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Long-Term Observational Study of Chronic Granulomatous Disease About 41 Patients From Tunisia and Comparison to Other Long-Term Follow-Up Studies

Clinical pediatrics, 2022-10, Vol.61 (9), p.629-644

2022

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Containment of Local COVID-19 Outbreak Among Hematopoietic Stem Cell Transplant Recipients and Healthcare Workers in a Pediatric Stem Cell Unit

Journal of clinical immunology, 2021-10, Vol.41 (7), p.1523-1526

2021

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Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients

Blood, 2011-11, Vol.118 (19), p.5108-5118

2011

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Langerhans cell histiocytosis of the cervical spine in a child: A case report and review of the literature

Pediatric hematology oncology journal, 2022-12, Vol.7 (4), p.161-164

2022

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Diagnostic challenge in a series of eleven patients with hyper IgE syndromes

Frontiers in immunology, 2023-01, Vol.13, p.1057679-1057679

2023

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PB2543: CIRCULATING MICROVESICLES AS POTENTIAL CELLULAR BIOMARKERS FOR THROMBOTIC RISKS IN BETA THALASSEMIA

HemaSphere, 2023-08, Vol.7 (S3), p.e0427349-n/a

2023

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Full Genome Characterization of Respiratory Syncytial Virus Causing a Fatal Infection in an Immunocompromised Patient in Tunisia

Pathogens (Basel), 2022-07, Vol.11 (7), p.758

2022

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A membranous nephropathy in a 5 year-old boy: and if that’s not all? A nephrology quiz

Journal of nephrology, 2024-04, Vol.37 (3), p.821-825

2024

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Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome)

Clinical and molecular allergy CMA, 2012-04, Vol.10 (1), p.6-6, Article 6

2012

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First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby

Journal of pediatric hematology/oncology, 2021-11, Vol.43 (8), p.e1055-e1058

2021

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Incidence and risk factors for osteonecrosis of the femoral head in five hundred and ten sickle cell disease paediatric patients

International orthopaedics, 2023-12, Vol.47 (12), p.2941-2952

2023

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Clinical features and predictors of osteoarticular manifestations in common variable immunodeficiency

Clinical rheumatology, 2023-11, Vol.42 (11), p.3123-3129

2023

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Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ) 0 -Thalassemia among Tunisian family

Annals of clinical biochemistry, 2023-03, Vol.60 (2), p.81-85

2023

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Prevalence and predictive factors of splenic sequestration crisis among 423 pediatric patients with sickle cell disease in Tunisia

Blood cells, molecules, & diseases, 2020-02, Vol.80, p.102374-102374, Article 102374

2020

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Successful Haploidentical Stem Cell Transplantation with Post-Transplant Cyclophosphamide in a Severe Combined Immune Deficiency Patient: a First Report

Journal of clinical immunology, 2016-07, Vol.36 (5), p.437-440

2016

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Predictors of autoimmune hemolytic anemia in beta-thalassemia patients with underlying red blood cells autoantibodies

Blood cells, molecules, & diseases, 2019-11, Vol.79, p.102342-102342, Article 102342

2019

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Reversion of neurovirulent mutations, recombination and high intra‐host diversity in vaccine‐derived poliovirus excreted by patients with primary immune deficiency

Journal of medical virology, 2024-09, Vol.96 (9), p.e29918-n/a

2024

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Clinical Features of Candidiasis in Patients With Inherited Interleukin 12 Receptor β1 Deficiency

Clinical infectious diseases, 2014-01, Vol.58 (2), p.204-213

2014

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Hypertransaminasemia revealing a clinically silent muscular dystrophy in a child with sickle cell disease

Annals of hematology, 2018-11, Vol.97 (11), p.2261-2262

2018

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Growth and Endocrine Function in Tunisian Thalassemia Major Patients

Mediterranean journal of hematology and infectious diseases, 2018-05, Vol.10 (1), p.e2018031-e2018031

2018

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Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study

Scandinavian journal of immunology, 2019-06, Vol.89 (6), p.e12763-n/a

2019

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A nine-month-old-boy with Atypical Hemophagocytic Lymphohistiocytosis

Mediterranean journal of hematology and infectious diseases, 2017-10, Vol.9 (1), p.e2017057-e2017057

2017

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Cutaneous Manifestations of Primary Immunodeficiency Diseases in Tunisian Children

Mediterranean journal of hematology and infectious diseases, 2018-11, Vol.10 (1), p.e2018065

2018

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A 9month-old-boy with atypical hemophagocytic lymphohistiocytosis

Mediterranean journal of hematology and infectious diseases, 2017-10, Vol.9 (1), p.e2017057

2017

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A 9month-old-boy with atypical hemophagocytic lymphohistiocytosis

Mediterranean journal of hematology and infectious diseases, 2017-10, Vol.9 (1), p.e2017057-e2017057

2017

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Long-Term Observational Study of Chronic Granulomatous Disease About 41 Patients From Tunisia and Comparison to Other Long-Term Follow-Up Studies

Containment of Local COVID-19 Outbreak Among Hematopoietic Stem Cell Transplant Recipients and Healthcare Workers in a Pediatric Stem Cell Unit

Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients

Langerhans cell histiocytosis of the cervical spine in a child: A case report and review of the literature

Diagnostic challenge in a series of eleven patients with hyper IgE syndromes

PB2543: CIRCULATING MICROVESICLES AS POTENTIAL CELLULAR BIOMARKERS FOR THROMBOTIC RISKS IN BETA THALASSEMIA

Full Genome Characterization of Respiratory Syncytial Virus Causing a Fatal Infection in an Immunocompromised Patient in Tunisia

A membranous nephropathy in a 5 year-old boy: and if that’s not all? A nephrology quiz

Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome)

First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby

Incidence and risk factors for osteonecrosis of the femoral head in five hundred and ten sickle cell disease paediatric patients

Clinical features and predictors of osteoarticular manifestations in common variable immunodeficiency

Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ) 0 -Thalassemia among Tunisian family

Prevalence and predictive factors of splenic sequestration crisis among 423 pediatric patients with sickle cell disease in Tunisia

Successful Haploidentical Stem Cell Transplantation with Post-Transplant Cyclophosphamide in a Severe Combined Immune Deficiency Patient: a First Report

Predictors of autoimmune hemolytic anemia in beta-thalassemia patients with underlying red blood cells autoantibodies

Reversion of neurovirulent mutations, recombination and high intra‐host diversity in vaccine‐derived poliovirus excreted by patients with primary immune deficiency

Clinical Features of Candidiasis in Patients With Inherited Interleukin 12 Receptor β1 Deficiency

Hypertransaminasemia revealing a clinically silent muscular dystrophy in a child with sickle cell disease

Growth and Endocrine Function in Tunisian Thalassemia Major Patients

Challenges in investigating patients with isolated decreased serum IgM: The SIMcal study

A nine-month-old-boy with Atypical Hemophagocytic Lymphohistiocytosis

Cutaneous Manifestations of Primary Immunodeficiency Diseases in Tunisian Children

A 9month-old-boy with atypical hemophagocytic lymphohistiocytosis

A 9month-old-boy with atypical hemophagocytic lymphohistiocytosis

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