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Annals of Neurology|February 12, 2014
Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan AfricaModibo Sangaré, Brant Hendrickson, Hammadoun Ali Sango, et al.
Molecular Cytogenetics|February 14, 2026
Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insightsRim Khelifi, Houcemeddine Othmane, Houda Ajmi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2017
Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiencyAhmed Khattab, Shozeb Haider, Ameet Kumar, et al.
Nature Genetics|June 1, 2010
Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromesEnza Maria Valente, Clare V Logan, Soumaya Mougou-Zerelli, et al.
Frontiers in Medicine|August 4, 2022
Development and implementation of the AIDA international registry for patients with Schnitzler's syndromeJurgen Sota, Antonio Vitale, Ewa Więsik-Szewczyk, et al.
Frontiers in Medicine|June 27, 2022
Development and Implementation of the AIDA International Registry for Patients With Undifferentiated Systemic AutoInflammatory DiseasesFrancesca Della Casa, Antonio Vitale, Giuseppe Lopalco, et al.
Rheumatology (Oxford, England)|July 14, 2026
Effectiveness and probability of full disease control with canakinumab in familial Mediterranean fever: real-world data from the AIDA NetworkAntonio Vitale, Valeria Caggiano, Jessica Sbalchiero, et al.
Rheumatology (Oxford, England)|April 2, 2025
Predictors of proteinuria, amyloidosis and kidney failure in familial Mediterranean fever: data from the International AIDA Network RegistryAntonio Vitale, Valeria Caggiano, Jessica Sbalchiero, et al.
Frontiers in Immunology|May 27, 2024
Risk for cancer development in familial Mediterranean fever and associated predisposing factors: an ambidirectional cohort study from the international AIDA Network registriesAntonio Vitale, Valeria Caggiano, Abdurrahman Tufan, et al.
Internal and Emergency Medicine|October 12, 2023
Clinical and laboratory features associated with macrophage activation syndrome in Still's disease: data from the international AIDA Network Still's Disease RegistryPaola Triggianese, Antonio Vitale, Giuseppe Lopalco, et al.
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