» (2020)، وقد استُشهد به 678 مرة. 49 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل، منهم باحثون من مؤسسات في فرنسا.
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Immunodeficiency and Autoimmune Disorders
- Blood disorders and treatments
- T-cell and B-cell Immunology
- Autoimmune and Inflammatory Disorders Research
- Tuberculosis Research and Epidemiology
المنشورات (124)
- Autoimmunity and inborn errors of immunity: a complex coexistence
- Auto-antibodies neutralizing type I interferons in ~10% of Moroccan patients with life-threatening COVID-19
- STAT1 gain-of-function in 12 Moroccan patients: Clinical and genetic insights
- Major histocompatibility complex class II deficiency in Morocco: a 26-year retrospective cohort study
- Case Report: IL2RA (CD25) deficiency: first reported cases in Morocco
- Rare STAT1 variants in Moroccan tuberculosis patients: insights into host genetic susceptibility
- Clinical, Immunological and Genetic Features of STAT3-HIES Patients: A Multisystemic and Heterogeneous Presentation
- Complications of Bacillus Calmette-Guérin vaccine in patients with inborn errors of immunity
- Case Report: Different faces of LRBA deficiency in five Moroccan families
- Gastrointestinal stenosis: an underrecognized complication of CARMIL2 deficiency
- From T-cell defect to tumorigenesis: Epstein–Barr virus–associated smooth muscle tumors in ITK deficiency
- STAT2 R148 variant: A 16th-century founder mutation and clinical response to high-dose JAK inhibitor therapy
- Case Report: A novel homozygous splice-site variant in the C3 gene causing complete complement C3 deficiency in two unrelated Moroccan patients
- Chronic granulomatous disease: A multicenter study from the MENA region
- Wiskott-Aldrich syndrome: clinical, immunological, and genetic characterization of the first Moroccan cohort
- Rediscovering Kaposi Sarcoma in North Africa: Thirteen years of HIV-negative cases and survival insights from Morocco
- Clinical and Etiological Profile of Bronchiectasis in Morocco
- From underdiagnosis to genetic confirmation: unveiling Primary Ciliary Dyskinesia in Morocco
- Clinical and Radiological Profile of Cystic Fibrosis Associated Bronchiectasis: A Descriptive Study of 19 Patients in Morocco
- Primary immune regulatory disorders in two children with autoimmune cytopenia (a challenge for the pediatrician): case report
- Clinical, immunological, and genetic landscape of common variable immunodeficiency in Morocco: a nationwide multicenter study
- Autoimmune manifestations in children with inborn errors of immunity in Morocco: A study from the national registry
- Major Histocompatibility Complex Class II Deficiency Beyond Infancy
- Application of whole-exome sequencing to predict inborn errors of immunity in pediatric severe infections and sepsis
- Case Report: A novel CIITA mutation causing MHC class II deficiency: first reported case in Morocco
- Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case report
- Prevalence of pathogenic variants of inborn errors of immunity in critically ill children admitted to the pediatric intensive care unit for sepsis: A Moroccan cohort study
- Exploration of the Clinical and Immunogenetic Profile of Patients with Agammaglobulinemia: About 47 Cases
- Defects in Innate and Intrinsic Immunity in Morocco: A Retrospective Analysis of the Genetic Landscape and Clinical Correlations
- Exploring the landscape of congenital and idiopathic neutropenia in Moroccan children: a comprehensive retrospective analysis
- Correction: Hypercalcemia and co-occurring TBX1 mutation in Glycogen Storage Disease Type Ib: case report
- Clinical manifestations of 42 Moroccan patients with chronic granulomatous disease
- CHARGE Syndrome in a Six-Month-Old Male Infant: A Case Report
- Allogeneic Hematopoietic Stem Cell Transplantation for Primary Immunodeficiencies in Morocco
- Lymphocytophagy Is a Serious Complication of Severe Combined Immunodeficiency
- ZNF341-Related Autosomal Recessive Hyper-IgE Syndrome: A Case Series of Four Patients
- Variation of HLA-DR Expression in Patients with HLA Class II Deficiency: A Retrospective Study at Ibn Rochd University Hospital
- Complement Deficiencies in Morocco: 6 Confirmed Cases and Variants
- Diagnostic of Chronic Granulomatous Disease: Experience of Ibn Rochd University Hospital
- Defects in Innate and Intrinsic Immunity in Morocco: Genetic Variants and Their Clinical Impact
- Primary ciliary dyskinesia in Morocco: first seven genetically confirmed cases
- When Recurrent Infections Don’t Always Reveal a Primary Immunodeficiency
- Assessment of IL-13, IL-31 Levels and Disease Severity in Children with Atopic Dermatitis
- Human genetic and immunological determinants of SARS-CoV-2 infection and multisystem inflammatory syndrome in children
- Innate immunodeficiencies: a group of primary immunodeficiencies predisposing exclusively to common diseases
- Impact of COVID-19 on child tuberculosis hospitalization
- Les cytopénies auto-immunes de l’enfant : Quand penser au déficit immunitaire primitif ?
- Phenotypes of 126 Moroccan HIES patients according to NIH Score
- Multisystem Inflammatory Syndrome in Children (MIS-C) Associated With COVID-19 Infection in Morocco
- Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia
- Mendelian Susceptibility to Mycobacterial Disease (MSMD): Clinical, Immunological, and Genetic Features of 22 Patients from 15 Moroccan Kindreds
- Mendelian susceptibility to mycobacterial disease: an overview
- Atypical Cutaneous Viral Infections Reveal an Inborn Error of Immunity in 8 Patients
- Classification of Common Variable Immunodeficiency Using Measurement of B-cell Subsets in Moroccan Patients
- Acute generalized exanthematous pustulosis induced by isoniazid and pyrazinamide in a child
- Hyperimmunoglobulinémie E et Déficits Immunitaires Héréditaires
- Classification of common variable immunodeficiency through immunological and clinical phenotyping in Moroccan patients
- Un cas de pustulose exanthématique aiguë généralisée à l’isoniazide et à la pyrazinamide : défi thérapeutique
- Orientation diagnostic devant une neutropénie héréditaire de l’enfant : Revue narrative de la littérature
- A partial form of inherited human USP18 deficiency underlies infection and inflammation
- Genetic Diagnosis of Inborn Errors of Immunity in an Emerging Country: a Retrospective Study of 216 Moroccan Patients
- HPV-Related Skin Phenotypes in Patients with Inborn Errors of Immunity
- Chronic upper airway inflammation related to high Th2 cytokines in Mendelian susceptibility to mycobacterial disease case
- [Autoimmune lymphoproliferative syndrome: a case report].
- Intriguing Acute Abdomen and Covid-19 in children : A case report
- Pediatric multi-systemic inflammatory syndrome complicated by severe cardiac and renal involvement
- Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents
- Pediatric Demodicosis Associated with Gain-of-Function Variant in STAT1 Presenting as Rosacea-Type Rash
- Clinical and Immunological Features of 96 Moroccan Children with SCID Phenotype: Two Decades’ Experience
- Severe Combined Immunodeficiency Disorder due to a Novel Mutation in Recombination Activation Gene 2: About 2 Cases
- Prédisposition génétique aux infections fongiques cutanéomuqueuses
- Genetic basis of common variable immunodeficiency: from common to variable
- Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification
- Human T-bet Governs Innate and Innate-like Adaptive IFN-γ Immunity against Mycobacteria
- Homozygous STAT2 gain-of-function mutation by loss of USP18 activity in a patient with type I interferonopathy
- Candidose cutanéo-muqueuse chronique avec mutation gain-de-fonction du gène STAT1 associée à des infections herpétiques et à mycobactérie
- Recurrent Meningitis
- Recurrent Pneumonia
- A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity
- Disruption of an antimycobacterial circuit between dendritic and helper T cells in human SPPL2a deficiency
- IFN-γ and CD25 drive distinct pathologic features during hemophagocytic lymphohistiocytosis
- The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies
- Poikiloderma with Neutropenia in Morocco: a Report of Four Cases
- Syndrome d’activation macrophagique compliquant une lymphohistiocytose familiale
- Le profil clinique et immunologique de 15 patients Marocains atteints de syndrome hyper IgM
- Human Genetics of Tuberculosis of the Nervous System
- Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases
- Dual T cell– and B cell–intrinsic deficiency in humans with biallelic RLTPR mutations
- Alanine-scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss- or gain-of-function variants
- X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations
- Bécégites de l’enfant : diagnostic, classification et exploration
- Utility of the QuantiFERON®-TB Gold In-Tube assay for the diagnosis of tuberculosis in Moroccan children
- First 3 cases of glycogen storage disease type 1b diagnosed in Morocco: genetic and clinical features
- Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome
- The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies
- Inherited and acquired immunodeficiencies underlying tuberculosis in childhood
- Pott's disease in Moroccan children: clinical features and investigation of the interleukin-12/interferon-γ pathway
- First Report on the Moroccan Registry of Primary Immunodeficiencies: 15 Years of Experience (1998–2012)
- Chronic Granulomatous Disease in Morocco: Genetic, Immunological, and Clinical Features of 12 Patients from 10 Kindreds
- Péricardite purulente et infiltration colique à Salmonella enteritidis compliquée d’invagination intestinale aiguë dans un cas de déficit en IL-12Rβ1
مجلات النشر
- Journal of Human Immunity × 12
- Journal of Clinical Immunology × 11
- Frontiers in Immunology × 8
- The Journal of Experimental Medicine × 5
- Clinical & Experimental Immunology × 4
- La Tunisie Médicale × 4
المنشورات حسب السنة
- 202620
- 202523
- 20246
- 202310
- 20227
- 20216
- 20203
- 20193
- 20183
- 20175
التعاون العلمي
المؤسسات الشريكة : Université Mohammed VI des Sciences et de la Santé · Mohammed V University · Centre Hospitalier Universitaire Mohammed VI · Centre Hospitalier Universitaire Hassan II · Université Hassan II Mohammedia
بلدان المؤلفين المشاركين : فرنسا
المؤلفون المشاركون
- Ahmed Aziz Bousfiha
- Ibtihal Benhsaien
- Jalila El Bakkouri
- Zahra Aadam
- Leïla Jeddane
- Abderrahmane Errami
- Aziz A. Bousfiha
- Naima Amenzoui
- Zineb Jouhadi
- Jilali Najib
- Asmaa Drissi Bourhanbour
- Fatima Adnane
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
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