Inherited IL-12p40 Deficiency

Carolina Prando, Arina Samarina, Jacinta Bustamante, +43

Medicine

Bcg VaccinationImmunodeficienciesIl-12p40 DeficiencyImmunologyGenetic Epidemiology +18

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

Imen Ben‐Mustapha, Khaoula Ben-Farhat, Naouel Guirat-Dhouib, +10

Journal of Clinical Immunology

HistocompatibilityPrimary ImmunodeficiencyAutoimmune DiseaseGenetic DisorderGenetics +11

Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III

A. Mili, Ilhem Ben Charfeddine, Ons Mamaï, +14

Journal of Human Genetics

GlycoproteomicsBiochemistryNatural SciencesBioanalysisGlycobiology +9

Epidemiology and clinical profile of pathogens responsible for the hospitalization of children in Sousse area, Tunisia

Inès Brini, Aida Guerrero, Naïla Hannachi, +10

PLoS ONE

Clinical SymptomsRespiratory Virus ImmunityMalariaRespiratory ComplicationsPediatric Lung Disease +24

Phenotypic spectrum of fucosidosis in Tunisia

Hadhami Ben Turkia, Néji Tebib, Hatem Azzouz, +8

Journal of Inherited Metabolic Disease

Effect of Family Empowerment Education on Pulmonary Function and Quality of Life of Children With Asthma and Their Parents in Tunisia: A Randomized Controlled Trial

Maha Dardouri, Jihène Sahli, Thouraya Ajmi, +4

Journal of Pediatric Nursing

AsthmaFamily HealthChild Well-beingFamily InvolvementChild Health +8

Primary ciliary dyskinesia gene contribution in Tunisia: Identification of a major Mediterranean allele

Rahma Mani, Sabrina Belkacem, Zohra Soua, +21

Human Mutation

GeneticsGenetic EpidemiologyDiagnosisPathologyPcd Genes +14

Inherited IL-12p40 Deficiency: Genetic, Immunologic, and Clinical Features of 49 Patients From 30 Kindreds (vol 92, pg 109, 2013)

Carolina Prando, Arina Samarina, Jacinta Bustamante, +44

Primary ImmunodeficiencyInflammationAllergyImmunodeficienciesIl-12p40 Deficiency +10

Assessing the impact of a family empowerment program on asthma control and medication use in children with asthma: A randomized controlled trial

Maha Dardouri, Jihène Bouguila, Jihène Sahli, +4

Journal for Specialists in Pediatric Nursing

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

Imen Ben‐Mustapha, Meriem Ben‐Ali, Najla Mekki, +9

Immunogenetics

Disease SusceptibilityMolecular Diagnostic TechniquesMendelian DisorderMendelian SusceptibilityPathogenesis +8