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Idiopathic pulmonary hemosiderosis and stroke secondary to protein C deficiency in a child with Down syndrome: a case report

Journal of medical case reports, 2023-03, Vol.17 (1), p.105-105, Article 105

2023

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Success of anti-CD20 monoclonal antibody treatment for severe autoimmune hemolytic anemia caused by warm-reactive immunoglobulin A, immunoglobulin G, and immunoglobulin M autoantibodies in a child: a case report

Journal of medical case reports, 2017-11, Vol.11 (1), p.321-321, Article 321

2017

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Vein of Galen Aneurysmal Malformation revealed by a severe heart failure and pulmonary hypertension in an infant

Journal of pediatric and neonatal individualized medicine, 2018-10, Vol.7 (2), p.e070239-e070239

2018

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Clinical and radiological findings of posterior reversible encephalopathy syndrome in children: About 16 children hospitalized in the pediatric department of a Tunisian tertiary care hospital

European journal of paediatric neurology, 2023-03, Vol.43, p.18-26

2023

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Acute disseminated encephalomyelitis: A retrospective study of 20 children in a pediatrics department in Tunisia

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2021-11, Vol.28 (8), p.638-646

2021

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Inherited IL-12p40 deficiency: genetic, immunologic, and clinical features of 49 patients from 30 kindreds

Medicine (Baltimore), 2013-03, Vol.92 (2), p.109-122

2013

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Coronary artery aneurysm in Kawasaki disease and its risk factors : a retrospective study about 65 Tunisian children

Annales de cardiologie et d'angeiologie, 2022-04, Vol.71 (2), p.86-89

2022

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Les complications coronaires de la maladie de Kawasaki et ses facteurs de risque : à propos de 65 cas d'enfants tunisien

Annales de cardiologie et d'angéiologie, 2022-04, Vol.71 (2), p.86-89

2022

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Epidemiological, Bacteriological, and Evolutive Features of Children Hospitalized for Infective Endocarditis in a Tertiary Tunisian Pediatric Department

Journal Of The Saudi Heart Association, 2023-01, Vol.35 (4), p.339-345

2023

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Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: Implication for diagnosis in North Africa

Gene, 2013-09, Vol.527 (1), p.316-320

2013

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Mutational Analysis of Agxt in Tunisian Population with Primary Hyperoxaluria Type 1

Annals of human genetics, 2017-01, Vol.81 (1), p.1-10

2017

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A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients

Journal of clinical immunology, 2016-08, Vol.36 (6), p.547-554

2016

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Clinical, Immunological and Genetic Findings of a Large Tunisian Series of Major Histocompatibility Complex Class II Deficiency Patients

Journal of clinical immunology, 2013-05, Vol.33 (4), p.865-870

2013

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X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations

Journal of clinical immunology, 2016-04, Vol.36 (3), p.187-194

2016

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Clinical and imaging features of malignant infantile osteopetrosis

Turkish journal of pediatrics, 2017, Vol.59 (4), p.452-457

2017

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Pseudotumoral acute cerebellitis associated with mumps infection in a child

World journal of clinical cases, 2017-08, Vol.5 (8), p.340-343

2017

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A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients

Immunogenetics (New York), 2014, Vol.66 (1), p.67-71

2014

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Molecular investigation of distal renal tubular acidosis in Tunisia, evidence for founder mutations

Genetic testing and molecular biomarkers, 2014-11, Vol.18 (11), p.741-748

2014

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Rhombencephalosynapsis diagnosed in childhood: Clinical and MRI findings

European journal of paediatric neurology, 2007-01, Vol.11 (1), p.35-38

2007

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Clinical and Genetic Heterogeneity of Inherited Autosomal Recessive Susceptibility to Disseminated Mycobacterium bovis Bacille Calmette-Guérin Infection

The Journal of infectious diseases, 2002-05, Vol.185 (10), p.1468-1475

2002

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Acute myocarditis associated with parvovirus B19 infection in a child

Pediatric infectious disease (Amsterdam), 2015-04, Vol.7 (2), p.53-55

2015

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Gaucher disease in Tunisia: High frequency of the most common mutations

Blood cells, molecules, & diseases, 2009-09, Vol.43 (2), p.161-162

2009

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Kawasaki disease, Mycoplasma pneumoniae infection and anaplastic large cell lymphoma: An uncommon association

Open journal of pediatrics, 2012, Vol.2 (3), p.250-252

2012

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Central precocious puberty and hypothalamic hamartoma

Tunisie Medicale, 2008-02, Vol.86 (2), p.187

2008

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Idiopathic pulmonary hemosiderosis and stroke secondary to protein C deficiency in a child with Down syndrome: a case report

Success of anti-CD20 monoclonal antibody treatment for severe autoimmune hemolytic anemia caused by warm-reactive immunoglobulin A, immunoglobulin G, and immunoglobulin M autoantibodies in a child: a case report

Vein of Galen Aneurysmal Malformation revealed by a severe heart failure and pulmonary hypertension in an infant

Clinical and radiological findings of posterior reversible encephalopathy syndrome in children: About 16 children hospitalized in the pediatric department of a Tunisian tertiary care hospital

Acute disseminated encephalomyelitis: A retrospective study of 20 children in a pediatrics department in Tunisia

Inherited IL-12p40 deficiency: genetic, immunologic, and clinical features of 49 patients from 30 kindreds

Coronary artery aneurysm in Kawasaki disease and its risk factors : a retrospective study about 65 Tunisian children

Les complications coronaires de la maladie de Kawasaki et ses facteurs de risque : à propos de 65 cas d'enfants tunisien

Epidemiological, Bacteriological, and Evolutive Features of Children Hospitalized for Infective Endocarditis in a Tertiary Tunisian Pediatric Department

Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: Implication for diagnosis in North Africa

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

Mutational Analysis of Agxt in Tunisian Population with Primary Hyperoxaluria Type 1

A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients

Clinical, Immunological and Genetic Findings of a Large Tunisian Series of Major Histocompatibility Complex Class II Deficiency Patients

X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations

Clinical and imaging features of malignant infantile osteopetrosis

Pseudotumoral acute cerebellitis associated with mumps infection in a child

A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients

Molecular investigation of distal renal tubular acidosis in Tunisia, evidence for founder mutations

Rhombencephalosynapsis diagnosed in childhood: Clinical and MRI findings

Clinical and Genetic Heterogeneity of Inherited Autosomal Recessive Susceptibility to Disseminated Mycobacterium bovis Bacille Calmette-Guérin Infection

Acute myocarditis associated with parvovirus B19 infection in a child

Gaucher disease in Tunisia: High frequency of the most common mutations

Kawasaki disease, Mycoplasma pneumoniae infection and anaplastic large cell lymphoma: An uncommon association

Central precocious puberty and hypothalamic hamartoma

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