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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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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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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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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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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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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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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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Myocardial and liver iron overload, assessed using T2 magnetic resonance imaging with an excel spreadsheet for post processing in Tunisian thalassemia major patients

Annals of hematology, 2017, Vol.96 (1), p.133-139

2017

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Bronchogenic cyst: An uncommon cause of congenital lobar emphysema

Respiratory medicine, 2008-11, Vol.102 (11), p.1663-1666

2008

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Budd-Chiari syndrome in a boy with β thalassemia major (a study of a new case)

Journal of pediatric hematology/oncology, 2013-04, Vol.35 (3), p.237

2013

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Effectiveness and acceptance of hydroxyurea in the treatment of severe forms of sickle cell disease: a prospective study of 65 cases

Tunisie Medicale, 2013-08, Vol.91 (8-9), p.544-550

2013

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Cytogenetic assessment of Fanconi anemia in children with aplastic anemia in Tunisia

Journal of pediatric hematology/oncology, 2013-10, Vol.35 (7), p.547-550

2013

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Neonatal heart failure revealing a cardiac rhabdomyoma with tuberous sclerosis

Tunisie Medicale, 2008-01, Vol.86 (1), p.75

2008

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Feminizing Adrenocortical Adenoma in a 5 Year-old Girl

Journal of Pediatric Endocrinology and Metabolism, 2009, Vol.22 (1), p.79-84

2009

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Hypocalcaemia due to hypoparathyroidism in β-thalassemia major. A study of a new case

Tunisie Medicale, 2011-03, Vol.89 (3), p.302-304

2011

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Diabetic acido-ketosis revealing thiamine-responsive megaloblastic anemia

Annales d'endocrinologie, 2009-12, Vol.70 (6), p.477-479

2009

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Surgical management of lifebuoy cataract

Indian journal of ophthalmology, 2023-06, Vol.71 (6), p.2575-2577

2023

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Optical Coherence Tomography Angiography in idiopathic retinal vasculitis, aneurysms and neuroretinitis (IRVAN) syndrome: A case report

European journal of ophthalmology, 2022-01, Vol.32 (1), p.NP144-NP148

2022

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Epidemiological, clinical, and therapeutic characteristics of Behçet's disease: a monocentric study in Tunisia

The Pan African medical journal, 2021, Vol.40, p.13-13

2021

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Attitudes of ophthalmologists towards pharmaceutical promotion

La Tunisie medicale, 2023-08, Vol.101 (8-9), p.670

2023

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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

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

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

Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988–2012)

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

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

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

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

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

Myocardial and liver iron overload, assessed using T2 magnetic resonance imaging with an excel spreadsheet for post processing in Tunisian thalassemia major patients

Bronchogenic cyst: An uncommon cause of congenital lobar emphysema

Budd-Chiari syndrome in a boy with β thalassemia major (a study of a new case)

Effectiveness and acceptance of hydroxyurea in the treatment of severe forms of sickle cell disease: a prospective study of 65 cases

Cytogenetic assessment of Fanconi anemia in children with aplastic anemia in Tunisia

Neonatal heart failure revealing a cardiac rhabdomyoma with tuberous sclerosis

Feminizing Adrenocortical Adenoma in a 5 Year-old Girl

Hypocalcaemia due to hypoparathyroidism in β-thalassemia major. A study of a new case

Diabetic acido-ketosis revealing thiamine-responsive megaloblastic anemia

Surgical management of lifebuoy cataract

Optical Coherence Tomography Angiography in idiopathic retinal vasculitis, aneurysms and neuroretinitis (IRVAN) syndrome: A case report

Epidemiological, clinical, and therapeutic characteristics of Behçet's disease: a monocentric study in Tunisia

Attitudes of ophthalmologists towards pharmaceutical promotion

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