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2. Insights into the clinical presentation of juvenile systemic lupus erythematosus: the PRAGMA monocentric cohort of 177 patients

7. ASAH1 pathogenic variants associated with acid ceramidase deficiency: Farber disease and spinal muscular atrophy with progressive myoclonic epilepsy

8. Farber disease (acid ceramidase deficiency) natural history study: Prospective and retrospective clinical data

9. Acid ceramidase deficiencypresenting as Farber disease: prospective and retrospective clinical data from an ongoing natural history study

12. Phenotypic variability and disparities in treatment and outcomes of childhood arthritis throughout the world: an observational cohort study

13. Farber disease (acid ceramidase deficiency): Data from an ongoing natural history study

18. Disease status, reasons for discontinuation and adverse events in 1038 Italian children with juvenile idiopathic arthritis treated with etanercept.

19. Proceedings of the 23rd Paediatric Rheumatology European Society Congress: part two: Genoa, Italy. 28 September – 01 October 2016

20. Farber Disease (Acid Ceramidase Deficiency): The First Natural History Study of This Rare Disease Involving Symptoms Which Can Mimic JIA

21. Phenotypic variability and disparities in treatment and outcomes of childhood arthritis throughout the world: an observational cohort study

22. Disease status, reasons for discontinuation and adverse events in 1038 Italian children with juvenile idiopathic arthritis treated with etanercept

23. Insights into the clinical presentation of juvenile systemic lupus erythematosus: the PRAGMA monocentric cohort of 177 patients.

24. Chronic recurrent multifocal osteomyelitis presenting with Tolosa-Hunt syndrome in a 13-year-old boy.

25. Recurrent macrophage activation syndrome in spondyloarthritis and monoallelic missense mutations in PRF1: a description of one paediatric case.

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