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Acta Tropica|March 29, 2011
Neglected tropical disease (NTD) control in health systems: the interface between programmes and general health servicesBruno Marchal, Monique Van Dormael, Marjan Pirard, et al.Plos Neglected Tropical Diseases|September 3, 2010
Interactions between Global Health Initiatives and country health systems: the case of a neglected tropical diseases control program in MaliAnna Cavalli, Sory I Bamba, Mamadou N Traore, et al.BMC Medical Genomics|March 5, 2024
Heterozygous truncating variant of TAOK1 in a boy with periventricular nodular heterotopia: a case report and literature review of TAOK1-related neurodevelopmental disordersAnna Cavalli, Stefano Giuseppe Caraffi, Susanna Rizzi, et al.Journal of Clinical Medicine|September 13, 2025
Paroxysmal Dyskinesias in Paediatric Age: A Systematic ReviewGiulia Pisanò, Martina Gnazzo, Giulia Sigona, et al.Neuropediatrics|November 14, 2024
Sensory-Motor Polyneuropathy in an 11-year- old Girl with a Pathogenic Variant in SMC1A: A Case ReportAngelica De Luisa, Carlo A Cesaroni, Marzia Pollazzon, et al.American Journal of Medical Genetics. Part A|August 6, 2025
Prolonged Follow-Up in a 30-Year-Old Male With a Novel Pathogenic Variant in MSL3: A Case Report and a Brief Review of the LiteratureGiulia Pisanò, Carlo Alberto Cesaroni, Susanna Rizzi, et al.Children (Basel, Switzerland)|November 27, 2025
A Boy with a Novel Variant in <i>TCF20</i>: An Expanded Phenotype and a Brief Review of the LiteratureDiletta Ziveri, Carlo Alberto Cesaroni, Gianluca Contrò, et al.Neurogenetics|April 23, 2024
Early-onset dysphagia and severe neurodevelopmental disorder as early signs in a patient with two novel variants in NARS1: a case report and brief review of the literatureCarlo Alberto Cesaroni, Gianluca Contrò, Carlotta Spagnoli, et al.Neurogenetics|February 24, 2025
Axonal motor polyneuropathy in a 13 years old Girl with a de Novo variant in ADNPSara Scaccini, Carlo Alberto Cesaroni, Stefano Giuseppe Caraffi, et al.Journal of Clinical Medicine|January 10, 2026
Feeding-Triggered Seizures in a Newborn with <i>AP1S1</i>-Related MEDNIK Syndrome: Expanding the Phenotype of a Hyper-Rare DiseaseAnna Cavalli, Francesca Peluso, Daniele Frattini, et al.Pageof 2